mejbcart’s Newsletter

Oats, memory, the genetically modifying SARS-CoV-2 injections, and the Epstein files.

mejbcart — Tue, 13 Oct 2026 01:18:05 GMT

This wild medley of topics will start with the 2012 Nobel Prize for GPCR related proteins, which went to Stanford researchers:

https://news.stanford.edu/stories/2012/10/nobel-prize-work-g-protein-coupled-receptors-paves-way-drug-discoveries

A motif of just THREE consecutive amino acids Glu/Asp(D)-Arg(R)-Tyr(Y), present among hundreds of amino acids in sequences of those proteins, appears to be crucial for the GPCR activation. More on it can be found in this article “The Highly Conserved DRY Motif of Class A G Protein-Coupled Receptors: Beyond the Ground State“ https://www.sciencedirect.com/science/article/abs/pii/S0026895X24043918 That combination of Asp(+ charge)+Arg(- charge)+Tyr(hv=photon of 280nm), i.e. electric dipole coupled with light, which makes GPCR’s work, deserves truly a respect, in my opinion and was always my fascination. GPCR family members include: rhodopsin , histamine H₂ receptor, cannabinoid-2 (CB2) receptor, alpha2A adrenergic receptor, gonadotropin-releasing hormone receptor and many others, all functionally very important proteins. This reminder is to point out, again (after a long break of not posting), HOW a specific decisive FUNCTION can be performed thanks to the smallest pieces of any protein. I do believe, one of the reasons for this is the fact, that even single amino acids, like glycine (the ‘cousin’ of the lethal synthetic GMO-related glyphosate) can function as neutrotransmitters. The ‘22 post of mine went deeper into that issue:

And now imagine billions of people are being forced ever since end of 2020, to produce via the injected synthetic universal Spike gene, a non-human patented synthetic protein, the Spike with ~1273 residues, harboring countless motifs while interfering with the ORIGINAL intended human functions. That’s the biggest human tragedy in our latest history.

Now to the oats. This short post is about the only recently (after 2020…) appearing in the news RW-9 peptide ‘RDFPITWPW’ derived from OATS. PubMed lists only 6 articles explicitly mentioning it: https://pmc.ncbi.nlm.nih.gov/search/?term=RDFPITWPW There is another article at https://europepmc.org/article/PMC/PMC9294724 describing the general dietary-nutraceutical properties of oats, which have an influence on an important pathway related to SARS-CoV-2, i.e. angiotensin-2. Here a scheme I’m pasting from that article:

The “Characterization and Exploration of the Neuroprotective Potential of Oat-Protein-Derived Peptides in PC12 Cells and Scopolamine-Treated Zebrafish“ lists that neuroprorective peptide ‘RDFPITWPW’ (among 2 more) as a potential prevention of neurodegenerative diseases, like for example Parkinson’s, Alzheimer’s (AD), multiple sclerosis diseases. The fact, that scopolamine can induce those diseases in fish, isn’t so impressive, given, that fish won’t tell you in which year it was born, or where it is currently heading, BUT the absolutely detrimental fact of scopolamine on human brain and consciousness is real, and can be found ‘nicely’ described in 2 Epstein files: https://www.justice.gov/epstein/files/DataSet%209/EFTA00163098.pdf and https://www.justice.gov/epstein/files/DataSet%209/EFTA00865569.pdf . The second file was send to Epstein in 2015 and was titled: “Scopolamine: Powerful drug growing in the forests of Colombia that ELIMINATES free will”. The first one from 2022 titled “A Very Serious Cry For HELP! Please Read!” describes an absolutely heinous case of scopolamine application on a victim who ‘lost his memory’ afterwards. While looking into Epstein files from very begin, I noticed that ‘something’ was changed in these particular 2 entries, a name and that personal note to J.E. disappeared..

VAERS reports list all sorts of exotic diseases after the GENETICALLY MODIFYING covid injections (example: Alice in Wonderland Syndrome) but it does NOT have Alzheimer’s(!), thus estimation of the extend on this issue is not possible, by DEFINITION. At least Parkinson’s related symptoms are there, so for the ~500 affected listed individuals, possibly multiplied by 100, the oats could be of some help, I’d hope. Btw, one needs to be added, I’m not advertising here for the oats, in particular since: https://organicconsumers.org/100-percent-oat-products-tested-positive-glyphosate/ Just making sure, everyone tries to find the best resource as possible.

So why is that ‘RDFPITWPW’ peptide so important, suddenly? Let’s look at the SARS-CoV-2 SPIKE amino acid sequence, which is being produced in human bodies, possibly indefinitely, given the synthetic character of the non-digestible mod mRNA injected into many victims. NIH software package BLAST (changed since 2020..) shows the following while comparing the original Spike sequence (https://www.ncbi.nlm.nih.gov/protein/1796318598) and a sequence which includes that ‘good’ RW-9 peptide added to some other oats Glutenin-like avenins and Gliadin-like avenins peptides, apparently involved with coeliac immune response (from https://pmc.ncbi.nlm.nih.gov/articles/PMC4744869/pdf/FNR-60-30324.pdf):

Query  73   R-D-FPITWPW  77    <<=RW-9 peptide
            + + + I WPW        <

This level of IDENTITY between RW-9 and Spike 2020 is unprecedented, in particular since exactly that tryptophan rich section in Spike IKWPWYIWLG is also connected with the high homology between the HIV-1 gp-160 protein and Spike, described in:

The bad ‘coeliac-like’ parts of Spike (sequence in Sbjct line) from those homologies are rich in glutamines and prolines, for example:

Query  39   QPLQYQPY  46
              + YQPY
Sbjct  501  NGVGYQPY  508
Query  2     QYQPYPEQQ  10
               Q Y  QQ
Sbjct  1003  SLQTYVTQQ  1011
Query  10   QEPFVQ  15
            QE F Q
Sbjct  779  QEVFAQ  784
Query  65   QQQMRDFPIT  74
            QQ  RD   T
Sbjct  563  QQFGRDIADT  572
Query  21   VQQEQPFQQPFMQQQPFMQP  40
            V+Q  P Q   +    +  P
Sbjct  407  VRQIAPGQTGKIADYNYKLP  426

both residues known to play a significant roles in the pathophysiology of Parkinson's disease.

As mentioned in my previous old posts (basically confirming what Dr. David Martin is saying from the begin of 2020), the Spike 2020 sequence has ~37% IDENTITY with the in 1987 by DUPHAR INTERNATIONAL RESEARCH B.V (acquired by Wyeth in 1994, which then became one with Pfizer in 2009) patented peplomeric protein from the infectious bronchitis virus (https://www.ncbi.nlm.nih.gov/protein/832948). Many of the homologies related to specific diseases, between then and 2020 ‘version’ are preserved. For example, the extremely unique tryptophan and cysteine rich section at the C-terminal of Spike:

Query  1056  ILDIDSEIDRIQGVIQGLNDSLIDLEKLSILKTYIKWPWYVWLAIAFATIIFILILGWVF  1115 <=1987 sequence
             +++I  EIDR+  V + LN+SLIDL++L   + YIKWPWY+WL      I  +++   +      IDENTITIES
Sbjct  1176  VVNIQKEIDRLNEVAKNLNESLIDLQELGKYEQYIKWPWYIWLGFIAGLIAIVMVTIMLC  1235 <=2020 Spike

Query  1116  FMTGCCGC  1123 <=1987 sequence
              MT CC C
Sbjct  1236  CMTSCCSC  1243 <=2020 Spike

the apparently new, but actually OLD furin site, just inserted in other ‘strategically important’ place:

Query  682  TTPSSPRR-RSFIEDLLFTSVESVGLPTDDAYKNCT-AGPLGF  722  <<=1987
            T  +SPRR RS     +     S+G     AY N + A P  F
Sbjct  676  TQTNSPRRARSVASQSIIAYTMSLGAENSVAYSNNSIAIPTNF  718  <<=2020

or the amyloid polypeptide:

Query  819   QQIQDVVNKQSAILTETMASLNKNFGAISSVIQEIYQQLDAIQANAQVDRLITGRLSSLS  878  <<=1987 
              ++QDVVN+ +  L   +  L+ NFGAISSV+ +I  +LD ++A  Q+DRLITGRL SL 
Sbjct  946   GKLQDVVNQNAQALNTLVKQLSSNFGAISSVLNDILSRLDKVEAEVQIDRLITGRLQSLQ  1005 <<=2020
                                  SSNNFGAILSSTNVGS <<---AMYLIN=islet amyloid polypeptide (IAPP)

While we are being plagued for a long time possibly with patented viruses related not only to lung diseases, why only now all the precious peptides so similar to the genetically expressed pieces of the Spike? Btw. all without human consent, thus illegal.

Is it because exactly these peptides can be used to produce more of the building blocks of the Spike, thus increase the Spike burden, or is it because somebody really wants to help people regain their memories???

Scopolamine strongly affects the GPCR receptors integral to the parasympathetic nervous system, the central nervous system (CNS), influencing everything from heart rate and glandular secretions to memory and cognition. Epstein files are worth forgetting (for many involved..) but on the other hand they are extremely precious, since the scopolamine’s ‘free will’ effect, is nowhere to find. That’s what the official science reports on it, for example: ‘Clinically, the compound has long been used for the prevention of motion sickness and postoperative nausea and vomiting, as well as for ophthalmological procedures requiring mydriasis and cycloplegia.’ or more on memory related effects: ‘Experimental and clinical studies demonstrate that scopolamine induces transient cognitive impairment. This property has led to its widespread use as a pharmacological model of Alzheimer’s disease, enabling investigation of cholinergic contributions to cognitive decline.“ Both quotes are from an article titled ”Exploring the Evolving Role of Scopolamine in Pharmacotherapy: From Cognitive Impairment to Neuroplasticity?―A Narrative Review” (https://pmc.ncbi.nlm.nih.gov/articles/PMC13075120/) and hint towards an inconvenient suggestion: neuroplasticity, or a memory replacement??

And while (‘thanks’ to the genetic modifications of humanity via synthetic genetic material, mod mRNA injections!) we are reading countless stories like this one:

Makis Health - by William Makis (Cancer Researcher)
NEWS: The Julie Powell story - 49 year old author wished death on the unvaccinated. Then she died suddenly.
I remember reporting Julie Powell’s “sudden death…
Read more
19 days ago · 138 likes · 37 comments · William Makis

in the same time the scientific and industrial community have the audacity to offer the victims more of the gene therapies, this time openly calling out the right name of the agenda: https://www.genomeweb.com/precision-medicine/gene-therapy/gnw-heart-disease-obesity-chronic-conditions-20261013/ titled “Biotechs Are Betting on Gene Therapy for Heart Disease, Obesity; Will Patients?“

Thank You for reading and the almost 2 years patience since the last post!

Closing with a dramatic piece:



Evolutionary Dynamics: brought to you by Jeffrey Epstein, with connections to SAR-CoV-2 Spike genetically modifying injections.
mejbcart — Tue, 29 Jul 2025 02:40:44 GMT
9/26/2026: De-worming, KRAS and NSCLC cancer, with link at the end of the post.
8/4/2026: Dr. David Martin and Mikki Willis discuss the corruption of the most recent Senate ‘Fauci hearing’ in which he was citing 111 times the 5th Amendment.. Link to the short dicussion at the end of this post.
4/10/2026: How Palantir with its Foundry now monitors the genetic modifications of ‘covid pandemic’: https://blog.palantir.com/leveraging-palantir-foundry-to-monitor-genetic-mutations-of-covid-19-56a2392d26d2 . From interview titled “Moderating Human Behavior: Palantir Insider REVEALS Company’s Sick Plans for A.I.“ at https://www.brighteon.com/ec89c4c6-e6c1-42e2-b196-e5ab7c59b3eb ( Alex Karp at 4:56) 
2/18/2026: the final goal for Epstein and his entire clan was, and as long as nobody is arrested, still is 'the s.c. ‘digital health’ (https://www.justice.gov/epstein/files/DataSet%2011/EFTA02658424.pdf and more at the end) with ‘great scientists’ names like: Nandan Nilekan (and team/Aadhaar), Geoff Ling (DARPA), Paul Greengard (Nobel Laureate, Rockefeller), Linda Buck (Nobel Laureate, Fred Hutchison Cancer Center), Yann LeCun (convolutional nets, Facebook), Todd Park (former CTO of the USA), including WEF Global Future Council on Blockchain, WEF Global Future Council on Neurotechnology and Brain Science, with Lauder Foundation, Mayo Clinic, Kaiser Permanente, Stanford (Shenoy Lab), Caltech (Koch Lab).
2/11/2026: How ‘american’s’ of Russian origin who influence MIT science are connected with Epstein, with 3 links here and rest at the end of this post: from 2010 https://www.justice.gov/epstein/files/DataSet%2011/EFTA02422408.pdf , from 2014  https://www.justice.gov/epstein/files/DataSet%2011/EFTA02421173.pdf and  https://www.justice.gov/epstein/files/DataSet%209/EFTA00284908.pdf
2/9/2026: 2015 Epstein’s email about cancer in  https://www.justice.gov/epstein/files/DataSet%209/EFTA00710399.pdf  and direct involvement of its subject in SARS-CoV-2 https://www.nature.com/articles/s41392-023-01719-7   Great summary of many Epstein files by Prof. Homburg attached at the end of this post. The top ‘science magazine’ Nature publishes https://www.nature.com/articles/d41586-026-00388-0 paper with ‘list of nearly 30 top scientists,‘ in connection with Epstein, among them many completely unknown, yet the biggest names like Craig VENTER and others, completely ‘forgotten’. How strange!
2/5/2026: Jason Powers, a substack writer uncovers the genetics obsession in Epstein files, link to his newest post is added  at the end. Also some of the Epstein files related to RNA, cloning, genetic experimentation, including involvement in Pfizer FINANCING, briefing into CRISP technologies by Deutsche Bank are also listed at the end of this post. 
1/31/2026: Important link at the end to an interview of Bannon with Epstein, who was placed on the board of the Rockefeller Foundation to ‘manage’ the finances within the interdisciplinary sciences, thanks to a good friend, David Rockefeller (https://www.justice.gov/epstein/files/DataSet%209/EFTA00584942.pdf *). It’s also about Rothschilds..
12/12/2025 IMPORTANT. A must read by everyone who wants to understand this post. It is a 2012 hearing about economic planning of Virgin Islands with Jeffrey Epstein revealing his monumental money making idea using HUMAN GENES:  https://www.documentcloud.org/documents/23858163-virgin-islands-economic-development-hearing-2012-govuscourtsnysd59165318640/
added some changes at the very end, and more updates. It is a pity, that this ‘special’ post, caused some readers unsubscribing. On 8/5 I’m changing the front image of the post to 2017 National Geographic cover titled ‘The Next Human’, which features an article citing Prof. George Church from MIT (whose work is related to Epstein’s money). His EXTREMELY IMPORTANT statements expressed in that NG edition are copied and questioned, below in text. Here a statement from Epstein files: “The genetic manipulation of wild populations has been discussed as  a solution to a number of humanity’s most pressing ecological and public health concerns, including the eradication of insect-borne diseases such as malaria, the reversal of herbicide and pesticide resistance in agriculture, and the control of destructive invasive species“ (https://www.justice.gov/epstein/files/DataSet%209/EFTA01205594.pdf) . The same LIES of the scientific criminals as always.
: also a new post, an extensive summary by Strange Sounds Substack about Palantir and Epstein is added below. 
Is the title connected with the delay of the finally showed up files everyone would like to see? Don’t know, but this below, shall we know. After very long break (am very sorry!) this finally next post, will be a short one, touching two topics, the 5 years long still ongoing story of the Sars-CoV-2 and its Spike genome, story never even remotely touched by the new administration (similar to JE files..), story connected to military operations (similar to JE files..), and the most recent debate about the lost/changed files of the national importance, discussed by many, among others by a journalist Jon Rappoport in his post at:   
Jon Rappoport
Epstein and Harvard; boom
Read more
a year ago · 89 likes · 26 comments · Jon Rappoport
With one word, is there a connection between covid related issues, including the Pfizer and MOD-e-RNA covid GENE therapies and J. Epstein who had some friends among top geneticists out there?? Rappoport points to a summary at https://www.prnewswire.com/news-releases/jeffrey-epstein-science-financier-changes-the-course-of-evolution-at-harvard-211218581.html, with a quote:
NEW YORK, June 12, 2013 /PRNewswire/ -- Ten years ago the Program for Evolutionary Dynamics was founded at Harvard with a $30 million dollar grant from a financier called Jeffrey Epstein. Since then, the Program, under the direction of Martin Nowak, a professor of Mathematics and Biology at Harvard (https://ped.fas.harvard.edu/files/ped/files/nowakcv_jan2017.pdf), a Wellcome Trust Senior Research Fellow 1992-1998, has changed the way in which evolution is studied and utilized.
This old article points to the 22 years old establishment of digital genetics (linear sequences of given numbers of nucleotides), based on mathematics. The program dealt first with viral infection models, based on small amount of genetic material, with conditions leading to destabilization of chromosomes, and ever since ~2002  (timeline of SARS-CoV), it ended up with more investigations of cancer.   
“In 2012 for example, the Program developed the first mathematical model of how colon cancer cells become immune to inhibitor therapy. The research showed how the KRAS gene is not activated from inhibitor drugs, making cells resistant, but rather a small percentage of cancer cells with an inherantly activated KRAS gene are immune from the start and evolve to predominance as other cancer cells are destroyed by the inhibitor drug. The discovery was critical because instead of applying drugs in sequence to fight resistance, using a cocktail of inhibitor drugs to capture both activated KRAS gene cells and those without, came into focus. In 2010, the Program published a study showing that most solid tumors contain 40 to 100 genetic mutations, but on average only 5 to 15 actually drive tumor growth. The findings highlighted the importance of targeting only a minority of tumor cells for effective inhibitor treatment.“ This one image shows which genes are KRAS dependent, and those who know SARS-CoV-2 Spike, recognize some of them here (copied from https://www.mdpi.com/2072-6694/15/6/1635):
Harvard open statements about Epstein’s funding money at:  https://ogc.harvard.edu/files/ogc/files/report_concerning_jeffrey_e._epsteins_connections_to_harvard_university.pdf
do not mention any scientific details, page which in 2026 disappeared! The recently released Epstein files clarify better that topic, for example in: https://www.justice.gov/epstein/files/DataSet%209/EFTA01116320.pdf .  The name of Prof. Martin Nowak (evolutionary theory and viral dynamics), in the now disappeared Harvard files, appears in it 123 times, and the big, so important name (in covid ‘times’) of Prof. George Church, collaborating with Nowak, 15 times.
The money expert Epstein was tortured with the very same scientific interests as the father of his girlfriend Ghislaine, Mr. Ian Robert Maxwell, born in Ukraine, the ‘chameleon of all names’, also known as John Ludvik, or Ján Ludvík Hyman Binyamin Hoch or Ivan du Maurier or Leslie du Maurier as Candace found out at https://candaceowens.com/video/the-epstein-files-dead-men-tell-no-tales-an-introduction/). Some of Maxwells family history connecting to Epstein can be found at:  https://rumble.com/v6ws7ny-house-of-maxwell.html?mref=5grgb&mrefc=5 and his power in the area of scientific publishing: https://docs.lib.purdue.edu/cgi/viewcontent.cgi?article=8480&context=atg further goes into Welcome Trust business: https://rogue-scholar.org/records/ystd4-npt46 .
 "Mathematics in evolutionary biology is an exciting new field," Jeffrey Epstein remarked, whose foundation supports cutting edge science across the United States. "It reveals patterns that are otherwise hard to detect."
Yes, that must be it, his one and only Little Saint James, U.S. Virgin Islands must have been behind the scientific goal of all the rich men, and poor girls, placed on Lolita Express heading towards the beaches in order to go down the rabbit hole of mathematics in human genes expression…. Here some of the citations of Prof. M. Nowak papers (https://www.martinnowak.com/publications) related to the RNA based theory of evolution (is that why one and the same mod mRNA SPike genome for the entire world?), and how to influence it:
”Using an analysis based on game theory, we can predict the situations in which cooperation, selfishness, or a mixture of the two is beneficial to the future evolutionary success of RNAs.” or “The dynamics of RNA assembly in a complex mixture of sequences is a frequency-dependent process and mimics such scenarios.“ or “In some cases, we find that mixtures of different RNAs reproduce much better than each RNA type alone, reflecting a molecular form of reciprocal cooperation.“, from https://www.pnas.org/doi/full/10.1073/pnas.1525273113 titled “Dynamics of prebiotic RNA reproduction illuminated by chemical game theory“
“The question of how complexity and cellular life arose on early earth remains unanswered. As we discussed in the introduction, prominent experimentalists within the field have over the years attempted to make efficient RNA polymerases [8, 9, 20, 70]. The premise behind this approach is that once there is an RNA replicase, it will kickstart Darwinian evolution and hence allow for mutations and natural selection to generate complexity in the familiar way.“ The severity of this statement is currently full in heinous action, that’s the SELF-replicating mod mRNA injections containing RNA-dependent RNA polymerase obtained from a Venezuelan equine encephalitis virus, currently injected into pets since summer 2024: 
FOCAL POINTS (Courageous Discourse)
The Genetic Integrity of Humanity Was Sabotaged by mRNA — Now Our Pets Are Being Used as Self-Amplifying RNA Vectors
By Nicolas Hulscher, MPH…
Listen now
a year ago · 230 likes · 31 comments · Nicolas Hulscher, MPH
“These include previously unrecognized putative cancer drivers (RPS15, IKZF3), and collectively identify RNA processing and export, MYC activity, and MAPK signalling as central pathways involved in CLL.“ at https://pubmed.ncbi.nlm.nih.gov/26466571/ titled “Mutations driving CLL and their evolution in progression and relapse“ where CLL stands for chronic lymphocytic leukaemia.
“While other genetic polymers may have preceded RNA, it is generally accepted that an “RNA world” evolved at some point. In this world, RNA acted as both information carrier and enzyme (Woese, 1967; Crick, 1968; Orgel, 1986; Joyce, 1989, 2002; Ellington and Szostak, 1990; Cech, 1993; Sievers and von Kiedrowski, 1994; Johnston et al., 2001; Steitz and Moore, 2003; Hughes et al., 2004). Evidence supporting the RNA world theory comes from several sources, including the
discovery that RNA forms the catalytic core of the ribosome (Nissen et al., 2000) and the discovery of RNA molecules that catalyze nucleic acid chemistry (Wilson and Szostak, 1999). A particularly noteworthy RNA molecule, evolved from a ligase ribozyme, catalyzes template-directed RNA polymerization, demonstrating a step toward a replication enzyme (Bartel and Szostak, 1993; Johnston et al., 2001). In a recent experiment, Lincoln and Joyce (2009) constructed paired RNA catalysts that can synthesize copies of each other when supplied with the right chemical precursors.“ from https://pmc.ncbi.nlm.nih.gov/articles/PMC2827768/pdf/nihms170295.pdf  Please note, the RNA ‘origin’ story develops ~50 years AFTER DNA discovery and it central role in reproduction.
one of many emails between Nowak and Epstein: https://www.justice.gov/epstein/files/DataSet%209/EFTA00714285.pdf and one at https://www.justice.gov/epstein/files/DataSet%209/EFTA01187403.pdf pointing to “Genome-Wide RNA Polymerase II Profiles and RNA Accumulation Reveal Kinetics of Transcription and Associated Epigenetic Changes During Diurnal Cycles.” 
Almost every gene mentioned in 3. is connected with SARS-CoV-2 activity. Who would thought that behind so much in depth theories there is this dirty Epstein’s money, as the very cause of these investigations? Prof. G. Church and M.A. Nowak in 2017 published together an article titled: ”Evolutionary dynamics of CRISPR gene drives” (https://www.science.org/doi/10.1126/sciadv.1601964), which should explain everything what happened ever since 2020. Just one quote from it:”The alteration of wild populations has been discussed as a solution to a number of humanity’s most pressing ecological and public health concerns. Enabled by the recent revolution in genome editing, clustered regularly interspaced short palindromic repeats (CRISPR) gene drives—selfish genetic elements that can spread through populations even if they confer no advantage to their host organism—are rapidly emerging as the most promising approach.” Also the mentioned edition of NG that year published Church’s statements, quote: “People get hang up on Darwin and DNA but most of the selection today is occurring in culture and language, computers and clothing. In the old days, in the DNA days, if you had a pretty cool mutation, it might spread in the human race in a hundred thousand years. Today if you have a new cell phone or transformative manufacturing process, it could spread in a week“!!!!! He is talking about synthetic genes from a ‘transformative process’, I do believe. Indeed, after the covid genes introduction via the nanos in the shots, starting from already the clinical trials, the covid spread was pretty fast! But he knew more, something about Iphones…. Oh, did you have a hair loss after the covid infection (shedding) or injection? Or eyes issues? Or hearing issues with strange features in which a digital sound becomes way more prevalent than analog, like the one from your own family members?? Try to go to VAERS and search for hearing issues, you will have NO digital rights to see the result!!!!  Well, that NG 2017 image, has it all.
If it is still not clear, here a quote from recent paper clarifies the essence of Prof. Nowak’s work: “Here we engineered an orthogonal alphaviral RNA replication system to evolve RNA-based devices, enabling RNA replicase-assisted continuous evolution (REPLACE) in proliferating mammalian cells. This system generates a large, continuously diversified library of replicative RNAs through replicase-limited mode of replication and inducible mutagenesis.“ and also “Collectively, this work establishes a powerful platform for advancing mammalian synthetic biology and cell engineering applications through directed evolution.“ in https://www.nature.com/articles/s41589-024-01783-2 .
Nowaks’ KRAS gene is worth to look into, despite of some chinese scientists writing about it in 2024, quote: “For decades, KRAS has always been a huge challenge to the field of drug discovery for its significance in cancer progression as well as its difficulties in being targeted as an “undruggable” protein. KRAS regulates downstream signaling pathways through protein–protein interactions, whereas many interaction partners of KRAS remain unknown.“(https://pmc.ncbi.nlm.nih.gov/articles/PMC11575137/). Despite of this, the uniprot entry about KRAS is very extensive:  https://www.uniprot.org/uniprotkb/P01116/entry . As usual, let’s look at few NIH BLAST outputs comparing SARS-CoV-2 Spike with KRAS, a GTPase of the following catalytic activity: ( GTP + H2O ) = ( GDP + phosphate + H+ ) with its switch I, motif ‘YDPTIEDSY’ binding effector proteins, depending on catalytic activity (Query line represents KRAS amino acide sequence, Sbjct the Spike2020):
the below alignment is not perfect, it BUT covers ~1/3 of total KRAS length
Query  76   EGFLCVFAINNTKSFEDIHHYREQIKRVKDSEDVPMVLVGNKCDLPSRTVDTKQAQDLAR  135
            EGF C F +  +  F+  +    Q  RV       +VL       P+     K++ +L +
Sbjct  484  EGFNCYFPL-QSYGFQPTNGVGYQPYRV-------VVLSFELLHAPATVCGPKKSTNLVK  535
Query  136  SYGIPF  141 <YDP  1140
the effector region 'YDPTIEDSY' is only covered by BLAST the following way:
Query  26    NHFVDEYDPTIEDSYRKQVV---IDG  48 <YDP-TIE-DSYRKQVVIDGET  50     <YDPLQPELDSFKEELDKYFKN  1140   <YDPTIEDSYRKQVVIDG--ET-CLLD  40  <
there are many more homologous fragments for this 188 residues long protein, related to cancers, growth stimulation, proliferation and survival, all energy dependent. A good structural overview of KRAS is at https://pmc.ncbi.nlm.nih.gov/articles/PMC6965201/ . One needs to keep in mind that if the KRAS substrate, ‘energy’ molecule GTP, is required for RNA synthesis, which then can drive cancer progression, every single step of which is energy driven, then how on earth the sudden appearance of the in muscle injected synthetic spike mod mRNA gene requiring 3x1273 more energy molecules, genetically not coordinated with any other living process in form of DNA gene corresponding with that RNA in the time of the injection, suppose to stay unnoticed? It won’t, here just one publication talking about this: https://www.preprints.org/manuscript/202507.2155/v1 titled “Synthetic mRNA Vaccines and Transcriptomic Dysregulation: Evidence from New-Onset Adverse Events and Cancers Post-Vaccination”. It would be a good example, if it was not for the false title with the deceptive usage of the word ‘vaccines’…
There is also another disturbing common issue around KRAS and the Spike genome:
“Insight into the Complexity of the i-Motif and G-Quadruplex DNA Structures Formed in the KRAS Promoter and Subsequent Drug-Induced Gene Repression” at https://pubs.acs.org/doi/10.1021/jacs.7b02046
which sounds like we have something similar here: “Potential G-quadruplexes and i-Motifs in the SARS-CoV-2” at https://pubmed.ncbi.nlm.nih.gov/34101725/
That, at the end leads to prions, according to Dr. Seneff and others:
and https://stephanieseneff.net/wp-content/uploads/2025/02/Seneff_Corona_2022.pdf
citing the “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs” at https://pmc.ncbi.nlm.nih.gov/articles/PMC9012513/
Finally “The regulation and functions of DNA and RNA G-quadruplexes” (https://pmc.ncbi.nlm.nih.gov/articles/PMC7115845/pdf/EMS86249.pdf ) illustrates how important these features are.
The viral work of Prof. Nowak involved mainly HIV-1, where he collaborated in 90-ies with the ‘covid hero’ Dr. A. Fauci, involving experiments quantifying the RNA amounts during infections for vaccines development, or maximizing virus production in the face of rapid killing of infected target cells, or measuring in plasma HIV RNA while testing different drugs (why didn’t ‘they’ measure the RNA inside of HUMANS before and AFTER covid injections, that’s a BIG QUESTION!!!). Funding for these works, already in those times, came also from the very same Welcome Trust, playing essential role in covid19 drugs and vaccines development: 
T-W. Chun, .., M. A. Nowak & A. S. Fauci (1997). “Presence of an inducible HIV-1 latent reservoir during highly active antiretroviral therapy.” Proc. Natl. Acad. Sci. USA 94: 13193-13197.
J. D. Lifson, M. A. Nowak, .., A. S. Fauci & V. M. Hirsch “The extent of early viral replication is a critical determinant of the natural history of simian immunodeficiency virus infection.” J. Virol. , Dec. 1997, p. 9508–9514
M. A. Nowak,, .., A. S. Fauci, V. M. Hirsch & J. D. Lifson (1997). Viral dynamics of primary viremia and antiretroviral therapy in simian immunodeficiency virus infection. J. Virol. 71: 7518-7525.
 Some of his paper scripts at that time were reviewed by  Drew Weissman, the 2023 Nobel Prize winner so greatly prized for his mod mRNA work which finalized in universal covid Spike gene therapies applied on the entire world population, without consent, thus illegally.. In 2015 article titled “mRNA: Fulfilling the Promise of Gene Therapy” at https://www.cell.com/molecular-therapy-family/molecular-therapy/fulltext/S1525-0016(16)30267-2 was published by Drew Weissman¹ dreww@upenn.edu ∙ Katalin Karikó² katalin.kariko@biontech.de , the very same scientists, who completely decimated innate immunity via introduction of foreign genetic material into human bodies, across the entire world, now, after 2020, the same people changed their language and only talk about: “therapeutics and vaccines—a realization crucial to the rapid development of the life-saving mRNA COVID-19 vaccines during the deadly pandemic.:” No more ‘mRNA gene therapy’ in 2020, with the synthetic version of mRNA, properly called mod mRNA, as if the word ‘GENE THERAPY’ got suddenly after 2020 highly classified, in the very same time of its application by the MD’s and ‘science priests’ around the globe. That classification of the ‘therapy’ itself, is not the only issue, the families of the people dying after the injections, have the right to know the bitter truth of the ‘white clots’ being pulled from blood vessels by many surgeons, and certainly by MANY embalmers who are trying to raise the alarm, and are being SILENCED, even by the ‘most friendly truth telling media’: 
Clotastrophe
Tucker, Glenn, Megyn, and Joe
By Tom Haviland…
Read more
a year ago · 22 likes · 18 comments · Laura Kasner
H. Clifford Lane also appears in Nowak’s papers, Fauci’s best body… Around 2002 the interests of Prof. Nowak shifted from viral related issues and genetic chromosomal instabilities more towards cancer research. His membership in the ‘prestigious’ EDGE club (https://www.edge.org/memberbio/martin_nowak) with countless other top scientists (https://www.edge.org/people) and artists, for example https://www.edge.org/memberbio/marina_abramovic, means basically common interests in the fields of genetics (CRISP hero https://www.edge.org/memberbio/jennifer_a_doudna), physics, mathematics, psychology, ‘art’, if one dares to call it this way in this case:
 
History and military are equally represented by the EDGE club. Here https://www.edge.org/memberbio/yuval_noah_harari takes the lead, for whom we humans, are ‘hackable animals’! It is the deepest irony that this monster teaches at the Hebrew University of Jerusalem, in such a special place. Given  the interests of Prof. Nowak which were condensed around darwinian evolution, one special publication needs more attention. It’s title “Primordial sex facilitates the emergence of evolution“  and location: https://pmc.ncbi.nlm.nih.gov/articles/PMC5832742/pdf/rsif20180003.pdf . The meaning of sex, according to Nowak is basically information, quote:” In biology, sharing information content between two individuals is considered a defining property of sex. The implications of this information-sharing ability among protocells, which is a form of ‘primordial sex’, have not received much attention”. Protocell is a self-organized, endogenously ordered, spherical collection of lipids proposed as a rudimentary precursor to cells during the origin of life. Excuse me??? Did anyone see the nanolipid spheres injected into billions of arms??? According to this definition, people were injected with protocells, the new origin of life, premordial sex!!! Here one publication specifying the definition https://pmc.ncbi.nlm.nih.gov/articles/PMC2649781/ title “Porous Nanoparticle Supported Lipid Bilayers (Protocells) as Delivery Vehicles“ or another one, more fundamental, explaining the basics and how important it is in RNA based world THEORY: https://biologyinsights.com/what-are-protocells-and-why-are-they-important/ with a quote: “Protocells are also connected to the RNA World Hypothesis regarding the origin of life.” 
Did anyone notice that we live in REALITY which was PROCEEDED BY CREATION hence now ’we the people’/the planet, and NOT some kind of THEORY our bodies need to give a proof of by genetically modifying injections?? Our bodies, so far, run physically FORWARDs in time, NOT backwards, in my view.
This conformation of Dr. David Martins preaching in covid times, presented here, needs more attention, in particular because people are coming out with even more terrifying news:
https://rumble.com/v6wnez0-this-is-an-extinction-level-event-cia-mkultra-whistleblower-james-martinez-.html
please listen starting at ~13:00. This amount of personal precision would need to have connections with Palantir, being essential in those times, alone because of collecting ALL personal data (if PCR tests, then equally peoples genomes) in regard to who, where and when got ‘the shot’: https://www.palantir.com/newsroom/press-releases/cdc-partners-with-palantir-to-bolster-the-fight-against-covid-19/ Another quote from 2021 Palantir’s pages: “Palantir was commissioned in mid-2020 by the Department of Health and Human Services to build Tiberius, a software platform it uses to track vaccine production, distribution, and administration across the United States.“ Thus it is Palantir/Thiel+Karp who know who got genetically modified and who not, and that includes the ‘special batches’ for those who were wiped out with higher probability. The question is, were the batches pre- or postdetermined.., i.e. were they preplanned for specific populations? Looks like Epstein contributed to some extend to this ‘outcome’, which once again, is terrifying:
FOCAL POINTS (Courageous Discourse)
The mRNA Triple Threat: Genetic Collapse, Instant Biological Damage, and the Pet Vector Danger
By Nicolas Hulscher, MPH…
Listen now
a year ago · 105 likes · 12 comments · Nicolas Hulscher, MPH
Thus it is maybe no wonder to see in 2014 on Forbes such a subtitle:”Peter Thiel Appeared To Meet With Jeffrey Epstein, Report Says—Latest Billionaire With Epstein Ties”. Now the current big AI era will ‘live from these data’, the only problem is, there is not enough energy to run the zillions of computer centers. Tons of new material on Palantir was posted today (8/6/25) at:
Strange Sounds
All those geniuses obsessed with the Deep State ended up ushering in an actual Deep State…
Palantir is winning big right now! Two days ago, Palantir topped $1 billion in revenue for the first time and, last week, the company also secured a $10 billion software and data contract with the U.S. Army…
Read more
a year ago · 1 like · 1 comment · Strange Sounds
and another one on 9/5/2025 from Patrick: 
Patrick Wood's Technocracy News: The Quickening Report
Palantir Is The Biggest Existential Threat To America 
Read more
a year ago · 19 likes · 3 comments · Patrick Wood
Oh, last serious question, to those sexually exploited, mutilated, hurt, humiliated, who never come out with their stories because of shame, what would you prefer if you never got affected, to go over the torture and have a chance of healing afterwards and slapping the face of the felon with a smile of FORGIVENESS, or to be genetically modified in your entire body, including the HEART AND THE BRAIN, and loose your identity for good, with no chance of even remotely to forgive?? This question about bodily assault, excludes children (different type of torture includes hunger with an example: https://old.bitchute.com/video/HQQMpKRO2QtJ/ ), because in such cases, there should be NO forgiveness, just my own opinion. 
Update: 8/13/2025
A new Documentary is available for those who want more details on historical facts about covid genetically modifying injections, with specific emphasis on the horrific stories of the injured. The title, unfortunately deceiving (because not touching the word gene therapies, only towards the end we start to get the most important message): “Inside mRNA Vaccines“
 https://www.brighteon.com/9f6c7ade-7af6-41e8-a0b6-55a72b6add21
And there is more about the key figure who keeps all the genetic data on it all:
https://old.bitchute.com/video/wd4dVc2R6C5m/
and that little section of the SARS-CoV-2 Spike genetic code encoding this amino acid string:
G-W-T-A-GAAAYY  (in https://www.ncbi.nlm.nih.gov/protein/YP_009724390.1)
now ‘engraved’ in who knows how many human genomes:
FOCAL POINTS (Courageous Discourse)
The Genetic & Biological Assault on Humanity
by Nicolas Hulscher, MPH…
Listen now
a year ago · 85 likes · 14 comments · Nicolas Hulscher, MPH
with questions on the final application of all these data:
https://unlimitedhangout.com/2025/08/investigative-reports/from-project-2025-to-the-paypal-presidency-school-choice-fin-tech-for-a-blockchain-social-credit-economy/
According to Whitney Webb, in the age of Palantir, you do not need Jeffrey Epstein, all the smart data are here already, in the clouds available in seconds: https://www.brighteon.com/da4ab06c-f763-4996-94fe-ff11d60d29ed , thus one could end the worst crimes out there pretty fast, if one would like to… BUT, it does not happen, yet! WHY? Seth and Todd are discussing in depth the issue here:
Man in America
Challenging the Narrative of Operation Warp Speed: 5D Chess or Mass Betrayal?
When President Trump recently called Operation Warp Speed “one of the most incredible things ever done in this country,” I felt my stomach turn…
Listen now
a year ago · 7 likes · 4 comments · Man in America
From very begin of covid plandemic it was known, that the universally injected Spike genome integrates into the human genome: “Further evidence supports controversial claim that SARS-CoV-2 genes can integrate with human DNA“ (https://www.science.org/content/article/further-evidence-offered-claim-genes-pandemic-coronavirus-can-integrate-human-dna) and now HHS is so protective that all the covid PCR tests collecting the entire human genomes are apparently stored and kept in secret, or maybe sold to the pharma companies?? The ‘program’ description is at https://www.palantir.com/assets/xrfr7uokpv1b/1EE4kLUXymcHCQ68Xo2OzQ/8cbc5cc985ff4c3cddffdeb292c2967a/Emergency_Preparedness__Response__and_Recovery.pdf and an important podcast on it can be found at https://uncutnews.ch/corbett-interview-schockiert-palantir-nutzte-ki-um-buerger-nach-ethnie-und-gehorsam-zu-sortieren/ . 
Update 9/29/2025: a new check of my own post indicates that the link to  Program for Evolutionary Dynamics was CHANGED to LITERALLY laughable “https://contactanycelebrity.com/cac/contact-ghislaine-maxwell/“. Thank you a new reader who liked this post after which I noticed that change!
Update 11/7/2025 New research at https://unlimitedhangout.com/2025/11/investigative-reports/cold-harbor-eugenics-epstein-and-big-tech/ connects more dots in terms of Epstein, scientists and the future of eugenics. 
Update 11/22/2025 Dr. Boris Nikolic, M.D is not only important figure related to Epstein’s will and distribution of his >500mln$ after his death, but equally to scientific works with Prof. Nowak and R. Langer, big MIT researchers: https://www.flagshippioneering.com/news/press-release/editas-medicine-raises-120-million-advance-genome-editing , essential in the new genetically mutilated human world.
Update 1/31/2026: 1/31/2026: Epstein on the board of the Rockefeller Foundation to ‘manage’ the finances within the interdisciplinary sciences, thanks to a good friend, David Rockefeller: 
Update 2/5/2026: 
DCFPRESS Post
Epstein's Obsession: Designer Babies, Genetic Editing & Mengele-Level Evil for PROFIT
Listen now
9 months ago · 1 like · 3 comments · Jason Powers
Update 2/7/2026: One of the released Epstein files explaining Nowak’s speculations about creating biological matter without GOD, strangely coincides with Epstein pulling the plug on his involvement in Evolutionary Dynamics program: https://www.justice.gov/epstein/files/DataSet%2010/EFTA02016026.pdf
Update 2/9/2026: Prof. Homburg’s summary in German
Update 2/11/2026: 
https://www.justice.gov/epstein/files/DataSet%209/EFTA00750620.pdf
https://www.justice.gov/epstein/files/DataSet%2010/EFTA02081116.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00701249.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02418369.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00995604.pdf
Update 2/19/2026:
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02642995.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA01209136.pdf with a quote: “Bill Heiman has some ideas on how to create a business around this and to monetize the concepts / plant to human translational research and don’t worry he’s incredibly discrete. And discreet. Also Geoff Ling the former head of DARPA and total genius is also my good friend and very supportive - didn’t give a ton of detail but he says he will do whatever or even help run, advise, etc. he knows how to make science fiction science fact.“
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02365490.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02352454.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02658424.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA01029069.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02365313.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA01029072.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02658658.pdf
are we talking Larry Ellison in the files below??
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02658584.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02365376.pdf
and the GOALKEEPER was/is(?) Obama (Brain Initiative)..:
https://www.justice.gov/epstein/files/DataSet%2010/EFTA01620719.pdf
2/22/2026: how important RNA science in 2010 was for Epstein: https://www.justice.gov/epstein/files/DataSet%209/EFTA00748238.pdf
OVER. 
THANK YOU FOR BEING OUT THERE AND READING.
the Epstein file ‘dump’ is strange, has multiple version of the same similar file. In this case this one:  https://www.justice.gov/epstein/files/DataSet%209/EFTA01071423.pdf
Here more of the files mentioning the BIG masters in synthetic biology, genetics, cloning, redesigning HUMANS, i.e. Craig Venter and George Church:
 https://www.justice.gov/epstein/files/DataSet%209/EFTA01156115.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00736376.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00749351.pdf
https://www.justice.gov/epstein/files/DataSet%2011/EFTA02380379.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00734558.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00717710.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00629471.pdf
https://www.justice.gov/epstein/files/DataSet%2010/EFTA01866406.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00606986.pdf
https://www.justice.gov/epstein/files/DataSet%209/EFTA00583634.pdf
Pfizer was on Epstein list too:  https://www.justice.gov/epstein/files/DataSet%2011/EFTA02539825.pdf and https://www.justice.gov/epstein/files/DataSet%2011/EFTA02692886.pdf and placebo effect known by Pfizer  https://www.justice.gov/epstein/files/DataSet%209/EFTA00823009.pdf and autophagy https://www.justice.gov/epstein/files/DataSet%2010/EFTA02077324.pdf
https://www.justice.gov/epstein/files/DataSet%2010/EFTA02011631.pdf
CRISPR/CAS9 briefing : https://www.justice.gov/epstein/files/DataSet%2010/EFTA01462770.pdf
https://www.justice.gov/epstein/files/DataSet%2010/EFTA01447777.pdf
https://www.justice.gov/epstein/files/DataSet%2010/EFTA02011631.pdf
Update 8/4/2026:
Update 9/26/2026: https://www.sciencedirect.com/science/article/abs/pii/S0304383519301442 “Drug library screen reveals benzimidazole derivatives as selective cytotoxic agents for KRAS-mutant lung cancer“ based on fenbendazole info which came from the extremely important (for every CANCER patient) post: 
Surviving Healthcare
418. IS CANCER A PARASITE? AN INTERVIEW WITH THE ELUSIVE WILLIAM SUPPLE, PHD, WHO WRITES THE FENBENDAZOLE SUBSTACK
READER RESOURCES: THE APOCALYPSE ALMANAC: Hidden cures in our dystopian age. Check out the “Cure Cancer in Your Kitchen” chapter. FULLSCRIPT SUPPLEMENTS: top quality and economical…
Listen now
7 months ago · 2160 likes · 336 comments · Robert Yoho, MD



HUMANITY in 2025 with prayers for LA=haina2.0, the genetic Spike fallout continues, insulin and H5N1. 
mejbcart — Mon, 13 Jan 2025 08:50:10 GMT
"You'll own nothing and you'll be happy": a phrase from 2018 predictions for 2030 published by the World Economic Forum (WEF)
=> my answer: for a normal human it would apply only if you are dead or mentally impaired, in which case the normality needs questioning…
The post starts below the divider bar, first some updates, quite a few and THANK YOU for ‘checking in’ :)
Update 7/16/2025: Here s the reason for the Palisade fires, quote “Another 'Conspiracy Theory' Comes True: California Bill Passes To Buy Fire-Ravaged Palisades For Low-Income Apartments“ from https://www.zerohedge.com/political/another-conspiracy-theory-comes-true-california-bill-passes-buy-fire-ravaged-palisades  5G cities anyone???
Update 4/8/2025: apparently unrelated BUT actually not, it is about the same/related  technology used on 9/11: 
9/11 Revisionist
A 9/11 truther movement celebrity meltdown, take two
Wow, what an interesting week it’s been. So much happening, so much 9/11 talking points, a buzz on social media…
Read more
2 years ago · 3 likes · 9/11 Revisionist
Update 3/26/2025: “ADAM CAROLLA WAS RIGHT: 75 Days After CA Wildfires, FOUR Building Permits Have Been Issued in the Palisades” at https://www.thegatewaypundit.com/2025/03/adam-carolla-was-right-75-days-after-ca/
Update 3/12/2025: Dr David Martin summarizes the covid19 genetic assault on the entire world human population: https://rumble.com/v6qfh5a-dr-david-martin-the-dark-truth-behind-the-mrna-revolution.html  PROHIBIT ALL mod mRNA injections NOW, THANK YOU from the bottom of my heart to all MD’s who finally officially talk about the lethal effects of GENE THERAPIES (Dr. Cole, Mr. Hultscher, Dr. Janci Lindsay and more..) : https://old.bitchute.com/video/rgbbpTwazYMa/
Update 2/8/2025: WARNING II, from the 2ndsmartestguyintheworld, extremely important:
2nd Smartest Guy in the World
God Help US
From day one this Substack has been extremely critical of President Operation Warp Speed aka President Trump for his totally misguided and murderous PSYOP-19 scamdemic response…
Read more
2 years ago · 87 likes · 31 comments · 2nd Smartest Guy in the World
WAKE UP and STAND UP AGAINST the continuation of covid crimes… 
Update 2/4,5/2025: about officially un-predicted weather in CA capitol, extremely windy, on days with no wind there are ‘alarms’,  on day like today, no alarm… 180 deg opposite ‘predictions’… Dr. David Martin talks: https://rumble.com/v6h9bqm-dr-david-martin-covid.html
Update 1/31/2025: More essential clues on PALANTIR, predictive+PERSONAL (everyones’ God given genes) ‘med-I-cin-e’, in a post from CHR, which unfortunately never talks ‘GENE THERAPIES’, instead is deceiving with the word ‘vaccine:
The Defender
Investigation: Healthcare Driven by AI Technology Will Lead to More Mass Surveillance of Americans
by Brenda Baletti, Ph.D…
Read more
2 years ago · 17 likes · 5 comments · The Defender
Update 1/29,30/2025: Day No 1 Senate Hearings of Mr. RF Kennedy Jr, who states 'GENES DO NOT CAUSE DISEASES' : absolutely right, assuming a human with own original given by birth UNTOUCHED genes (and no gene cutting enzymes applied like in SYNTHETIC BIOLOGY).
Day No 2 RF Kennedy Jr. states: "Absolutely I support" it is about gene therapies being evolution in science NIH/FDA is working so hard on (Sen. Scott)!!!???
=> HHS is about health and since genes do not cause diseases why the hell humanity suddenly needs gene therapies Mr. RFK??? To make us HUMANS to WHAT, APES back 'again'??  More on news about real wars at the very end of this post.
Update 1/27/2025: Just as AI had a significant ‘fault’ in fueling covid propaganda, so it is possibly involved in CA fires, and now it get’s back to covid, a military operation. Everyone not shutting down the ‘cloud’ operations on own computer, Iphone, etc., is feeding the beast, now worth ~500bln$, oh no, much less now for the chinese version… AI’s combination of Microsoft, OpenAI (https://blogs.microsoft.com/blog/2025/01/21/microsoft-and-openai-evolve-partnership-to-drive-the-next-phase-of-ai/) and military operations, not even going into health or porn, is described here: https://www.972mag.com/microsoft-azure-openai-israeli-army-cloud/. from wi-ki, about Sam:
”Altman is an apocalypse preparer.^[9]^[105] He said in 2016: "I have guns, gold, potassium iodide, antibiotics, batteries, water, gas masks from the Israel Defense Forces, and a big patch of land in Big Sur I can fly to."^[9]” And here is how a good researcher on that topic sees it: https://www.brighteon.com/bb60b285-5dc7-4f7d-a85b-b42e5b88a222
Update 1/24/2025: reminder related to the first (https://www.brighteon.com/ce26574b-0c97-4a04-b7d7-cde46abe3234) and the second part of this post: https://www.kla.tv/30724
Update 1/21-23/2025: WARNING No 1!!!!! 500BLN for gene therapies on cancer sick patients (NOW for the many covid injected victims who went to get these ILLEGAL COVID GENE THERAPIES), according to AI specialists currently in this big DATA BUSINESS, who are saying, it was all possible only thanks Trump…. BUT the project started in 2024 though, so it was Biden in fact!!! It is about WAR(p) S(p)EED.  To cause a cancer pandemic thanks to gene modifications treatments via covid mod mRNA shots and now to offer yet another mod mRNA therapy to  apparently heal it, is a CRIME beyond imagination, committed by EXPERTS… The death of the TOP OpenAI programmer last Nov connected with copy rights violations applied in current AI models is described below. The 40 executive orders can be found at: https://www.thegatewaypundit.com/2025/01/here-is-full-list-presidential-actions-trump-signed/ and an extremely important comment on the WHO intended withdrawal in James Rogulski’s post titled “President Trump "Intends" to #ExitTheWHO“. Shouldn’t anything around health be discussed with HHS head first?? Oh, he is not there yet!!! 
Update 1/20/2025: first news ‘Biden pardoned Fauci’! What?? After SO MANY covid genetically modifying injections deaths and injuries, so many hospitals intentional deaths of un-jabbed, ‘side’ effects of the entire covid agenda, which will never end??? That NEEDS TO BE UN-PARDONED, NOW, hopefully, or maybe not, let’s exercise forgiveness. Here is what Dr. David Martin says today, https://www.brighteon.com/a4e810bc-03c4-4360-80ab-92af2a7d410b , and why that pardon is for period between Jan 1st 2014 and Jan 20th 2025, is explained here: 
Strange Sounds
This is how you know they're guilty...
Biden pardons his family for all nonviolent federal crimes committed from January 1st, 2014 to today…
Read more
2 years ago · 6 likes · 2 comments · Strange Sounds
With prayers for PEACE in DC today. Many good plans were revealed, but how about stopping the illegal thus criminal covid gene therapies? From www.globalsecurity.org, quote: ‘Ukrainian Minister of Health Viktor Liashko ordered the destruction of a number of dangerous pathogens across Ukrainian biolab facilities, including anthrax, the plague, tularemia, cholera and other deadly diseases. A day later, the MoD held a press briefing to reveal that a network of over 30 US-funded biolabs has been operating across Ukraine, with some of the facilities feared to be engaged in the production of chemical weapons, and others sending serum samples of "Slavic ethnicity" patients to the Walter Reed Army Institute of Research in Silver Spring, Maryland under the pretext of testing for COVID-19 treatment methods, for reasons as yet unknown.’, things need to be looked into…
Update 1/19/2025: In regard to War(p) S(p)eed2.0 possibility, at the very end of this post.
Update 1/18/2024: George Webb an investigative journalist, mentions in his post today among other Deep Seek, Berggruen Institute, WEF. ScaleAI (established by a second generation chinese-american A.Wang) was performing a life fire exercise named FireAId on 1st Of Jan ‘25 in LA(!!). It is worth listening, but with a grain of critical thinking, in particular because the entire event is now getting a ‘chinese touch’, like covid19, now extending into a ‘wild fire’.
George’ Webb Task Force Orange Journal
Deep Seek And Destroy - Part Five - Scale AI And AI Drone Warfare
You probably don’t know the youngest American ever to become a Billionaire or his company, Scale AI. But his name is Alexsandr Wang, and Scale AI does the AI training and data labeling for drone surveillance imagery for the Department of Defense and NATO for the Ukraine War…
Read more
2 years ago · 23 likes · 2 comments · George Webb
Update 1/17/2025: https://unlimitedhangout.com/2025/01/investigative-reports/the-cdc-palantir-and-the-ai-healthcare-revolution/ summarizes the second part of this post very well, connecting more dots. The sanity ‘will not return until’ we see the very last picture in this post…
Update 1/16/2025 : From Peggy Hall substack, analysis of the ‘new normal fires’ which are burning the roofs first, ‘creeks in those ‘fires’ are devoid of life, no aquatic insects, frogs, turtles, fish, nothing, even when the creeks are 6 to 8 feet deep. They’ve electrocuted the creeks’ says Mr. Brame:
The Healthy American, Peggy Hall
HOUSES GONE but TREES STILL STANDING?! Interview with Forensic Arborist Robert Brame
We’re now a full week into these devastating fires raging through Los Angeles, and the situation has been nothing short of heartbreaking. I’m so grateful to have my friend, Healthy American and forensic arborist Robert Brame back on my channel for an updated interview…
Listen now
2 years ago · 64 likes · 33 comments · Peggy Hall
This should terrify everyone! Targeted annihilation of living creatures consisting of water AND metals!!! Did anyone find the missing human bodies in LA fires?
A note to the second part of this post, covid19 and health related issues, where I mentioned PALANTIR. It partnered with ‘One Health’ in 2022, which now forms a cross agency CDC + USDA +DOI for pathogen surveillance, pandemic preparedness and vaccine development. Also in 2024 PALANTIR partnered with ORACLE (https://www.oracle.com/news/announcement/oracle-and-palantir-join-forces-to-deliver-mission-critical-ai-solutions-to-governments-and-businesses-2024-04-04/). In 2024 Moderna and OpenAI started Collaboration To Advance mRNA Medicine. Equally OpenAI and Palantir are exchanging services, and data, too by now. What happened is a creation of a huge bowl of private citizen data, coming from injured and deceased genetically modified HUMANS, which became an ILLEGAL new source for an automated future. Do we need to wonder when a cold-bloody murder of a coding genius Suchir Balaji who worked for OpenAI and blowed the whistle on Sam Altman, is now totally covered up by police, lawyers, medical examiner and will be possibly totally suffocated by the new incoming SF mayor, a friend of Altman, OpenAI owner?
Update 1/15/2025: Mike and Dane are explaining more details about LA fires: https://www.brighteon.com/f515db12-fbd5-4392-8f2d-8af62e43c304 can only add to it, we also got all or nothing temperature scenarios, example: CA Sac valley, in summer months with 100F, current winter time coastal temp. of ~60F, with night temp. ~10F less than coast. 
Updates 1/14/2025:
 https://www.npr.org/2025/01/14/nx-s1-5232808/robert-f-kennedy-jr-rfk-hhs-confirmation-hearing-abortion-vaccines mentions Gov. Green, involved in LA-haina devastation AND in the Samoa MANDATORY vaccination campaign in 2019, quote:”Hawaii Gov. Josh Green, a Democrat, calls Kennedy "dangerous." Because once people find out the entire truth, he will be in a different place…
Gov. Newsom announces “Reimagining LA 2.0” initiative, aligning with the city’s preparations for global events while addressing ‘wildfire’ recovery needs. (https://x.com/houmanhemmati/status/1878521212772696082?mx=2)
Those victims need equally help: https://rumble.com/v696d8y-fema-evicting-hurricane-helene-victims-during-snowstorm.html
Updates 1/13/2025: happening constantly as the new info flows in, for example on water, Resnicks and Newsom… All in text below.
Fires in LA started around the 1/7/2025, 1/8/2025 leaving thousands homeless, with death toll rising. How many of those victims really do have nothing right now?? It is a tragedy! Schwab, listen, nobody is happy right now, are you getting this? 
Any motif? Is there something what needed to be erased, like Diddy’s past, in order to build back better, smart cities, to relink the attention and gain TIME after the recent Cybertrack story? Whatever, Please Pray for everyone down there and their eyes opening and not to get desperate in case of loosing entire livelihoods. Condolences for those who lost their loved ones. 
On other note. FIRE does not exist without OXYGEN, CO2 would extinguish it immediately. Gov. Newsom, the label on every Fire Extinguisher says: It contains CO2. To blame increasing CO2 (climate ‘change’) for the presence of fires right now defies any logic. Increasing CO2 levels should make less fires, not more. And of course our food is here thanks to CO2: https://x.com/Donuncutschweiz/status/1878392730520543508 , https://x.com/Donuncutschweiz/status/1877690604492116408 , and everything else. Life without carbon doesn’t exist, and I do not mean graphene, the exotic material with superconductor properties.
Please look at these pictures at: https://www.nationalgeographic.com/environment/article/los-angeles-palisades-california-fires-photos (was free for me only the first time, no more access now..) which make the point: fires which start from inside of the houses, wooden objects, are NOT because of CLIMATE CHANGE, which ‘comes from outside’. Many LA fire pictures show structures burning inside with standing walls untouched from outside, where did ‘the energy’ come from? ABOVE? Mr. Shellenberger (who got his FOX voice, Tucker Carlson voice), who can’t distinguish the difference between wind and fire and defines Jan as fire season(??), question, would a full Palisades water reservoir have prevented melting of all these cars? Not, if you have a targeted huge flow of energy deliberately applied by all the communication networks. Arsonists, fireworks anything out there, will not generate the energy needed to melt metals, glas. And even this corruption: https://usaherald.com/billionaire-power-couples-control-of-californias-water-amid-wildfire-crisis/, proceeded by this corruption: https://sjvsun.com/news/politics/fundraising/resnicks-deliver-hefty-sum-to-defend-newsom-from-recall/, followed by this corruption: https://ballotpedia.org/Gavin_Newsom_recall,_Governor_of_California_(2024), ending with the current corruption in LA fires, does not explain the energy deficit, (no not the green energy!) caused by the difference of melting temperatures of all the materials involved in the current unbelievable fires. It is high school physics, and many PhD’s didn’t get it immediately on 9/11…
It is just strange, that LA’s MSM broadcasting epicenter on Mount Wilson with transmitting towers of nearly every Los Angeles TV station, many of its FM radio stations, was rescued immediately, quote: “a fire suppressant was dumped from a tanker, quickly knocking down the flames and reducing the immediate danger.”, and the same didn’t apply to civilians, for days??? And note, it was not water, but rather fire suppressant (CO2?) used down there… FCC Chairwoman Jessica Rosenworcel said that the impact of the fires on communications has been minimal (from https://wirelessestimator.com/articles/2025/mount-wilson-towers-remain-intact-as-fcc-reports-minimal-communication-disruptions-from-deadly-la-fires/). It sounds like the communications are more important than humans in 2025. And how many other strategic points were rescued, except for private houses?? And truly, would like to know what the Starlink satellites are seeing from far above… After looking at many of these fires, with the latest report at:
there is this elephant in the room completely blocked out by the powers. Possibly this post will end like the Lahaina post, without any/or ‘erased’ attention.. And today addition by Greg:
The Reese Report
Directed Energy Weapons Burning Homes to Ash
Listen now
2 years ago · 163 likes · 40 comments · Greg Reese
All the revealed human corruptions are a prelude feeding MSM, and do not EXPLAIN the current real burning process in all fires, ever since ~2015, or actually ever since 2001 on 9/11. The government corruption witnessed in LA is huge, and reported at: https://www.zerohedge.com/political/why-was-pacific-palisades-reservoir-empty-it-gets-worse, includes funding cuts for Fire Departments, and especially in substack post titled ”Palisades Fire - Deep Seek And Destroy? by George Webb, a different dimension of the destruction is presented. In this post you can see how a really burned forest looks like, there is nothing left from the trees, except for the charcoaled stem:  https://kitten.substack.com/p/are-microwaves-from-aerial-sources. Peggy Hall reports on fires also for years, with the most recent at: 
The Healthy American, Peggy Hall
LA FIRESTORMS: Incinerated Cars Yet Shrubbery Untouched 🤔
Read more
2 years ago · 26 likes · 13 comments · Peggy Hall
Another summary worth reading: 
OUTRAGED’s Newsletter
PG&E and fires?
https://www.washingtonpost.com/local/dc-politics/dc-lawmaker-says-recent-snowfall-caused-byrothschilds-controlling-the-climate/2018/03/18/daeb0eae-2ae0-11e8-911f-ca7f68bff0fc_story.html…
Read more
2 years ago · 93 likes · 48 comments · OUTRAGED HUMAN
 strangesounds.substack.com pointed out today to looting by Tom Cruises' and Will Smith’s Scientologists, yes from the same church community which painted lot of their roofs with blue colors: https://rumble.com/v31rnu-scientology-gold-base.html  , and that despite of the recommendation by the Nobel prize winner, ‘cool’ laser Stanford physicist, Steve Chu, who was telling everyone to paint the roof white because of climate ‘change’…
Yes, the same physicist just recently signed a letter with 76 other Nobel prize winners to reject RF Kennedy’s Jr nomination as HHS secretary! One more example of global ‘warning’ agenda, we are just too many here on this round spinning ball: https://x.com/Donuncutschweiz/status/1879068434702520822 . The same place Satnford, sorry Stanford, comes always in a spotlight, ever since ~1975 and the first conference where decisions were made, on a Nobel prize level to change this world, beyond recognition:   https://old.bitchute.com/video/IbYBEI99IjEE/. The list of their names on the first GMO support letter is here: https://www.supportprecisionagriculture.org/view-signatures_rjr.html
And what is this: 
Must admit, only substack publishes the ‘controversial’ fires stories, in official MSM this one fire aspect, geoengineering, is still completely suppressed, exactly like the fact about universal covid-19 GENE THERAPIES. Why? Without that part, even all the fixed human errors and admitted corruption will not halt the coming ‘climate agenda’ caused by exactly that never revealed fact, ongoing geoengineering, for decades, reported by Dane Wigington ever since. How to fight that deception? Ask questions.  
Which climate change exactly is capable of melting those cars, like nothing seen before ever since 9/11? Which climate change ‘feature’ burns totally a collection of differently oriented houses and leaves the near standing trees almost untouched at speeds of 100mph?  Even with the dramatic 4deg C temperature increase, where does the energy come from to melt that steel at ~2250degC in these fires? Note, why the hell, so many of the plastics are untouched in the same time? The cases of left over car tires include intact ones:
or the ones which ‘evaporate’:
: 
These are partly IDENTICAL questions everyone should have already asked in 2001 on 9/11, in Santa Rosa, Chico, Paradise, LA-heinous fires.  The accumulating human ‘mistakes’, or deliberate actions strangely happening right before the LA fires, all this is not explaining the real reason of such absolute but also targeted devastation. The point is, if the fires have unnatural features, proceeded by many sketchy plain evil actions, like cancelling fire insurances, isn’t it logical that the event must have been engineered, pre-planned? Geoengineered? Like covid19, BIO-engineered??? Like 9/11? Like that event shown on the blatant Economist cover image below from Dec 19th 2024 in an article titled “The world ahead 2025“, putting at the top skyscrapers, in LA, maybe??? The image is from https://www.economist.com/the-world-ahead/2024/12/19/the-world-ahead-2025
That Saturn story was created by The Prisoner and is available at https://www.brighteon.com/959e4468-89ed-4883-a5ab-dfd7cf91c83d
The infernos are being commented everywhere, here some of them:
 ‘Somebody’ wants us all HUMANS, all out, no matter how poor or rich, good or bad.  This page is listing the names involved in it: https://nemosnewsnetwork.com/they-really-do-want-to-reduce-the-population/. People need to become aware of the for decades ongoing geoengineering: https://www.brighteon.com/6a4d6975-9ba0-477a-b013-549fee9a5c18  with more on the most recent from Dane Wigington: 
who is pointing to the 1970 publication titled: “Forest Fire as a Military Weapon. A June 1970 Report of study commissioned by the Department of Defense.” with the following diagram
from the document at: https://www.geoengineeringwatch.org/documents/GeoengineeringWatch%20-%20Vietnam%20War%20Forest%20Fire%20As%20A%20Military%20Weapon.pdf Doesn’t it explain the ‘unusual' timing and weather conditions of the current event in LA, described 55 years ago?
Mr. Wigington notified Mr. News-om(g) more then 10 years ago about that issue, no response. Here from some professionals about building materials at: https://titanstuccoaz.com/f/is-stucco-fire-resistant/ , quote “The most fire resistant forms of siding are brick, stone and metal.” Well, no more now. A new type of energy downs it all, BUT strangely leaves many trees barely touched. From which direction came the fire on this picture below? Screen snapshot from FOXnews at https://www.thegatewaypundit.com/2025/01/just-palisades-wildfire-reaches-brentwood-where-kamala-harris/, where you can see a wider section. The forest stands untouched, the house explodes in flames. Clearly it is NOT the vegetation which feeds the fire, it is the content of the burned structures. Here is a good source of who is feeding the money for new types of nanomaterials with ‘exotic features’ https://www.nano.gov/sites/default/files/Keeler.pdf
and for application of nanomaterials in construction, electronics, agriculture (thus water, soil and air) just search in browser and you get for example, quote:”The construction sector is responsible for 25 % of global greenhouse gas emissions and consumes 50 % of the world's energy. This paper addresses the use of nanomaterials in housing construction, comparing their influence at the technical-structural level. Materials such as titanium dioxide, carbon nanotubes, nanosilica, nanocellulose, nanoalumina, and nanoclays were analyzed.” (https://www.sciencedirect.com/science/article/pii/S2666016424002573) 
Facit: The very same ‘climate change’ justifies usage of materials which are feeding it. Search every of those materials MSDM data sheets and you will find: ‘Flammability: No data available’, Explosive properties: Not available, and from NIST, for example on the nTO2: Flammability (solid, gas): not applicable…. Really???
Please, be aware of the presence of weaponry (https://www.brighteon.com/7fd311e4-8c00-430c-b422-497531c9190b) which goes beyond the horizon of daily TV imagination, and no, the fires are not about the 'little fish’, that’s or a lack of complete knowledge or intentional deception about the real reason of the crime blamed on human corruption, negligence and DEI:
another even deeper dive into the arena is presented by Dr. Greer:
 
and the most recent one about incredible mind and soul, Maxwell Chikumbutso (it was posted on Ron’s Substack ):
Will leave the hot topic right now (updates will be added at the begin) and go back to the still ongoing covid related human trauma. 
When you read books like “Corona false alarm“ by Dr. K. Reiss and Prof. S. Bhakdi or ‘The Real Anthony Fauci’ by RF Kennedy Jr., and so many more by now, and then you realize: “The federal government has provided about $4.6 trillion to help the nation respond to and recover from the COVID-19 pandemic.“  (https://www.gao.gov/products/gao-23-106647) while asking who took all the money, you need to check what is happening now. Guy Hatchard, PhD just published in Expose an article titled: ”Because of the “success” of covid, New Zealand has introduced a Gene Technology Bill”, with the first sentence: “The dream of biotechnology, which promised a new age of health and human achievement..“ Also “The bill’s introduction is believed to be driven by trade negotiations with the US, which wants New Zealand to deregulate biotechnology to pave the way for similar deregulation in Europe.”
Even VAERS (https://www.medalerts.org/vaersdb/index.php), the most corrupt reporting system of all, lists millions of injuries, thousands of dead bodies, and now call that all a ‘success’?? And there are some who despite of all the dead bodies still want more testing of synthetic genetic materials on HUMANS, with the most essential in the last 2 minutes:
The person here on the left at: https://www.prageru.com/presenters/calley-means, is the one behind RF Kennedy Jr. drop out from his run last year…
Moderna, CIA and religious circles has a common hero, J. Robert Kerrey:  https://investor.tenethealth.com/governance/person-details/default.aspx , https://www.adventisthealth.org/news/2024/march/adventist-health-and-tenet-healthcare-finalize-acquisition-of-central-coast-hospitals/ , and here more of the faces who do profit from gene therapies: https://boisedev.com/news/2024/05/31/sun-valley-allen-2024/  
Let’s start with Mod-E-RNA injections production CIA based facility https://resilience.com/meet/team/. Search for their funds (RESILIENCE GOVERNMENT SERVICES, INC. =RGS) at: https://www.usaspending.gov/search/  gives ~280mln from DOD and only ~15mln from HHS, whereby all HHS contracts between Apr 2020 and July 2024 were strangely not related to SARS-CoV-2 but rather to MAB (monoclonal antibodies) for BOTULINUM NEUROTOXIN SEROTYPE G,F. HHS contracts between 2009 and 2013 were for smallpox and contracts from DHS for 6.5mln in May 2021 (early time of covid injections) for Resilience partners  ‘JOINT VENTURE RAP TO CONTINUE COMMUNITY ENGAGEMENT AND RISK COMMUNICATIONS CERC SUPPORT‘.. That can’t be for the donuts after covid jabs, etc., as seen on TV’s, because that was ‘brought to you by Pfizer’. Examples of spending by NIAID can be investigated here: https://www.usaspending.gov/federal_account/075-0885. Money flow speaks for the actions, and their consequences.
And like many government tasks, once you’ve done something with an expiration date, it’s a time to say good-bye: https://www.aminext.com/blog/2024/12/27/am-i-next-no-love-at-resilience-government-services/ . There are some exceptions though, like Dr. Fauci, a Jesuit born on the 24th of Dec.
Why did the big money went for botulism research at RGS in the years where it was corona virus causing the biggest ‘p(l)andemic’ in human history? Quick check for Spike2020 and bacterial Botulin toxin similarities (strangely almost identical in size with Spike, 1296 vrs. 1273) shows, again, as always, quite a portion, in particular the ACE2 Receptor Binding Domain portion:
Query  516   SIENLSSDIIGQL---ELMPNIERFPNGKKYELDKYTMFHYLRAQEFEHGKSRIALTNSV  572                     +I ++ +DI+ +L   E    I+R   G+   L  Y     +RA E     + +A T  + 
Sbjct  972   AISSVLNDILSRLDKVEAEVQIDRLITGRLQSLQTYVTQQLIRAAEI-RASANLAATK-M  1029  Query  573   NEALLNPSRVYTFFSSDY  590   P0DPI0.1 Botulin
             +E +L  S+   F    Y        <<
Bacterial Botulin toxin, BoNT from A to F, with A being the most lethal (https://www.uniprot.org/uniprotkb/P0DPI0/entry) blocks the neurotransmitters release while interacting with human SNAP25 protein. One of the pioneers in crystallography, the good old Bill wrote with his team years back a paper describing that protein: Crystal structure and biophysical properties of a complex between the N-terminal SNARE region of SNAP25 and syntaxin 1a. KMS Misura et al. with WI Weis. J. of Biol. Chem. 276 (44), 41301-41309. They also worked on: “The structure of a membrane fusion mutant of the influenza virus haemagglutinin.” WI Weis et al. with DC Wiley. The EMBO J. 9 (1), 17-24 1990. (https://scholar.google.com/citations?user=pbkgvawAAAAJ)
Unfortunately one can’t ask the 2 PI’s more questions, both are dead, William I Weis died in 2023 (https://med.stanford.edu/news/all-news/2023/11/william-weis-obituary.html) and his old MIT friend, Don C Wiley was murdered in 2001 (https://en.wikipedia.org/wiki/Don_Craig_Wiley). Well, MSM says it was an accident. Yes, in particular with Wiley finding new ways to help the human immune system battle such viral scourges as smallpox, influenza, HIV/AIDS and herpes simplex. 
It appears that SARS-CoV-2 is indeed connected with botulism: https://pmc.ncbi.nlm.nih.gov/articles/PMC8149469/  “Botulism during SARS-CoV-2 pandemic: The importance of differential diagnoses“. The same Salicylanilides like sal30 inhibit the most lethal toxin BoNT-A as well as the viral activity of SARS-CoV-2 (https://pmc.ncbi.nlm.nih.gov/articles/PMC9592073/). And here is where these Botulism funds are crossing with the nicotine remedy during covid19 :”Could treatment with botulinum toxin protect against subsequent infection with COVID-19?”(https://pubmed.ncbi.nlm.nih.gov/34144245/) What? One toxin against even worse one in order to apparently ‘rescue’ the human body??? At least in the abstract the authors admit “The recent mention of a potential protective effect of nicotine in COVID 19, by blocking ACh, attracted our attention and guided the present study.“ but their task was to inject the clueless victims with the botulin toxin, no nicotine for them… That’s called ‘science’. NEVER, EVER, anything NATURAL, since that is ‘not in line with’ whoever pays for the studies. The entire medicine, made by Rockefellers et al., is NOT A SCIENCE, but rather an OIL based drugs intoxication.
The Mod-E-RNA financial endeavor is connected with one of the most influential company, Palantir: https://en.wikipedia.org/wiki/Palantir_Technologies , thus this should immediately ring the bell:
https://blog.palantir.com/leveraging-palantir-foundry-to-monitor-genetic-mutations-of-covid-19-56a2392d26d2 
But that’s not all, their software package called Palantir, is helping many companies to chase their data, among others PG&E, most probably readings from smart meters. One can imagine such data during fires must be invaluable! And when one adds to it the health status of the owners, that’s even better! Maybe? Just a speculation.
Identical words for 2 different things are being used everywhere, to confuse and hide. So Palantir No2, their software is described at:
https://pmc.ncbi.nlm.nih.gov/articles/PMC7549125/pdf/nihms-1521379.pdf
and it does  the ‘Characterization of cell fate probabilities in single-cell data with Palantir using Human Cell Atlas Project43.’, among many others. 
A source code description of that Palantir No 2 package at:
https://palantir.readthedocs.io/en/latest/notebooks/Palantir_sample_notebook.html
lists an example of its application with: ‘function plots the expression of HSC gene CD34, myeloid gene MPO and erythroid precursor gene GATA1 and dendritic cell gene IRF8’ 
Is the CD34 gene involved somewhere in covid19? Yes, big time, here some examples: https://pmc.ncbi.nlm.nih.gov/articles/PMC8400074/, and from https://www.ahajournals.org/doi/10.1161/circ.142.suppl_3.14741, quote:
“Early data from the SARS-CoV-1 epidemic indicated that CD34+ cells in the lung could also be a target of infection and that destruction of lung CD34+ progenitors could account for persistence of pulmonary manifestations.”
Is GATA1 active in covid19??? Yes, it plays a role in neutrophil disregulation, Alzheimers and memory loss: https://pmc.ncbi.nlm.nih.gov/articles/PMC10500457/ and https://pmc.ncbi.nlm.nih.gov/articles/PMC10286240/
Are MPO genes involved in covid19?? Yes, again involving neutrophils, oxidative stress: https://pmc.ncbi.nlm.nih.gov/articles/PMC7436665/, https://pubmed.ncbi.nlm.nih.gov/34186206/ , https://pmc.ncbi.nlm.nih.gov/articles/PMC9809351/ 
And IRF8 genes, are they involved in covid19? Yes, most importantly in processes involving type I interferons (IFNs), thus playing a central role in initiating antiviral immune response: https://pmc.ncbi.nlm.nih.gov/articles/PMC8635750/
So where is that Palantir package used? Possibly here:
https://www.palantir.com/offerings/palantir-for-hospitals/ and here:
https://www.healthcare.digital/single-post/palantir-launches-healthstart-developer-platform-for-healthtech-startups-to-build-faster  and in many more places.
Any Privacy of data? “Confidentiality, privacy, and general practice: GPDPR and the brave new world of ‘big data’ in 2021 by Paquita de Zulueta ¹“(https://pmc.ncbi.nlm.nih.gov/articles/PMC8378569/) quote: ”We also know that the NHS has links with commercial technology giants and the corporate sector. For example, NHSX holds the extensive NHS COVID-19 data store, which has contracts with Palantir Technologies, a US company known more for supporting spy agencies, militaries, and border forces, as well as with Amazon, Google, and others to provide data analysis and management.”
Not only that. Palantir in 2020 was described at https://pmc.ncbi.nlm.nih.gov/articles/PMC7378370/: “Surveillance capitalism,” regardless, has blended into the commons architecture in the form of “capitalist platforms” such as Amazon, Apple, Google, and Facebook, as well as data analysis start-ups such as Palantir and Clearview AI. These businesses enable "value-creating interactions between external producers and consumers, providing an open, participative infrastructure for these interactions and setting governance conditions for them.” ¹”
Just few snippets of Palantir’s powers. 
Dec 2, 2023: The Lancet Diabetes & Endocrinology; The Lancet Digital Health; ... levels of success. 
On Nov 21, 2023, NHS England announced the award of a 7-year, £330 million contract to Palantir Technologies UK to create a ... Attempting to profit from customer data in this way would be illegal and would undermine the trust that is necessary to work in ... Palantir NHS contract raises criticisms - The Lancet
If you want to dive in more details to see what’s cooking at palantir go here and read their patents: 
 https://patents.justia.com/assignee/palantir-technologies-inc
but you need to know that’s not all. The most important patents are SECRET, behind the special ‘Invention Secrecy ACT’ (‘law’ signed in 1951). It’s because with a military agent in every patent office the special ‘national security’ items, new inventions, needs to be ‘protected’.. The true great things for humanity are classified with the only new owner: military. At least part of medical Palantir research is out: https://www.palantir.com/offerings/federal-health/
============================
FLU and diabetes.
Similar to the last post, let’s look at the NIH BLAST comparison of the Insulin A6XGL2 (INS) with Hemagglutinin  WYN03019.1 (HEM)
Query  12  ALLALWG--------------PDP------AAAFVNQHLCGSHLVEALYLVCGERG---F 48 INS
            LL LWG               +P       ++ +NQ L  +  + +   V G+RG   F 
Sbjct  187 DLLILWGIHHSNNAEEQTNLYKNPITYISVGTSTLNQRL--APKIATRSQVNGQRGRMDF 244 HEM  Query  49  FYTPKTRREAEDLQGSLQPLALE--------G-SLQ-KRGIVEQ-CCTSIC  88 INSULIN
           F+T     +A   +     +A E        G D   K G VE   C   C 
Sbjct  245 FWTILKPDDAIHFESNGNFIAPEYAYKIVKKGDSTIMKSG-VEYGHCNTKC  294 WYN03019.1 or 
Query  22   AAAFVNQHLCGSHLVEALYLVCGERG---FFYTPKTRREAEDLQGSLQPLALEGSLQKRG  78
            +++ +NQ L  +  +     V G+RG   FF+T     +A   +     +A E +      
Sbjct  216  TST-LNQRL--APKIATRSQVNGQRGRMDFFWTILKPDDAIHFESNGNFIAPEYAYK---  271 Query  79   IV---EQCCTSI--CSL-YQLENYCN  98
            IV   + ++  I  + + Y     CN 
Sbjct  272  IVKKGD-ST--IMKSGVEY---GHCN  291  
Query  52   PK--TRREAEDLQGSL  65 A6XGL2
            PK  TR +    +G + 
Sbjct  227  PKIATRSQVNGQRGRM  242 WYN03019.1  
Query  64   SLQPLAL  70
             ++ PL + 
Sbjct  309  NIHPLTI  315 
there is also a homology at the C-term, HA2 
ALEG-SLQK--RGIVEQCCTSICSLYQLENYCN
    G SL     G + QC   IC MMAGLSLWMCSNGSL-QC--RICI
The above is like taking the entire human insulin section of 98 amino acids which increases cell permeability to monosaccharides, amino acids and fatty acids, which accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver, and literally blending it into HA1 portion of hemagglutinin from Influenza A virus H5N1 (strain A/Texas/37/2024, at https://www.ncbi.nlm.nih.gov/protein/WYN03019.1?report=fasta).. That’s the portion which is extremely positive charged at the C-terminal and which is capable of crossing membranes.
What is the purpose of all this? Bill and Don would know for sure. Somebody will find out, one day.
Will stop the analysis here and send out the post, which will be updated, for those who are interested.
THANK You for reading. Any comments would be very much appreciated.  
A song, which this crazy, evil world really needs: Psalm of love (song in polish).
And lastly, a DOCUMENTARY which explains a LOT of what is happening right now:
The background on this image from:
 https://uncutnews.ch/wir-laden-sie-herzlich-ein-unsere-arbeit-mit-ihrer-spende-zu-unterstutzen-vielen-lieben-dank-dafur-freuen-sie-sich-auf-neue-und-interessante-videos/ 
should be LA fires, given that Mel Gibson’s house burned down totally and Diddy’s still standing. And what did Gibson sad just recently? Ivermectin heals cancers.. 1/29/2025 Bombshell about cancers: 
George’ Webb Task Force Orange Journal
Tempus AI In A Pelosi Teapot
When Nancy Pelosi engages in insider trading, she trades on insider knowledge. What insider knowledge does she have about the Cancer AI firm Tempus, based in Chicago? Cancer, cancer vaccines, and AI for cancer vaccines seem to be on everyone’s mind these days. Nobel Prize winner and Google Deep Mind AI executive Dennis Hassabis gave a speech yesterday…
Read more
2 years ago · 35 likes · 2 comments · George Webb
Mel says, it is actually much, much worse, it is about the missing children: https://www.brighteon.com/f8b2290a-17ff-4b3d-9a97-1f901d09f23c
More cancer cures hints: https://rumble.com/v6duwrs-known-and-suppressed-cures.html
Well, and today this, from controlled opposition, A. Jones about Gates and Trumps 3 hour long dinner just recently: https://x.com/Donuncutschweiz/status/1880869047535083869
There is that first word by Gates ‘intriguing’… Facit, become the unbelievable Thomas, and once you are sure what is going on, say something.. Well, it’s getting real HUMANS, here from Nature:
https://www.nature.com/articles/d41586-025-00231-y
“‘Never seen anything like this’: Trump’s team halts NIH meetings and travel“
I hope one day NIH will really start doing something for the HUMAN BEINGS!
Thank You Mr. President! Well there are some other extremely important voices out there too:



How Substack works.. It's about covid19 and HxNy comment.
mejbcart — Tue, 07 Jan 2025 19:53:44 GMT
Update 1/8/2025: A story which WILL NOT GO AWAY, with Tom Haviland at https://usawatchdog.com/embalmers-keep-finding-fibrous-cv19-vax-clots-tom-haviland/ 
Update 1/7/2025, this post was send out at 11:53AM, and at 3:39 PM : my complaint described here must have been heard, I can post comments on Dr. McMillan’s substack;)) Thank You!!! Well, I’ll keep this post, the word was written already, so won’t erase the contents here, which are too IMPORTANT, for me, for everybody.
First, Happy, HEALTHY, Blessed New Year to everyone. Please forgive, but this short note actually will be about something very disturbing, for a long time already. Namely, the suppression of free speech, here on this platform and everywhere else for that matter, with an extreme example just recently touched by Dr. Nagase:
Logical Surprises
A New Year and the Closing Series for This Substack
Today’s article is about what I observed in an ER doctor who survived an attempted murder and near death in Red Deer regional hospital. But first a bit about the reasons and the timing to end my substack this winter…
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2 years ago · 74 likes · 46 comments · Daniel Nagase MD
Freedom of speech should prevail, no matter what. But it seems like some writers, MD’s in particular, are actually silencing indirectly people who talk TOO MUCH about covid19 genetically modifying injections. And that issue is HUGE, way beyond what one can imagine:
Strange Sounds
The creation of personalized bioweapons?
Yes, I know, this article was written almost 27 years ago... I just picked an article among others. So keep in mind that it isn’t the first time a country has attempted to make weapon/germ of sorts to only affect one part of a population. Many have tried and it remains a mystery if one has ever developped this weapon successfully. They are probably impr…
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2 years ago · 23 likes · 19 comments · Strange Sounds
and from Jason today, few more hints, about the plot, that thickens:
DCFPRESS Post
Reference: CIA, In-Q-Tel mRNA "Vaccines"
Link: https://x.com/myhiddenvalue/status/1875357688626131289…
Listen now
2 years ago · 4 likes · 2 comments · Jason Powers
Since the suppression of that lifesaving info is criminal, you might be having my last post, in case ‘they’ (buS-kcatS, bacwards please) cancel me and do not allow posting any more. It’s clear for many, but just in case, that HxNy stands for the cumulative flu viruses, with the most recent touched also in my last post, the H5N1.
If you have some comments to point to something offensive in that what I’ll describe below, PLEASE let me know in comments. Let’s start. Dr. Philip McMillan publishing under Vejon COVID-19 Review  posted today a video titled: “CARDIAC Arrest EXPLOSION: What’s Behind the Surge?”
I wanted to comment with thanks for the important info, BUT the comment editor does not allow it any more. That’s a second time in the last few days. Well why did he blocked me? Or what blocked me? Maybe that’s why. In his latest posts, in one titled:
“What's Behind Von Der Leyden's SEVERE Pneumonia?”, I commented the following:
“Doc, please stop the covid19 story, and answer that ONE QUESTION: HOW MANY covid19 shots did she get??????????? That's essential, since as you will see, will be in my next hopefully soon post, H5N1, any flu, any of those viruses targeting lung tissue, have a timely reason. Why covid injections first? To embed the Spikes, GLYCO-proteins in as many cellular membranes as possible. Also if the genetic code persists, why was it made of a single stranded POSITIVE RNA type? So now negative-sense, single-stranded, segmented RNA genome of HxNy viruses, all of them, can generate proteins binding to the very heavily glycosylated Spike ankered in the membranes and allow entry, on top of all the membrane proteins binding to the scialic acid and related sugars, thus POTENTIATING the infection immensely....That type of RNA must have a special meaning, which needs more thinking... Is that why everywhere there is a talk about H5N1, in particular here:
https://www.nist.gov/news-events/news/2025/01/nist-develops-genetic-material-validating-h5n1-bird-flu-diagnostic-tests
That just in addition to the other things you are mentioning, unfortunately NOT telling much about the already genetically modified human bodies after the covid Pfizer/Mod-E-RNA shots.
I'm not MD, just logically I'd say, those currently sick people need huge amount of enzymes deactivating/chewing up the Spikes AND deglycosylating agents which will prevent the sticking and opening of all cells... ZERO sugar diet, of course.. And they need it FAST with VitC+Mg in the same time to give as much energy as possible to get over this fight. Just in case graphene is involved, inhale H2O2... That's all only my op-IN-I-on, after HUGE education by many alternative MD’s, in particular the Vic C hero Dr. Thomas Levy, who used to be a cardiologist. Can’t mention the RIP Linus of course, the one laughed at and equally suppressed.
In Dr. McMillan’s video of today he mentions another article showing that Japanese study I was talking about in my recent post:
and announces he will have an explanation for that japanese study.
AND look what happens now: I CAN’T COMMENT ANY MORE under his posts….
Co-inc-I-dence? Since as said, that happened 2-ice just recently, I hope there is maybe or change in rules of publishing here, or indeed people are fed up with my comments.
Please, let me know if You think the same. 
Closing with a favorite piece of music giving strength to FIGHT in this 2025 year so memorable alone because of that 1996 publication at: https://ia601605.us.archive.org/35/items/WeatherAsAForceMultiplier/WeatherAsAForceMultiplier.pdf titled “Weather as a Force Multiplier: Owning the Weather in 2025“
 
Thank YOU for reading and any comments, if you like.
That was my FASTEST written post ever. Look what adrenaline can do!
Just arrived, from Sayer Ji. An announcement by Mr. Sugarmountain (German translation of Zuckerberg), well, with new haircut, or actually lack thereof, and the news about NO more ‘screw you freedom’: 
Sayer’s Substack
Mark Zuckerberg’s Free Speech U-Turn: Will Meta Confront Its Legacy of Censorship and Restore Justice?
Mark Zuckerberg’s recent address on free speech marks a critical juncture in the battle over global censorship. While Meta’s CEO acknowledges the need to “restore free expression” and criticizes censorship pressures from governments worldwide, which I have…
Listen now
2 years ago · 3 likes · Sayer Ji


Insulin sequences within the universally injected Spike? Clock gene, Ozempic, cancer, wars and the last call of the lost Bifidos: STOP ALL RNA-based products, NOW.
mejbcart — Wed, 25 Dec 2024 09:06:53 GMT
This will be a very long post, won’t fit in an email, so please read it on substack directly. THANK YOU and MERRY CHRISTMAS;)) Christmas is about one Special Child and consequently about all Children, this post is about Children and their future, or lack of, despite of the title, on top of what is going on behind the scene already: https://rumble.com/v62er3n-save-the-babies-a-documentary-on-cps-child-trafficking.html
Update 2/7/2026: Epstein’s interest in RNA world, directly affecting the gene activation of the circadian clock, topic of this post: https://www.justice.gov/epstein/files/DataSet%209/EFTA01187403.pdf
Update 3/9/2025: Methylene Blue, a substance being used for mitochondrial dysfunction seems to cause lot of controversies. Here is Dr. Levy’s protocol for Spike detox has it on its list where it is well justified: https://www.tomlevymd.com/articles/omns20230204/Resolving-Colds-to-Advanced-COVID-with-Methylene-Blue .
Update 2/6/2025: Sorry readers, if you are still there, this update is about indirect health, of those Palestinians, who are about to become HOMELESS, it is BAD, related somewhat to the first video here:
Unreported Truths
The Presidency is not performance art
This isn’t why I voted for him…
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2 years ago · 134 likes · 117 comments · Alex Berenson
and if that was not enough, add to this that: https://caitlinjohnstone.com.au/2025/02/05/only-3-of-jewish-israelis-think-trumps-ethnic-cleansing-plan-for-gaza-is-immoral/
Update 2/3/2025: Sport events in the era of ‘post covid injections’: https://old.bitchute.com/video/MQHQMbtnjR8A/ => anger, agressivity, hate.
Update 1/26/2025: Protein Glycation discussed in this post is also responsible for the dark spots on the skin^1,^2,^3,^4,^5,^6 . Dr. Steven Gundry is known for treating it quite well with natural polyphenols. 
Update 1/16/2025: Moderna announces in Apr ‘24: https://investors.modernatx.com/news/news-details/2024/Moderna-and-OpenAI-Collaborate-To-Advance-mRNA-Medicine/default.aspx , with broad adoption of ChatGPT Enterprise. Well OpenAI is connected with not only massive corruption, but now also with a COLD BLOODY murder of Suchir Balaji!!! The deepest crimes are merging.
Update 1/2/2025: BLESSED HAPPY, HEALTHY NEW YEAR to everyone!!!) Post unrelated: Salary of PhD working on H1B visa for NIH in 1997 was ~1600$/month, i.e. ~19,000/year, while in the same time average federal worker income was ~38,000$/year according to https://babel.hathitrust.org/cgi/pt?id=uiug.30112075337979&seq=436 Yes, foreign workers are the modern SLAVES in this money governed world!
Update 12/28/2024: a must interview about new hit on RFK Jr.: https://tuckercarlson.com/tucker-show-aaron-siri and the newest 2025 ‘indirect’ hit: https://tuckercarlson.com/tucker-show-bernard-hudson
Update 12/27/2024: few informative videos were added in text, one by Dr.Eric Berg revealing how to restore your weight/muscle mass and more, with home made yogurt using L. Reuteri.
Update 12/29/2024: pubmed search at https://www.ncbi.nlm.nih.gov/pmc/?term=EDTA+and+antibiotic points to many publications about restoring antibiotic sensitivity and many more health issues related to heavy metals poisoning.
Update 12/30/2024: For everyone who needs pharmacies, A MUST interview: https://tuckercarlson.com/tucker-show-brigham-buhler
After the worldwide illegal application of Fauci’s+ NIH+Co. universal SAS-CoV-2 Spike gene therapy, finally attention is being paid to never seen before cancers, with ‘new biology‘ (https://old.bitchute.com/video/CNzDYGgP4r5F/). Most recent confirmation of incorporation of the foreign DNA contamination into the human genome is now out: https://dailysceptic.org/2024/11/25/dna-contamination-of-mrna-vaccines-can-integrate-into-human-dna-top-molecular-scientist-confirms/. Similar to the influence  of a foreign transplanted organ into a patient, here we got some examples of changes in human behavior caused by the covid gene therapies: https://old.bitchute.com/video/XZIuKIiGdGrI/. But that’s not the only ‘new normal’, there are skyrocketing deaths tolls among all age groups, newborn included, all professions, teachers, pilots, soldiers, young students, elderly, all are affected. It’s absurd to pick that out, but increasingly disturbing death rates among many populations somehow mirror the completely different arena, armed conflicts, shown below. Since the diagram ends in 2022 it does not include deaths in Ukraine in the last 2 years and the ~44.000 killed in Gaza with less than half of it completely innocent children (first part  www.youtube.com/watch? then add v=gEo813rYm8g) : 
and one more horror story at: https://tiktokgenocide.com/uploads/6-yo-child-displaced-legless and anothe tip of in-humanity at https://old.bitchute.com/video/HQQMpKRO2QtJ/ . It seems link the hidden crimes never end, 3 examples of which are discussed at: https://www.brighteon.com/be048ad3-8170-4e50-8385-236e3037f14f , here https://uncutnews.ch/whistleblower-tony-aguilar-enthuellt-missstaende-in-gaza-und-wehrt-sich-gegen-angriffe/ and here: 
Seymour Hersh
KILLING FOR KILLING’S SAKE IN GAZA
Gaza has become a killing field—that is the view of a well-informed Israeli veteran who was an enthusiastic supporter of the initial Israeli response to the Hamas attack of October 7, 2023. He believes that Israeli Prime Minister Benjamin Netanyahu, the mastermind of the all-out retaliatory bombing and ground attack there, is now a contemporary Colonel Kurtz, the psychotic killer of Francis Ford Coppola’s…
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2 years ago · 72 likes · Seymour Hersh
And how many children, in US alone, died after the so ‘safe and effective’ covid19 genetically modifying injections? Other news like ABC says this: “Nearly 120,000 children in US have lost a primary caregiver to COVID-19: Internal CDC data”. Were the parents possibly equally covid injected?
Is it all a coincidence that the increasing death trends are reaching peaks everywhere, as if the insanity by the partially lost 1p36 gene is really happening? The first BNT-162B2 ‘side effect’ admitted by Pfizer on its list with >1000 side effects, is the 1p36 gene deletion, characterized by an intellectual disability, behavioral problems, etc.  Question, do vaccines delete entire genes? NO, TARGETED GENE THERAPIES DO. Therapies with foreign synthetic genetic material, equipped with the good old biology mimicking properties, a lab made patented concoctions, all subject of the most ‘modern science’, paid by the richest in the world and supported by Nobel prize winners who now have the guts to stand in the way of Trump’s HHS nomination. The same tactics of Nobel prize winners happened in the past with the introduction of genetically modifying plants and a trial of hindrance of the proper labeling of the synthetic GMO food, now leading to an explosion of chronic diseases across the globe.. If you are not interested in news connecting politics and science, please jump to the first divider bar below for analysis touching Spike science related to diabetes;)
First a warning about our current situation from Dr. David Martin: https://rumble.com/v6091q8-dr-david-martin-bioweapons.html (VERY IMPORTANT).
At least in terms of real health science in US there is a hope with this one nomination of RF Kennedy Jr as HHS secretary. Already anti-movements to MAHA are out there, with some of its faces at: https://committeetoprotect.org/about/,  https://ctpedfund.org/board-members/ , https://www.eenews.net/articles/health-care-organization-launches-stop-rfk-war-room/ ,  https://www.wfyi.org/news/articles/former-vp-mike-pence-wants-senate-republicans-to-reject-rfk-jr--trumps-pick-for-hhs and the most involved into ‘arrangements’ of the mod mRNA shots production Scott Gottlieb says he’s against RFK Jr. for HHS: ‘It will cost lives in this country’”. Gottlieb together with Mark McClellan (Johnson&Johnson, https://healthpolicy.duke.edu/people/mark-mcclellan-md-phd), running also the Global Alliance for Genomics and Health https://www.ga4gh.org/our-community/organisational-members/#{“organisation”:{“page”:”21”}}  (toggle the last numbers between 1 and 51, to see for example google, Intel, BMGF, LabCorp producing right now the H5N1 tests, this time…) both were very active during covid. 
The just assassinated Russian general Igor Kirillov, No 1 specialist on nuclear, bio and chemical weapons, had Gottlieb(Pfizer/FDA) and McClellan plus Steven Hahn from the Flagship Pioneering Inc.(Mod-E-RNA) on his list of the criminals involved in production and the biggest money making scam around the most dangerous covid 'vaccines' in connection with Ukraine biolabs (https://rumble.com/v60xgnw-scott-ritter-moscow-assassination-ignites-russian-retaliation-ukraine-hidde.html). Dr. Andrew Huff was talking and writing so much about it (https://rumble.com/v28ex34-dr.-andrew-huff-on-ecohealth-metabiota-the-cia-and-the-biden-connection.html).
On 12/12/2024, a new RFK front opposition was assembled: 77 Nobel prize winners.. One of them is Dr. Drew Weissman, who with Dr. Kariko won the 2023 Nobel Prize for the mod mRNA invention, applied in majority of all covid19 genetically modifying injections (Pfizer, Moderna). Dr. Kariko didn’t sign the opposition letter though, why? And then Dr. Baltimore ( interaction between tumor viruses and the genetic material of the cell) did, and so did Joseph L. Goldstein ( regulation of cholesterol metabolism) and Harold E. Varmus (cellular origin of retroviral oncogenes), and Stanley B. Prusiner ( discovery of prions – a new biological principle of infection) signed too, but then Michael Levitt (multiscale models for complex chemical systems) this time didn’t, just wonder why? Many of those are the same people who signed on a support of the precision agriculture using GMO’s (https://www.supportprecisionagriculture.org/view-signatures_rjr.html) to genetically change the human food supply! All these top scientists know exactly what mRNA does, they did the first science on it, and now they allow others to drive a crime beyond human imagination, only in order to cover up for revelations like this: https://x.com/Donuncutschweiz/status/1871556592187150536
Fight for the truth is not easy, very important reminder of 2019 story. RFK’s health related Samoa visit in June 2019 was strangely followed by measles ‘incubation’ exactly the next month after, measles epidemic in Oct/Nov/Dec ‘19, with by 20th Dec 94% population vaccinated in a ‘Mandatory door-to-door vaccination trial..’ MSM is blaming RFK Jr for the deaths not mentioning that it was the vaccinated, who were dying. 1g of Vit C, every 2 hours, and up to 100,000 IU of Vit A for 3 days was the solution to the tragedy according to a local hero, Kennedy’s collaborator Edwin Tamasese who started that protocol, and was later on arrested and sued for that(!). Luckily all charges were dismissed, obviously due to fraudulent accusations. The only truthful report on the details of what happened one can find at: https://childrenshealthdefense.org/defender/lsamoa-medical-freedom-hero-court-case-dismissed/ written by RF Kennedy Jr. himself. It is not known, but possible, that a test of Baric’s measles-covid19 vaccine combo was performed down there already in 2019 while using inactivated measles virus carrying the synthetic “codon-optimized for Homo sapiens“ SARS-CoV-2 spike glycoprotein (https://www.ncbi.nlm.nih.gov/nuccore/MW090971.1) Arkmedic's blog post from 2022 at 
Arkmedic's blog
The Killing Fields of Samoa
Malo Lava…
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4 years ago · 518 likes · 340 comments · Dr Ah Kahn Syed
indicates that it was also a test for human compliance, with the deaths statistics 1 in 67 and not 1/10,000 like it used to be in case of measles. Back to covid issue with the hope that all the other in the past so PRO-COVID individuals, in particular this controversial choice:
2nd Smartest Guy in the World
BLACK FRIDAY SALE: STOP the mRNA SHOTS--NOW!
With the possible exception of RFK Jr., not a single one of President Trump’s “health” appointments to date is against the Modified mRNA slow kill bioweapon “vaccines…
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2 years ago · 39 likes · 14 comments · 2nd Smartest Guy in the World
who are now appointed as ‘health’ candidates, will help to lead that, what Americans really wanted, real MAHA, which can be as simple as delivery of the basic vitamins A,B,C,D,E and necessary minerals, nutraceuticals with healthy fats and proteins, without synthetic patented genetic materials and infinity of toxic chemicals in our food, air and water… I can only shout the same: STOP the mod mRNA NOW, in any form, in any product, in particular, after finding out that scientists knew already in the 50-ies that bacterial Bifido species DO NOT GROW AND MULTIPLY in the presence of RNA building blocks (more on it below the second divider). Every OLD citation below, going back >70 years and answering todays’ questions in regard to covid shots side effects, kind of indicates a premeditated action by the medical and scientific community. 
Another terrifying message by RFK’s team shown in a documentary titled ‘Authorized to kill’ (https://live.childrenshealthdefense.org/chd-tv/videos/vaxxed-3-or-authorized-to-kill-movie/ ) uncovers that the hospital’s covid protocols were killing ‘accidentally’ predominantly the covid unvaccinated, to propagate lies. Thus it is no wonder, many ‘covid installers’ are on the highest alert. And the irony goes way deeper than we even imagine, from TeamKennedy.com:”Dr. Anthony Fauci, now a private citizen, enjoys taxpayer-funded security costing more than $15 million since his retirement in January 2023 — complete with U.S. Marshals, a chauffeur-driven limousine, and armed protection. Meanwhile, Robert F. Kennedy Jr. was denied Secret Service protection for all but 43 days of his campaign. Even after multiple extremely alarming threats to his life, the Biden administration ignored the long-established practice of affording protection to high-profile candidates.” Other source reports on 12/5/2024: “Rumors of President Biden considering a blanket pardon for Dr. Anthony Fauci have sparked a wave of outrage and concern.” A pardon can be only issued for somebody who committed a crime, in this case, Anthony Fauci, the top U.S. public health official on infectious diseases, who won the 2021 Dan David Prize – one of the most prestigious Israeli academic awards. The pardon would not be for enriching himself and others (https://www.jewishledger.com/2020/11/the-jewish-connection-to-the-covid-vaccines/ , https://x.com/Donuncutschweiz/status/1864573924681621791), but rather for the deaths and injuries during the covid response and in particular for the deaths the genetically modifying injections caused and are causing, to this day.
The very first BNT-162B2 mentioned ‘side effect’, the 1p36 gene deletion (https://www.malacards.org/card/chromosome_1p36_deletion_syndrome) is worth few more  thoughts. This ‘side effect’ like everything else in the human body, is related to main energy source, the glucose. 2014 article with the title “Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype“ points to obesity and impaired glucose metabolism with countless other pathologies resembling some of the ‘covid19’ symptoms. Pancreas is producing not only insulin but also the 2 most anti-inflammatory, anti-cancerous enzymes, trypsin and chemotrypsin, and it can do it only while having its own energy supply divided between those processes. Will that have an effect on the current diabetes/cancer outbreak? You tell me. There is no official routine genetic testing of the covid injected, only that most recent bombshell from Kevin at: 
Nepetalactone Newsletter
Hacksawing your Hypothesis
Several weeks ago I was about to upload this bombshell paper. Nepetalactone Newsletter is a reader-supported publication. To receive new posts and support my work, consider becoming a free or paid subscriber…
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2 years ago · 43 likes · 6 comments · Anandamide
But actually hidden in plain sight, the work on it is being done, reported for example in this publication “Curation and reporting of pathogenic genome-wide copy-number variants in a prenatal cell-free DNA screen“ (https://www.gimjournal.org/action/showPdf?pii=S1098-3600(24)00157-6) with the conclusion: ”This framework for genome-wide fetal-CNV reporting carefully prioritizes findings with the potential to affect reproductive decision making” mentioning 1p36 as a ‘comon microdeletion’!! In fact, the entire biotechnology field with companies like Gingkoworks, which just ‘swallowd’ Metabiota, are working on human cell programming and ‘biosecurity’. Gingkoworks recent goal of mammalian cell engineering and induced pluripotent stem cell (iPSC) engineering is to create cells that produce and deliver therapeutic molecules—such as hormones, for ‘fighting diabetes’, among others. Their (BIO-INSYNC) project will utilize implantable bioelectronic devices in which engineered cells will produce therapeutic molecules on demand and/or measure disease biomarkers in real time. The ‘health care’ provider will monitor and CONTROL the patient via smartphones… A suggestion to get blood sugar values <100, rather fast.. Friend of mine is using grams of VitC, together with grams of the best magnesium salt, per day, both dissolved in water and sipping on it, every 2 hours...The values dropped from 130 to ~80, within ~2 months. No need for drugs.  
The drama of the official medical practices go now in this direction “IS Assisted Dying Being Rushed Due to Covid Complications?“ for anyone who can even bear to listen to it at: 
Vejon COVID-19 Review
IS Assisted Dying Being Rushed Due to Covid Complications?
The debate over assisted dying is nothing new. It’s a topic that has surfaced repeatedly, yet the context in which it’s being discussed today feels particularly troubling. As the UK Parliament prepares to vote on an assisted dying bill, I can’t help but feel that this discussion is happening at the wrong time and under the wrong circumstances…
Listen now
2 years ago · 39 likes · 11 comments · Dr Philip McMillan
Search in VAERS (https://www.medalerts.org/vaersdb/index.php) for diabetes related deaths after the covid shots and its boosters ends with ‘only’ 193.  For exactly the same list of diabetic symptoms, but asking for not recovered cases, VAERS responds: “Found 1,423 cases where Vaccine is COVID19 or COVID19-2 and Symptom is “Diabetes insipidus or Diabetes mellitus or Diabetes mellitus inadequate control or Diabetes mellitus insulin-dependent or Diabetes mellitus management or Diabetes mellitus non-insulin-dependent or … Diabetic cardiomyopathy or .. etc., etc.” and “Did Not Recover“. Thus INSULIN related issues after covid shots can end up with ~13% probability of DEATH, at least. The total death rate for all listed symptoms in all VAERS entries related to covid and bivalent shots is ~2.3%, and that represents possibly only ~1% of all real cases, with the rest not being reported. In the meantime, official science admits, that diabetic patients infected with coronavirus disease 2019 (COVID-19), so frequently affecting none other but the ‘vaccinated’, often have a higher probability of organ failure and mortality (https://link.springer.com/article/10.1007/s11033-023-08504-3). The homology between the amino acids sequence of the Spike2020 (produced by HUMANS after the injected Spike genome) and insulin is extremely important. Just a small section of the only 21 amino acid long insulin amino-acid sequence of its A-chain and the Spike2020 (with 2 homolog sections to it)
Query  83    CC-TSICS  89     INSULIN
             CC TS CS     <<< IDENTITIES
Sbjct  1236  CCMTSCCS  1242   Spike2020
and continuation of the above Spike fragment
             CCTS-ICS     INSULIN
             CC++  C+     IDENTITIES
 CCMTSCCSCLKGCCSCGSCC     Spike2020
shows a cysteine pattern which can’t be a random event. Below is shown the 2D insulin sequence with the cysteines from A and  B chains building cystine bridges (a) and their role in 3D fold of the synthetic monosaccharide-responsive insulin (https://pmc.ncbi.nlm.nih.gov/articles/PMC8158166/). More on that not trivial process of glucose interacting with insulin at  https://www.ncbi.nlm.nih.gov/books/NBK279029/:
Human insulin has its corresponding homologs within other organisms, example of which is described in this report “A minimized human insulin-receptor-binding motif revealed in a Conus geographus venom insulin.“ The overlap of those two is:
Query  1  GVVEHCCHRPCSNAEFKKYC   Conus-insulin A chain (con-insulin)
          G+VE+CC   CS      YC   <Human insulin A chain
also !!!!      CYIQNCPLG    <<<HUMAN OXYTOCIN <<
Query  1  TFDTPKHRCGSEITNSYMDLCYR          Conus-insulin B Chain 
           F    H CGS +  +   +C            <Human insulin B Chain
The above sequence identity coverage is enough for the con-insulin to strongly bind also the human insulin receptor and to activate its receptor signaling. The difference is in the timing. Conus gets its pray by extremely rapid hypoglycemic shock caused by that con-insulin. The goal of the studies? A design of ultrarapid-acting therapeutic insulins (https://www.rcsb.org/structure/5jyq)… Question: like the one ‘homolog’ causing the Hyperglycemia in acute respiratory distress syndrome COVID-19??? Joking.. Oh really? I’m not sure.
And then add to this above this fact:”Two Birds with One Stone: Possible Dual-Role of Oxytocin in the Treatment of Diabetes and Osteoporosis” (https://pmc.ncbi.nlm.nih.gov/articles/PMC4530313/) so now you know why Fauci needed a pardon!!! Human oxytocin has also a role in affecting glucose and insulin homeostasis, as well as regulating body weight balance, thus why on earth giving people Ozempic??
A search of the ‘Human Urine PeptideAtlas’ at https://peptideatlas.org/builds/human/urine/  for that insulin fragment ‘‘CCTSICS” within available human urine data base from 2022, gives 2 hits matching that human insulin fragment, whereby when you do the search within the 2013 data, you will find none, the same with 2010 data base. Why do people in covid times pee out their own insulin pieces? The atlas content increased 15-fold between 2010 and 2022, thus, or the data became more available or indeed the human body is changing. A search for that equivalent Spike2020 piece ‘CCMTSCCS’ is in none of the data bases. BUT, the largest piece of it, the tetrapeptide ‘CCMT’ can be found 9 times within the 2022 data base, 1 time in 2013 data base and ZERO times in 2010. Just for a heck, let’s search for the HIV-homolog piece in Spike, the  “KWPWYIW’ peptide. None of the data bases has it in full length, and the largest ‘KWP’ can be found 52 times in the 2022 data base, 5 times in 2013 and only 1 in the 2010 data base, whereby that one piece comes from mannan-binding lectin serine protease 2 isoform X2, connected with sodium conservation in the kidney, salivary glands, sweat glands, and colon, which involves aldosterone, the hormone keeping the pedals on blood pressure regulation. A truly strange result appears when you search the urine data bases for the C-terminal Spike2020 pentapeptide ‘KLHYT’. All the pre-2020 years had it only in just one protein (Dolichyl-diphosphooligosaccharide--protein, DDOST glycosyltransferase), present on all organs, associated with aging and hyperglycemia. The same ‘KLHYT’ search in 2022 data base results in two HUMAN proteins, the DDOST from 2010 and 2013 AND in 2022 a new one, protocadherin, a calcium-dependent cell-adhesion protein present mainly in the brain and reproductive organs, ~40% identical with Spike2020, when using custom BLAST parameters in that search using small fragments! Is there any publication out there finding a connection between those 2? Yes, this one: “Early suppression of antiviral host response and protocadherins by SARS-CoV-2 Spike protein in THP-1-derived macrophage-like cells“ at https://pubmed.ncbi.nlm.nih.gov/36341352/. And here the last sentence from its abstract, quote: “Our study highlights the intrinsic pathogenic role of the S protein and sheds some light on the potential drawbacks of its utilization in the context of vaccination strategies.“ No matter at which Spike2020 brick you look at, the end will lead to a premeditated crime. 
Another provocative fact. Were the experiments in 2019 using miR-455-3p molecules modulating high-glucose-induced inflammation in SV40 driven mouse cells and mimicking a diabetic nephropathy (https://pmc.ncbi.nlm.nih.gov/articles/PMC6949587/) a pretest for 2022 research with this title: ‘The emerging role of miRNAs in the pathogenesis of COVID-19: Protective effects of nutraceutical polyphenolic compounds against SARS-CoV-2 infection’ (https://pmc.ncbi.nlm.nih.gov/articles/PMC9346380/#B106 ), in which exactly the same micro-RNA from homo-sapiens labelled as ‘hsa-miR-455-3p’ were able to interact with SARS-CoV-2 genome (part of it got universally injected into human beings) and while having their expression regulated by polyphenols, play an effect on the covid infection??? 
Injections of mod mRNA in order to later on try to ‘heal’ it with methods found BEFORE the massive injections? Scientists who spend their entire life in disconnected from LIFE labs, possessed by their carriers (https://en.wikipedia.org/wiki/List_of_RNA_biologists) have this ‘diabolic dream’, quote: “By utilizing an appropriate delivery vehicle, these small non-coding RNA could be envisioned as a promising biomarker in designing a practical RNAi-based treatment approach of clinical significance.” (https://pmc.ncbi.nlm.nih.gov/articles/PMC9249409/ ) One of those, Dr. Kornberg, signed the anti-RF Kennedy letter with following remark:
 A complete library of all the covid-19 mrRNA genes AND THE RELATED DISEASES can be found at https://pmc.ncbi.nlm.nih.gov/articles/PMC9288248/ and that one particular miR455 gene itself, is described more in detail at https://www.genecards.org/cgi-bin/carddisp.pl?gene=MIR455 . How many ‘covid patients’ or better, covid injected victims and their shedded upon followers, have the following related to MIR455 gene issues: Silicosis, Dental Pulp Disease, Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Salivary Gland Adenoid Cystic Carcinoma, Skin Carcinoma??? How about this “New onset of palmoplantar keratosis triggered by COVID‐19 vaccination“ (https://pmc.ncbi.nlm.nih.gov/articles/PMC9874741/)? Dr. Kornberg, any comments??? And this is NOT A JOKE, just came in: https://expose-news.com/2024/12/17/japanese-begin-trial-for-drug-to-grow-new-teeth/… To grow new teeth because of Dental Pulp Disease??? Do you see this ‘create a problem’-’reaction (while enriching themselves)-’solution (more money)’, by one and the same ‘hand’ aiming the ‘old human’ extinction in every single step of this strategy? 
Clearly the fact that the top of the ‘scientific cream’ is standing up against RF Kennedy tasks, becomes clearer and clearer, in particular when the signee like Kornberg has his views, few quotes: “The second longstanding challenge that I wish to address is future pandemic preparedness.”, “The solution to this problem will come from RNA therapy.”, ”So small interfering RNA drugs are not only therapeutic but also preventative. They are prophylactic. They will immunize an individual against infection for a period of weeks, if not longer.” (https://technode.com/2022/09/22/beyond-expo-nobel-laureate-roger-kornberg-on-new-solutions-to-health-challenges/) What about INNATE immunity for the lifetime? Oh, does not exist any more, the science magicians erased it, for good, just on time during covid19 crimes. And pre-paid media like ‘Mother Jones’ is parroting the new ‘science’ lies loud and wide: https://www.motherjones.com/politics/2020/05/anti-vaxxers-have-a-dangerous-theory-called-natural-immunity-now-its-going-mainstream/
Allow a very basic ‘sugary’ sidetrack, with some important findings about the Bifido bacteria story, maybe not new to everyone, but worth to consider. 
So the more sugar, (whether in pure injested form or derived in process of gluconeogenesis from injested foods, https://bodyhealth.com/blogs/news/the-science-behind-perfectamino-amino-acid-utilization) and its synthetic analogs, of all sorts in the human body, GLUCOSE in particular, the more insulin, which is also a growth hormone (https://pubmed.ncbi.nlm.nih.gov/18465354/ ), is needed in order to transport it inside the cell to give it energy in form of ATP. That energy molecule ATP is an RNA nucleotide with three phosphate groups attached (https://www.ncbi.nlm.nih.gov/books/NBK560599/ and https://bio.libretexts.org/Bookshelves/Introductory_and_General_Biology/Concepts_in_Biology_(OpenStax)/04%3A_How_Cells_Obtain_Energy), thus isn’t it already intuitive that messing with RNA building blocks will affect energy, to even start with?? 
The missing metabolic pathway of ascorbic acid (Vit C) production from glucose in the human body is a big hindrance in funneling the glucose into that so needed VitC,  constantly used up, in largest quantities in the adrenal cortex and the medulla, where it is required in catecholamine biosynthesis. In stress, which includes cancer, it is essential. If that L-gulono-γ-lactone oxidase (GLO) gene had not have been mutated, the regulation of the oversupplied sugary nutrients in humans (https://diabetesjournals.org/care/article/44/2/618/35482/Effects-of-Vitamin-C-Supplementation-on-Glycemic, https://pmc.ncbi.nlm.nih.gov/articles/PMC3254006/ , https://pmc.ncbi.nlm.nih.gov/articles/PMC9182772/) would look very different, in particular, after the major crops for sugar resources were entirely genetically modified, and even the natural resources, like honey, is polluted with chemicals sprayed on us for decades (‘The Dimming’ by Dane Wingington). Dr. Thomas Levy considers humans to be genetic mutants because of the lost ability of VitC production from glucose, present in all other animals, except for only few. His health protocolls are attached at the very end of this post.
Proteins do not consist of sugars, DNA/RNA do, similar to phosphor, element found only in DNA/RNA, but not in proteins. Proteins are getting COATED with sugars in an enzyme supported targeted posttranslational modification process called glycosylation, or they can be randomly glycated. Glycation happens with DNA too, with equally severe consequences, which include reduced transcription of the affected gene and change in resulting protein activity. It appears that even RNA is glycosylated, since 2021 discovery (https://pubmed.ncbi.nlm.nih.gov/34004145/)... Sugars also bind to lipids forming the s.c. glycolipids, components of cellular membranes, including the one which determine the very unique personal feature, the blood type.. All that on top of the universal glycolysis, breakdown of sugar for the ATP production, also involved in carcinogenic reprogramming using the genes indicated in the rectangles below (https://iubmb.onlinelibrary.wiley.com/doi/epdf/10.1002/iub.1251)
With the ever increasing dietary sugar amount in human bodies, an IRREVERSIBLE overcoating in the glycation process happens, which will lead to a change/loss of proteins function, DNA function, entire organ function. In case of hemoglobin, to a reduced OXYGEN delivery to the body (https://pubmed.ncbi.nlm.nih.gov/22985301/). Thus ‘oversweeting’ the essential breathing molecules, the hemoglobins, leads to larger difficulty of getting the oxygen into tissues, all due to the hemoglobin forever being ‘coated’ (chemically bound) with the sugars. No matter how much fresh air is around you, one would need to wait ~4 months for the new red blood cells producing fresh ‘unsweetened’ hemoglobin, which can ‘breath’ again (via binding and carrying O2), unless.. a natural way to stop that sugar sticking is utilized. Substances which interfere with advanced glycation end (AGEs) products, by blocking it are: benfotiamine, luteolin, pyridoxal-5-phosphate, and carnosine. PQQ, R-lipoic acid, and taurine enhance mitochondrial resistance to glycation-induced oxidative stress (https://www.lifeextension.com/magazine/2017/5/combat-sugar-toxicity). Going back to the SAD diet. If you do not change your food, the higher glycated hemoglobin (HbA1c), related to liver health, blood pressure, triglycerides, among others,  will give you the new normal, the opposite of building back better, a chronic metabolic disease (https://pmc.ncbi.nlm.nih.gov/articles/PMC8049785/).  The overglycated hemoglobin leading to a sweet non-functional ‘paradise’ inside, is called diabetes. In that state, you literally pee the sugar out of your body (urine in diabetics TASTES SWEET). Hopefully the above ruined the appetite for those crispy do-nuts or chocolate prezels;) If not, please continue reading. 
Then we got the HIGH-fructose corn syrup everywhere, and the blood sugar monitors are telling you only the glucose part, not the fructose. Does it matter? Both sugars use many the same enzymes for their metabolism, and ~54% of the fructose is converted into glucose in the liver, so do we have the problem here? Fructose is insulin pathway independent, but not when it turns into glucose.. Also there is something like fructose intolerance, which luckily can be treated with VitC and folic acid (https://pmc.ncbi.nlm.nih.gov/articles/PMC9708598/). Well, bad news, quote: “recent transcriptome investigations, demonstrated that the fructose metabolism is altered in patients with SARS-CoV-2 infection.” Further: “We therefore hypothesize that the poor prognosis of cancer patients caused by SARS-CoV-2 may therefore be mediated through fructose metabolism.“ (https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1012412). How comes? Fruits, veggies, the main source of fructose, were always essential for healthy diet, so was there any distinction between these different fructose sources, like the natural and man-made?? And now the fructose metabolic pathway got somewhat changed?? Oh, what do the Bifidos eat? Fructose from a good diet of veggies and fruits, bifidos do not utilize glucose the usual way, their enzyme portfolio is different. Given the current missing Bifidos tragedy, who is going to convert the fructose into moles and moles of ATP (https://pmc.ncbi.nlm.nih.gov/articles/PMC4923077/) in human bodies!!?? 
Glucose, carried by 9 out of GLUT1 to 14 types of receptors (https://pmc.ncbi.nlm.nih.gov/articles/PMC9368955/pdf/ijms-23-08698.pdf), the main being GLUT4, is regulated by insulin and its receptors, and it is the ‘raw material’ for ribose, deoxyribose, building blocks of genetic material DNA/RNA (https://www.ncbi.nlm.nih.gov/books/NBK560599/), which include the pseudouridine with cancerous properties. How much carbohydrates/sugars is needed in order to sustain/renew OWN targeted glycosylation, cellular membranes restoration, energy production and DNA/RNA production, that unique own DNA everyone was born with??? Not much, all what blood can carry at once is ~5g. Ask Okinawa citizens how much do they eat? Not much, sea veggies most, and they live LONG!!! How much sugar do Americans consume, every day? Well, they have to, there is not much with little sugars in stores to get… And where does this excessive sugar/carbohydrates go? Into liver, turning it with time into FATTY liver, which then tries to convert and store more and more of it, but when the saturation moment comes, liver/pancreas say ‘no more hoarding’ and ignore the growing sweetness while forming ‘insulin resistance’. Where else that sugar is being used for?? Not only for always the same own DNA/RNA ‘replacement’ production in apoptosis events but also everywhere where the FOREIGN GENETIC MATERIAL is being produced, NO 1, your GUT MICROBIOME. Right now everyone carries less and less of the good bacteria, and more, and more of the bad ones (thanks to the genetically modifying foods and the accompanied chemicals like glyphosate which by itself is an antibiotic!). To a level where in covid injected victims and diseased patients, the Bifio-species are gone (https://bmjopengastro.bmj.com/content/bmjgast/9/1/e000871.full.pdf) But WHY Bifidos? This fact is extremely concerning since, quote:”Bifidobacterium is one of the most abundant genera in adults, but its predominance is even more pronounced in infants, especially during lactation, when they can constitute the majority of the total bacterial population.” (https://pmc.ncbi.nlm.nih.gov/articles/PMC5722804/). Dr. Sabine Hazan is the top expert on investigating the lost Bifidos issue in connection with covid19, here one of her interviews: https://x.com/Donuncutschweiz/status/1873255128095953283 .
So if the Bifidos are all gone, thanks to covid genetically modifying injections (the RNA viruses were here for a long time, so it can’t be them..), with what are human guts being filled these days? Chronic constipation is caused by a relative decrease in obligate bacteria, (e.g. Lactobacillus, Bifidobacterium, and Bacteroides spp.) a parallel increase of potentially pathogenic microorganisms (e.g. Pseudomonas aeruginosa and Campylobacter jejuni) (https://pmc.ncbi.nlm.nih.gov/articles/PMC4951383/), thus that must be the reason why the definition of clinical constipation changed from 1 bowel movement per day to 2 per WEEK (per Dr. Nuzum’s)!!! Is that some kind of a new normal UN march into the sustainability direction, in order to save water, paper, etc., while making the human bodies to unattractive baloons causing the obesity epidemic? It is becoming clear that human guts are being filled with antibiotic resistant strains of bacteria, alone due to the worldwide glyphosate pollution, with bifidos being part of it, in particular after adding synthetic genetic mod mRNA to it, and wiping out the rest totally..
Bifidospecies are among the first species colonizing the new growing infants body, that’s the predominant type of bacteria allowing the full utilization of MOTHERS’ (in all mammals including HUMAN) MILK, the food for every baby. Good overview about breastfeeding can be found here: https://articles.mercola.com/sites/articles/archive/2024/12/30/power-of-breastfeeding.aspx
Those who can’t digest diary/milk in general, are LACTOSE-intolerant. Lactose, a disacharide which consists of a galactose and glucose, must be split/digested by the lactase enzyme, which is missing in the intolerant individuals, leading to fermentation, gas production in the guts and to a hindered glucose production. Bifido species improve that lactose digestibility and the fact that they are the ‘first foreigners’ in the human body (wish Biden would invite those all over the borders!), makes them essential in immune system development (https://pmc.ncbi.nlm.nih.gov/articles/PMC9002861/).
 Glucose binds 1/5 weaker hemoglobin than galactose and 1/10 weaker than fructose in the blood, thus the least sticky sugar becomes the fuel for the entire body, a real energetic efficiency. In end effect, seems like covid19 targets everybody but the babies most, by not allowing them to utilize their own mothers milk for the growth, while wiping out the friendly life support, the bifidos. Just recently it was shown that bacterial ‘communication’, the quorum-sensing pathway had the strongest effect on the ability of Bifidobacterium to promote glucose homeostasis, suggesting its role in regulating other intestinal microbiota (https://pmc.ncbi.nlm.nih.gov/articles/PMC11622461/). That master conductor role in energy distribution within the microbiome must have been targeted in covid19 injections design, alone via application of plasmids carrying antibiotics resistance. Wait, there is more evil behind.
Another possible reason why the injections are being responsible for that specific annihilation, is because of unlimited supply of Spikes which by DESIGN require/bind lipids, essential building blocks for all gut bacteria. Scientists claim that happens in particular during viral assembly (https://pmc.ncbi.nlm.nih.gov/articles/PMC8486083/pdf/main.pdf), but whether that assembly happens or not, the lipids will bind to the Spike first! And where within Spike??? Well, exactly to that most sulfur rich fragment of Spike so similar to the insulin: 1235-CCMTSCCSCLKGCCSCGSCC-1254. How strange!  Scientists tell you in the title that “Polyunsaturated ω-3 fatty acids inhibit ACE2-controlled SARS-CoV-2 binding and cellular entry“ (https://www.nature.com/articles/s41598-021-84850-1) but only deep in text “Among them, linolenic acid, eicosapentaenoic acid (EPA), and linoleic acid had the highest binding affinity to spike protein.” Thus the good fats, in particular the ones building the brain, little baby needs most, the ones with the most ‘curly’ structure on this planet are gone, not the hard trans-fats from McDonald’s. Who else needs those good PUFA’s EPA/DHA’s? Bifido single wall gram-positive, the most electric bugs of all (https://news.berkeley.edu/2018/09/12/gut-bacterias-shocking-secret-they-produce-electricity/) to build their own membranes, to multiply and give the butyric acid everyone needs, the vitamins, and in particular the live saving Vit B2, riboflavin, (https://pmc.ncbi.nlm.nih.gov/articles/PMC5751248/#sec1-ijms-18-02645, https://pmc.ncbi.nlm.nih.gov/articles/PMC4919986/pdf/MBT2-9-441.pdf), the one without which no chicken/egg would exist on this planet.. 
That lactase enzyme, allowing the baby to get its energy (to grow) from mothers milk, which is tearing apart the lactose (https://www.uniprot.org/uniprotkb/P09848/entry) via this simple reaction:
H2O + lactose = beta-D-galactose  + D-glucose 
is huge, it has 1927 amino acids but it is only that ONE negatively CHARGED residue E=Glu which determines that capability of that reaction, this SINGLE POINT mutation of that E at the position 1749 in this ‘NDPPIYVT→E←N’ piece will make you to be able or to enjoy that ice cream or be lifted up by an excessive gas production… 
The third reason why Bifidos are disappearing in Covid times saturated with synthethic RNA molecules, the most surprising, to me, comes from 1950 publication titled “INTERRELATIONSHIPS BETWEEN RIBOSE AND DESOXYRIBOSE COMPONENTS OF NUCLEIC ACIDS“(https://pmc.ncbi.nlm.nih.gov/articles/PMC385957/pdf/jbacter00605-0061.pdf). What do the bifido species are munching on and what kills them in lab conditions? They need DNA and it is RNA, which kills them, brutally speaking. Here a quote: “In addition to DNA, thymidine, or vitamin B12, Lactobacillus Bifidus is able to utilize for growth desoxyadenylic acid, desoxycytidylic acid, desoxyguanylic acid, thymidylic acid, or hypoxanthine desoxyriboside. Utilization of DNA or the desoxyribonucleotides is inhibited by adenylic acid and ribonucleic acid, and to a lesser degree by guanylic acid, cytidylic acid, and uridylic acid. Utilization of the desoxyribosides of hypoxanthine and thymine is not markedly inhibited by the ribose compounds.” Why is that?
“Competition between the desoxyribose and ribose nucleotides for a nucleotide phosphatase is offered as a possible explanation for the observed inhibitory effects.”
So once again: “The growth of L.Bifidus in the presence of DNA was found (Skeggs et al., 1950)1 to be inhibited competitively by yeast ribonucleic acid (RNA).” Here the diagram how fast that growth inhibition happens:
With knowledge like this for almost 75 years, it must be a clear premeditation of the ‘RNA world’, the ‘new eugenic evolution’, to produce synthetic mod RNA which does not get degraded and reaches the entire digestive system. To decimate species needed for human life means to stay against creation. One of the magician’s example: ”Building blocks for 'RNA world' made from simple ingredients” at https://www.nature.com/articles/nature.2016.19901 with the subtitle: Chemical assembly bolsters theory that life might have begun with RNA. If that was the case, Bifidos would embrace the RNA as their food and not die out in masses like the above 1950 diagram shows. Another source at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC385940/pdf/jbacter00628-0019.pdf found that if ascorbic acid and vitamin B12 were omitted from bifidos growing medium, growth did not occur aerobically. 
Bifidobacteria can be greatly propagated/multiplied in cows milk, which can also be fed to little babies. Right now even that part is being targeted, with a much larger motif behind:  https://childrenshealthdefense.org/defender/bird-flu-panic-ramps-up-california-declares-state-of-emergency/. Incredible talk, not about bifido though, but covering some other essential bacteria, like L. Reuteri and what do they do to human bodies, how to propagate them and make your own yogurt with them can be found here:  
After listening to the above story, truly NOBODY needs Oz-em-PIC, any more. The in that video featured Dr. Davis exlplains the benefits of many probiotics at https://drdavisinfinitehealth.com/super-gut/.
Humanity is really on crossroads of existential survival, in particular California, with H5N1 bird flu emergency inflicting HUMANS, which must be connected with studies which make the bovine version https://www.science.org/doi/epdf/10.1126/science.adt0180 switchable to humans. That gain/loss of function achievement by the ex head of JCSG comes on top of already countless patents for covid-19 genetically modifying injections (20240140993, 11845777,20210139543←self assembling ferritins https://patents.justia.com/patent/20210139543 . Anyone got huge ferritin to neutrophile ratio during ‘covid19’??? So how to make the next great plandemic with one or 2 point mutations in comparison to the old hemaglutinin is out, and possibly embedded into the Self-Amplifying-mod mRNA/mRNA products which are about to be tested on humans by Arcturus  Therapeutics (ARCT-2304). The Japanese population is already on its way to the annihilation with that new already approved and being applied never ending gene therapy. The utilization of the Company’s proprietary STARR® self-amplifying mRNA and LUNAR® delivery technologies, are  GENE THERAPIES! (Sourced from: https://ir.arcturusrx.com/news-releases/news-release-details/arcturus-therapeutics-announces-second-quarter-2024-financial). Moncef Slaoui, the chief of the Operation Warp Speed is on it too, again… Thus this time, a GENE THERAPY forever, with SA-mRNA described in some of their long patents list: https://www.lens.org/lens/search/patent/list?q=Arcturus Therapeutics, Inc. , with some on the technology https://www.lens.org/lens/patent/106-955-279-178-346/frontpage?l=en and in this one https://www.lens.org/lens/patent/144-359-614-274-210/sequences?si=&t=AA which yesterday was readable, today not…. BARDA Biodefense program support of $63.2M in 2022 already with trials right now (!!) in 2024  (https://ir.arcturusrx.com/node/12936/pdf) for a gene therapy with a synthetic genetic sequence one can’t find anywhere, is just illegal. One can only speculate, that the new injections are maybe having the 2 mutations which allow for exactly that human transmission, to apparently protect them from it…. That’s my speculation. And if the timing of the solution proceeds the incident, we know, it is/was a plan…. Today a new post reviews the clinical studies with much more info on these even more questionable type of synthetic RNA injections: 
DoorlessCarp’s Scientific Literature Reviews
Self-amplifying mRNA (saRNA) Part 1: The Japanese registration documents
Reading time…
Read more
2 years ago · 14 likes · 2 comments
Back to Kevin McKernan’s news, the DNA contamination issue of covid Pfizer/Mod-E-RNA injections. SV40 was known to cause cancer (https://embryo.asu.edu/pages/asilomar-conference-1975) and was involved in the first genetic experiments with transferring viral genes into E.Coli bacteria. Ask Dr. Baltimore, he knows best! Oh, the chance is gone, Dr. Baltimore passed away on 6th Sep ‘25.
When looking at the SV40 entire genome (https://www.ncbi.nlm.nih.gov/nuccore/NC_001669.1) one cysteine rich section sticks out, the one in the small t-antigen protein (174 amino acids, code NP_043128.1), and here is what BLAST comes up with when comparing Spike2020:
Query  50   EKMKKMNTLYKKMEDGVKYAHQPDFGGFWDATEVFASSLNPG---------------VDA  94
            E+ K    ++ +++   K     DFGGF + +++      P                 DA
Sbjct  773  EQDKNTQEVFAQVKQIYKTPPIKDFGGF-NFSQILPDPSKPSKRSFIEDLLFNKVTLADA  831
Query  95   MYCKQWPECAKKMSA-NCIC  113 SV40 small t antigen 
             + KQ+++C   ++A + IC      <
There is a special work written by B. Robson at https://www.sciencedirect.com/science/article/pii/S0010482520300627 showing that this ‘added’ piece in the first Subjct line ‘KRSFIEDLLFNKV’, representing the Spike2020 amino acid sequence is required for SARS-CoV-2 cell entry.. How do these viruses ‘remember’ so much about SV40 and then insert just one piece which makes them so welcome into the human body, again, under a different name? I’m sure again, Dr. Baltimore, and Dr. Fauci (born on the 24th of Dec.), for sure, can answer that! Amazing coincidences indeed.
The SV40 early promoter has 6 repeat motifs 5'-CCGCCC-3' essential for its in vivo activity (https://pubmed.ncbi.nlm.nih.gov/3004974/ ) and strangely that’s the complementary middle piece (read backwards and exchange C→G, and G→C) in that Moderna patented sequence  ‘CTCCTCGGCGGGCACGTAG‘. Spike sequence does not have that exact SV40 repeat motif, but it has this ONE pattern, into which some CRISP tools could bite in and get that T out, maybe?? That’s the Spike’s genome fragment from the entry at https://www.ncbi.nlm.nih.gov/nuccore/NC_045512
25081 tgcttcagtt gtaaacattc aaaaagaaat tgaCCGCCTC aatgaggttg ccaagaattt
In any case, Spike2020 homologies between the SV40 large T antigen are the same and very disturbing for most part, with even more fragments, except for the C-rich section, here just one example:
Query  427  PIDSGKTTLAAALLELCGGKALNVNLPLD------RLNFEL-GVAIDQ  467 NP_043127.1
            P+   KT++  ++  +CG  +   NL L       +LN  L G+A++Q
Sbjct  728  PVSMTKTSVDCTMY-ICGDSTECSNLLLQYGSFCTQLNRALTGIAVEQ  774 Spike2020
 Let’s not imagine a horror scenario with this question, is the strange ‘shedding’ from the covid injected some kind of SV40 coupled transmission in which the promoter  might interact with Spike, which simulates the LTA?? Just a speculation, but the fact that SV40 ORI with the LTA protein is responsible for horizontal transmission (from one organism to the other) was described already in 2007 (https://pmc.ncbi.nlm.nih.gov/articles/PMC1941725/)?? The part relating SV40 LTA proteins (and so the Spike2020) to cancer, via glucose metabolism pathway, was also described: ”The SV40 Large T Antigen-p53 Complexes Bind and Activate the Insulin-like Growth Factor-I Promoter Stimulating Cell Growth” (https://aacrjournals.org/cancerres/article/68/4/1022/542775/The-SV40-Large-T-Antigen-p53-Complexes-Bind-and). Kevin McKernan talks about the shedding more at: https://uncutnews.ch/selbstverstaerkender-impfstoff-die-gefahr-replizierender-dna-plasmide-die-von-geimpften-auf-andere-uebergehen-koennten/ On 12/23/24  SV40 DNA from Pfizer and Mod-E-RNA was found in the blood of 75 ‘vaccinated’ Australians, plus the autopsies of the covid injected with SV40 DNA present in their cancerous organs are out there too..  
Regarding this glucose dependent growth alert in these covid times, there is that strange GIANT consortium (The Genetic Investigation of ANthropometric Traits), (not sure Francis Collins is in it https://portals.broadinstitute.org/collaboration/giant/index.php/GIANT_consortium), which is very much interested in Type II Diabetes according to “Functional genomics of human skeletal development and the patterning of height heritability“ (https://www.cell.com/cell/fulltext/S0092-8674(24)01256-X). The fact, that this GIANT consortium is affiliated with BROAD Institute (MIT, Harvard), so heavily involved in design of covid19 genetically modifying injections, is very much concerning, but maybe justified. Maybe? Here is what the scientists are telling us about us, humans, with just one picture, from top science journal (https://www.nature.com/articles/d41586-024-04194-4), mind you, there is no woman…:
and just for fun, kind of inverted evolution in terms of size, this would actually correspond more with the NIH+Co gigantic interests:
substantiated by more old pictures, movie, documents, from a source, I’ll leave out for now, and only share this thought, maybe NIH+Co. are taking the biblical Goliath and David story somewhat seriously..?? Most recent very thorough resource at https://strangesounds.org/2019/12/7-proofs-ancient-giants-earth-video.html points to places with definite proof of giant’s existence.  
There are reporters out there, like Timothy Alberino who very actively researches that topic, even more concealed than ‘aliens’: https://rumble.com/v6xzds0-the-hidden-bones-of-giants-and-nephilim-what-is-the-smithsonian-hiding-in-i.html?mref=5grgb&mrefc=5
Since genetics, and glucose, determine this ‘dimensions/energy feature’, as shown on this one point mutation event above and as a consequence utilization of mothers milk for growth, one needs to consider this most recent nature genetics paper “A multilineage screen identifies actionable synthetic lethal interactions in human cancers“ (https://www.nature.com/articles/s41588-024-01971-9) saying in the first sentence, quote “Cancers are driven by alterations in diverse genes, creating dependencies that can be therapeutically targeted.“ This quote talks about alteration in genes in different people though. Since your genes always stay the same since your birth, why didn’t you have that cancer years back? In addition to epigenetic changes of gene’s expression thanks to good or toxic chemicals, how about inserting NEW GENES, like pieces of Spike, like SV40, for example via covid shots? Also the lifetime of a plain DNA molecule can be thousands of years, when left alone and properly stored, but not when adding DNA/RNA restriction/digestive enzymes, which cut and paste the original genetic material to a level of a wild zoo, the end result of which is shortened lifespan…. Effects on human bodies of random genetic mutations caused by radioactive radiation are known very well. Please listen to this short section, if you are bored by now,  around 31:50 at https://www.bitchute.com/video/5G8ObLVkONL1, it is about the possible life span of Marshal Islands inhabitants before and after 1960, a difference of ~150 years, ‘thanks’ to mutations caused by a nuclear radiation. Anyone more Jasons, Ukraine labs, lost nuclear material?? 
That point of building genetic material using sugars, as one component, is also connected with using one very specific amino acid GLYCINE derived from SERINE for that production in the s.c. ONE CARBON metabolism, which is essential in cancer (https://www.nature.com/articles/nrc.2016.81). And since serine is the building block for glycine production, that simple nonpolar amino acid is linked to cancer as well (https://www.science.org/doi/10.1126/science.1218595). One of these links is the fact that phosphatidylserine, defined as negatively charged lipid, is a part of an intracellular layer of normal cell membrane, but in cancer, it ends up in increased cell surface exposure, following immune suppression and cancer growth.
In the meantime, FDA prepares for the future: “Final FDA Guidance Lays Path for Drugmakers to Establish Circulating Tumor DNA as Trial Endpoint“ at https://www.genomeweb.com/cancer/final-fda-guidance-lays-path-drugmakers-establish-circulating-tumor-dna-trial-endpoint. Is that the cDNA injected into the billions of arms??? That must be why Gottlieb wants RF Kennedy Jr out so much… Please pray for RFK Jr.’s mission to be accomplished.
Dr. Jack Kruse, a well known surgeon (student of the late Robert O. Becker, father of electromedicine) is touching the Ozempic blues and all so ‘sweet’ GLP-1 agonists, Glucagon-Like Peptide-1, a 30- or 31-amino-acid-long peptide hormone derived from the tissue-specific posttranslational processing of the proglucagon peptide (https://diabetesjournals.org/clinical/article/38/4/390/35426/Switching-Between-Glucagon-Like-Peptide-1-Receptor), in this podcast at: 
Dr. Kruse goes even further and combines the SV40 cancer story with JFK 1963 assassination:
GLP-1, described at https://www.uniprot.org/uniprotkb/P01275/entry is a potent stimulator of glucose-dependent insulin release. Upon food intake GLP-1 (brown helix below, that’s what Ozempic is ‘mimicking’) is excreted by intestine lining and with glucose around it binds its receptor (green) while stimulating pancreas to produce insulin. 
 
So many people wish to loose some weight. Well, we can’t change the gravity constant, but when you ‘get covid’, the weight loss comes with it, thus no need for Ozempic. Besides, before ever ‘going on it’ you better check this list of 266 (!) drugs interacting with Ozempic:  https://www.drugs.com/drug-interactions/semaglutide,ozempic-index.html
There are some ‘drug oriented’ scientists, who didn’t see the above list and think diabetics might need Ozempic, summarizing their findings (https://pmc.ncbi.nlm.nih.gov/articles/PMC10500111/pdf/HSR2-6-e1549.pdf) with the title “The impact of preadmission/prediagnosis use of GLP‐1 receptor agonists on COVID‐19 mortality in patients with diabetes: A systematic review and meta‐analysis“. GLP-1 RA drugs, which stimulate insulin production are reported by few more groups to have positive outcome in covid19 treatment. But more insulin also leads to insulin resistance, since cells do have only given amount of the receptors on their surfaces… And that’s just a ‘mild issue’, the weight loss program can also end up with cancer, paralized stomach or blindness (https://childrenshealthdefense.org/defender/ozempic-semaglutide-vision-loss-study-side-effects/)… And this : https://x.com/Donuncutschweiz/status/1869332782440390978 tells really enough in order to sue Novo Nordisk for their product.
Search of PubMed (https://www.ncbi.nlm.nih.gov/pmc) for published articles involving two keywords ‘SARS-CoV-2 insulin’ results in 19710 publications connecting the greatest PLAN-demic with the NO 1 ‘energy’ hormone of the humankind, insulin, amino acids sequence of which was decoded by the geneticist Frederick Sanger in 1951. Insulin amino acid residues from its B chain, Tyr16, Tyr26, F24 and F25, His10 and Glu13 participate in its receptor binding (https://pmc.ncbi.nlm.nih.gov/articles/PMC8513149/pdf/main.pdf). They are  marked below with * under the amino acid sequence (single letter code) of the B chain overlapped with the Spike2020:
1       10        20
FVNQHLCGSHLVEALYLVCGERGFFYTPKT INSULIN CHAIN B
         *  *  *       ***  <= INSULIN residues binding the insulin receptor 
overlap with Spike2020:
FVNQHLCGSHLVEALYLVCGERGFFYTPKT   INSULIN, CHAIN B
 VN   + + L  A Y  +  RG +Y  K    IDENTITIES
CVNLT-TRTQLPPA-YTNSFTRGVYYPDKVFRSSVLHSTQDLFLPFF-SNVTWFHAIHV  <=SPIKE2020
and continuation of Spike sequence from the above
FVNQHLCGSHLVEALYLVCGERGFFYTPKT  INSULIN, CHAIN B
F    L   H  + L+L     +FF +  T
FRSSVL---HSTQDLFL-----PFF-SNVTWFHAIHV <=SPIKE2020
The coverage of 11 in total residues identical or homolog to insulin in the TWO Spike fragments, and the fact that the same residues binding the insulin receptor are among them, seems to be strange. It is almost as if the mimic of insulin allows Spike fragments binding to the insulin receptor on the cell surface, thus allowing for easier viral entry, maybe? Well this publication at https://pmc.ncbi.nlm.nih.gov/articles/PMC9756566/pdf/main.pdf titled “Insulin may promote SARS-CoV-2 cell entry and replication in diabetes patients“ indeed describes the clinical findings confirming that..
Some basics from 1922 at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2417009/pdf/brmedj06741-0003.pdf : 
→ ratio of how much CO2 is exhaled in breathing to how much O2 is left (also proportional to lung quality/size being indicator of longevity!!!) was reported to be 1 for carbohydrates diet, 0.7 for fats and 0.8 for proteins. That ratio indicates the level of glucose oxidation. Removal of pancreas (in the experimented dogs!) ends with diabetes, in which the value of 1 falls below 0.7, due to impaired carbohydrate digestion. What else happens in the victimized dogs? Acetone bodies and sugar appear in urine, glycogen from liver disappears and in the heart it grows way above the normal. Fat disappears from the liver and the blood. Administration of insulin rescues the pancreas-less victim. 
The ‘pre-designed’ presence of sugar in all foods driving the insulin spikes, is an evil tactics of food industry. But now it is in the hands of smart scientists: “‘Smart’ insulin prevents diabetic highs — and deadly lows“ or exactly quote “Scientists have designed a new form of insulin that can automatically switch itself on and off depending on glucose levels in the blood. In animals, this ‘smart’ insulin¹ reduced high blood-sugar concentrations effectively while preventing levels from dropping too low.“ And that’s how the ‘smart’ crystals look like (https://www.nature.com/articles/d41586-024-03357-7): 
This is NOT how classical symmetry looks like, 1-,2-,3-,4-,6-fold symmetry!
Insulin, the OLD one, has MANY FUNCTIONS (https://www.uniprot.org/uniprotkb/P01308/entry) and it is not only about carbohydrates, but equally about regulation of lipid formation/breakdown. That’s because of that fat conversion in the liver when in oversupply. Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver. It is the main anabolic hormone of the body, and it is a fat storage hormone, which inhibits lipase, the fat burning enzyme. The regulation of the metabolism of carbohydrates, fats, and proteins by promoting the absorption of glucose from the blood into cells of the liver, fat, and skeletal muscles, is an indication for a masterminded insulin driven energy distribution. That’s from wi-ki and uniprot, reinterpreted.. Not much about the brain. Why? When you look at the latest PET Japanese study of covid un-jabbed (A and B) vrs. jabbed (C and D) at https://pubs.rsna.org/doi/epdf/10.1148/radiol.230743 (the entire study is at https://pubmed.ncbi.nlm.nih.gov/37724969/), you see there is LOT of the unhealthy sugar derivative ¹⁸Fluorine-fluorodeoxyglucose (POOR patients!) in the brain AND you have a lot of that ‘sugar’ in the heart of the jabbed in C and D, exactly there, where it should NOT be, like in A and B, hearts of the unjabbed:
That 1922 study explained already partly what we see here.. The above pictures indicate a LACK OF insulin in heart tissue, which would ‘take away’ the sugar from those jabbed ‘diabetic’ hearts… Heart has one of the highest concentrations of ACE2 receptors to which the sugar-hungry Spike will bind. Does this maybe indicate that the FFG-sugar binds the Spike instead? Another experiment, from 1927 at https://pmc.ncbi.nlm.nih.gov/articles/PMC1514894/pdf/jphysiol02513-0044.pdf  is helping in understanding exactly that situation “THE ACTION OF INSULIN ON THE ASEPTICALLY PERFUSED HEART.“ quote:
“accelerated disappearance of sugar, from the fluid perfusing an isolated mammalian heart, under the influence of insulin, is a real phenomenon, and is not connected with bacterial contamination of the perfusion fluid. …a large acceleration of sugar disappearance may occur without any significant acceleration of the heart beat. From analogy with the effect of insulin on skeletal muscle it would be expected that part of the glucose so disappearing is stored as glycogen;“ More on the details at https://biologyinsights.com/aerobic-respiration-pathways-atp-yield-and-cellular-functions/
Now to some homologies between human pro-insulin entire sequence of 110 amino acids (we covered one part only) and the SARS-CoV-2 Spike sequence, the one genes of which were injected into billions of arms, illegally, because without a consent to undergo GENE THERAPIES. The NIH BLAST software finds the following identities, most important one, the already discussed cysteine rich C-terminal section of human insulin A6XGL2  (uniprot code), and here more:
'GIVEQ-CCTSICS-LYQLENYCN being a SEQ1 in 2001 filed patent for 'Use of insulin for the treatment of cartilaginous disorders.' by GENENTECH.

the first 24 N-terminal insulin amino acids, representing the signal for expression:
MALWMRLLPLLAL--LALWGPDPAA-A expression signal of INSULIN
M ++  LLPL+++  + L     ++ +
MFVFLVLLPLVSSQCVNL-----TTRT expression signal of SARS-CoV-2 SPike

is =>15/24*100%~62% IDENTICAL with Spike2020 signal!
it means that the expression of SPike2020 is maybe somewhat synchronized with insulin secretion, to allow for the max steal of the building blocks necessary to assemble SPike2020, and NOT insulin?? Just a thought..

And even more homolog insulin fragments:

Query  33   SHLVEALYLVCGER  46 Insulin
              L+ A   VCG +
Sbjct  515  FELLHAPATVCGPK  528 Spike2020
Query  46  RGFFYTPKTRREA  58   Insulin
           RG +Y  K  R +
Sbjct  34  RGVYYPDKVFRSS  46 Spike2020
Query  52   PKTRREAEDLQGSLQPLALEGSLQKRGIVEQ  82 Insulin
            P  R   EDL      L  + +L   G ++Q
Sbjct  812  PSKRSFIEDL------LFNKVTLADAGFIKQ  836 Spike2020
Query  54   TRRE-AEDLQGSLQPLALEGSLQKRG  78  Insulin
            ++R   EDL  +   LA  G +++ G
Sbjct  813  SKRSFIEDLLFNKVTLADAGFIKQYG  838 <<< Spike2020's 'hammer' section
Query  17   WGPDPAAAFV  26 Insulin 
            W    AA +V
Sbjct  258  WTAGAAAYYV  267 Spike2020
Query  29    HLCGSHLVEALYLVCGERGFFYTPKTRREAE  59
             H   +H+     +V     +F T +   E +
Sbjct  1083  HDGKAHFPREGVFVSNGTHWFVTQRNFYEPQ  1113
part of furin site:
Query  56   REAEDLQGSLQPLALEGSLQKRGIVEQCCTSI  87
            R A  +  S   +A   SL     V     SI
Sbjct  682  RRARSV-ASQSIIAYTMSLGAENSVAYSNNSI  712
Query  64   SLQPLALEGSLQKRGIVEQCCTSICSLYQLENY  96
            +L PL+      K   VE+       +YQ  N+
Sbjct  292  ALDPLSETKCTLKSFTVEK------GIYQTSNF  318

Since NIHs BLAST can't any better, here by hand the entire PATENTED cystein rich section in Spike2020 overlapping the homolog PATENTED section of HUMAN insulin:

GIVEQCC-TSICS-LYQL--------ENYCN          <<CCMTSCCSCLKGCCSCGSCCKFDEDD        <<CTSI-CSLYQLENYCN   <<CSCGSCCKF---DEDD     <<
Genentech patent at https://www.lens.org/lens/patent/026-563-655-881-535/fulltext specifies how much of amino acid sequence is needed in order to preserve the ‘insulin character’. Patent calls for minimum 15 resides in Chain A, we got 11 overlapping residues. Short way to go CRISP addicts! Here some of their recent claims:  https://www.npr.org/sections/shots-health-news/2024/12/13/nx-s1-5227283/crispr-rare-genetic-disorders-gene-editing, https://www.nature.com/articles/s41587-024-02512-9
An example of BLAST alignment of the above closely related insulin and insulin growth factor (IGF-1) with uniprot code of P05019, both of HUMAN origin:
Query  28   QHLCGSHLVEALYLVCGERGFFYTPKTRREAEDLQGSLQPLALEGSLQKR----GIVEQC  83
            + LCG+ LV+AL  VCG+RGF++               +P    GS  +R    GIV++C
Sbjct  51   ETLCGAELVDALQFVCGDRGFYFN--------------KPTGY-GSSSRRAPQTGIVDEC  95
Query  84   CTSICSLYQLENYC  97  <<< INSULIN 
            C   C L  LE YC
Sbjct  96   CFRSCDLRRLEMYC  109  <<< IGF-1
and one more fragment
Query  49   FYTPKTRREAEDLQGSLQPLALEGSLQKRGI  79
            +  P T + +        P +  G  QK G+ 
Sbjct  135  YQPPSTNKNTKSQRRKGWPKTHPGGEQKEGT  165
since insulin also affects the natriuretic peptide, is Spike there somewhere too?
Query  57   VVPPQVLS-EPNEE-AGAALSPLPEVPPWT  84  P01160  Natriuretic peptides A
            V+PP +L+ E   + + +AL       +WT
Sbjct  860  VLPP-LLTDEMIAQYT-SALLAGTITSGWT  887 Spike2020
Query  57   VVPPQVLSEPNEEAGAALSPLPEVPPWT  84   P01160  Natriuretic peptides A
             + P   S +   AGAA   ++ + P T
Sbjct       YLTPGDSSSGW-TAGAAAYYVGYLQPRT Spike2020

ANGIOGENIN (P03950) a ribonuclease involved in ALS and Parkinson, critical in cancer growth and supply of new blood vessels, which is controlled by glucose concentration. Here its 2 active centers and how well they align in the homolog section of Spike2020:
           active site *, that H below is histidine
Query  28    SRYTH-FLTQHYDAKPQ  43   ANIOGENIN
             S  TH F+TQ+    PQ       IDENTITIES
Sbjct  1097  SNGTHWFVTQRNFYEPQ  1113 Spike2020
     active site * histidine138
Query  135  LPV--HLDQ  141           ANGIOGENIN
            +PV  H DQ                IDENTITIES
Sbjct  620  VPVAIHADQ  628           Spike2020
all coincidence???
As one can see that cystein rich section (in bold), containing the by Fauci patented HIV-1 drug with the pattern CxxxxC (cysteine plus any 4 amino acids plus cys again), aligns equally well if not better with Spike2020 than with the physiologically related HUMAN growth factor.
With so many common blocks between HUMAN insulin and countless other proteins which depend on it and the universally injected VIRAL Spike2020, question, will that sudden synthetic production of a new universally injected synthetic gene affect insulin production and the processes glucose is involved with??? The full insulin 110 amino acids uniprot entry P01308 compares following way with Spike:
That's what BLAST comes up with, overlap over almost the entire length of the insulin, it ignores the important fragments which were listed before:
Query  23   AAFVNQHLCGSHLVEALYLVCGER--GFFYTPKTRREAEDLQVGQVELGG--------GP  72
            A F+ Q+      + A  L+C ++  G+   P    +    Q     L G        G 
Sbjct  831  AGFIKQYGDCLGDIAARDLICAQKFNGLTVLPPLLTDEMIAQYTSALLAGTITSGWTFGA  890
Query  73   GAGSLQPLALEGSLQKRGI  91
            GA    P+A++ + +  GI
Sbjct  891  GAALQIPFAMQMAYRFNGI  909
That entry P01308 actually defines the PRO-insulin as heteroDIMER consisting of:
25-54 insulin B chain  FVNQHLCGSHLVEALYLVCGERGFFYTPKT
57-87 C peptide           EAEDLQVGQVELGGGPGAGSLQPLALEGSLQ
90-110 Insulin A chain GIVEQCCTSICSLYQLENYCN
          ->Zn-binding site of Insulin Bchain
            * H=His
Query  22  SHLVE---ALYLVCGERGFFYTP-KT  26 Insulin B-chain
           ++  +   A Y  +  RG +Y P K
Sbjct  34  TR-TQLPPA-YTNSFTRGVYY-PDKV  38 Spike2020
Insulin chain B binds ZINC at the His10 position (pdb code 1G7A), and is important for proper functioning of insulin‑secreting cells (https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0038-1676241.pdf). ZINC is essential for β-cell function, insulin action, glucose homeostasis and the pathogenesis of diabetes and its complications (https://pmc.ncbi.nlm.nih.gov/articles/PMC4573932/). Everything known about Zinc in drug industry can be found at: https://go.drugbank.com/drugs/DB01593#BE0005831 and another resource is at https://jn.nutrition.org/article/S0022-3166(22)14102-7/fulltext. ZINC is responsible in our bodies for a proper functioning of >300 enzymes!!!!! Imagine a car and how far can it get without 300 ESSENTIAL parts in it….
Going back to glucose oxydation and CO2 dependence (breathing and energy), gluconeogenesis requires bicarbonate as substrate and that brings the fastest enzyme in the human body into the play, carbonic anhydrase, which catalyses reversible transformation CO₂ + H₂O ↔ HCO₃⁻ + H⁺and which also won’t happen without zinc (https://pmc.ncbi.nlm.nih.gov/articles/PMC7717713/). The No 1 source of zinc in our diets is meat, shelfish and legumes. If you ever notice your fingernails are starting to get vertical streaks like this:
or also at: https://zinc.truecellularformulas.com/drz or here another one: https://drjockers.com/test-zinc-levels-home/
that’s a time to go to your local farmer and reward him for nice piece of beef and some beans, or get a can of oysters every day… Lack of zinc will effect your strength to fight off diseases, you are ‘delivered’ without that crispy element… A good overview of how Zn affects diabetes can be found at: https://pmc.ncbi.nlm.nih.gov/articles/PMC4573932/pdf/40199_2015_Article_127.pdf
Since it is about BREATHING and energy, the fastest enzyme in the human body, and how does it relate to covid or its SPIKE, so heinously used as a pretext for all covid injection materials, one needs to look into it closer. First the comparison of insulin receptor https://www.uniprot.org/uniprotkb/P06213/entry with Spike2020:
Query  1168  AHDFTVKIGDFGMTRDIYETDYYRKGGKGLLPVRWMAPE  1206 <<=insulin receptor
             A +  +K+ +F    D +   YY K  K      WM  E
Sbjct  123   ATNVVIKVCEFQFCNDPFLGVYYHKNNKS-----WMESE  156 <<-Spike2020

Query  717  SQILKELEESSFRKTFEDYLHNVV  740
            SQIL +  + S R   ED L N V
Sbjct  803  SQILPDPSKPSKRSFIEDLLFNKV  826

Query  1285  EIVNLLKDDLHPSFPEVSFFHS  1306
              +++  +D   P F  V++FH+
Sbjct  46    SVLHSTQDLFLPFFSNVTWFHA  67
Query  242  NCSQPDDPTKCVACRN  257
            N   PDD T CV   N
Sbjct  422  NYKLPDDFTGCVIAWN  437
Query  279  RCVNFSF  285
            +CVNF+F
Sbjct  537  KCVNFNF  543
Query  868   HLMWQEPKEPNGLIVLYEVSY  888
             HLM      P+G++ L+ V+Y
Sbjct  1048  HLMSFPQSAPHGVVFLH-VTY  1067
Query  91   FRVYGLESLKDLFPNLT  107
            FRV   ES+   FPN+T
Sbjct  318  FRVQPTESIVR-FPNIT  333
Query  972  IGSIYLFLRKR  982
              S+Y + RKR
Sbjct  347  FASVYAWNRKR  357
Query  1235  QPYQGLSNEQVLKFVMDGGYLDQPDNC--PERVTDLMR-MCWQFN  1276
             QPY+ +    VL F +    L  P     P++ T+L++  C  FN
Sbjct  506   QPYRVV----VLSFEL----LHAPATVCGPKKSTNLVKNKCVNFN  542
and this special one KIGDFGMTRDIYETDYYRKGGK of functional importance^1:
Query  16   YYRKGGK  22
            YY+K  K
Sbjct  144  YYHKNNK  150
insulin receptor shares ~30% identity with GLP-1. Spike comparison
with 6X18_6 (pdb):Glucagon-like peptide 1 receptor P43220.2
Query  60   TEDPPPATDLFCNRTFDEYACWPDGE-PGSFVNVSCPWYLPWASSVPQGHVYRFCTAEGL  118
            T+ PP  T+ F    +     +PD     S ++ +   +LP+ S+V   H        G 
Sbjct  22   TQLPPAYTNSFTRGVY-----YPDKVFRSSVLHSTQDLFLPFFSNVTWFHAIHVSGTNGT  76
Query  119  WLQKDNSSLPWRD  131  P43220.2 = GLP-1
              + DN  LP+ D
Sbjct  77   K-RFDNPVLPFND  88  Spike2020
Query  453  SSGATAGSSMY  463 GLP-1
            SSG TAG++ Y
Sbjct  255  SSGWTAGAAAY  265 Spike2020
Query  110  YRFCTAE--GLWLQKDNSS  126 GLP-1
            ++FC     G++  K+N S
Sbjct  133  FQFCNDPFLGVYYHKNNKS  151 Spike2020
Query  113  CTAEGLWLQKDNSSLPWR  130
            CT   + +  D  +  WR
Sbjct  617  CTEVPVAIHADQLTPTWR  634
Query  47    FDEYACWP  54
             +++Y  WP
Sbjct  1206  YEQYIKWP  1213
Query  85   CTAEGLWLQKDNSSLPWR  102
            CT   + +  D  +  WR
Sbjct  617  CTEVPVAIHADQLTPTWR  634
Facit from all of these BLAST comparisons above: certain single amino acids left after a complete digestion of every piece of food are precursors for many neurotransmitters allowing for all the ‘connections’ within the entire body, every new protein within human body is made from SINGLE AMINO ACIDS, produced only after a complete healthy digestion. Thus ignoring the fact that the Spike synthetic gene steels SO MUCH building materials, and that maybe at all times, is just mindblowing. I’m not even talking about a foreign gene embedded into a human genome here!
Some of the glucose binding GLUT receptors from 1 to 12, regulated by the insulin, https://pmc.ncbi.nlm.nih.gov/articles/PMC9368955/ in addition to glucose and other sugars bind also melatonin and oxidized VitC, depending on the organ, how frequently it is used, how much energy it needs, etc.. GLUT-4 in particular has its name “insulin-responsive glucose transporter” for its relocation from intracellular vesicles to the plasma membrane upon insulin signaling. Disruption of the regulated GLUT4 trafficking is associated with obesity and the type II diabetes mellitus. Accessive sugars can do the same to GLUT4 what HIV protease inhibitors, like Ritonavir, which all cause acute insulin resistance and result in increased diabetes incidence among AIDS patients treated with these inhibitors! (https://onlinelibrary.wiley.com/doi/epdf/10.1002/pro.2858).
When melatonin and VitC bind and affect the glucose receptors? Melatonin for example, is excreted mainly in the night, so one should expect titles like these: “Switching diseased cells from cytosolic aerobic glycolysis to mitochondrial oxidative phosphorylation: A metabolic rhythm regulated by melatonin?“ (https://onlinelibrary.wiley.com/doi/abs/10.1111/jpi.12677), or “Melatonin and Pathological Cell Interactions: Mitochondrial Glucose Processing in Cancer Cells“ (https://pubmed.ncbi.nlm.nih.gov/34830375/) or “Anti-Warburg Effect of Melatonin: A Proposed Mechanism to Explain its Inhibition of Multiple Diseases“ (https://pubmed.ncbi.nlm.nih.gov/33466614/) or “Melatonin Signaling a Key Regulator of Glucose Homeostasis and Energy Metabolism“ (https://pmc.ncbi.nlm.nih.gov/articles/PMC6651071/pdf/fendo-10-00488.pdf) and so many more. Melatonin, the open pandora box in covid times (https://pubmed.ncbi.nlm.nih.gov/33741691/) currently leads to a situation where you won’t get even the 20mg supplementation in your health store any more, sold out. Great, people finally got it! 
The mentioned oxidized Vit C form has its name: Dehydroascorbate (DHA) (https://watermark.silverchair.com/32-6-545.pdf ). It inhibits the uptake of 2-deoxy-D-glucose and of 3-O-methyl-D-glucose by human blood neutrophils (https://www.nature.com/articles/s41467-021-26829-0.pdf ) On the other hand this link makes the difference between health and disease : “2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA“. Not only that, dehydroascorbate has a special function  (https://pubmed.ncbi.nlm.nih.gov/19686035/) linking the ascorbate metabolism with oxidative protein folding. VitC upon entry in CNS system functions as a neuromodulator, enzymatic cofactor, and reactive oxygen species (ROS)scavenger; it also stimulates differentiation, which is the reason why Dr. Paul Marik uses the infusions of that vitamin to fight septic shock, which will be always also involving glucose (https://pmc.ncbi.nlm.nih.gov/articles/PMC4126260/pdf/nihms609574.pdf). The literally cruel witch hunt behind Dr. Marik’s EXPERIMENTAL covid findings, was and still is, mindblowing, ending with countless published ‘science’ papers claiming the totaly opposite, Vit C is useless in covid disease.. Dr. Marik is not alone with his recommendation of VitC therapy, I’m attaching at the end protocol of Dr. Thomas Levy, who asked to distribute it far and wide. It is unprecedented, but it looks like the fight for the HUMAN BODY becomes the last battle on this planet. Here the same top journal fabricating the EUA for covid injections, now claims, VitC will kill you when you have covid and land in ICU: https://www.nejm.org/doi/full/10.1056/NEJMoa2200644 . Please, do NOT land in ICU. Here one article describing VitC usage in other diseases, including sepsis (https://pmc.ncbi.nlm.nih.gov/articles/PMC9708598/).
 Also this discussion with Dr, Merik and Steve Kirsch might be of interest: https://rumble.com/v5yagjq-vsrf-live-156-the-sepsis-epidemic.html
As much as insulin production is important, so is its degardation. Insulin-degrading enzyme (IDE), is a Zn2+-metalloprotease, involved in the clearance of insulin and amyloid-beta and many other short peptides(refs 1-3), all requiring zinc. Loss-of-function mutations of IDE in rodents cause glucose intolerance and cerebral accumulation of amyloid-beta, whereas enhanced IDE activity effectively reduces brain amyloid-beta (refs 4-7) (from abstract at https://www.rcsb.org/structure/2G54) Thus the new marker for Alzheimer disease is insulin, as reported in article with this title:”Glucose Metabolism is a Better Marker for Predicting Clinical Alzheimer’s Disease than Amyloid or Tau”.
 The synthetic crazy expensive monster OZEMPIC (https://pdb101.rcsb.org/global-health/diabetes-mellitus/drugs/incretins/drug/semaglutide/semaglutide) paralyzing human stomachs is based on chemical mutilation of the natural sequences of GLP-1, the one patented by Dr. L. Walensky, husband from Dr. R. Walensky, who introduced the so ‘safe and effective’ Spike synthetic genes… First Ozempic with only the blue being natural:
Now the GLP-1-RGR in 2016 patented sequence from Dr. L. Walensky so similar to Spike2020 (https://www.ncbi.nlm.nih.gov/protein/APN27348):
  HDEF-ERHAEGTFT-SDVSSYL-EGQ------AAKEFI-AWLVKG+RGR   GLP-1+RGR << husband
  +  F E       T +D+  ++ +        AA++ I A    G
  KRSFIEDLLFNKVTLADAG-FIKQYGDCLGDIAARDLICAQKFNG   Spike2020     << wife
  =============
  ^^^^^^^^^^^^^
fragment so needed for SARS-CoV-2 infection!!!!
“Stabilized insulinotropic peptides and methods of use”
That’s the title of that patent filed already in 2011 (https://www.lens.org/lens/search/patent/list?q=US%209296805)
Do we need to wonder why the GLP-1 imitating Ozempic suppose to be so helpful in covid19? Some explanation how it works at: https://pmc.ncbi.nlm.nih.gov/articles/PMC8425441/ with the title “The role of GLP-1 receptor agonists during COVID-19 pandemia: a hypothetical molecular mechanism“. Or just lets throw few more titles:
“ACE2 and SARS-CoV-2 Infection: Might GLP-1 Receptor Agonists Play a Role?“
“Anti-inflammatory effects of GLP-1 in patients with COVID-19“
“Friend or foe? ACE2 inhibitors and GLP-1R agonists in COVID-19 treatment“
There are more drugs based on GLP-1 3 D structure, here another candidate, at: https://pdb101.rcsb.org/global-health/diabetes-mellitus/drugs/incretins/drug/tirzepatide/tirzepatide , the one Mr. Musk is ‘on’, apparently. If you ever really need help with loosing weight, maybe the best is no 1, eat less and only organic, no 2 get enough of all the single amino acids (the blue ones) from which your body will assemble the GLP-1 on its own… There are also resources offering the natural GLP-1 peptide (nonpatented, thus cheap..), mentioned in this interview: https://www.brighteon.com/139f5139-ef1a-496a-8165-26f8e7986016. 
GLP-1 and GLP-2 are parts of larger protein GLUCAGON (https://www.uniprot.org/uniprotkb/P01275/entry) a counterregulatory hormone of insulin, it stimulates insulin release depending on glucose availability and it regulates the glucose levels in the blood. GLP-1 has growth-promoting activities on intestinal epithelium, suppresses satiety and stimulates glucose disposal in peripheral tissues, regulates the hypothalamic pituitary axis by influencing LH, TSH, CRH, oxytocin, and vasopressin secretion. GLP-2 acts from the stomach down to colon, while affecting nutrient absorption, and disposal. GLP-2 as also an intestinal-derived peptide stimulator of small bowel epithelial proliferation. Here the sequences of those two parts from glucagon:
92-128 : GLP-1   HDEFERHAEGTFTSDVSSYLEGQAAKEFIAWLVKGRG
146-178 : GLP-2 HADGSFSDEMNTILDNLAARDFINWLIQTKITD
Walensky’s patent states, quote:”invention provides stably cross-linked insulionotropic polypeptides having superior and unexpected benefits in the treatment of conditions involving abnormal glucose homeostasis, e.g., type 2 diabetes and conditions relating to type 2 diabetes. Such benefits include, but are not limited to, extended polypeptide half-life, enhanced alpha-helicity, improved thermal stability and protease resistance, increased functional activity and pharmacologic properties, improved bioavailability when administered by any route”
The difference between NovoNordisk patent and the entire GLP-1 length is the ‘HDEFER’ sequence which was left out in Ozempic. NovoNordisk has also patents for the GLP-2 related peptides, which overlap with Spike in that important ‘KRSFIEDLLFNKV’section, all summarized below:
HADGSFSDEMNTILDNLAARDFINWLIQTKITD   Novo Nordisk Patent/NPS Pharmaceuticals,
HADGSFSDEMNTILDNLAARDFINWLIQTKITD    GLP-2  /2L63
      HAEGTFTSDVSSYLEGQAAKEFIAWLVRGRG  HUMAN Semaglutide peptide  7KI0
      HAEGTFTSDVSSYLEGQAAKEFIAWLVRGRG  4ZGM GLP_1
HDEFERHAEGTFTSDVSSYLEGQAAKEFIAWLVKGRG  => GLP_1 NATURAL P01275
and this is BLAST alignment of the GLP-2 (ONLY 33 AA’s) with Spike2020:
Query  18   AARDFINWLIQTKIT  32   GLP-2
            + R FI  L+  K+T
Sbjct  813  SKRSFIEDLLFNKVT  827  Spike2020
Query  14   LDNLAARDFI  23
            L ++AARD I
Sbjct  841  LGDIAARDLI  850
Query  5     SFSDEMN  11
             SF +E++
Sbjct  1147  SFKEELD  1153
Query  16   NLAARDFI--N  24
            NL  R+F+  N
Sbjct  188  NL--REFVFKN  196
Query  20   RDFI-----NWLIQTKIT  32
            R FI     N     K+T
Sbjct  815  RSFIEDLLFN-----KVT  827
Query  22    FINW-----------LI  27  GLP-2
             +I W           LI
Sbjct  1209  YIKWPWYIWLGFIAGLI  1225 <
There is another insulin issue in connection with Spike. When searching the https://peptideatlas.org/builds/human/phospho/202204/APD_Hs_all.fasta for PRRAR motif, that peptide shows up ‘>PAp07149871 HDSPDPSPPRRAR‘, which is a part of https://www.ncbi.nlm.nih.gov/protein/Q9BRD0.1 s.c. human spliceosome with 3 identical PRRAR sites and couple of highly homologous to it, the same so frequent FURIN SITE, inserted also in Spike2020:
Query  145  HDTPDPSPRRAR  156  Q9BRD0.1 BUD13  
            + T   SPRRAR
Sbjct  674  YQTQTNSPRRAR  685 Spike2020
Query  116  NRHFRHDTPDSSPRRVRHGTPDPSPRKDR  144
            N  +  D P  +     + T   SPR+ R
Sbjct  657  NNSYECDIPIGAGICASYQTQTNSPRRAR  685
Query  185  SDTSPPRRAR  194
            + T+ PRRAR
Sbjct  676  TQTNSPRRAR  685
Query  228  PRRARHGSS  236
            PRRAR  +S
Sbjct  681  PRRARSVAS  689
that on top of many other highly relevant sections, just few :
Query  579   WPGYRWDG  586
             WP Y W G
Sbjct  1212  WPWYIWLG  1219 <
This BUD13 protein splicing RNA, affects the s.c intron retention while regulating gene expression. Deficiency in BUD13 dampens the interferon 1 response, as result of which macrophages can’t withstand vesicular stomatitis virus (VSV) infection (https://www.cell.com/molecular-cell/fulltext/S1097-2765(18)31030-X and https://pubmed.ncbi.nlm.nih.gov/30639243/). Only recently it was discovered that RNA splicing affects also insulin regulation (https://news.feinberg.northwestern.edu/2020/07/02/new-role-for-rna-splicing-in-insulin-regulation/) via the s.c. clock gene (https://www.genecards.org/cgi-bin/carddisp.pl?gene=CLOCK), playing a central role in the regulation of circadian rhythms. That possibly ties with the developing embryo, without too much light, and the bifidos playing the central role in this process… The clock stands for ‘Circadian Locomotor Output Cycles Kaput’,  and it is very strange that ‘they’ put that word Kaput in this name, which means ‘damaged’ in German…
This clock protein (mouse https://www.uniprot.org/uniprotkb/O08785/entry and human form at https://www.uniprot.org/uniprotkb/O15516/entry) has incredible functions, from rhythms in metabolism and behavior to sleep, body temperature, blood pressure, endocrine, immune, cardiovascular, and renal function. Basically the energy derived from the Krebs cycle of every cell, is divided into all actions, depending on LIGHT, which implies timing during the day/night! Isn’t that the MELTONIN effect on covid related issues???
And it also plays an essential role in cancer: https://www.nature.com/articles/s12276-021-00681-0 . It appears that melatonin promotes adipocyte proliferation by forming a Clock/HDAC3/c-Myc complex and subsequently drives the circadian amplitudes of proliferation genes (https://pubmed.ncbi.nlm.nih.gov/27987529/). The c-MYC cancer connection needs to be kept in mind, for later. 
To close this medley, one mention about the NIH project titled: All of Us, after ~9 years of research, which was to collect genetic and health data from one million volunteers…, changes.
Research Program (previously known as the Precision Medicine Initiative Cohort Program^[1]) is a research program created in 2015 during the tenure of Barack Obama with $130 million in funding that aims to make advances in tailoring medical care to the individual. And now the news from today 10/16/2024: 
“All of Us Program to Delete Genetic Ancestry, Trait, Health Info From Participant Accounts” => so suddenly no more medical care for individual???? Further:
“In an email sent to participants on Wednesday, All of Us said genetic ancestry and trait DNA results will be deleted from their accounts effective Nov. 22.
Health-related DNA test results will remain available as PDFs in an updated system beginning in January of next year, but only if participants log on to view them before Nov. 22. The PDFs, too, will be deleted from participants' accounts at the end of 2025.“
Also, quote (https://www.genomeweb.com/research-funding/all-us-program-delete-genetic-ancestry-trait-health-info-participant-accounts):
“"We know these are big changes to how we share DNA results," the organization wrote in its email to participants. "As a research program, we are always learning and growing. We do our best to listen to our participant partners and adapt to changes in our program. Despite these changes, our vision remains the same: to drive discoveries that lead to better health and provide you with information that matters to you."“
What do ‘they’ know what we don’t AFTER the introduction of the genetically modifying covid injections, which btw, do ‘not work’ at all (https://www.science.org/content/article/missing-immune-cells-may-explain-why-covid-19-vaccine-protection-quickly-wanes)?? 
LAST note about another INSULIN offender:
https://staging1.stetzerelectric.com/wp-content/uploads/Milham-Stetzer-2013-Dirty-electricity-chronic-stress-neurotransmitters-and-disease.pdf
And the promised Dr. Levy’s Protocoll, which he kindly provided to everyone:
++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++
Persistent Spike Protein (PSP) Protocol
Thomas E. Levy, MD, JD
January 31, 2024
The protocols for PSP syndrome (Long-Haul COVID and/or post-COVID vaccine syndrome) are similar for both prevention and resolution, differing primarily in dosing and clinical aggressiveness in the application.
For PSP Prevention and Health Optimization
Super 8 supplementation
[To reduce increased intracellular oxidative stress and optimize intracellular vitamin C levels]:
Vitamin C, 3,000 to 9,000 mg daily
Magnesium chloride, 1,000 to 3,000 mg daily
Vitamin D3, 3,000 to 10,000 international units daily
Vitamin K2, 500 micrograms daily
[To optimize mitochondrial production of ATP]:
Niacinamide 1,000 to 3,000 mg daily
Riboflavin 400 mg daily
Coenzyme Q10, 600 to 900 mg daily
Methylene blue, 25 mg daily
Above supplements are virtually non-toxic, and dosages can be adjusted up (or down) as desired and depending on how well one feels.
For chronic PSP syndrome
Super 8 supplementation, and, depending on availability to the patient:
Any of the bio-oxidative therapies, singly or combined (available at Riordan Clinic, Wichita, KS):
• Vitamin C, 25 to 100 gram infusions (with 25 to 50 mg of hydrocortisone if possible)
• Hydrogen peroxide infusions (0.15% concentration in D5W)
• Ozone autohemotherapy; EBOO (extracorporeal blood oxygenation and ozonation) if possible
• Ultraviolet blood irradiation
• Hyperbaric oxygen therapy (1.5 to 2.0 atmosphere pressures)
Hydrogen peroxide nebulization (3% or less, depending on patient tolerance)
15 minutes daily until clinical resolution
EDTA chelation (CalciumDisodium EDTA) intravenously or a quality oral EDTA supplement, as directed by the treating medical professional
Ivermectin 3 to 6 mg daily and zinc picolinate 50 mg daily
Nattokinase 200 to 400 mg twice daily
D-dimer testing is essential for the optimal clinical management of the patient. It should be 500ng/cc or less. Higher levels indicate increased blood clotting in the body, caused by the persistent attack of the spike protein on blood vessel receptors. Clinical resolution cannot be considered complete as long as this blood test remains elevated.
Many high-quality nutrient supplements can be taken as well. However, these recommendations are advanced as critical baseline components of an effective anti-spike protein regimen. The importance of these specific recommendations, along with their scientific validation, can be found in the resources listed below.
Hydrogen Peroxide Nebulization
https://www.tomlevymd.com/articles/omns20200821/Curing-Viruses-with-Hydrogen-Peroxide:-Can-a-simple-therapy-stop-the-pandemic?
and
https://www.rvr.medfoxpub.com/ (complimentary book)
Ultraviolet Blood Irradiation and D-dimer testing
https://www.tomlevymd.com/articles/omns20230927/Persistent-Spike-Protein-Syndrome:-Rapid-Resolution-with-Ultraviolet-Blood-Irradiation
and
https://riordanclinic.org/2023/11/ultraviolet-blood-irradiation-new-hope-for-chronic-covid/
Bio-oxidative Therapies
https://www.tomlevymd.com/articles/omns20230310/Resolving-Persistent-Spike-Protein-Syndrome
Methylene Blue
https://www.tomlevymd.com/articles/omns20230204/Resolving-Colds-to-Advanced-COVID-with-Methylene-Blue
EDTA, heavy metal toxicity, and Super 8 Supplementation
https://www.tomlevymd.com/articles/omns20231103/Heart-Failure-or-Therapy-Failure?-Toxins-Cause-Cardiomyopathy
Vitamin C synergy with Cortisol (hydrocortisone)
https://www.tomlevymd.com/articles/omns20211211/Vitamin-C-and-Cortisol:-Synergistic-Infection-and-Toxin-Defense
If there is anyone still reading, THANK YOU for SO MUCH patience:)))))))
Wish you a MERRY CHRISTMAS one more time, since you read to this point, with 3 hours of nice music, no classic this time…
or wait, can’t do without it:
                                                              THE END
Literature:
https://pmc.ncbi.nlm.nih.gov/articles/PMC8657738/
https://pmc.ncbi.nlm.nih.gov/articles/PMC7999557/
https://thedermreview.com/gundry-md-polyphenol-dark-spot-diminisher-review/
https://www.nutritionadvance.com/nutrition/top-food-sources-polyphenols/
https://www.lifeextension.com/magazine/2015/6/protect-your-skin-from-age-related-glycation
https://www.sciencedirect.com/science/article/pii/S102194981630179X



The war on human genes, Cholesterol, LNPs and Covid genetically modifying injections, now also in the CRISPED patients.
mejbcart — Sat, 17 Aug 2024 05:48:34 GMT
Update 2/9/25: C15:0 (pentadecanoic acid) is a healthy and essential odd-chain saturated fatty acid, a ‘new’ healthy saturated fat for long-term metabolic, heart, immune, and liver health ,i.e. or healthy aging, for lowering cholesterol level, to be only in milk and its products, yogurt, butter => fight for healthy cows!:) ^18.
Update 9/27/2024: 
DCFPRESS Post
USRTK FOIAs: Links File #1 (embeds)
First, I want to thank the U.S. Right to Know website for their efforts and files shared. Of course, they have done, like others did with the Pfizer documents, a great deal for all normal people and investigators, paving the way to see what goes on inside our government via their emails…
Read more
2 years ago · 2 likes · Jason Powers
Update 10/1/2024: Reminder, Mod-E-RNA and Pfizer covid injections contain CHOLESTEROL. Here some knowledge by Robertson and Burnett in experimenting with tumour-grafted rats, who showed that intravenous injections of cholesterol in sodium oleate cause the tumours in the injected animals to grow twice as fast as in the controls, all the rats having been grafted at the same time and with the same tumour (ROBERTSON, T. B. and BURNETT, T. C. “The influence of lecithin and cholesterin upon the growth of tumours.”  Jour. Exper. Med., 1913, xvii, 344-352.)^17
 With so many critical hot summer ‘24 events, drops in, drops out, official lack of proof for women identification (according to the Olympics organizer Thomas Bach), with contradictory news everywhere, maybe the few left out tired readers show some interest in that tiny, so sticky innocent, cholesterol..? THANK YOU for choosing this sub-stack, even after a very LONG pause, which now will be substituted with a long post;). Before anything else though, just want to remind everyone this speech, which was suppressed on every single MSM, a speech very similar to the one RFK Jr. gave few weeks before that Aug 2020, in Sacramento CA, a speech you won’t find anymore, anywhere, so lets go back at least to the Berlin 2020 speech:
If people had listened to it, or read the book ‘The Real Anthony Fauci‘ by RFK Jr., and took into their hearts all the contents, we wouldn’t be here, where we are today… 
Some history first. Julian Huxley, British evolutionary biologist, eugenicist and director of the International Union for Conservation of Nature/Unesco(United Nations Educational, Scientific and Cultural Organization), aligned with Rockefeller Foundation, said in 1947:
‘we’ll be improving the genetic quality of the human population through selective breeding, the population has to be controlled and the unfit have to go’, which partly explains where we are today:
On July 22nd ‘24, an email send out by MIT Technology Review announces a Roundtable titled: “CRISPR Babies: Six years later“ with a short introduction, quote:
”Gene-editing can correct or improve the DNA of human embryos, essentially opening the door to ‘technological evolution’ of our species. But in 2018, a premature attempt to use gene-editing led to a prison term for the researcher involved.” 
Where do the gene therapies stand today? There are many, many extremely rich people, who finance the Creators Overwrite, while changing and mixing up the genetic footprint of what was given to us by God, so let’s take the recent actor on the political scene, JD Vance. Thanks to the illegal gene therapies of the War(p) S(p)eed, the amount of ‘those in need’ (injured) raises with every day, and here is where some of Vance’s endeavors come in: “Kriya Announces Exclusive License and Collaboration Agreement with Everads to Advance Gene Therapies for Prevalent Diseases in Ophthalmology Including Geographic Atrophy“ and from its CEO quote: ”We are excited about the potential to advance a gene therapy that blocks both complement C3 and C5, which are validated biological targets for the treatment of geographic atrophy,” said Shankar Ramaswamy, M.D., Co-Founder and CEO of Kriya.” And no, geographic atrophy is not loosing weight depending on where you stand on the planet earth… And who is the gene specialist Shankar? A younger brother from Vivek, friend of JD Vance.  Half a year after introduction of the illegally ‘approved’ genetically modifying covid injections:”Battelle (please remember that, or read Leonard G. Horowitz books), investors including J.D. Vance, launch gene therapy startup, AmplifyBio” (https://www.dispatch.com/story/business/2021/05/05/battelle-investors-including-j-d-vance-launch-gene-therapy-startup/4935970001/). What does the AmplifyBio do? The answer is in the title of this link, https://www.amplify-bio.com/amplifybio-and-rnav8-bio-announce-strategic-partnership-to-support-mrna-therapeutic-developers-from-sequence-design-to-gmp-manufacture/ . Two important quotes from it:
-”Together (AmplifyBio+RNAV8), this partnership creates a one-stop shop for mRNA sequence/chemistry engineering, in vitro performance screening, in vivo (diseased vs. healthy) model data generation, and mRNA production volumes ranging from micrograms to 100+ grams.”
-”Comprising a team of experts hailing from prominent backgrounds at Moderna, Pfizer, and Resilience, the company stands at the forefront of innovation in this field.”
Isn’t that a continuation of Warp Speed sickening the entire humanity? Check out this, to see the real truth of what happened in the last 4.5 years(!!!): https://www.brighteon.com/a5b31f9e-b523-4171-b875-1d795cbfbcbb
or this professional collection of major political facts, can equally help in understanding the bigger picture:
Resilience, the manufacturer of Mod-E-RNA shots was covered here:  
All what one needs to know, are the CIA ties in all of it, extremely well covered in the mentioned RF Kennedy’s Jr. book, and also covered in this post:
 
How does the cholesterol fit into that GMO’s covid crime scene?
One would think, the so demonized cholesterol, the biggest enemy of all, not a protein, not a genetic material would escape all of the above. Since it is synthesized enzymatically by >20 enzymes in the liver (diet delivers ~20% of daily cholesterol needs), with each of them expressed by a GENE, it does not escape anything. Cholesterol as the most vital rigid membrane lipid of all (https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2013.00031/full), ~(25-30)% of which builds the dry mass of the brain, serves as precursor for sex hormones, for all fat soluble vitamins, Vit D including (this implying everything related to the immune defense of the human body), it is located in every single cell membrane, and all of it is genetically driven (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474947/). That does not even include all the genes involved in cholesterol transportation and degradation (https://www.pnas.org/doi/epdf/10.1073/pnas.96.20.11041). How to find all those involved genes??? By genetic screening of specific cells and later on targeted controlling and monitoring the levels of specific short length RNA types (https://www.cell.com/action/showPdf?pii=S1550-4131%2809%2900157-0). If you monitor RNA’s, because they imply, influence and result in genetic control, can those short internal HUMAN mRNA signals be affected by the CDC/FDA/Fauci et al. mandatory injected covid19 Spike synthetic mod mRNA? What will happen when you CHANGE these RNA’s? The entire information of the genetic control is a ‘reset’, a ‘great’ one indeed…. 
Cholesterol can do so much more. It binds to bacterial toxin’s via just single dipeptide Thr-Leu (TL) capable of lysing an entire cell, all described in article titled “Only two amino acids are essential for cytolytic toxin recognition of cholesterol at the membrane surface“ (https://www.pnas.org/doi/10.1073/pnas.0911581107 ). How many of the TL-dipeptides are embedded in the synthetic, patented Spike sequence? SIX, which makes the impression of Spike being a well designed cholesterol catcher, similar to the HIV-1 envelope glycoprotein precursor gp160, with equally SIX ‘TL’ dipeptides.
There is a link between heat shock proteins (HPSs) and cholesterol. HSPs affect folding of many other proteins in a temperature dependent manner affecting cancer, neurodegenerative, cardiovascular, and autoimmune diseases. Everyone has some antibodies to some of the HSPs, like to Hsp60, Hsp70, but we also have some antibodies to cholesterol (https://pubmed.ncbi.nlm.nih.gov/15488946/). Strangely, during HIV-1 infection the Hsp70 and cholesterol antibodies go over the roof (https://pubmed.ncbi.nlm.nih.gov/15488946/). The same Hsp70 has a strong affinity towards negatively charged phosphatidyl serine lipids, but only on membranes of cancer cells, not the normal ones (https://www.nature.com/articles/s41598-023-46131-x). And all of it is cholesterol dependent. Despite of all of this, cholesterol is an ‘evil doer’, which the Global Center for Health (In?)Security at: https://www.unmc.edu/healthsecurity/transmission/2023/05/30/covid-19-can-cause-new-cholesterol-problems-what-to-know/
decided to connect with a ‘global warning style’ message, quote: “They found that unvaccinated people who had been infected with SARS-CoV-2 were significantly more likely to develop high cholesterol and other unhealthy levels of blood fats than people who had not been infected.“??? It almost sounds like the SARS-CoV-2 virus could be put on the McDonald’s menu list…  
It is also the very first time, that ‘disease preventing injections’ of covid19 Pfizer and Mod-E-RNA genetically modifying concoctions, have cholesterol^3 on their ingredients list. The only other injecrtion material with cholesterol in it is Shingrix, which replaced Zostavax in Nov 2020 ( https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf)... So ‘somehow’ the new covid mod mRNA based injections now suppose to protect from high cholesterol, by not giving you covid19, while having the cholesterol in them..? Imagine the despair of those cardiologists who might need to end their statins prescriptions. And let’s not mention here EU’s established guidelines for statin drugs, which the Germans ‘HEaLth minister’ now intends to put on drugs list of 5 years old children. There is no mention that sugar consumption correlates with heart diseases more than cholesterol,  that smoking chemicals (NOT nicotine though…) and high blood pressure does the same. Just insane, and evil.
Are there maybe other connections between the universally injected synthetic Spike genes embedded into a matrix of novel lipid-nanoparticles and cholesterol??  The Sep 2021^2  study, titled “Cholesterol Hinders the Passive Uptake of Amphiphilic Nanoparticles into Fluid Lipid Membranes“, stated: ”membrane cholesterol, at biologically relevant concentrations, hinders the molecular mechanism for passive NP penetration within fluid bilayers, resulting in a dramatic reduction in the amount of NP incorporated.”, where NP stands for synthetic engineered nanoparticles… Doesn’t it indicate, maybe,  that the more cholesterol the better protection from nano’s? Thus, could we say, human body essential building block, cholesterol, is not so good for the gene therapies to work optimally because it functions as a stronger barrier against the nanos cell membrane penetration and thus gene delivery? At least this one is sure, cholesterol modulates the NPs abilities (https://www.nature.com/articles/s41565-023-01455-7) thus looking into ‘cholesterol business’ makes sense.
Let’s switch for a moment to N. Harraris’ way of thinking, so to make the universal illegal covid gene therapy more effective, let’s give the foreign non-human Spike genes, we’ll inject into everyone, some cholesterol, and take it away from the real humans… That’s absurd (!), yet countless scientific groups, claim that statin drugs, that usually block the cholesterol production in the liver, thus represent neurotoxins due to prevention of continuation of brain regeneration, were beneficial for ‘covid19’ disease! Just few examples, out of many: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233054/ and one more with only ‘in-hospital conditions’: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463212/ and one group  with ‘yes but no’ strategy: https://www.nejm.org/doi/full/10.1056/NEJMoa2309995. Countless publications link covid19 with acetylcholine and its related enzymes and many confirm the protective role of choline (eggs as the no 1 source) during covid-19 disease (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532804/ or  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775685/), and yet, the statins, essential in affecting neurotransmission, are the everydays’ bread of ‘health care’ system, in particular in covid times... There are many health professionals who question ‘cholesterol hysteria’, among them is a danish  researcher Uffe Ravnskov, who says ““The cholesterol campaign is the greatest medical scandal in modern time“. His lifelong work with lot of precious resources is summarized at http://www.ravnskov.nu/uffe/ and it only confirms what was just recently published by Dr. Mercola at: https://articles.mercola.com/sites/articles/archive/2023/05/27/just-say-no-to-statins.aspx 
Linus Pauling was known for his unified theory of cardio-diseases in which vitamin C deficiency leads to body using cholesterol taking over the role of collagen, normally used to heal the blood vessels. There is another great resource going more in depth on the VitC/statins/cholesterol topic: https://jeffreydachmd.com/2016/12/linus-pauling-heart-disease-prevention-with-vitamin-c/ , and it describes the NIH role in this coverup… Little shorter version of the link between lipoprotein A and VitC, challenging the ‘cholesterol theories’ of heart diseases by Pauling, can be found at: https://www2.lbl.gov/Science-Articles/Archive/pauling-and-vitamin-c.html
Cholesterol suppose to be involved in prion disease while playing a role as cofactor in the conversion of the naturally present in brain prion protein (PrP)  into its pathogenic form (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871914/). With that 2022 study, here comes a new solution, in 2024 (https://www.science.org/doi/10.1126/science.ado7082): “Brainwide silencing of prion protein by AAV-mediated delivery of an engineered compact epigenetic editor“ with the following quote:”This study represents the ﬁrst demonstration of AAV-mediated delivery of an epigenetic editor that can programmably methylate DNA in the brain for durable, potent silencing of a target gene”. Further “When coupled to a prion protein–targeting zinc ﬁnger domain and delivered to the mouse brain through AAV, CHARM methylates the prion gene promoter and achieves up to 80% brainwide reduction in neuronal prion protein, far exceeding the minimal reduction required for therapeutic beneﬁt.“ The CHARM stands for Coupled Histone tail for Autoinhibition Release of Methyltransferase, and AAV for Adeno-Associated Virus. While cutting and pasting the major DNA ‘editor’ histone H3, the science geniuses actually reduced only the NATURAL PrP protein without indicating the mental/emotional/ status of their experimental molestation object, the mouse… The ‘epigenetic editor’ is a new name, again, like covid ‘vaccines’, for GENE THERAPY…
Who has this key to GENETICALLY get rid of prions? BROAD Institute and MIT, the main players in covid genetically modifying injections, i.e. the ones, who contributed to the problem in the first place.
The many faces of cholesterol and the covid thrill do not end here, ~10 years ago chinese scientists found out that ivermectin binds to the Farnesoid X receptor (FXR) responsible for cholesterol homeostasis (https://www.nature.com/articles/ncomms2924). Ivermectin decreased serum glucose and cholesterol levels. And in 2023 the beloved Welcome Trust and Oxford Uni members determined that FXR controls the ACE2 transcription thus must have direct effect on SARS-CoV-2 infection (https://www.nature.com/articles/s41586-022-05594-0). What a cascade of events, ivermectin controls FXR, FXR controls ACE2, SARS-CoV-2 depends on them all, and now we got the metabolism-modulating drugs repurposed for COVID-19, like statins and metformin (https://www.nature.com/articles/s41392-023-01510-8), without ever mentioning the universal cure for it all, ivermectin:
2nd Smartest Guy in the World
Ivermectin for Parkinson's Disease - MS, Stroke, Chronic Pain, Anxiety, Depression, and Schizophrenia? Modulated through P2X4 Receptors
At the end of this article there will be a synergistic protocol which may more potently treat all of the various diseases featured in the following article…
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2 years ago · 126 likes · 38 comments · 2nd Smartest Guy in the World
In the meantime we find that “Serious errors plague DNA tool that’s a workhorse of biology“ (https://www.nature.com/articles/d41586-024-02280-1) and everything else related to Gene Therapies applied without human consent, being dangerously redirected towards a new phenomenon, birds with no symptoms of coughing or sneezing, landing on cows, later on humans giving rise to the new covid-2.0: https://expose-news.com/2024/07/11/is-another-pandemic-is-being-orchestrated/. This time it is equally serious: BARDA gives Mod-E-RNA $176 million to support late-stage development for an mRNA-based influenza vaccine (https://investors.modernatx.com/news/news-details/2024/Moderna-Receives-Project-Award-through-BARDAs-Rapid-Response-Partnership-Vehicle-Consortium-to-Accelerate-Development-of-mRNA-based-Pandemic-Influenza-Vaccine/default.aspx), Nature article announces that EU bought already 700,000 doses of a flu vaccine manufactured by UK biotech CSL Seqirus, with the option to buy another 40 million (https://www.nature.com/articles/d41586-024-02237-4), and then there is that very questionable member of the birdflusummit who in a phone request for more information, shows, that she knows nothing about the bird flu: https://birdflusummit.com/ in Oct24. The old CSL news from 2022 which describe their product: https://newsroom.csl.com/2022-10-05-CSL-Announces-Positive-Preclinical-Data-for-Self-Amplifying-Messenger-RNA-sa-mRNA-Influenza-Vaccine-Candidates might point to the smiling Bill Gates face while talking about the next one… Is that what EU bought already, self amplifying mRNA? The covid19 story of the last 4.5 years indicated that the real issues started AFTER starting the applications of covid genetically modifying injections, and this time, it shall never end..? Just in case the science geniuses will come out with SELF-amplifying mRNA of Hemagglutinin (https://www.uniprot.org/uniprotkb/O92929/entry), which probably will be the mass murder, one has to look at its amino acid sequence and its conserved motif in HIV-1 and  partly in SARS-COV-2 Spike. and what one can see is disturbing, to say the least:
Query  312  PLTIGECPKYVKSNRLVLATGLRNTPQRERRRKKRGLFG  350 O92929
            P+  G C  Y             N+P+R R    + +  
Sbjct  665  PIGAGICASYQTQT---------NSPRRARSVASQSIIA  694 <==Spike FURIN SITE
a Spike homolog fragment in H5N1 is ~150 residues long(!!):

Query  23   YHANNSTEQVDTIMEKNVTVTHAQDILERTHNGKLCDLNGVKPLILRDCSVAGWXLGNPM  82
            YH NN +      ME    V  + +          C    V    L D         N  
Sbjct  145  YHKNNKSW-----MESEFRVYSSANN---------CTFEYVSQPFLMDLEGKQGNFKNLR  190

Query  83   CDEFLNVPEWSYIVEKTSPAN---DLCYPGHFNDYEELKHLLSRIN--HFEKIQIIPKSS  137
               F N+  +  I  K +P N   DL  P  F+  E L  L   IN   F+ +  + +S 
Sbjct  191  EFVFKNIDGYFKIYSKHTPINLVRDL--PQGFSALEPLVDLPIGINITRFQTLLALHRSY  248

Query  138  WSNHDASSG--VSSACPYLGRSSFFRNVVWLIKKN  170
             +  D+SSG    +A  Y+G   + +   +L+K N
Sbjct  249  LTPGDSSSGWTAGAAAYYVG---YLQPRTFLLKYN  280
and BLAST won't do it, again, so with no shifts, by hand, the fragment binding fats, like in the Spike, the cluster of cysteines at its C-terminal, every one conserved: 
GLSLWM---CSNGSLQ-CRICIYFCEF <= H5N1
 LCC-MTSCCS--CLKGCCSCGSCCKF <= SARS-CoV-2 Spike
all these similarities are extremely worrisome, given that SARS-CoV-2 is positively stranded RNA corona-virus, and H5N1 negatively…. What’s the implication of that??? 
BUT the last homology indicates at least this one (https://pubmed.ncbi.nlm.nih.gov/35336938/): “Identification of SARS-CoV-2 Spike Palmitoylation Inhibitors That Results in Release of Attenuated Virus with Reduced Infectivity“, that the saturated fat palmitate is a good start, the best possible the ascorbyl palmitate version, supporting the cell membranes with the fat soluble Vit C….
With the consequences of the past not even digested properly yet, VAERS system (https://www.medalerts.org/vaersdb/index.php) reports only 2 cases of prion disease after covid injections, one of then was fatal. Due to multiple names for one and the same or related disease (deceptive strategy) there are also ‘93 cases where Vaccine is COVID19 or COVID19-2 and Symptom is Creutzfeldt-Jakob disease’, 53 of which were fatal!!! That’s >50% fatality rate. This post below summarizes the cause of the covid crime related to just one of the diseases the gene therapies cause, but it does not mention that there is already a solution for the problem, by the same players, which indicates, that everything around covid injections is and was a PLAN, a PREMEDITATED MURDER.
2nd Smartest Guy in the World
UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases
The genetically modified humans are suffering from VAIDS. Perhaps the single most horrifying feature of these slow kill bioweapon “vaccines” is found in the prion disease symptom of VAIDS that is transmittable. This latest communicable mis-folded protein disease may not just spread through, say, intercourse, but, rather, far more worryingly, it may be…
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3 years ago · 183 likes · 68 comments · 2nd Smartest Guy in the World
Once again, both Pfizer and Mod-E-RNA covid19 gene based injection materials contain cholesterol in their LNP composition^3..* 
A 2018 study (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984996/) titled “The Chemical Potential of Plasma Membrane Cholesterol: Implications for Cell Biology“ measured for the first time the chemical potential of the membrane bound cholesterol and related its increased chemical potential to the activation of transcription factor STAT3. This very same factor affects the pathogenesis of covid19, according to https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937040/, https://pubmed.ncbi.nlm.nih.gov/34626364/ and many more.  The 2020 article at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545020/, indicates that STAT3 phosphorylation of one of its serines is the cause of the covid-19 pathogenicity (https://www.nature.com/articles/s41598-023-46628-5). What else the STAT3 gene is involved with? It is activated by a member of a large family of phosphatidylserine (PS)-dependent kinases (https://pubmed.ncbi.nlm.nih.gov/17583567/), which also contribute to many cancer types, among other skin cancers..
When we talk SARS-CoV-2, we need to keep an eye on HIV-1 too, alone due to the repeatable character of the ‘covid19 infections’. So, generally, is HIV-1 involved in cholesterol issues? Yes, it is, NIH admits it at:  https://hivinfo.nih.gov/understanding-hiv/fact-sheets/hiv-and-high-cholesterol. Is STAT3 involved in HIV-1? Yes, it is, here a AAAS report at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514100/ titled “Insertional activation of STAT3 and LCK by HIV-1 proviruses in T cell lymphomas“. How about Monkeypox, any cholesterol connection? Yes, there is, just one example at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10751291/. And Influenza, the most recent crystal ball prepared like covid19, by BARDA et al.? Also here, yes, there is, described in 2022 for example at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513517/ and titled “Modulating cholesterol-rich lipid rafts to disrupt influenza A virus infection“. 
 Oh, actually, just recently, the autopilot changed the direction, WHO decided to choose the Monkeypox as the next threat, again..
So why all these viral infections are so cholesterol dependent? Because many types of both DNA and RNA viruses have their GENETIC material protected by LIPID bilayers which have to fuse with human cells, thus interact with human cell membranes, which contain the essential cholesterol, which in turn regulates fluidity, dielectric properties, permeability, i.e. function of the natural human cellular borders. The average cell membrane contains 10-30% of cholesterol, the membranes within the cell (endoplasmic reticulum, Golgi apparatus, and mitochondria membranes) have less cholesterol, i.e. <10%, that’s in order to facilitate cholesterol sensing and homeostatic feedback.. The cell types with high cholesterol level of ~50% are red blood cells and the myelin membranes of Schwann cells isolating nerve axons, in which the ratio of cholesterol/phospholipids (PL) is >1. The highest level of Cholesterol is in eye lens (that’s why its UV spectrum is important), >50%. At ~66% of cholesterol content, crystals form, which can be seen in old individuals and in atherosclerotic arteries. The higher the cholesterol level in the membrane, the higher its hydrophobicity and rigidity ( https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645210/ ) and thus higher protection from synthetic lethal nanos.
One of the first known extremely cholesterol-lowering dipeptides was the in 2015 described simple Phenylalanine-Proline (FP in single amino acid code) (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469013/). How many of those dipeptides are in the Spike sequence encoded by the synthetic genes injected into billions? FOUR ‘FP’ cholesterol lowering dipeptides are being build from single amino acids phenylalanine (F) and proline (P) for the production of every single toxic patented Spike. It is almost as if the universally injected Spike production on its own supports the synthetic statins, once the Spike gets degraded back into those peptides.
STAT3 has a huge list of functions (https://www.uniprot.org/uniprotkb/P40763/entry), including synaptic plasticity and cognition, thus was found to be involved in Alzheimers (https://pubmed.ncbi.nlm.nih.gov/33859760/ , https://pubmed.ncbi.nlm.nih.gov/30617153/). When a mouse is missing one of the isoforms of STAT3 and apolipoprotein E, it ends up with an enhanced atherosclerotic plaque formation (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771242/). Further the ApoE protein transporting lipids in plasma and interstitial fluid, together with few other factors is also deeply involved in Alzheimers, and in the so called exotic ‘episotic memory’ issue. One of the best known experts on Alzheimers, Dr Rudolph E Tanzi (Harvard) worked for decades on genetics involved in that brain disorders. The following publications (available at https://scholar.google.com/citations?user=2Qlrv_cAAAAJ) by Rudolph E Tanzi point to the ‘other factors’ accompanying ApoE in episodic memory:
-Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. S Barral, T Bird, A Goate, MR Farlow, R Diaz-Arrastia, DA Bennett, Neurology 78 (19), 1464-1471 also
-Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes G Jun, AC Naj, GW Beecham, LS Wang, J Buros, PJ Gallins, JD Buxbaum. Archives of neurology 67 (12), 1473-1484. 2010
Is covid19 involved in any of those APOE ‘episodic memory’ involved genes?? Here a small list of the studies and where they are located:
-”Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family”(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014500/)
-”ApoE4 associated with severe COVID-19 outcomes via downregulation of ACE2 and imbalanced RAS pathway” (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910247/)
-”APOE interacts with ACE2 inhibiting SARS-CoV-2 cellular entry and inflammation in COVID-19 patients” (https://www.nature.com/articles/s41392-022-01118-4)
-CLU→”Serum Clusterin Concentration and Its Glycosylation Changes as Potential New Diagnostic Markers of SARS-CoV-2 Infection and Recovery Process”(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11049940/)
-PCALM→”Paradoxical relationship between proton pump inhibitors and COVID-19: A systematic review and meta-analysis” (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058681/)
-BIN1→”BIN1 rs744373 SNP and COVID-19 mortality” (https://pubmed.ncbi.nlm.nih.gov/33521641/ )
If all the genes related to Alzheimers (oh, FDA blocked the ApoE4 genetic tests for early Alzheimers detection, because it was not a drug, how strange, and covid19 PCR tests are?) were investigated by Dr. Rudolph E Tanzi, and now they all also relate to the first universal gene therapy in form of covid19 injections, will there be a continuation of the scientific work by Dr. Tanzi?  He connected Alzheimers with cholesterol and plaque buildup, he works in the same place where Dr. Rochelle Walensky does, and he does not mention in a single article among others the Alzheimers MERCURY or the ALUMINUM connection, but hey, he just published:
Gene therapy for CNS disorders: modalities, delivery and translational challenges. J Gao, S Gunasekar, Z Xia, K Shalin, C Jiang, H Chen, D Lee, S Lee. Nature Reviews Neuroscience, 1-20, 2024.
And will this plan fix the covid19 related episodic memories, lets be honest, most probably caused in part by the universal covid19 gene therapy injection and its shedding, also called ‘long covid19’? The german Dr. Tillenburg has the same opinion (https://report24.news/dr-tillenburg-long-covid-nur-ein-versuch-von-nebenwirkungen-der-impfung-abzulenken/). Just 2 reports on the memory issues during covid19 infection:
-”Episodic long-term memory in post-infectious SARS-CoV-2 patients.”(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598275/)
-”Rapid vigilance and episodic memory decrements in COVID-19 survivors”(https://pubmed.ncbi.nlm.nih.gov/35128398/)
Well, time will tell if the episodic memories, like ‘what did I want here?’, ‘where did I put it again?’, ‘is it mine or..?’, ‘where am I?” will disappear, even in case of the so fall prone Joe... The above could explain Biden’s bizarre 'freezing' episodes, Fauci’s et al. sudden memory loss in all the hearings, all in regard to details of covid19 operation. As a side note, was it a coincidence that the only two, so famous US presidential covid injected candidates, one of which isn’t any more, didn’t want the 3rd legitimate candidate, RFK in their debate?? Please, judge for yourself the quality of the answers to the same questions, by RFK, Jr.:
https://x.com/RobertKennedyJr/status/1806462171892895808
The mentioned APOE protein exists in few forms in human bodies which differ by just few amino acids, yet they play an essential role in specific diseases. That’s what official world data base on proteins states about one out of the three isoforms:”Thus APOE*4 gene dose is a major risk factor for late onset AD (Alzheimer Disease) and, in these families, homozygosity for APOE*4 was virtually sufficient to cause AD by age 80. The mechanism by which APOE*4 participates in pathogenesis is not known” (https://www.uniprot.org/uniprotkb/P02649/entry). What are the differences between APOE-4 and APOE-2? According to Prof. Boyd Haley (https://emeramed.com/boyd-haley-phd-curriculum-vitae/) people with APOE-2 isoform never have AD and the only difference between the two are cysteines in APOE-2 replaced with two arginines in APOE-4. The cysteines in APOE-2 are known to bind mercury (Hg), while arginines can’t. Prof. Haley was not able to get any NIH grants which would allow him investigating the mercury involvement in the Alzheimer disease while looking into this APOE-2,4 issue. The official explanation for that was always dodged. In the meantime EU team of scientist publishes “Mercury Ion Binding to Apolipoprotein E Variants ApoE2, ApoE3, and ApoE4: Similar Binding Affinities but Different Structure Induction Effects“ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404194/) and say quote “Hg(II) ions bind all three ApoE variants with approximately the same binding affinity, around 4–5 μM. This indicates similar binding sites with similar binding ligands in all protein variants.“ Thus no mercury involvement in Alzheimer, in contrary to what Prof Haley says for years! What does the EU team is using in order to determine whether Hg binds or not? Fluorescence and CD spectra, both sensitive only to global structural changes, nothing with absorption of heavy metal. So while the difference in isoforms is only Cys→Arg exchange in 2 positions, which the study says do not bind the Hg in both forms, instead histidine, still the question is why only the cysteine containing isoform is free of AD, exactly the isoform which contains cysteines? The histidines binding the Hg are both on the same positions in the pro-AD and non-AD patients, thus all this in fact indicates, Hg is not involved in AD… How clever. Also a new phenomenon is being introduced here namely, quote: ‘the differences in structure induction’ between the three ApoE variants might conceivably be connected to the APOE-ε4 gene being a risk factor in mercury intoxication… That’s a 2022 publication, where NOTHING in science makes sense any more. Equivalent to saying a 16-24 piece of DNA can detect infection caused by a virus consisting of 30,000 other pieces and that only in one of its components, because the PCR method doesn’t detect the lipids, proteins, metals, the water, all in a virus, normally!
It is literally a shame to be a ‘life sciences’ scientist, in particular in med-I-cin-e, ever since 2020…. 
Myeloperoxidase (https://www.uniprot.org/uniprotkb/P05164/entry) can influence the oxidation status of the LDL’s and it is equally capable of loosing its binding partner iron (Fe) to mercury (Hg). It was known for a long time, that oxidation of fats, lipids is influenced by chelating agents: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC345326/pdf/pnas00613-0283.pdf and that this process involves immune system (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC304787/) and it is connected with the earliest well-defined lesion in atherogenesis. 
The war on cholesterol goes even into the chicken and eggs business, putting the cholin, the dietary cholesterol supply, in danger. It is thus not only because of the potential H5N1:
Arkmedic's blog
One Flew over the Chickens' Nest
A private government report obtained this week in response to questions over the decision to kill over 500,000 chickens in Victoria, Australia shows that the people making the decision had no verifiable evidence of a high risk infectious outbreak. The chicken farms that were claimed to be infected were so distant from any possible bird source that it …
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2 years ago · 369 likes · 154 comments · Dr Ah Kahn Syed
Cholesterol structure in comparison of what Mod-E-RNA or Pfizer throw into their formulas looks following:
Please look above at the cholesterol and now at the testosterone and estrogen below:
and now at the pathway of testosterone production, from cholesterol (!)_
 remember the direction of these arrows, meaning,  the amount of testosterone is cholesterol dependent(!). Further down the line there is also DHEA and thyroid hormones, everything about human energy. And below just to throw in, how hydrogenated fats look like, in comparison with cholesterol (https://en.wikipedia.org/wiki/Fat_hydrogenation):
Cholesterol’s UV spectrum, ‘proceeds’ DNA/RNA/proteins in its wavelength absorption:
  
That above spectrum alone allows one to imagine a cellular cholesterol fortress surrounding all the essential building blocks of every cell and guiding those extremely energetic photons towards other pi-converting, properly positioned cell compounds, with the healthiest cells emitting the least amount of biophotons all the way down around (350-360)nm…. 
Over the years the officially ‘recognized as good’ cholesterol levels went from 280 or less, as normal, to 250, then to 220, now in 2024 the ‘new normal’ is ~200mg/dl, and according to some real sick fanatics, it should be even much less than that.. How about zero..? Since function of human livers didn’t change in those years, at least theoretically, sizes of human brains didn’t change/shrink, hopefully, there is a reason why these new cholesterol limit values are becoming constantly lower, and lower, and lower… This page https://www.ahajournals.org/doi/pdf/10.1161/CIR.0000000000000624 lists the names of MD’s, who made these guidelines and which drugs/statin manufacturers, among others Merck and Pfizer, possibly affected ‘their opinion’….
Statin drugs are not only neurotoxins but on top of it antibiotics, according to Dr. Thomas Lewis lectures (Harvard). His most recent post at: 
Thomas’s Substack
Cholesterol Fun Facts - 2
My mentor at Harvard Medical School was decades ahead of his time 20 years ago. And, sadly, what he knew and conveyed to me still puts him in the lead even though he is long retired…
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6 months ago · 9 likes
explains more.. There are natural good antibiotics, but also bad ones, like glyphosate which kills only special bacteria^1 leaving sometimes in peace the really bad ones, like the endotoxin producing strains, or diminishing the good Lacto and Bifido species. Also according to Dr. Lewis, the no 1 condition leading to mortality due to low cholesterol are the s.c. mood disorders ending in ‘violent deaths’, suicides.. In addition, the underlying infections in Alzheimers, are frequently connected to the presence of certain pathogens, 3 in particular: Herpes virus, Chlamydia Pneumonia and Spiroki. Judith Miklossy in her 2016 study at https://pubmed.ncbi.nlm.nih.gov/27314530/ titled “Bacterial Amyloid and DNA are Important Constituents of Senile Plaques: Further Evidence of the Spirochetal and Biofilm Nature of Senile Plaques“ points actually to the disease caused by presence of foreign DNA in human brain. That’s what happened in 1944 when Avery, MacLeod and McCarty, Rockefellers fellows, discovered how to transform a mixture of 2 types of pneumonia bacteria, one living type and one dead type, into just one type. All what was needed was to add the gene from the dead bacteria into the culture of the living ones, in order to transfer the living type into the dead type. Shocking but true, and T. Avery went unnoticed in the history for his discovery. Isaac Asimovs book ‘The Genetic Code’ describes these historical facts of molecular biology/genetics. ‘So what are the covid Mod-E-RNA and Pfizer shots again??? FOREIGN Genetic material containing TRANSLATION, affected by TRANSFORMATION information. The question is, transformation of humans into WHAT??? Genetic aspect of living nature is grounded on every specie having its own ‘footprint’, if left untouched, that footprint prevails, changing its appearance depending on the environment, but mixing different footprints of different species, that’s where eugenics comes in.
It is unfortunate that Alzheimers’ research money is favoring mainly plaque/amyloids related reasoning (being only diagnostic markers of the AD disease) leaving out some of the true actors on the AD scene, to comedians:  
It is only little bit unsettling to hear from MIT researchers (again..) about their cell’s study^4 in which they report cholesterol-metabolising bacteria from Oscillibacter species, which encode the conserved cholesterol-metabolizing enzymes, lowering its levels and thus linking its absence with Cardio Vascular Disease. Bugs, good for the heart but what about the brain???  Maybe no more needed, and Elons chips instead?? 
So we know statin drugs lower VitK2 amounts, lower Testosterone, increase risk of type 2 diabetes, lower CoQ10, raise liver enzymes, lower the energy level, lower DHEA, worsen memory, increase shingle risk and also increase risk of erectile dysfunction, and since so many people are ‘on them’ while in the same time immense number of people have cardiovascular issues, now comes a solution^5: “How Gene Editing Could Help Solve the Problem of Poor Cholesterol“! Who owns the best-seller called lipitor? Pfizer. In the meantime all the good news about statins and covid19 were crashed by this short summary with 18 supporting citations: https://www.bmj.com/content/368/bmj.m1182/rr-21. It’s final sentence:”There are therefore good reasons to stop statin treatment of patients with severe Covid-9 infection, also because at least 20 statin trials have been unable to lower mortality with statistical significance (7) and because more than 20% of statin-treated people suffer from serious side effects (6,7).” Science is never settled, that’s for sure.
Despite of the huge statin dilemma, fraud actually, New Zealand got its first ‘edited’ patient^6 in 2022, a case reported in article titled “Edits to a cholesterol gene could stop the biggest killer on earth“!! A killer which is essential for brain survival, for every single cell in the body? Who is behind it? US biotechnology company Verve Therapeutics, which injected a version of the gene-editing tool CRISPR in order to modify a single letter of DNA in the patient’s liver cells. Sekar Kathiresan, is the geneticist who started Verve three years ago and is the company’s CEO, the same who worked at Broad Institute in Cambridge, Massachusetts, on heart issues…  Verve’s plan is to test it on much more people. What the article says is, quote:
”One reason Verve’s base-editing technique is moving fast is that the technology is substantially similar to mRNA vaccines for covid-19. Just like the vaccines, the treatment consists of genetic instructions wrapped in a nanoparticle, which ferries everything into a cell.” WHAT? The ‘gene editing’ of now real humans is substantially similar to covid 'injections??? 
Further the article states:
“While the vaccine instructs cells to make a component of the SARS-CoV-2 virus, the particles in Verve’s treatment carry RNA directions for a cell to assemble and aim a base-editing protein, which then modifies that cell’s copy of PCSK9, introducing the tiny mistake.  In experiments on monkeys, Verve found that the treatment lowered bad cholesterol by 60%. The effect has lasted more than a year in the animals and could well be permanent.” Sir, and what happened to the monkey and its brain??? Silence.
Apr ‘24 news at https://www.biopharmadive.com/news/verve-pcsk-liver-enzyme-pause-trial/711936/ announce:”Verve pauses base editing trial, shifts strategy after treatment side effect”.. Is there a single healthy human on this planet with less than half of the necessary cholesterol in brain? The problem with all these trials is one never hears back from the participants personally… Maybe because they are gone???? Also, who gives the money like the $267 millions to this guy Kathiresan, so that he can shrink the human brain by 60% without telling what is he going to replace it with….??? Let’s calm down.. 
One of the largest human plasma proteins Apolipoprotein B (https://www.uniprot.org/uniprotkb/P04114/entry), among its countless functions, processes cholesterol efflux, homeostasis, metabolic process and its transport. It was THE PROTEIN of interest when in 1987 Baylor College of Medicine in Houston discovered organ specific in-frame stop codon  (https://www.jstor.org/stable/1700694) in its mRNA, responsible for two forms of APOB: APOB100 (in liver) and the shorter APOB48 isoform (small intestine). That first in 2001 (!!) discovered RNA ‘editing’ resulted from the DEAMINATION of C → U at nucleotide position 6666 (C 6666 ) in the APOB mRNA, which causes the change of a glutamine to a translational stop codon ^7. The APOB sequence can be also found at https://www.ncbi.nlm.nih.gov/nuccore/NM_000384.3 . Just wonder, that natural ‘editing’ won’t exist when U is replaced with the synthetic N1-methypseudouridine..? Many thanks to 2 very kind ANL scientists who gave me the copy of that article describing the first RNA editing at the position C6666 (!), related to cholesterol… That number, 6666 position in mRNA sequence, how unique it is, like the earth speed around the sun 66,616 mph, or the tilt axis on its orbit of 90-23.4=66.6 or even the DNA tilt in the Polymerase-beta, equally ~22 deg…, and like the triangle on Trump Tower with 6x6x6 trees along its each side. How unique!
It is indisputable, that many people were put on statin drugs in recent years^8, more than two times, since 2017. Here another source on it^10. Was it all on purpose??
How all the cholesterol issues and covid gene modifying injections are reflected in VAERS system?A search in an expert mode of the VAERS data at: https://www.medalerts.org/vaersdb/findfield.php
indicates, that there is NO LLT SYMPTOM entry for anything cholesterol related, except for cholestasis and its related liver injury. Searching for those 3 cholestasis ‘allowable entries’ gives 6 deaths among 37,647 deceased victims in total as of 5/31/2024 (that’s how long I’m working on this post…). A manual search for the keyword ‘statin’ of the first 20 VAERS reports pages reveals total of 22 dead covid injected patients who were on some kind of statin drugs.. Assuming this trend over the rest of the data base, and given that each page contains ~10 entries with 1 death accompanied by statin drugs on each page, that can be extrapolated to ~10%, at least, of all covid injected and deceased, who died while being ‘on statin’ drugs. If that extrapolation is true, seems like the papers relating covid19 with supporting statin drugs, should be clarified, supporting in which direction, survival or death??
Vaers lists 17 deaths related to Antiphospholipid syndrome(APS) and the antibodies against this lipid, among in total 1008 registered cases. Early on in covid injection campaign Sep ‘21 paper titled: “Pfizer–biontech COVID-19 RNA vaccination induces phosphatidylserine autoantibodies, cryoglobulinemia, and digital necrosis in a patient with pre-existing autoimmunity“ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486180/) pointed out that autoantibodies to one of the most important cancer markers, phosphatidylserine (https://www.mdpi.com/2072-6694/14/10/2536) are the cause of that APS syndrome!! The studied case described a progression of the s/c digital necrosis within ~1 month pictured below_
 
Why would human body generate antibodies against one of the essential compounds in it??? A similar case in terms of symptoms, from 2017 though (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518967/) indicated a huge dose of norepinephrine, with the same outcome. This 2021 study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396423/ talks about ‘Vasopressor-Induced Digital Ischemia’ with the same outcome (be aware, pictures are terrifying). With that, a help is on its way: https://www.nature.com/articles/d41586-024-02157-3 “Bionic leg moves like a natural limb — without conscious thought“… How much cruelty the medical cartels need to possess in order first to mutilate the human being and then having the audacity to offer a fix for it, all the time?  
Back to the APS cases, related to covid injections and also to overdose of the neurotransmitters, is it the antibodies or vasopressin (Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH₂) or norepinephrine, all ending with the same ‘black legs’ outcome? How many Spikes are being produced per second in the human body after the Mod-E-RNA and Pfizer injections? Trillions. Is the below homology maybe responsible for the ‘overproduction’ of vasopressin-like peptides after the Spike digestion? Maybe, or just a coincidence….?
CYFQNC--PR-G  VASOPRESSIN
C FQ C  P  G  <
That CYSTEINE-X-X-X-X-CYSTEINE sequence motif in vasopressin CYFQNCPRG , where X stands for any amino acid, represents Faucis’ favorite Jesuits HIV cure patented peptide, with the motif CxxxxC!
That ‘digital’ phenomenon involving autoimmune reaction, points also to now an impossible application, “Targeting phosphatidylserine for Cancer therapy: prospects and challenges’ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415799/)/. Even more disturbing digital necrosis pictures are presented in this ‘22 study at https://www.emjreviews.com/hematology/article/digital-necrosis-as-initial-manifestation-of-multiple-myeloma-an-unusual-case-report/ titled “Digital Necrosis as Initial Manifestation of Multiple Myeloma: An Unusual Case Report“.
No wonder this report ‘predicts’ the future, its title: “2024—First Year the US Expects More than 2M New Cases of Cancer“ at : https://www.cancer.org/research/acs-research-news/facts-and-figures-2024.html
Phosphatidylserine supplement is also used for improving memory and cognitive function and now it is related to possible autoimmune reactions!? 
Just recently I met a 65+ female, who after ONE covid injection, got the same issue, but, only the right leg became completely black, from toes to the knee. While in hospital, she got the message, amputation. That’s where her ‘inner voice’ came through, as a Christian, and she decided to go home and heal herself with her plants. After ~4 years, that leg which was supposed to be amputated is still there, grey in color though, but in much lesser extend it was at the begin. And she walks perfectly fine! The question left: how a greyish looking human body actually work??? 
Another recent victim: Wojcicki with small cell lung cancer (SCLC), which is known to be stimulated by a small peptide called bombesin with a sequence ‘QRLGNQWAVGHLM’ . Is it partly present in the injected genes encoding the Spike? A BLAST comparison indicates a presence of few bombesin homolog pieces in Spike: 
That all what BLAST finds:
Query  5      QRLGNQWAVGHLM  9 Bombesin
                  NQ AV
Sbjct  606    TNTSNQVAVLYQD 610 Spike

and that's what eyes can see, i.e found 'by hand', almost 100% identity:
Query  1     QRL-GNQW--AVGHLM  13 Bombesin
             Q++ +NQ+  A+G++
             QKLIANQFNSAIGKIQ    Spike
and few more with less homology:
Query  1     QRLGNQWA--VGHLM   Bombesin
             QDVVNQNAQALNTLVK  Spike
QUERY  1     Q--RLGNQW-AVG-HLM  Bombesin
             QSKRV--DFCGKGYHLM  SPIKE
Can the expression of trillions of the injected Spike genes (initiated by covid genetically modifying injections), after their digestion, deliver countless bombesin homologs, and this somehow trigger and contribute to that pathogenic cancerous condition??? You be the judge. Is it unusual to see NOW BNT116 tests of a new ‘miracle’ cure for the non-SCLC cancers, by the same criminals who invented BNT162B2: https://www.annalsofoncology.org/article/S0923-7534(22)03170-2/fulltext ???  
To all of these tragedies, we got some unpractical facts, for example the good healthy oils, olive oil for example, is now double the price in comparison to pre-covid times.. According to the Dr. Daniel Amen, healthy fat diet leads to 42% smaller chance of getting Alzheimers, with healthy protein diet that values sinks to 21%, a simple carbohydrate diet with bread, pasta, potatoes, sugar leads to 400% increased risk of getting Alzheimers…
Is that why Broad / MIT was preparing the crimes for quite a while already while giving the path to the first CRISPED patients with ‘too much cholesterol’? Only because among others, according to the late Dr. Pauling, they do not have enough VitC??? Is that why all the MD’s in USA (governed by Rockerfellers et al.) are calling the same type of product once like ‘vaccines’ (in order to get enough patients to be eliminated/injured) and once like ‘gene therapy’ for apparently trying to repair the collateral damages? I’d almost dare to say, covid injections purpose was to make the takers immune to almost anything human…, and that MD’s these days’ ‘vaccinate’ in order to CRISP the victims afterwards, whether they know it or not. 
Never forget who introduced WAR(P) S(P)EED operation, all leading to the for decades prepared and now full employed erasing of the Creator given human genome and replacing it with CRISPED organoids, straight from the labs of the new false ‘creators’. Never forget the names which forced you to become genetically modified...  How strange, all of the above was written BEFORE the 13th of July, the birthday of Julius Casear, or was something else there?
We were told to get genetically modified in order to get anti-bodies, and now:
https://www.nature.com/articles/d41586-024-02010-7 “What causes long COVID? Case builds for rogue antibodies“ with quote: ““The findings suggest that antibodies might drive some symptoms of long COVID — although how that process works is unclear, and the results will need to be replicated in larger studies.” How similar to the lack of protection during the transmission. As always, more funds are needed, to continue the research and buy more time for even larger collateral damage by keeping people in dark. And now, the casino house with the living roulette’s fights starts to fall apart, Plotkin admits issues with injections https://www.nejm.org/doi/full/10.1056/NEJMp2402379 . 
Cholesterol issues go far deeper than all of this above. The literature below has a collection of papers, including Dr. Kariko’s work, connecting cholesterol with radioresistance of biological matter. Last but not least commercial cholesterol antibodies represented by short peptides, can be found these days in genetically modified tomatoes (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538285/) and of course are also partly embedded in Spike sequence. The evil never ends.
The  US Disinformation Governance Board should consider a serious investigation into the hate/war of/on cholesterol! 
Enjoy your eggs, butter, olive oil, fish oil, as long as you can;)
 Closing this chaotic post with a link to Dr. Thomas Binder’s precious remarks on covid injections containing synthetic foreign genetic material: https://www.brighteon.com/04635967-e615-4c70-9fa0-19eae92d583d
and a link to extremely disturbing, just one out of many facts, leading to annihilation of police forces in US: https://www.brighteon.com/6a1631d9-16f4-4615-9e83-e68352c1fa56 . What are they going to replace it with? AI driven robots or young  ‘illegal immigrants’ trained as special forces in communist countries???
Thank you for your patience and getting that far!
Literature.
   1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261966/pdf/PRP2-8-e00601.pdf
E. Canepa et al. “Cholesterol Hinders the Passive Uptake of Amphiphilic Nanoparticles into Fluid Lipid Membranes“  J. Phys. Chem. Lett. 2021, 12, 35, 8583–8590 https://pubs.acs.org/doi/10.1021/acs.jpclett.1c02077
Ewelina Musielak et al. “Synthesis and Potential Applications of Lipid Nanoparticles in Medicine“ Materials (Basel). 2022 Jan; 15(2): 682. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780297/
https://www.cell.com/cell/abstract/S0092-8674(24)00305-2
“How Gene Editing Could Help Solve the Problem of Poor Cholesterol“ https://time.com/6239076/high-cholesterol-crispr-gene-editing/
July 2022 “Edits to a cholesterol gene could stop the biggest killer on earth“ https://www.technologyreview.com/2022/07/12/1055773/crispr-gene-editing-cholesterol/
Liam P. Keegan et al. “THE MANY ROLES OF AN RNA EDITOR“ Nature Review. Genetics, Vol2, 2001. p. 869.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203693/
Increased radioresistance of ejras‐transformed human osteosarcoma cells and its modulation by lovastatin, an inhibitor of p21ras isoprenylation
AC Miller, K Kariko, CE Myers, EP Clark, D Samid
International journal of cancer 53 (2), 302-307. https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.2910530222 
IN collection at https://scholar.google.com/citations?user=PS_CX0AAAAAJ
“US Trends in Cholesterol Screening, Lipid Levels, and Lipid‐Lowering Medication Use in US Adults, 1999 to 2018“ https://www.ahajournals.org/doi/10.1161/JAHA.122.028205
Dandan An et al. “The role of lipid metabolism in cancer radioresistance” 
Clinical and Translational Oncology Volume 25, pages 2332–2349, (2023)
https://link.springer.com/article/10.1007/s12094-023-03134-4
“Cancer radioresistance is characterized by a differential lipid droplet content along the cell cycle“ https://celldiv.biomedcentral.com/articles/10.1186/s13008-024-00116-y
https://journals.lww.com/pn/fulltext/2024/06000/radioresistance_via_lipid_metabolism__intrinsic,.1.aspx
GIGAVLKVLTTGLPALISWIKRKRQQX“Radioresistance via lipid metabolism: intrinsic, acquired, and tumor microenvironment.”
https://journals.lww.com/jno/fulltext/2023/09000/cholesterol_metabolism_and_tumor_radiotherapy.2.aspx
“Radioresistance of Human Cancers: Clinical Implications of Genetic Expression Signatures” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579106/
“Novel insight into metabolic reprogrammming in cancer radioresistance: A promising therapeutic target in radiotherapy” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910008/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524424/pdf/canmedaj00414-0049.pdf
https://daveasprey.com/the-ultimate-biohacking-fat-c150-explained/
https://www.greenvalleynaturals.com/learn/article/do-dairy-foods-contain-the-most-powerful-anti-aging-factor-yet-discovered?optout=1



Stanford, Penn, MIT et al. dream, genetically modified world. More Spike2020 companions, with ADAM33, no EVE yet...
mejbcart — Tue, 19 Mar 2024 19:50:50 GMT
Imagine, all the sepsis cases could have been prevented by applying a super fast, huge dose of intravenous Vitamin C^18 and few other essential nutrients!!!
Change: Updates now will be attached at the very end of each post, except for this one, keep an eye on the good old Penn’s director Amy Gutmann (https://www.kla.tv/28574), Dr. Henry Daniell (https://www.dental.upenn.edu/faculty/henry-daniell/ ), Dr. Black’s lab (https://hosting.med.upenn.edu/blacklab/). THANK YOU.
This post is to honor all injured victims of covid gene based injections, in particular a teacher, who after loosing all extremities, still laughs, the story comes from Dr. Makis post: 
COVID Intel - by Dr.William Makis
mRNA Injury Series - SEPSIS epidemic in COVID-19 mRNA Vaccinated young healthy adults - Sepsis deaths are up 30% in the UK - 12 recent cases
April 21, 2023 - Pearland, TX - Sherri and David Moody are both COVID-19 Vaccinated Teachers in Texas. Sherri was admitted to hospital with dehydration which turned into a life-threatening condition that included pneumonia, sepsis, and ultimately septic shock…
Read more
3 years ago · 126 likes · 51 comments · Dr. William Makis MD
and there are many more just unthinkably horrifying incidents, including multiple injuries and 3 deaths in my own family, all covid injections related plus personally witnessing just recently a man in shorts, supported by a female, barely walking towards the store, with both legs of dark purple color…  A list of just newly deceased young people in connection with the covid gene modifications via the injections, can be found and translated at: https://report24.news/ploetzlich-und-unerwartet-das-sterben-hoert-nicht-auf/
There are too many injured people, alone on the streets! Just one quote from 2007 article^1: “Organ damage in sepsis involves an alteration in gene expression, making gene transfer a potential therapeutic modality.“ It is about using SV-40 vectors for pulmonary gene therapy..
The question is, to mutilate humanity to a point of no return, requires planning, precision and devotion, to do evil. This post will show just incredible flat admission of that precision (below the 3rd divider bar), while using NIH BLAST bioinformatics software for analysis of specific protein sequences and the universally injected Spike’s synthetic patented gene, expressing this toxic non-human protein. There are also many links for theme validation with clear words in the links title, so no need to read it all.. Also, Spike2020 as always, is the very first Spike version from the official NIH SARS-CoV-2 data base at https://www.ncbi.nlm.nih.gov/nuccore/NC_045512, the one which with tiny modification, was injected into billions of people.. How important is that Adam and Eve theme in the human history and in all of this, is wonderfully expressed in this piece by the polish composer Piotr Rubik:
Why is the contamination of the covid injections with the SV40 promoter now so popular (https://covid19criticalcare.com/covid-vaccines-genome-integration/)? Is it because the https://www.snapgene.com/plasmids/basic_cloning_vectors/SV40_promoter contains very special restriction enzyme called SexAI :
present in rCutSmart^™ Buffer among 210 other DNA chopping dream tools of geneticists? Try to search SexAI with any engine, you will get everything else connected with the first 3 letters, but the SV40 promoter map.. SexAI can be purchased at https://www.neb.com/en-us/products/r0605-sexai . That is now in bodies of how many and it is all over the MSM, like https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-vaccines/
Geneticists intentionally are sticking to FDA re-definitions of covid19 ‘vaccines’, which now include GENETIC MODIFICATIONS, because that’s their ‘daily bread’, money.
That SexAI insertion is on top of two examples of short amino acid strings inside of the expressed Spike toxin: ‘SSS-G-WTA-GAAAYY‘ or this one, from my first posts: ‘ALLAG-TITS-G-WTF-GAGAA‘ (sequences 254-266 and 886-893 from file https://www.ncbi.nlm.nih.gov/protein/1796318598). Dr Fauci, did the covid breeding bats attend some LBGT introduction course, in order to adjust to the global warm(n)ing changes with all these ‘biologically imprinted words’ (in form of single amino acid code) now so deep in human flesh? 
Hands expression reflects the content of our intentions, some engage left, some right with few image examples below. First one is from a student from Stanford, the second well known Dark Act proponent https://www.huffpost.com/entry/obama-signs-dark-act-to-invalidate-vermonts-landmark_b_57a644c7e4b0ccb023727b2d, the one who chose Biden, who then chose himself,  and the third one from other places. Links to the first one https://stanfordmag.org/contents/caption-this, and the last one from https://www.usatoday.com/story/news/nation/2023/05/03/satancon-boston-2023-convention/70168925007/)
They all say, these hands signs are just a gesture, to express love. Love? 
Human heart is the place where love grows and also lot of blood flows, and that’s why Sherry Moody still laughs(!!), so thank YOU for that wonderful example of valuing what’s most important in life. What ‘they’ definitely do not like is, when YOU FORGIVE them their evil (ironically backwards live…), in particular, when intended..’They’ want you to be miserable, angry, crying for years, and some do indeed.
So Stanford ‘lives’ from In-nova-t-I-on, researching/doing something what has to be new, not from non patentable nature made by the Creator. The overwrite of CREATION is well illustrated in this short abstract in one of the top scientific magazines, link at: https://www.nature.com/articles/nature16162 . The title: “Exploring the repeat protein universe through computational protein design“. There, Dr.’s John A. Tainer &David Baker et al. say: ”.. it is possible to design novel repeat proteins with precisely specified geometries, opening up a wide array of new possibilities for biomolecular engineering.” The end of that sentence should have been “new possibilities for biomolecular GENETIC engineering“. That was in 2015. Now ~10 years later, we have billions of human victims injected with genetically modifying materials, without consent (thus ILLEGAL!), containing synthetic genes of one and the same NON-human, toxic, patented Spike protein of the SARS-CoV2 coronavirus, whose only parts (not the entire active infectious virus) can be found in the Pdb Data Bank. The result of the covid tragedy called, mildly speaking, universal Spike gene therapy, until this day was not investigated properly, that’s why this illegal agenda explodes like the chinese balloons and now ends with just few recent announcements, like:
https://www.medicalcountermeasures.gov/BARDA “Project NextGen: Next Generation Medical Countermeasures“
https://www.statnews.com/2024/03/13/hemophilia-treatment-gene-therapy-use-of-hemgenix-roctavian/ “Hemophilia gene therapies arrived after 40 years of struggle. Where are the patients?“ 3/13/2024 
https://www.wsj.com/health/pharma/doctors-can-now-edit-the-genes-inside-your-body-4c8e1aea “Doctors Can Now Edit the Genes Inside Your Body” It sounds like science fiction, but dozens of people have undergone gene editing for cardiovascular disease and other conditions“. 3/11/2024 
https://www.technologyreview.com/2024/01/18/1086791/brain-dead-man-gene-edited-pig-liver/ 1/18/2024
that pure evil, comes from the top of the scientific establishment https://www.theguardian.com/environment/2024/jan/19/nobel-laureates-call-on-eu-to-relax-rules-on-genetic-modification “Nobel laureates call on EU to relax rules on genetic modification.“
with the explosion of cancers, in particular among the covid jabbed victims, the establishment is now keen on collecting the NEW genetic footprint of those victims, here their next trap:  https://kffhealthnews.org/news/article/chemotherapy-drug-overdose-fluorouracil-common-gene-test-lifesaving/
A new documentary at https://brokentruth.com/epidemic-of-fraud/  (Truth is a bitter Pill HCQ) was pointed out by Steven Kirsch, the covid ninja fighter: 
Steve Kirsch's newsletter
Two "must see" films
The Unseen Crisis This film, documenting the stories of the vaccine injured, is free if you are an Epoch Times subscriber. Otherwise, it is $4. For example, Maddie de Garay was permanently disabled within 24 hours after her Pfizer shot in the clinical trial with 1,131 kids (aged 12-15) getting the shot. 1 in 1,000 kids being permanently disabled due to t…
Read more
3 years ago · 334 likes · 78 comments · Steve Kirsch
Due to brokentruth promotion of Wellness Company selling drugs, be it as great as HCQ or Ivermectin, but with Dr. McCullough not telling consistently the entire truth about covid genetically modifying injections, things should be questioned, as always. So let’s say, analysis of part truths is still good, at some point lies will be filtered out.
Brokentruth movie mentions the congress woman Anne Eshoo, who established BARDA, the NO 1 decision maker in early 2020 covid response (directed by Rick Bright), crashing the Hydroxychloroquine based cure for the ‘new disease’. Just recently Mrs. Eshoo discussed the future of science in SLAC, the most unique Stanford project: https://www.flickr.com/photos/slaclab/albums/72177720314995447/ consuming lot of earth’s Helium supply, luckily still down to the earth..
Stanford is like a giant magnet attracting all the hummingbirds to a sweetest feeder. An example, caged guests (except for the one honorable James Baker III) at the memorial service for G.Shultz, who died at 100 in ‘21, with H. Kissinger in the front raw, who had no idea that he will be dead in 2 years too, equally at 100 ^2:  
So the U.S. Rep. armenian Congress woman Anna Eshoo cares for Stanford a lot, it’s like her own child, which develops new things super fast for people in need, few examples:
https://news.stanford.edu/2024/02/21/new-rna-editing-tool-enhance-cancer-treatment/
https://med.stanford.edu/genetherapy.html (Program in Human Gene Therapy works on a variety of viral and non-viral vector systems, with major disease models of hemophilia, hepatitis C and B viral infections, and diabetes.)
https://online.stanford.edu/courses/xgen201-principles-and-practices-gene-therapy
https://stanmed.stanford.edu/scientists-are-refining-crispr-for-wider-applications/
https://biox.stanford.edu/research/seed-grants/interdisciplinary-initiatives-program-seed-grant-humanize-and-deimmunize (To increase the precision/efficacy of gene therapy and cell therapy, one promising approach is to use engineered intracellular proteins, such as transcription factors, to control cells.)
The entire research program https://biox.stanford.edu/research/research-projects, has NO organic carrots, red beets, grass fed beef, no Vit C, clean F-free water or raw milk, none of it, that’s history, instead, everything else unthinkable, which started with an initiative of just few people (https://biox.stanford.edu/about/biox-history). That was ~ quarter century ago with Condoleezza Rice et. al, Silicon valley money including the non-vanishing Bermuda-based entity, Atlantic Philanthropies... These days BioX endeavors include even taking into custody ‘free-flying’ birds (https://biox.stanford.edu/research/seed-grants/brain-activity-during-visual-motor-coordination-free-flying-birds), no one is spared. The final sentence of the birds imprisonment trial: ”In addition, the results will yield much-needed control strategies for search and rescue robots flying in turbulent wind.” Ha, here comes the wind, straight from the Stanford young global specialty: https://stanfordmag.org/contents/the-weather-man 
The persistence of the money supply to ‘adjust’ any biological world into a synthetic man-made LAB product, later on patented, is just not only insane, but it is a HUGE issue of ethics, personal believes, to that level that in 2010 Dr. Fauci wife participated in 'Ethical' Committee initiated by Obama, it was about Synthetic Biology, which now includes HUMANS: https://bioethicsarchive.georgetown.edu/pcsbi/sites/default/files/PCSBI-Synthetic-Biology-Report-12.16.10_0.pdf
Let’s close with last example from Satnford: https://news.stanford.edu/2021/09/03/researchers-develop-hypercompact-crispr/
In the meantime, number of injured covid genetically affected takers of the injections is growing, with the newest:
https://www.nature.com/articles/d41586-024-00720-6 “Why are so many young people getting cancer? What the data say“
 https://twitter.com/TuckerCarlson/status/1768033041568727391
And all that, while FDA secretly and illegally approves more and more of those, with their agents constantly migrating between their FDA homeland and corporation security:
https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-products/approved-cellular-and-gene-therapy-products
with industry and academia, running the gov’s show,  planning ahead:
https://deepcell.com/press-release/deepcell-raises-73-million-series-b-round-to-advance-its-ai-powered-single-cell-analysis-platform/
https://www.nature.com/articles/d41586-024-00775-5 “Building a heart atlas: researchers map organ in stunning detail“
https://www.nature.com/articles/s41587-024-02172-9 about genetic variants of p53..
https://www.science.org/doi/10.1126/scitranslmed.adj9283 “Genome-wide repeat landscapes in cancer and cell-free DNA“
https://www.thelancet.com/journals/lanmic/article/PIIS2666-5247(23)00378-6/ “Benchmarking CRISPR-BP34 for point-of-care melioidosis detection in low-income and middle-income countries: a molecular diagnostics study“
https://onlinelibrary.wiley.com/doi/10.1002/jgc4.1890 “Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis“
And this one, the 201 event organizer, JHI, gets it just one time, again:
https://www.hopkinsmedicine.org/news/newsroom/news-releases/2024/03/junk-dna-no-more-johns-hopkins-investigators-develop-method-of-identifying-cancers-from-repeat-elements-of-genetic-code
‘Junk DNA’ No More: Johns Hopkins Investigators Develop Method of Identifying Cancers from Repeat Elements of Genetic Code.
These elements represent six families: transposable elements, SINes, satellites, LTRs, LINEs, and RNA elements, most of them were discussed in regard to the genetic changes by covid injections, some already in 2020. It was PREDICTABLE, and now it is official.
The global concentration on genes applications, modifications, tests, collections, is, as if the entire medical research suddenly cares about one thing only, genes related issues, which was already before but in particular AFTER the universal covid genes based agenda. 
One of the previous posts: 
mentioned a cross shaped protein, named LAMININ (https://www.uniprot.org/uniprotkb/P24043/entry), glycosylated, like Spike, and regulating integrin mediated signalling pathway. Since Spike contains the same signature motif of all integrins, the ‘RGD’ tripeptide, thus laminin must ‘somehow’ affect the covid19 condition. Indeed 2022 paper^3 observed quote:”Serum levels of laminin in COVID-19 survivors 6 months after discharge were significantly higher than those in the controls.” In short, more laminins, more ‘covid19’.. Please note here, the paper writes about COVID19, the virus, but the official NIH virus sequence has only 3 proteins with this motif, one of which is expressed by the injected Spike genome. Thus what generates more of the integrin motifs, natural infection on the mucus membranes or genetic construct with never ending Spike production in CELLS OF ALL POSSIBLE ORGANS?
Further laminin participates in 22 officially known fundamental biological processes, from cell membranes organization, to neuronal, embyo/brain development, which should have been a huge ‘STOP"‘ for anything Spike related in the global ‘covid rescue plan’. Yes, it should have been, but no, it wasn’t, NIH/CDC/FDA lead the dec-i-sion.
The now discussed Spike-laminin plot includes other covid country club proteins. For example, the LAMR1( https://www.uniprot.org/uniprotkb/P08865/entry), which binds laminin and is worse then the Khazars, it has 10 alternative names, not just 2, here few of its sections homologous with Spike:
Query  74   VSVIS--SRNTGQRAVLKFAAATGATPIA  100 LAM-R1
            VSVI+  +  + Q AVL         P+A
Sbjct  595  VSVITPGTNTSNQVAVLYQDVNCTEVPVA  623 Spike2020
Query  11    KEEDVLKFLAAGTHLGGTNLDFQ----MEQYI  38 LAM-R1
             KE D L  +A   +L  + +D Q     EQYI
Sbjct  1181  KEIDRLNEVA--KNLNESLIDLQELGKYEQYI  1210 Spike2020
Query  202  YFYRDPEE  209 LAM-R1
            Y Y+ P++
Sbjct  421  YNYKLPDD  428 Spike
here quickly the LBGT section of Spike2020, manual alignment:
Query  272  ATEDWSAAPTAQATEWV-G  282 LAM-R1
            ++  W+A   A    ++ +
Sbjct  254  SSSGWTAGAAAYYVGYLQP  264 Spike2020
and here the Biden's singing bird: 
DW-SAQPA---TEDWS-AAPTAQATEWVGATTDWS LAM-R1
 + SA  A   T  W+  A +A    +   +  ++
QYTSALLAGTITSGWTFGAGAALQIPF---AMQMA Spike2020
LAMR1 is not only part of ribosomes, it functions as receptor for many viruses, bacteria and pathogenic prion proteins, it is everywhere, in nucleus, cytosol, cytoplasm, exosomes.. Thus its binding to the for microvessel formation responsible antigenic, glycosylated laminin (40 glycans!), is just one of its tasks. The ‘sweet’ Lam-in-ins’ complicated network of interactions keeps the entire space between cell membranes and collagen matrix ‘in space’^5:

What else binds laminin proteins? Sounds religious, but it is not, or maybe, it is the LUTHERAN BLOOD GROUP Glycoprotein^6, which has a long history going back to the gene on the human X chromosome responsible for color blindness^7. It is a red blood cell receptor binding the laminin^8,^9 and is involved in vaso-occlusion in sickle cell disease, when body produces too much of it. That laminin very high affinity interaction with the Lutheran antigen contributes to many other processes, organogenesis, erythropoiesis, smooth muscle development, malignant transformation and tumor metastasis^10. The Lutheran antigen (https://www.uniprot.org/uniprotkb/P50895/entry) has again quite few homologies with SARS-CoV-2 Spike, using normal BLAST (Query is the Luther, Subjct the Spike2020, the lines inbetween are the identical parts) and manual alignment, to name just few:
Query  57    GTHDHYMLEWFLTDRSGARPRLASAEMQ----GSELQVTMHDTRGRSP--------PYQL  104
             GTH      WF+T R+   P++ + +        ++ + + +     P          +L
Sbjct  1099  GTH------WFVTQRNFYEPQIITTDNTFVSGNCDVVIGIVNNTVYDPLQPELDSFKEEL  1152
Query  105   DSQGRLVLA-EAQVGDERDYVCVVRAGAAGTAEATARLNVFAK  146
             D   +   + +  +GD    +  + A      +   RLN  AK
Sbjct  1153  DKYFKNHTSPDVDLGD----ISGINASVVNIQKEIDRLNEVAK  1191

Query  435  SRTQNFTLLVQGSPE---LKTAEIE-----------PKADGSWREGD  467
            S+TQ  +LL+  +     +K  E +            K + SW E +
Sbjct  112  SKTQ--SLLIVNNATNVVIKVCEFQFCNDPFLGVYYHKNNKSWMESE  156
this corrected manually:
Query  361  LDPLELSEGKV-L-SLPL  376 
            LDPL  SE K+ L S  +
Sbjct  293  LDPL--SETKCTLKSFTV  308
BLAST alignment of the integrin motif 'RGD' in LUTHER
Query  290   LCRGDGSPSPEYTLF  304  LUTHER
             +C+   +  P   +F
Sbjct  1081  ICHDGKAHFPREGVF  1095 Spike2020
and here the same RGD manually, since BLAST won't do it
      QLLCRGDG----SPSPEYT  LUTHER
       ++ RGD     +P ++
      FVI-RGDEVRQIAP-GQTG  Spike
or also the special ACE2 RBD Spike fragment with larger piece of Luther
   VQLLCRGDGS-PSPE-YTLFRLQDEQ Luther
    Q+L  +D+S PS   ++   L +
   SQIL--PDPSKPSKRSFIEDLLFNKV Spike
The above first “RGD’ Luther motif overlaps with ‘HDG’, where the GD→DG inversion is an example of a frequent phenomenon in the Spike homologus insertions. The complexity of the invisible micro-world in our bodies goes beyond astronomy atlas, here another actor on the Luther scene, again blood related, and it is called spectrin^11, the heaviest part in red blood cells membranes. A 2001 publication^12 described how the erythroid alpha-spectrin gene mutation caused by exon skipping resulted in a amino acids deletion which in turn changed multimer formation stability and lead to thrombosis. There are 2 types of spectrin, alpha and beta chains (only ~27% seq ID) which have following homologies with Spike2020 (Sbjct lines), beta first (https://www.uniprot.org/uniprotkb/P11277/entry), heavily phosphorylated, thus lot of charge:
Query  422  QLARRFDRKAAMRETWLSENQRLVA  446 Spectrin Beta
            Q+A RF+      +  L ENQ+L+A
Sbjct  901  QMAYRFN-GIGVTQNVLYENQKLIA  924 Spike2020
Query  1542  QQLVEAAEI  1550
             QQL+ AAEI
Sbjct  1010  QQLIRAAEI  1018
Query  1412  TSVNRMLAKLKRVEDQVNVRKEELGELFAQV  1442 Spectrin Beta
             T  NR L  +  VE   N +     E FAQV
Sbjct  761   TQLNRALTGIA-VEQDKNTQ-----EVFAQV  785
Query  1917  SWMESIIR  1924 Spectrin Beta
             SWMES  R
Sbjct  151   SWMESEFR  158
Query  623   SNMAAGRKAQ--LEQSKR  638 Spectrin Beta
             +N+AA + ++  L QSKR
Sbjct  1022  ANLAATKMSECVLGQSKR  1039
Query  1567  DRLREAAAGRLQRLR  1581 Spectrin Beta
             DRL     GRLQ L+
Sbjct  994   DRL---ITGRLQSLQ  1005
also manual 
        FDEDDSEPVLKGVKLHYT C-terminus of SPike2020
        PQEEEGE--TAG         Spectrin
according to uniprot:

Spectrin is cleaved in Malaria infection in 2 spots:

Site 165-166 (Microbial infection) Cleavage; by P.falciparum SERA6 'QT'
Site 167-168 (Microbial infection) Cleavage; by P.falciparum SERA6 'QE'
both sites span the Spike furin site section
      ------------>.-.>
150-WTIILRFQIQDIVVQTQEG--RETRSAKDALL-170 --->Spectrin Beta
          GAGICASYQTQTNSPRRARSVAS        --->Spike2020

also the 'RGD' motif in Spike has high homolog section in spectrin:
Query  556  FGKHLLEVEDLLQKHKLMEADIAIQGDKVKAI  587 Spectrin Beta
            +G     + DL   +   ++   I GD V+ I
Sbjct  380  YGVSPTKLNDLCFTNVYADS-FVIRGDEVRQI  410 Spike
and now the alpha chain of spectrin, with lot of bound Ca+2, few phosphors and metals, all at https://www.uniprot.org/uniprotkb/P02549/entry
Query  1716  FQFFQDL-------DDEESWIEEKLIRVSS----------QDYGRDLQGVQNLLKK----  1754
             FQF  D         + +SW+E +    SS          Q +  DL+G Q   K     
Sbjct  133   FQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLEGKQGNFKNLREF  192
Query  1755  -HKRLEGEL---VAHEPAIQNVLDMAEKLKDKAAVGQEEIQLRLAQF----VEHWEKLKE  1806
               K ++G       H P I  V D+ +       +    I + + +F      H   L  
Sbjct  193   VFKNIDGYFKIYSKHTP-INLVRDLPQGFSALEPLVDLPIGINITRFQTLLALHRSYLTP  251
Query  1807  LAKARGLKLEESLEYLQFMQNAEEEEAWINEKNALAVRGDCG-DTLAATQSLLMKHEALE  1865
                + G     +  Y+ ++Q       + NE   +    DC  D L+ T+  L      +
Sbjct  252   GDSSSGWTAGAAAYYVGYLQPRTFLLKY-NENGTITDAVDCALDPLSETKCTLKSFTVEK  310
Query  1866  NDFAVHETRVQ------------NVCAQGE  1883
               +     RVQ            N+C  GE
Sbjct  311   GIYQTSNFRVQPTESIVRFPNITNLCPFGE  340

Query  1489  LIDERTKLGDYANLKQF-YRDLEELEEWISEMLP  1521
             L+D   K G++ NL++F +++++   +  S+  P
Sbjct  176   LMDLEGKQGNFKNLREFVFKNIDGYFKIYSKHTP  209

Query  264  ANLQRFKRDVTEAI  277
            +NL+ F+RD++  I
Sbjct  459  SNLKPFERDISTEI  472

Query  1402  GNCDQVESWMVARENSLRSDDKSSLDSLEALMKKRDDLDKAI---TAQEGKITDLEHFAE  1458
             GNCD V   +    N++    +  LDS       +++LDK     T+ +  + D+     
Sbjct  1124  GNCDVVIGIV---NNTVYDPLQPELDSF------KEELDKYFKNHTSPDVDLGDISGINA  1174
Query  1459  SLIADEHYAKEEIATRLQRVLDRWKALKAQLIDERTKLGDY  1499
             S++         I   + R+ +  K L   LID + +LG Y
Sbjct  1175  SVV--------NIQKEIDRLNEVAKNLNESLIDLQ-ELGKY  1206

Both RGD motifs by hand, BLAST won't do it:
     EKNALAVRGDCGDTLAATQSLLMK spectrin alpha
       ++ ++RGD    +A  Q+
     YADSFVIRGDEVRQIAPGQTGKIA Spike2020
when looking at spectrin a and b chains, it seems Spike2020 has more similarities to one or the other, than both chains on their own. It is also known that the first Arginine in ‘RGD’ motif in Spike suppose to bind ivermectin (https://www.futuremedicine.com/doi/10.2217/fvl-2020-0342), implying a possibly similar binding scheme in the above investigated malaria related proteins.
It all ABSOLUTELY DOES NOT LOOK RANDOM. Spectrin is also involved in hemolytic anemia, exactly the same symptoms reported in Dec ‘21 and in ‘22, only after introduction of the Spike gene therapies^13. A 2004 publication^14 with overlapping coauthor (J Aura Gimm) pointed to yet another Blood group antigen and Host cell receptor for virus entry, Glycophorin-A (https://www.uniprot.org/uniprotkb/P02724/entry), which binds sialic acid, it is a major intrinsic membrane protein of the erythrocyte. Like Luther antigen, it has high sequence homology with Spike, not only in the integrin ‘RGD’ motif section, but again at the ACE2 RBD domain:
Query  27   MHTSTSSSVTKSYISSQT--NDTHKRDTYAAT--PRAHEVSEIS  66 Glycophorin-A
            ++ S+S S  K Y  S T  ND    + YA +   R  EV +I+
Sbjct  368  LYNSASFSTFKCYGVSPTKLNDLCFTNVYADSFVIRGDEVRQIA  411 Spike's RGD motif 

or even better, overlap with even longer Spike section:

Query  27   MHTSTSSSVTKSYISSQT--NDTHKRDTYAATP--RAHEVSEISVRTVYPPEEETGERV-  81
            ++ S+S S  K Y  S T  ND    + YA +   R  EV +I          +TG    
Sbjct  368  LYNSASFSTFKCYGVSPTKLNDLCFTNVYADSFVIRGDEVRQI-------APGQTGKIAD  420
Query  82   ---QLAHHFSEPEITLIIFGVMAGVIGTILLISYGIRRLIKKSPSDVKPL  128
                L   F+   I+     +   V G      Y + RL +K  S+ KP 
Sbjct  421  YNYKLPDDFTGCVIAWNSNNLDSKVGGNY---NY-LYRLFRK--SNLKPF  464

and more overlapping sections:
Query  13   EIVSISASSTTGVAM---HTSTSSSVTKSY  39
            EI+ I+  S  GV+     T TS  V+  Y
Sbjct  583  EILDITPCSFGGVSVITPGTNTSNQVAVLY  612
by hand few special sections, ACE2 RBD domain: 
SPSDVKPLPS-PDTDVPLSSV  Glycophorin
NFSQILPDPSKPSKRSFIEDL Spike2020
The LBGT section of Spike2020: 
    VAMHTST-----SSSV-TKSYISSQTN
    LALHRSYLTPGDSSSGWT-AGAAAYYVG   
the furin site:
TSSSVTKSYISSQTNDTHKRDTYAATPRAH
  PIGAGICASYQTQTNSPRRARSVASQ
and expression signal:
MYGKIIFVLLL---SEIVSISAS
MF---VFLVLLPLVSSQCVNLTT
Glycoporin-A, is a receptor for HepatitisA Virus, it is a receptor for P.falciparum erythrocyte-binding antigen 175, in MALARIA. With its countless sugars and linked phosphors, has more interaction partners than amino acids, and with its genetic polymorphism in P.falciparum infection, it allows for resistance to malaria… 
Malaria? again? HCQ OR Ivermectin anyone? Red blood cells explosions all over? 
Well, Glycoporin is also used for SARS-COV2 detection, quote (https://www.nature.com/articles/s41467-021-22045-y#Sec2): “We have adapted this approach for detection of antibodies to SARS-CoV-2 by linking the RBD of the SARS-CoV-2 spike protein to IH4 via a short (GSG)2 linker to produce the fusion protein IH4-RBD-6H.” The same was done with antibodies to HIV p24, which when present in serum, crosslinked the p24 and agglutinated the red cells. 
Sounds like a real war against human blood, in particular the red cells.… Stay calm, just go down the food chain pyramid, who eats/degrades what. 
So what ‘eats’/degrades laminin, and even takes apart the collagen matrix on all organs?? MMP-9, Matrix Metalloproteinase-9, full of bound Ca2+ and Zn+2 ions, one of the latter inhibits the munching, the same protease which is also ESSENTIAL in malaria development:  https://ncbi.nlm.nih.gov/pmc/articles/PMC7123976/ “Etiopathogenesis and Pathophysiology of Malaria“, and in cardiovascular disease^16. This MMP-9 monster (https://www.uniprot.org/uniprotkb/P14780/entry) degrades collagen and more, but it is actually produced by the best human friends, the so normal alveolar macrophages and granulocytes, fighting the enemies. And what regulates that MMP-9 super soldier? 
A protein called RECK_HUMAN, yes that’s right, its link is at https://www.uniprot.org/uniprotkb/O95980/entry and is stands for the mouthful “Reversion-inducing cysteine-rich protein with 3 Kazal motifs”! It suppresses MMP9 secretion and directly inhibits its enzymatic activity (PubMed:9789069, PubMed:18194466), thus negatively regulating the soldier.
With that, we got the picture of the disaster painted on the wall, based on official data. In nutshell, and I kid you not: an aged armenian congress woman, very Stanford friendly, trailblazer, a true problem solver, indirectly contributes to a suppression of malaria wonder (BARDA’s fault to cut out Ivermectin/HQC) right at the begin of covid19 disaster so that only gene therapies will be allowed as the ‘cure’, while the only enzyme regulating the disaster got its name RECK_HUMAN and it has 3 Kazal-iam motifs, each of which has some homology with Spike2020, which now is all in human blood… Here the sequences of the 3 K(h)azal-ian motifs and how they overlap with Spike2020, using automated BLAST, not perfect (because the real BLAST is in Mod-E-RNA hands…), but still:
Kazal-like 1
627-673 TFTGLPCNCADQFVPVCGQNGRTYPSACIARCVGLQDHQFEFGSCMS
Query  592  TSFSIDCNVCSCFAGNLVCSTRLCLSEHSSEDDRRTFTGLPCNCADQFVPVCGQNGRTYP  651
            T  S+DC +  C   +  CS  L           R+ TG+          V  Q  + Y 
Sbjct  732  TKTSVDCTMYIC-GDSTECSNLLLQYGSFCTQLNRALTGIAVEQDKNTQEVFAQVKQIYK  790

Query  652  SACIARCVGLQDHQFEFGSCMSKDPCNPN  680
            +  I    G     F F   +  DP  P+
Sbjct  791  TPPIKDFGG-----FNFSQILP-DPSKPS  813
 2. Kazal-like 2 (part only, no time to fit it all…)
     698-752        TFDKFGCSQYECVPRQLACDQVQDPVCDTDHMEHNNLCTLYQRGKSLSYKGPCQP
Query  738  YQRGKSLSYKGPCQPFCR  755
            Y     L  K   +PF R
Sbjct  449  YNYLYRLFRKSNLKPFER  466
Kazal-like 3
       753-789 FCRATEPVCGHNGETYSSVCAAYSDRVAVDYYGDCQA
Query  733  NLCTLYQRGKSLSYKGPCQPFCRATEPVCGHNGETYSSVCAAYSDRVAVDYYGDCQAVGV  792
            N  TL   G    Y G C     A + +C       + +    +D  ++ Y     A G 
Sbjct  824  NKVTLADAGFIKQY-GDCLGDIAARDLICAQKFNGLTVLPPLLTDEMIAQYTSALLA-GT  881
Those who speak japanese would probably assume, it is a Khazar-motif….  Molecular biology, full of history, and fight. 
It all goes back to 1901, and a military general from WWI, named Karl LANDsteiner, Nobel Prize winner for Blood groups types. He also discovered, that addition of iodo-diazo group into serum albumins, causes that the original species specificity disappear. Rockefellers enjoyed the solutions of his brilliant mind. He also implied, there are so many blood types as there are humans… Every one of us is unique, every electron counts. Well, he is dead too, of course.
That’s not all, one more special name, by the molecular biologists, who ignore the Creator, but use a biblical name (no wonder there are projects out there like Mockingbird..) , ADAM33, another munching machine, from the title. Why not Adolf, or Barack, or Joe or even Donald, NO, it has to be ADAM33.
Officially it is a disintegrin and metalloproteinase domain-containing protein 33. Even in ‘pre-covid’ times it was heavily involved is severity of asthma. Lot of literature on it, for example showing how it chops down other important membrane proteins:
It almost looks like a snake, crawling down and eating all the eggs on the ground. Is it why, for environmental reasons, no eggs in White House this ‘24 Easter, they will paint the potatoes for the children…?
Take the ADAM33 sequence from https://www.uniprot.org/uniprotkb/Q9BZ11/entry, and run BLAST, its active site E346, nicely conserved in the first BLAST output, right next to the completely conserved tripeptide PIGA, with the letter ‘I’ being Isoleucine, the 666-th residue is the Spike amino acide sequence:
                        *<== ADAM's33 ACTIVE SITE E346 
Query  334  ELPIGAAATMAHE  346   ADAM33
            ++PIGA    +++
Sbjct  663  DIPIGAGICASYQ  675   Spike2020
               * that I=isoleucine, in the middle of the 'PIG' tripeptide is the 666-th residue in the Spike sequence (https://www.ncbi.nlm.nih.gov/protein/YP_009724390.1)

Query  380  PFPRVFSACSRRQLRAFFRKGGGACLSN  407
            PF+ VF+A     + A+ RK    C+++
Sbjct  337  PFGEVFNATRFASVYAWNRKRISNCVAD  364

expression signal from Spike2020
Query  706  MLLSVLLPLL  715 ADAM33
             +  VLLPL+
Sbjct  2    FVFLVLLPLV  11  Spike2020
COMPLETE furin site conservation(!!), being part of expression signal in ADAM33
Query  1      MGWPRRARGT  11 ADAM33
                 PRRAR  
Sbjct  681 QTQTNSPRRARSV  687 SPike2020
ADAM33, like Spike2020, is heavily ‘sugar coated’ and has that cysteine switch 131-CTCSGMSG-138, equally conserved in Spike2020. That motif in collaboration with the catalytic Zn+2 ions, inhibits its munching. Here some of the essential functional parts of ADAM33 and and their SIMILARITY within the Spike2020:
Disintegrin part:
Query  26    LCCFAHNCS  34 <<<---ADAM33
             LCC +  CS     <<<---IDENTITIES
Sbjct  1234  LCCMTSCCS  12 <<<---Spike2020
Query  3    LCGNGFVEAGEECDCGPGQECRDLCC  28
            L   GF++  +  DC +    RDL C
Sbjct  828  LADAGFIK--QYGDCLGDIAARDLIC  851
Query  11    AGEECDCGPGQECR-DLCCFAHNCSLRPGAQCAHGDCCVRCLLKPA  55
             A +  +C  GQ  R D C   ++    P +   HG   +     PA
Sbjct  1026  ATKMSECVLGQSKRVDFCGKGYHLMSFPQS-APHGVVFLHVTYVPA  1070

Peptidase part:
Query  237  LLEVANYVDQLLRTLDIQVALTGLEVWTERDRSRVTQDANA  277
            LL+   +  QL R      ALTG+ V  E+D+   TQ+  A
Sbjct  753  LLQYGSFCTQLNR------ALTGIAV--EQDKN--TQEVFA  783
Cysteine switch:
Query  131  CTCSGMSGLITLSRNAS  147
            C+  G S  IT   N S
Sbjct  590  CSFGGVS-VITPGTNTS  605
Query  181  HRDPGNKAGMTS  192
            H++  NK+ M S
Sbjct  146  HKN--NKSWMES  155
Query  75   QELLLELEKNHRLLA-PGYIETHYG  98
            ++LL     N+  LA  G+I  +YG
Sbjct  819  EDLLF----NKVTLADAGFIK-QYG  838

manualy the LBGT SPike2020 section:
  DHSELPIGAAATMAHEIGHS <<<-ADAM33
  SSSGWTAGAAAYYVGYLQPR <<<-Spike2020

Query  146  ASYYLRPW-PPR  156
            A+YY+  +  PR
Sbjct  263  AAYYVG-YLQPR  273

 ADAM33's cystein switch with Zn+2 binding to the last cysteine CTC*:
                        *
               VVLCT----CSGM----SGLITLSRN
               IMLCCMTSCCSCLKGCCSCGSCCKFD
The above is not all. A section of 100 residues in ADAM33 overlap quite well with Spike2020:
Query  146  ASYYLRPWPPRGSKDFSTHEIFRMEQLLTWKGTCGHRD-----PGNKAGMTSLPGGPQSR  200
            ASY  +   PR ++  ++  I      L  + ++ + +     P N +   +    P S 
Sbjct  672  ASYQTQTNSPRRARSVASQSIIAYTMSLGAENSVAYSNNSIAIPTNFTISVTTEILPVSM  731
Query  201  GRREARRTRKYLELYIVADHTLFLTRHRNLNHTKQRLLEVANYVDQLLRTLDIQVALTGL  260
             +     T     +YI  D T               LL+  ++  QL R      ALTG+
Sbjct  732  TKTSVDCT-----MYICGDST----------ECSNLLLQYGSFCTQLNR------ALTGI  770
Query  261  EVWTERDRSRV  271
             V  +++   V
Sbjct  771  AVEQDKNTQEV  781
AND this below, unprecedented, is defined as part of disintegrin in ADAM33, but in Spike2020 it is said to be all S-palmitoyl cysteines, in one publication^17, only..
Query  442   LCCFAHNCS-LRPGAQCAHGDCC  463 ADAM33
             LCC +  CS L+ G  C+ G CC
Sbjct  1234  LCCMTSCCSCLK-GC-CSCGSCC  1254 Spike2020
What that very C-terminal part of Spike actually represents is a cysteine cluster, like in ADAM33, where most probably metals bind, and not only fats… This cysteine rich Spike motif in earlier posts, was also related to venoms, something what was shared for the first time by Dr. Richard Bartlett (featured at 2:31 in https://rumble.com/v1hu7xr-the-truth-about-ivermectin-a-new-short-documentary-by-plandemic-filmmaker-m.html).
Isn’t somebody laughing wickedly right now, while watching the humanity to get literally disintegrated by ADAM33-like Spike2020, while buying out all lands, homes, animals, and offering worms for the rest??? Or even better, snakes: https://www.scientificamerican.com/article/snake-steak-could-be-a-climate-friendly-source-of-protein/
And wasn’t it Congress woman Eshoo who on January 30, 2008 (right on time before the collapse), endorsed the equally Stanford friendly, U.S. Senator Barack Obama for president? The same who in 2022 in a speech at Stanford, admitted:
"We've essentially clinically tested the vaccine on billions of people worldwide"
https://www.c-span.org/video/?519625-1/president-obama-speaks-threat-disinformation (source at 29.32). Oh, the humanity mutilating Stanford, takes something else from this speech: https://news.stanford.edu/2022/04/21/disinformation-weakening-democracy-barack-obama-said/ for promotions of its greatness. Lot of the world establishment was featured on the cover of Economist’s Christmas edition  in 2012 with Barack Obama floating in a canoe right into the EURO sign:
It is a great pity, that Stanford, a place on this planet, once geographically breathtakingly beautiful, turned into a death pit.
So far, it’s all a complicated net of no coincidences of actions in the right place and the right time, even on the microscopic level.
One more thought, inspired by an old article in Proc R Soc Med. from 1923 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2103460/pdf/procrsmed01359-0005.pdf, which makes a very interesting comparison of loosened teeth with a " Dental Sepsis", all preventable with the right living conditions, including proper living plant food with LOT of vitamin C..
This post needs to end, too long for email already, so no EVE yet..;))) 
STAY HEALTHY with LOT of good organic food, VitD3, VitC and LOVE. And stay tuned for the next episode, if time allows. And THANK YOU for checking in, without the boarding pass…
Update 3/21/2024 : “There is a new most expensive drug in the world. Price tag: $4.25 million“ https://www.technologyreview.com/2024/03/20/1089996/there-is-a-new-most-expensive-drug-in-the-world-price-tag-4-25-million/ The deception of this title from MIT news is explained in the first sentence: “There is a new most expensive drug ever—a gene therapy that costs as much as a Brooklyn brownstone or a Miami mansion, and more than the average person will earn in a lifetime.“ So we not only have deception in term of gene therapies called now ‘vaccines’, they are basically ‘drugs’!??
Repetition of an old but very important info from post titled “The 20 years of 'genomic medicine'. JP Morgan, is it about money or health?“
Update: 1/29/2024 The title “Cell-free DNA and RNA—measurement and applications in clinical diagnostics with focus on metabolic disorders” in Physiol Genomics 53: 33–46, 2021, implies, to what extend the medial cartel planned their future, while forcing the genetically modifying covid injections on billions of clueless citizens, ever since the end of 2020, the begin of that universal therapy, which started with changing the RNA pools of the human genome. The medical genocide goes that far, that SATNFORD, sorry Stanford, publishes proudly an article titled ‘The beat goes on’, in which since 2022 cardiothoracic surgeries are being performed with still beating hearts form cardiac arrest patients (the ones caused by the covid injections?) with astonishing success!!! A new field of ‘morpholome’ was invented, also in Satnford, sorry, stanford, which refers to variety of cell shapes taken on by an organism. Euan Ashley, Maddison Masaeli and Mahyar Salek (google AI expert) while analyzing the HEART CELL MORPHOLOME, want to differentiate deceased cells from others that have been ‘cured’(????) by gene-editing technology (Stanford Medicine, Issue 3, 2023). Between Apr 2023 and the print out date of that Stanford magazine (begin of ‘24), the amount of this sort of heart transplants, more than DOUBLED (https://med.stanford.edu/news/all-news/2023/04/beating-heart-transplant.html)
Another Stanford hero, https://profiles.stanford.edu/michael-ma, published in ‘22 statistics on infants heart transplants, https://pubmed.ncbi.nlm.nih.gov/35835207/, strangely covering the years 1994 to Sep 2019, and avoiding anything AFTER 2020 (WHY????), together 2552 infant heart transplants reported to UNOS.. If there is anyone who could help the embalmers to decipher the terrible clot issues, it would be this person specializing on multilevel obstruction of systemic and pulmonic arterial systems… Straight from Chemical Engineering to medicine, what an ideal transformation, unfortunately with ZERO input for the embalmers struggling with dead bodies of covid injected victims!!!
Update 3/26/2024: An old lecture by Rob Skiba, explaining the historical/religious background of the goals of the elites: 
and also this one: 
where he ends,  quote: ”I stand alone on the word of GOD, because in the sea of lies, that is our only compass.” Rob Skiba died of ‘covid’ in hospital on the 13-th of Oct 2021…
Update 9/9/2024: “Engineering cells for a new purpose” by Satnford elites describet at https://stanmed.stanford.edu/altering-cells-new-purposes/
Literature.
Luminita Eid et al. “Simian virus 40 vectors for pulmonary gene therapy.“ Respir Res. 2007; 8(1): 74.  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238754/
Mahsa Khoramipour et al. “Evaluation of the association between clinical parameters and ADAM33 and ORMDL3 asthma gene single-nucleotide polymorphisms with the severity of COVID-19” International Immunopharmacology, Volume 123, October 2023, 110707https://www.sciencedirect.com/science/article/abs/pii/S1567576923010329
https://stanforddaily.com/2021/10/07/secretaries-of-state-politicians-remember-george-shultz-at-memorial-service/
Hongwei Li et al. “Serum levels of laminin and von Willebrand factor in COVID-19 survivors 6 months after discharge“ Int J Infect Dis. 2022 Feb; 115: 134–141. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626146/
https://www.researchgate.net/figure/Domain-structure-and-self-assembly-of-laminin-111-A-Schematic-drawing-of-the_fig1_232280536
https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/blood-group-lutheran-system
https://www.omim.org/entry/303800#47
Wilson, E. B. The sex chromosomes. Arch. Mikrosk. Anat. Enwicklungsmech. 77: 249-271, 1911
https://www.jbc.org/article/S0021-9258(18)80596-8/pdf with “The Lutheran Blood Group Glycoproteins, the Erythroid Receptors for Laminin, Are Adhesion Molecules“
https://www.researchgate.net/publication/12194734_Lutheran_blood_group_glycoprotein_and_its_newly_characterized_mouse_homologue_specifically_bind_a5_chain-containing_human_laminin_with_high_affinity
C. Eyler & M. Telen “The Lutheran glycoprotein: a multifunctional adhesion receptor“ Transfusion. 2006 Apr;46(4):668-77. https://pubmed.ncbi.nlm.nih.gov/16584446/
Xiuli An et al. “Adhesive activity of Lu glycoproteins is regulated by interaction with spectrin”. Blood. 2008 Dec 15; 112(13): 5212–5218. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597615/
N J Wandersee et al. “Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis“ Blood. 2001 Jan 15;97(2):543-50. https://pubmed.ncbi.nlm.nih.gov/11154235/
Tyler A Finkenthal et al. “Autoimmune Hemolytic Anemia Exacerbation Associated With COVID-19 Infection and Markedly Elevated Inflammatory Markers“ Cureus. 2021 Dec; 13(12): e20416. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759712/ AND Hayder M. Al-kuraishy et al. “Hemolytic anemia in COVID-19“ Ann Hematol. 2022; 101(9): 1887–1895. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263052/
James C-M Leeet al. “Mechanism of protein sorting during erythroblast enucleation: role of cytoskeletal connectivity” Blood 2004 Mar 1:103(5) 1912-9. 
 Mauro Prato “Etiopathogenesis and Pathophysiology of Malaria“ Human and Mosquito Lysozymes. 2014 Sep 22 : 1–18. https://ncbi.nlm.nih.gov/pmc/articles/PMC7123976/ 
“Matrix Metalloproteinase-9: Many Shades of Function in Cardiovascular Disease” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858212/
https://www.cell.com/action/showPdf?pii=S1534-5807%2821%2900734-6
Paul E Marik et al. “Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Severe Sepsis and Septic Shock: A Retrospective Before-After Study“ Chest. 2017 Jun;151(6):1229-1238.https://pubmed.ncbi.nlm.nih.gov/27940189/
P. E. Marik was severely prosecuted for applications of VitC protocol in covid19 times to a level where he CRIED in front of one of the covid19 crimes hearings…



The white clots after the genetically modifying covid injections. Is it the -KV- to -PP- mutation, Fibrin/-ogen, or all of it?
mejbcart — Wed, 28 Feb 2024 23:50:27 GMT
Update 5/22/2024: Great discussion with the right language: https://uncutnews.ch/haeufigkeit-von-blutgerinnseln-steigt-radiologe-sieht-taeglich-alarmierende-befunde/
Update 4/8/2024: A ‘STRONG’ multinational team from UCLA/Stanford/University of North Carolina at Chapel Hill(!), Harvard and UK comes up with a publication https://www.pnas.org/doi/epdf/10.1073/pnas.2300644120 which ‘explains’ indirectly the non-digestable peptides which apparently are coming from viral fragments and affect the following ‘infection’, leading to cloths like no other coronaviruses.. Any comparison of these peptides with other coronaviruses? No, NONE. NO WORD about covid genetically modifying injections and the fact that the REAL onslaught of these fragments, which btw. are very conserved among the old and new corona viruses, comes from genetically modifying injections!!! Who participates? Specialists from places which came up with the covid injections and the SAX team from SSRL lab in Stanford. What an inconvenient bunch of LIES in a GLOBAL TRAGEDY. Few more FACTS about these fragments at the end of this post.
Update 3/2/2024: Heavy metal detox (including calcification being part of the clots ) presented in https://go2.thetruthaboutcancer.com/eastern-medicine/episode-3/ patent US6720356B2 with more details at the end of the post
Update 3/1/2024: Can’t respond to readers comments any more! SS, stands for sub-stack, backwards on two sections: bus-kcats, oh really???
Update 2/29/2024:  New canadian study “Genome-wide enhancer-associated tandem repeats are expanded in cardiomyopathy“ at https://www.thelancet.com/action/showPdf?pii=S2352-3964%2824%2900062-8 . A mention about sudden cardiac death in childhood and the performed whole genome analysis (NOW AFTER covid mod mRNA gene therapies on everybody!!!?) showed a rare tandem repeat expansions of CGG leading to the diseases.. How many CGG’s are in the Spike genome injected into billions, including children? Quick count: 5 at least..
The white clots in human bodies, MUST be seen by countless medical doctors investigating blood of their patients, surgeons cutting human bodies every day, embalmers dealing with deceased bodies, but still, except for the ‘Died suddenly’ documentary and the few new heroes on that intensifying topic, there are many questions left. The most important message here, about REMEDIES to this catastrophe, is at the very end of this post.
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The 2/22/2024 Highwire  episode 360 “The clot thickens” presents an interview with people researching the white clots in veins and arteries, including Dr. R. Cole, embalmer R. Hirschman and Thomas Haviland MSc., starting at ~1:16:45:
https://www.bitchute.com/video/0W0uyXi01JTl/
Here it needs to be added, this is NOT a promotion of Highwire, which until this day is following FDA redefinition rule, and like all MD’s, when talking about covid injections, illegally calls them ‘vaccines’.
The white clots were not quite there yet in 2020, when the SARS-CoV-2 was apparently ‘already killing countless victims’, since according to most of the embalmers’ testimonies, the clots came with the covid genetically modifying injections, ~6 months into 2021. The difference in the 2020 natural Spike from the SARS-CoV-2 (official NIH entry ever since 2020) and the Spike from the injections is the SYNTHETIC gene encoding it, which contains 2 mutations, making the final by ribosomes expressed Spike ‘stabilized’ in the cells membranes. That happens in all cells membranes crossed by the accompanying synthetic LIPID-nanos. Once again, a reminder, natural infection is caused by the SARS-CoV-2 Spike PROTEINS coming from OUTSIDE of the cells, from EXTERNAL sources proceeding the apparent integration of viral genetic RNA material. Covid genetically modifying injections, reverse that, they produce the synthetic, MODified SPIKE PROTEIN INSIDE of ALL ACCESSIBLE CELLS, not on the MUCUS on external surface of only specific tissues carrying the ACE2 receptor. The MANDATED (!!!) injected Spike protein production is only followed by GENETIC INTEGRATION FIRST, before any anti-body response can happen, which always, can only happen in the blood. The only virus reaching blood directly is Rabbies. Thus injection of viral, toxic, non-human Spike DIRECTLY INTO BLOOD, has to be called REPROGRAMMING of the human body for a synthetic immune response, that’s called gene modification treatment, or ‘gene therapy’. Here a short article titled: 
"mRNA: Fulfilling the Promise of Gene Therapy"
by Drew Weissman1 dreww@upenn.edu and Katalin Karikó2 katalin.kariko@biontech.de from:
https://www.cell.com/molecular-therapy-family/molecular-therapy/fulltext/S1525-0016(16)30267-2 That’s where they addmited the truth, which later on was totally derailed by the very same people and everybody else: “a realization crucial to the rapid development of the life-saving mRNA COVID-19 vaccines(???) during the deadly pandemic.“ from https://arstechnica.com/health/2023/10/after-being-demoted-and-forced-to-retire-mrna-researcher-wins-nobel/
So how about about this simplest clots explanation scenario, among many, so far: 
the synthetic, patented genetic CODE for the Spike, which ‘in ALL COVID-19 vaccines in the US encodes spike with K986P/V987P mutations to stabilize its prefusion conformation’^1 in all by nanos crossed membranes, that SYNTHETIC, NON-HUMAN Spike stays in the membranes of many tissues, but in particular inside of blood vessels, with constant motion, a flow, for long enough, narrowing them down, blocking the passages with sheer forces acting on blood while supporting its '‘phase separation’, build up from fibrin, platelets, binding to metals floating nearby, in particular Ca2+ deposits (that’s the color and hardness). Remember, the biggest amount of blood vessels, carrying oxygen, is in the BRAIN.
This process would NOT start if it was the natural ‘non-stabilized’ membrane Spike in 2020, not only because the VIRAL Spike always comes from OUTSIDE of the blood vessels, but also, because many embalmers do confirm the fact that 2020 was not the year of excessive clots, in particular thanks to (the worldwide responses) hard work of Thomas Haviland MSc: 
Vejon COVID-19 Review
Latest Research Findings on Embalmers Strange Clots
The scientific observation by Embalmers about unusual patterns and forms of clots has been largely ignored by the scientific community. Update from Thomas Haviland MSc, who has been surveying embalmers experience across the world. Why would multiple experts in their field make up these observations…
Listen now
3 years ago · 65 likes · 22 comments · Dr Philip McMillan
What happens to the blood when sheer forces are applied to it? The best answer to that comes from a biological dental office* applying a new healing technology called PRF (Platelet Rich Fibrin)^2 based on a phase separation due to differences in molecular weight in rotational motion, explained at: https://decisionsindentistry.com/article/applications-platelet-rich-fibrin-dentistry/
How do the fibrin clots look like when one trims the Platelet Rich Fibrin (PRF) membrane portion of the centrifuged blood, rich in stem cells, growth factors? Fig 4A from that PRF article:
and that’s what Msc Haviland show, and many saw it in ‘Died Suddenly’:
There are some clear differences in the 2 clots pictures above, but what the North Carolina at Chapel Hill writes in 2022 about the “Fibrinogen, Fibrin, and Fibrin Degradation Products in COVID-19“ (https://pubmed.ncbi.nlm.nih.gov/36029073/), which are the same clots? That’s the UNC, (employing also Ralf Baric) Blood Research Center from the same NCH who has the patent for MOD-E-RNA injections. Their summaries of the autopsies say, quote:
”Fibrin-rich deposits have also been reported in cardiac tissue both coincident with and independent from evidence of myocarditis [60, 61]”
Fibrinogen, fibrin deposition in intravascular and extravascular compartments,
and FDPs all appear to be biomarkers of severe COVID-19 as well as active players in pathogenic mechanisms, leading to poor patient outcomes. 
additional studies are required to define the causative mechanisms by which perturbations in fibrinogen, fibrin, and fibrinolytic pathways contribute to acute disease and the increasingly prevalent ‘long COVID’ !!!!!!! 
Indeed, a fundamental understanding of the contribution of fibrinogen to parental SARS-CoV-2 will likely provide a significant benefit in defining the pathophysiology of new SARS-CoV-2 variants as well as completely  new coronaviruses that emerge in the human population.
There is NOT A SINGLE WORD ABOUT covid genetically modifying injections (completely deceptively called ‘vaccines’ everywhere) expressing the patented Spike -PP- version which sits for nobody knows how long in membranes of all organs, blood vessels, etc. , wherever the nanoparticles reached their goal, not to mention binding of sugars, ligands while equally binding to degraded, misfolded own fragments or even the genetic aspect of the synthetic mod mRNA genes themselves. This paper was supported by a grant from the National Institutes of Health and National Heart Lung Blood Institute(R01 HL160046)... How convenient for NIH, which now cashes MILLIONS of $ for patents (co-owned by MODeRNA) on the genetically modifying injections!!!! And there was another 2021 study, titled “Characterization of the ‘White’ Appearing Clots that Cause Acute Ischemic Stroke“ (Journal of Stroke and Cerebrovascular Diseases, Vol. 30, No. 12 (December), 2021: 10612), claiming the same platelets and fibrin involvement. But it is not only min stream MSM-based science, even the study published by experts like  Dr.McCullough et al. titled “A Systematic Review of Autopsy Findings in Deaths after COVID-19 Vaccination“ does not touch the clots in a single word!!! The link to this study comes from todays CHD article at: 
https://childrenshealthdefense.org/defender/cureus-retracts-study-critiquing-covid-19-vaccine-censorship/, describing yet another retracted study which is not spending a single sentence on this issue.
Note, both first 2 MSM-based studies are NOT from 2020, but from the same time the embalmers start to raise voices about the issue. The only difference is, embalmers talk about ‘vaccines’, the official ‘science’ (which these days should change its name to sci-fi) about SARS-CoV-2 infections, not mentioning the covid injections at all, for clear reasons, a total GAG order by the gov!! 
Here is a blast form the past, about fibrin, discovered in 1666…:
The entire ‘modern mad-I-Sin-e’ is in a complete cover up of every single aspect of the covid, whether short or long, with not a single serious, proper study devoted to looking at the differences between the -KV- and -PP- forms of the toxic, synthetic Spikes. Maybe because it would also imply how many actually have the natural -KV- form….  
  This would also explain why all the geneticists, even the ones testifying in Senates, who still do work for medical cartels, will NOT SEQUENCE THE DIFFERENT SPIKES IN HUMAN BODIES. The very first SARS-CoV2 variant had just one single amino acid difference and yet, the entire dipeptide change -KV- to -PP- is suddenly forgotten??
What are the 3D SARS-CoV0-2 Spike crystallographic structures out there and do they point to maybe more than saying that the -PP- Spike version is the ‘prefusion’ version sitting in the membranes in much more stable way? In this study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109970/  titled “Multifaceted membrane binding head of the SARS-CoV-2 spike protein“ there is a complete mixture of  the 'natural -KV- and the artificial -PP- Spike mutants, for example:
6xlu, 7jwy, 6zge, 6zow, 6xm3 has the ‘SRLD-PP-EAEVQI’ modified sequence , and equally the 7jwy, 6zge, 6zow and 6xm3 all are the Spikes with -PP-mutation, except the natural forms in the Pdb Data Bank at https://www.rcsb.org/fasta/entry/6XRA , 6ZB4 , 6XR8, 6ZB5. Why are researchers mixing synthetic Spikes with natural version when they supposedly do research on natural infection only??? 
This part of their abstract is a total fall into a self inflicted net of questions: ”In contrast, all antibodies that target the spike head would block the membrane docking process that precedes ACE2 recognition. Together this illuminates the engagements of the spike protein with plasma, endocytic, ER or exocytic vesicle membranes that help to drive the cycle of viral infection, and offers novel sites for intervention.”
Emailing the senior author of this work and asking for an explanation, ended with no response from the Dep. of Biochemistry, University of Alberta, Edmonton, Canada..
Let’s switch to the fibrin-/-ogen issue of the blood, in particular the MODeRNA involvement. 
How much Mod-E-RNA is valuing the human genome while hacking the programmable, NOW DIGITAL biology was wonderfully admitted by its cooking Chef of the Flagship Pioneering and CEO & Moderna Co-founder Dr. Noubar Afeyan | Spotlight | Code 2022 on youtube, oh video does not exist, anymore…. Well, this link gives some info on it: https://www.fiercebiotech.com/biotech/shots-goal-to-deterministic-drug-development-flagship-ceo-moderna-chair-noubar-afeyan-pens 
And while MODeRNA was essential in starting the genetic attack, the industry flows with it, so look at the newest Pfizer Seagen purchase, which is all about: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658517/ peptide drug conjugates, the future of ‘med-i-Sin-e’, ALL looking like a Spike based connection of homing peptides, linkers and payloads, ALL originating from Spike, mind you, the injected and embedded one. You connect the new drug to whatever human part the Spike docked to, and you will get your cancer fixed, apparently. Not only there is fight for who has the rights to the new future https://www.jdsupra.com/legalnews/ptab-issues-final-written-decision-3424933/
but the fact, that https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452662/ Spike might be in every cancer tissue, possibly implies, that Bourla might be right saying every 3rd person on this planet will get a cancer in 2025…
Now to 866 aa’s long fibrin, https://www.uniprot.org/uniprotkb/P02671/entry with following features, binding a LOT of calcium:
Site 35-36`Cleavage; by thrombin; to release fibrinopeptide A ( at residues ‘RG‘)
Site 100-101`Cleavage; by plasmin; to break down fibrin clots (residues ‘KD’)
Site 121-122`Cleavage; by hementin; to prevent blood coagulation (residues ‘NN’)
Site 123-124`Cleavage; by plasmin; to break down fibrin clots (residues ‘RD’)
Binding site   791   Ca²⁺ (UniProtKB | ChEBI)
Binding site   793   Ca²⁺ (UniProtKB | ChEBI)
Binding site   795   Ca²⁺ (UniProtKB | ChEBI)
Binding site   797   Ca²⁺ (UniProtKB | ChEBI)
that section binding Ca+2 around the  781-800, with the specific residues binding the Calcium 791-793-795-797 D*aD*qW*eE* has its sequence:
NN←>MQFSTFDR<→D-A-D-Q-WEENCA
You see what happens when hementin cuts at ‘NN’, and further plasmin cuts at ‘RD’? The calcium looses their bonding partners, the entire net of amino acids holding calcium in place inside of the protein falls apart, the calcium goes free and accumulates. Btw. most of the digestive enzymes in general involve the smallest dipole moment out there, a pair of positive-negative residues, i.e. Arg-Asp=RD, or KD. This is like a micro knife, way better than graphene, which also cuts into all proteins and genetic material like RNA, DNA, the difference is graphene does it non-specifically, anywhere, anytime, unpredictable.
How ironic that Ca2+ fibrin section is encoded by ‘DADQWEEN’…. The one from UK with MEROPS digestive enzymes data base, owned by the Welcome Trust???
Direct comparison of the 866 residues long fibrin code P02671, with Spike (YP_009724390.1) has ~30% identities (Query line is fibrin, Sbjct is Spike2020):
20-35 Fibrinopeptide, nowhere to find by BLAST, so by hand
 ADS--GEGDFLAEGGG--VR    fibrin
PGDSSSG---WTAGAAAYYVGYL  Spike

here what BLAST comes out with:
Query  310  PGSSGTGGTATWKPGSSGPGSTGSWNSGSSGTGSTGNQN  348
            PG +G      +K      G   +WNS +  +   GN N
Sbjct  412  PGQTGKIADYNYKLPDDFTGCVIAWNSNNLDSKVGGNYN  450
                                          *<=glycosylation
Query  424   TRREYHTEKLVTSKGDKELRTGKEKVTSGSTTTTRRSCSKTVTKTVIGP-----DGHKEV  478
             T+R ++  +++T+  D    +G   V  G            V  TV  P     D  KE 
Sbjct  1105  TQRNFYEPQIITT--DNTFVSGNCDVVIG-----------IVNNTVYDPLQPELDSFKEE  1151
Query  479   TKEVVTSEDGSDCPEAMDLGTLSGI  503
               +   +    D    +DLG +SGI
Sbjct  1152  LDKYFKNHTSPD----VDLGDISGI  1172

Query  59   DWNYKCP---SGCRM  70
            D+NYK P   +GC +
Sbjct  420  DYNYKLPDDFTGCVI  434

and this is just mindblowing: FRAGMENT from S1 N-terminal portion, THE MOST DIFFERENT to all previous old corona Spikes, must be 'bat's fresh cloning':

Query  95   YQKNNKDSHSLTTNIMEILRGDFSSANNRDNTYNRVSEDLRSRIE-------VLKRKVIE  147
            Y KNNK       + ME     +SSANN   T+  VS+     +E        L+  V +
Sbjct  145  YHKNNK-------SWMESEFRVYSSANN--CTFEYVSQPFLMDLEGKQGNFKNLREFVFK  195
and continued with the sequence:
Query  148  KVQ-HIQLLQKNVRAQLV-DMKR----LE--VDIDIKIRSCRGSCSRALAR  190
             +  + ++  K+    LV D+ +    LE  VD+ I I   R     AL R
Sbjct  196  NIDGYFKIYSKHTPINLVRDLPQGFSALEPLVDLPIGINITRFQTLLALHR  246
BLAST puts no C-terminal section like, so here by hand:
        * * * - *
NNMQFSTFDRDADQWEENCA  fibrin
       FD + D   E
SCGSCCKFD-EDDS--EPVLKGVKLHYT spike C-terminal

BLAST aligns different portion instead, the ACE2 binding part of Spike:
                  ====>   *digestion of the 'DADQWEEN' aligns with ACE2 binding    
Query  777  YTSHNNMQFSTFDRDADQWEENCAEVYGGGWWYNNCQAANLNGIYYPGGSYDPRNNSPYE  836
            Y          F+RD         E+Y  G     C        Y+P  SY       ++
Sbjct  453  YRLFRKSNLKPFERDIS------TEIYQAG--STPCNGVEGFNCYFPLQSYG------FQ  498
Query  837  IENGVVWVSFR  847
              NGV +  +R
Sbjct  499  PTNGVGYQPYR  509
take that fibrinogen portion 95-147 so similar to Spike, with the RGD integrin motif in it(!!) : YQKNNKDSHSLTTNIMEILRGDFSSANNRDNTYNRVSEDLRSRIEVLKRKVIE
 SHSLTTNIMEILRGDF--SSA-NNRDNTYNRVS  FIBRINOGEN
           ++RGD     A ++   +       <<=IDENTITIES
 CFTNVYADSFVIRGDEVRQIAPGQTGKIAD     Spike RGD fragment
and search for PATENTED proteins containing that fibrinogen section, 100% of can be found in MANY patented items, among others for example:
nano-recombinant fibrinogen for fibrin sealants  Patent: US 9381232-B2 5 05-JUL-2016; BAE Systems Information and Electronic Systems Integration Inc.; NH
Regulated biocircuit systems.  Patent: US 11446398-B2 31796 20-SEP-2022 OBSIDIAN THERAPEUTICS, INC.; Cambridge, MA
AKX87622   289 aa  PAT 13-AUG-2015 DEFINITION  Sequence 973 from patent US 8999380. Modified polynucleotides for the production of biologics and proteins associated with human diseases. Patent: US 8999380-B2 973 07-APR-2015; Moderna Therapeutics, Inc.; Cambridge, MA
Let’s stop here. Forgive the sidewalk through this 2013 filed MODeRNA 411 pages long patent, which is NOT searchable any more, because of putting out pictures version of the file!!! Some important contents from it, between the divider bars below:
Patents mentions proteins like FactorIX, expression of VEGF with PSEUDO-U(!), VEGF with N1-methyl-Pseudo-U (the one in INJECTIONS), GCSF, hAPO-A1, plasminogen in HeLA cells, GALT, ASL (50kd), TAT (50kd), GBE (70kd),  ProTHROMBIN, CLP (148kd), TGF-beta1, OTC (40kd), LDLR IgG, hFactorXI, FactorVII, Insulin Glargine/Aspart/Lispro/GluLisine, Tissue Factor,  Human Growth Hormone, Human Erythropoietin, Lisosomal Acid Lipase, Glucocerebrosidase (59.7kd), Luciferase (60.7 kD), FactorVIII (for all U’s, natural, Pseudo and N1-methyl-pseudo). 
BLAST searches on >600 CHOSEN proteins as admitted by ModeRNA are: “Default parameters in the BLAST algorithm include, for example, an expect threshold of 10, Word size of 28, Match/Mismatch Scores 1, −2, Gap costs Linear. Any filter can be applied as well as a selection for species specific repeats, e.g., Homo sapiens.“, and that’s NOT WHAT NIH pages are offering as ‘DEFAULT’ in their BLAST, you get x1000 LESS sensitivity in search for identities/similarities! That’s a total NIH deception, but not for military protected MODeRNA patent files using very different BLAST then researchers at NIH!!! 
Admission of variant possibilities: “Such a library may contain 10, 10², 10³, 10⁴, 10⁵, 10⁶, 10⁷, 10⁸, 10⁹, or over 10⁹possible variants (including, but not limited to, substitutions, deletions of one or more residues, and insertion of one or more residues).“ ===> Long way to go variants!
Anti-viral polypeptide comprises or consists of from about 6 to about 100 amino acids, e.g., from about 6 to about 75 amino acids, about 6 to about 50 amino acids, about 6 to about 25 amino acids AND “ the anti-viral polypeptide is cytotoxic to a bacterium, fungus, protozoan, parasite, prion or a combination thereof. In certain embodiments, the anti-viral polypeptide is cytostatic and cytotoxic to a bacterium, fungus, protozoan, parasite, prion, or a combination thereof.” AND “the anti-viral polypeptide is cytostatic to a tumor or cancer cell (e.g., a human cancer cell).“
Genetic DETAILS: They harbor signatures like Kozak sequences which are commonly known to be involved in the process by which the ribosome initiates translation of many genes. Kozak sequences have the consensus CCR(A/G)CCAUGG, where R is a purine (adenine or guanine) three bases upstream of the start codon (AUG), which is followed by another ‘G’. 5′UTR also have been known to form secondary structures which are involved in elongation factor binding.
One paragraph is worth mentioning: ‘5′ UTR and Translation Initiation’ which points to the CONTROLLABLE PROGRAMMING OF HUMAN TISSUE: “For example, introduction of 5′ UTR of liver-expressed mRNA, such as albumin, serum amyloid A, Apolipoprotein A/B/E, transferrin, alpha fetoprotein, erythropoietin, or Factor VIII, could be used to enhance expression of a nucleic acid molecule, such as a mRNA, in hepatic cell lines or liver. Likewise, use of 5′ UTR from other tissue-specific mRNA to improve expression in that tissue is possible for muscle (MyoD, Myosin, Myoglobin, Myogenin, Herculin), for endothelial cells (Tie-1, CD36), for myeloid cells (C/EBP, AML1, G-CSF, GM-CSF, CD11b, MSR, Fr-1, i-NOS), for leukocytes (CD45, CD18), for adipose tissue (CD36, GLUT4, ACRP30, adiponectin) and for lung epithelial cells (SP-A/B/C/D).“ 
Let’s look at that SERUM AMYLOID A (SAA1) , expressed in liver upon cytokine stimulation, with description at: https://www.uniprot.org/uniprotkb/P0DJI8/entry , which describes its subcomponents (the reduction into pieces so much liked by molecular biologists then playing God, while living with an illusion they can ever be better in Creation…):
Region19-45 Important for amyloid formation; forms amyloid fibrils in vitro. Here its entire sequence:
MKLLTGLVFCSLVLGVSS—SIGNAL-
RSFFSFLGEAFDGARDMWRAYSDMREA— fragment responsible for amyloids formation and the rest:
NYIGSDKYFHARGNYDAAKRGPGGAWAAEVITDARENIQRFFGHGAEDSLADQAANEWGRSGKDPNHFRPAGLPEKY
whereby AANEWGRSGKDPNHFRPAGLPEKY is cleaved upon amyloid formation.
and here some of its BLAST comparisons outputs, with NIH default parameters, only:
Query  13   VLGVSSRSFFSF------LGEAFDGARD  34 SAA1
            VL  S++ F  F      + +  D  RD
Sbjct  551  VLTESNKKFLPFQQFGRDIADTTDAVRD  57 Spike
Query  39   YSDMREANYIGSDKYFHARGNY---DAAKRGPGGAWAAEVITDAR--ENIQRF  86 SAA1
            + ++RE  +   D YF+    +   +  +  P G  A E + D     NI RF
Sbjct  186  FKNLREFVFKNIDGYFKIYSKHTPINLVRDLPQGFSALEPLVDLPIGINITRF  238 Spike
Query  30   DGARDMWRAYS------DMREANYIGSDKYFHARGNYDA  62
            D     WR YS        R    IG++   H   +Y+ 
Sbjct  627  DQLTPTWRVYSTGSNVFQTRAGCLIGAE---HVNNSYEC  662
Query  31   GARDMWRA  38
             ARD+  A
Sbjct  845  AARDLICA  852

   MKLLTGLVFCS-LVLG-VSS       Signal for expression of SAA1
   MF-----VF--LVLLPLVSSQCVNL  Signal for expression of Spike
here few fragments all by hand
      RS---------FFSF--LGEAFDGARDMWRAYSDMREA
      RSSVLHSTQDLFLPFF-SNVTWFHAIHVSGTNGTKRFDNPVLPFND  Spike
or another way:
               RS-FFS---FLGEA-------FDGARD---MWRAYSDMREA
TTRTQLPPAYTNSFTRGVYYPDKVFRSSVLHSTQDLFLPFFSNVTWFHAIHVSGT  Spike

PGDSSSGWTAGAAA--------YYVG------L--Q-PRT----------F----L-LKY SPIKE 
PGGA---WAAEVITDARENIQRFF-GHGAEDSLADQAANEWGRSGKDPNHFRPAGLPEKY

and here comparison of SAA1 own fragments, similar to one another:

RSFFSFLGEAFDGARDM----WRAYSDM--REA   SAA1cont.1.
+ F    G  +D A+      W A      RE    IDENTITIES
KYFHAR-GN-YDAAKRGPGGAWAAEVITDARENIQ  SAA1cont.2.

KYF-HARGN--YD-AAKR--GPGG----AWA-AEVITDARENIQ  SAA1cont.1
++F H   +   D AA    G  G     +  A +     E     IDETITIES
RFFGHGAEDSLADQAANEW-GRSGKDPNHFRPAGL----PEKY   SAA1cont.3
              => usually cleaved upon amyloid formation
The above indicates SAA1 consists of domains with simiar properties..

And now by hand section of Spike having similar AA's composition to the amyloid

      RS---------F--FSFLGEAFDGARD---MWRA--YS--DMREA Amyloid SAA1
      RS         F  F F   + + +     +++A   S  +   + IDENTITIES
      RSSVLHSTQDLFLPF-F---S-NVT-----WFHAIHVSGTN--GT Spike 2020

and few other sections of Spike with similar character:

RSFFSF--LGEAF-DGARDMWRAYSDMREA ====SAA1
KRFDN-PVLP--FNDGV---YFA-STEK-S ====Spike 
or
RSFFSFLGEAF-DGA-----------RDMWRAYSDMREA ====SAA1
KRF-DNPVLPFNDGVYFASTEKSNIIRG-W-IF--GTTL ====Spike
and one more SPike fragment:
RSFFSFLGEAF-----DGAR--------DM-W-RAYSDM----R---EA ====SAA1
KDFGGFN---FSQILPDPSKPSKRSFIEDLLFNKVTLADAGFIKQYGDC
The above MODERNA sequence number 973 encodes  289 residues long human liver peptide. That’s HUMAN FGA (Fibrinogen alpha/beta chain family; pfam08702)  protein from 2004 NIH MGC Project (NOT accessible at the claimed site any more http://mgc.nci.nih.gov !!!).  Mammalian Genome Collection information can be found through the I.M.A.G.E. Consortium /LLNL at:  http://image.llnl.gov, equally no more to find! NIH data base still has it at https://www.ncbi.nlm.nih.gov/protein/AAH70246.1 , whereby it is EXTREMELY important to read the COMMENTS lines in this link! Note the DIFFERENT name for the 49-191 part of the sequence, NIH calls it also ‘Fib2’. 
>US_8999380_B2_973
MFSMRIVCLV LSVVGTAWTA DSGEGDFLAE GGGVRGPRVV ERHQSACK-DS
DWPFCSDEDW NYKCPSGCRM KGLIDEVNQD FTNRINKLKN SLFEYQKNNK
DSHSLTTNIM EILRGDFSSA NNRDNTYNRV SEDLRSRIEV LKRKVIEKVQ
HIQLLQKNVR AQLVDMKRLE VDIDIKIRSC RGSCSRALAR E-VDLKDYEDQ
QKQLEQVIAK DLLPVVNLQV TANNLLVARV TTEETPHLKA RAIKWQMRPE
VKPIMKEHIA PREAMLNLAL SEVSTLLLWG SLPCPPRLS       
BLAST-ing this 2004 MODeRNA sequence among non-patented proteins, gives:
- the 2005 sample from Tissue Procurement: CLONTECH from 2002 NIH MGC Project, 
- the 2021 289 residues long proteins from a Puerto Rican, an FGA sample derived from his blood B-lymphocytes submitted to The Center for Computational Biology, Johns Hopkins University…? His FGA had ONE mutation V→L. 
- next chimpansee sample had the same mutation but in addition, non homologous N→K, and 2 T→A mutations
- not the same but similar with the next orangutan sample.
The entire rest of fibrinogens are shorter or much larger samples. A 2005 much shorter version of NIH MGC human protein acquired by CLONTECH: https://www.ncbi.nlm.nih.gov/protein/AAI05804.1 ends exactly where the 2021 Puerto Rican sample got mutated, after the DLLP section :
Query  181  RGSCSRALAREVDLKDYEDQQKQLEQVIAKDLLPVVNLQ  219
            RGSCSRALAREVDLKDYEDQQKQLEQVIAKDLLP  + Q
Sbjct  181  RGSCSRALAREVDLKDYEDQQKQLEQVIAKDLLPSRDRQ  219
whereby completely different section appeared at the C-term: hlplhsslgdrarlhlktnktakkkkkkkkk, with 9 positive lysines at the very end!
Much longer 2015 FGA isoform https://www.ncbi.nlm.nih.gov/protein/ALQ33521.1 was from "pooled heart, liver, brain, testis and placenta tissues". That’s what Dana-Farber Cancer Institute was doing, alternative splicing of the same gene in different tissues. That’s where CDC director Walensky’s husband works, who carries the patent for part of the 2020 Spike… This longer FGA sample has after that DLLP section added following string of residues:
                                                                                 h lplikmkpvp dlvpgnfksq       241 lqkvppewka ltdmpqmrme lerpggneit rggstsygtg setesprnps sagswnsgss       301 gpgstgnrnp gssgtggtat wkpgssgpgs tgswnsgssg tgstgnqnpg sprpgstgtw       361 npgssergsa ghwtsessvs gstgqwhses gsfrpdspgs gnarpnnpdw gtlnlalsev       421 stlllwgslp cpprls
whereby the C-terminal portion of it was ‘almost;’ identical with the by MODeRNA in 2015 patented sequence AAH70246.1:
Query  261  PREAMLNLALSEVSTLLLWGSLPCPPRLS  289 MOD-eRNA 2015 patent
            P    LNLALSEVSTLLLWGSLPCPPRLS
Sbjct  408  PDWGTLNLALSEVSTLLLWGSLPCPPRLS  436 DANA-FArber 2015 (cancer?)sample
Now the Stunning: a 2023 chinese pedigree sample, fibrinogen alpha chain isoform alpha precursor, https://www.ncbi.nlm.nih.gov/protein/NP_068657.1, affected with Congenital dysfibrinogenemia due to variant of FGG gene, published in other work in J. Cardiothorac Vasc Anesth 37 (6), 942-947 (2023) in an article titled: “ Interaction Between Platelet and Fibrinogen on Clot Strength in Healthy Patients“, and many others, all related to the same sequence, which is ONE AMINO ACID different than KAI2536318.1, the 2021 to JHI submitted Puerto Ricarian blood sample, a T→A mutation :
Query  301  GPGSTGNRNPGSSGTGGTATWKPGSSGPGSTGSWNSGSSGTGSTGNQNPGSPRPGSTGTW  360
            GPGSTGNRNPGSSGTGGTATWKPGSSGPGS GSWNSGSSGTGSTGNQNPGSPRPGSTGTW
Sbjct  301  GPGSTGNRNPGSSGTGGTATWKPGSSGPGSAGSWNSGSSGTGSTGNQNPGSPRPGSTGTW  360
All what is needed now is to look at the literature history of that ‘pathological’ NP_068657.1 entry:
a)  Blomback,B., Hessel,B. and Hogg,D.   “Disulfide bridges in nh2 -terminal part of human fibrinogen.” Thromb Res 8 (5), 639-658 (1976)
b) Fretto,L.J., Ferguson,E.W., Steinman,H.M. and McKee,P.A. “Localization of the alpha-chain cross-link acceptor sites of human fibrin.” J Biol Chem 253 (7), 2184-2195 (1978)
c) Cottrell,B.A., Strong,D.D., Watt,K.W. and Doolittle,R.F. “Amino acid sequence studies on the alpha chain of human fibrinogen. Exact location of cross-linking acceptor sites.” Biochemistry 18 (24), 5405-5410 (1979)
d) Watt,K.W., Cottrell,B.A., Strong,D.D. and Doolittle,R.F. “Amino acid sequence studies on the alpha chain of human fibrinogen. Overlapping sequences providing the complete sequence” Biochemistry 18 (24), 5410-5416 (1979)
e) Fish RJ and Neerman-Arbez M. “Fibrinogen gene regulation” Thromb Haemost 108 (3), 419-426 (2012)
f) Hoppe B. “Fibrinogen and factor XIII at the intersection of coagulation,             fibrinolysis and inflammation.” Thromb Haemost 112 (4), 649-658 (2014)
which indicates a timely flow on information needed to develop what we are dealing with now.
That 2015 (filed in 2013) ModeRNA patent seems to be connected with all sorts of  Hereditary Hypodysfibrinogenemia, Hereditary Hypodysfibrinogenemia,  Congenital   dysfibrinogenem in China, Thromboembolic Pulmonary Hypertension in Turkey. 
One more pre 9/11 entry, a 2001 entry coded AAK31372.1 (LOCUS AF361104_1), equally encoding the fibrinogen alpha chain preproprotein, isoform alpha. The difference between the this 2001 and the in 2023 deceased samples NP_068657.1, the C-terminal is different, ‘LPCPP’ in 2001 →’PSLSP’ in 2023:
Query  601  YKMADEAGSEADHEGTHSTKRGHAKSRPVRGIHTSPLGKPSLSP  644  2023 NP_068657.1
            YKMADEAGSEADHEGTHSTKRGHAKSRPVRGIHTSPLGK    P
Sbjct  601  YKMADEAGSEADHEGTHSTKRGHAKSRPVRGIHTSPLGKLPCPP  644  2001 AAK31372.1
And now go to MEROPS data base (https://www.ebi.ac.uk/merops/cgi-bin/specsearch.pl) and try to find which enzyme digests the -PP- bond, rarely anything… 
Thus the pre-2001 fibrinogens were VERY STABLE, but no more now, in 2023!
Also remember, the synthetic Spike in the covid genetically modifying injections contains on purpose the -KV-→ -PP- undigestible modification….
Amyloid plaques possibly accumulate due to mercury inhibition of digestive enzymes which would take apart those amyloids. Low levels of mercury also HYPER phoshorylate the tau proteins, connecting tubulin with neurofibers. All enzymes related to brain build ups are always MERCURY inhibited. 
This chaotic post will end with this important summary from https://link.springer.com/article/10.1007/BF01683593 , a paper titled “In vitro inhibition of digestive enzymes by heavy metals and their reversal by chelating agent: Part I. Mercuric chloride intoxication“:
“The effect of mercury on alkaline phosphatase, lipase, aminotripeptidase and glycylglycine dipeptidase in the liver and digestive tract of Channa pynctatus is investigated in vitro. Mercury inhibits the activities of all these enzymes and the degree of inhibition increased with the increase in the concentration of the metal. Addition of EDTA, a chelating agent, restored the mercury inhibited enzyme activity and the degree of restoration was related to the concentration of the chelating agent.”
Seems like chelation first and then digestion, could be one way out here. This post had some of it while using EDTA:
In the https://go2.thetruthaboutcancer.com/eastern-medicine/episode-3/  at ~17:00 there is a practitioner who is using the following detox suppositories products (according to the patent https://patents.google.com/patent/US6720356B2/en :
Medicardium (Magnesium EDTA chelation for heavy metals and calcifications while removing lead, mercury, aluminum, cadmium, arsenic, uranium, nickel, barium, thallium, oxidized irom (Fe +3)
Xeneplex, i.e. Glutathione/organic cofee removing pesticides, petrochemicals, pharmaceuticls, molds, solvents, artificial colors, 
 Glytamins, herbs and amino acids for liver/gallstones/kidney stones/, bile sludge, parasites, candida, constipation
That biological dentistry can help anyone, including MD’s, with finding connections between the health status of ones mouth and any other organ in the human body, illustrated in a diagram at the very end of this post.
An update from 4/8/2024 needs one important addition. The ‘non-digestible’ Spike fragment which suppose to be responsible for the ‘super-binding’ mode to other proteins and possibly building the cloths: ‘KSTNLVKNKCVNFNFNGLTGTGVLTESNKK‘ has a very high homology with a 2001 PATENT EP 1074617-A2  for HUMAN ‘Primers for synthesising full-length cDNA and their use’… 
Thank you all readers (if any, given google searches for this substack…) for attention and your TIME!
Literature.
T.J.C. Tan et al. “High-throughput identification of prefusion-stabilizing mutations in SARS-CoV-2 spike“ Nature Communications Vol. 14, Article number: Apr 2003 (2023) https://www.nature.com/articles/s41467-023-37786-1
2017 Editor(s): Richard J. Miron & Joseph Choukroun “Platelet Rich Fibrin in Regenerative Dentistry: Biological Background and Clinical Indications: Biological Background and Clinical Indications“.
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Covid19 and what alpha-lipoic acid (ALA) can do for You? 
mejbcart — Tue, 20 Feb 2024 22:57:06 GMT
Update 2/21/2024: Substack is blocking sending of the comments on this post. So, dear readers, please have patience with responses to something I can’t get/see…. 
Update 2/23/2024: completely unrelated to this post, for those, who like to laugh with Robin Williams, collection of links at the end;) Also RFK on real history, which includes general vaccination (mentioned covid injections are not named properly) issues, at: https://articles.mercola.com/sites/articles/archive/2024/02/23/robert-f-kennedy-jr.aspx also reposting a link given today by Strange Sounds, how Congress works, last citation in the literature^14 .
Update 2/27/2024: Dr. David Martin at ICD summit explaining why and who is reponsible for the global genocide: https://www.brighteon.com/d37f1d61-059f-49eb-a16f-2175b25b742c
Can??? You can’t remember that, but this tiny ALA acid, Pubchem calls it 5-(1,2-Dithiolan-3-yl)pentanoic acid, is working inside of you like crazy from the first moment of your conception and it will until the last breath of your earthly existence, because it is a fundamental metabolite and a geroprotector (https://pubchem.ncbi.nlm.nih.gov/compound/864 ). Strangely the same Pubchem data base describes ALA as ‘irritant’ and ‘environmental hazard‘ which is like putting YOU, a HUMAN, in a bottle with 2 red warning symbols of ‘chemical safety’! That NIH chemicals data base defines for example Glyphosate as ‘corrosive’ and equally as ‘environmental hazard’! What an inconvenient truth in the glyphosate global warning... Few more words about this artificial amino-acid.
So the EPA decides how much of glyphosate to sprinkle us with, FDA checks how much of it can we eat, which then gets to the health specialists at NIH, and just in case you really get sick, then kindly call for help the disease epicenter at CDC.  There is also the Collaborative Initiative between NIH and FDA, to fast-track inventions, for the humans, according to their health: https://www.nih.gov/news-events/news-releases/nih-fda-announce-collaborative-initiative-fast-track-innovations-public. Since the levels of new synthesized chemicals grow exponentially with every day (like the timing of the S-EKG wave of heart diseased victims after the covid genetically modifying injections), that need to change the ‘approved levels’ of something ‘allowable’, represents a nice fast-track of falls into every loophole of that net of col-labor-at-I-on-s. 
And now, back to the middle-man, FDA and the so dangerous ‘environmental hazard’ alpha-lipoic acid (ALA).
Dr. Burton M. Berkson, was the principal investigator in using alpha lipoic acid intravenously as a drug, while working for  >20 years at the FDA^1. After experiencing remarkable recoveries of liver diseases ending up with no need for transplants, of diabetic neuropaties ending up with thousands of no more needed amputated extremities, and trying advocate for it as a ‘new drug’, he was utterly shut down and been told, the huge facilities like NIH, do not want to have rescued toes, because they would loose their patients, mind you, the toeless ones!!! Cutting of the extremities on the other hand would make lot of money, thus the alpha-lipoic acid had to be put on a shelf of ‘drugs bad for the business’. This came in an ‘off the record explanation’ for stopping every procedure which would involve alpha-lipoic acid. ALA would not only put out of business liver transplants^2, but equally diabetes drugs, while lowering blood sugar^3, heart drugs while dissolving plaques^4, while stimulating stem cells in the lungs^5 it would affect those drugs too, and while changing cancer metabolism from anaerobic to aerobic^6,^7, it would affect cancer drugs business.. Dr. Burtson ended up loosing his position at FDA, for a ‘drug’ which was too good to be true, now still available in all nutritional/supplemental stores, for our luck. 
A living prosecution of Dr. Berkson, as a professional with heart and consciousness ended up with not getting the s.c. ‘Black Craw Award’ for MD’s, who contributed to most deaths of their patients, in many hospitals, every month.. Adding to this the fact, that the NIH important directors KNOW about every such efficient cancer treatment, (in particular when it is completely natural and can’t be patented) but are NOT giving away this knowledge to anyone, letting everyone else DIE OF CANCER (including places like Stanford, Harvard, etc.), it seems like we are in a hell of satanic actions by a cruel death cult. In Deb 2024 Dr. David Martin explains why certain people are EXCLUDED from informed consent when talking medical experimentation: “We actually said, that we were actually in 1948, prohibit experimentation on humans at all costs. But, at exactly the same time 45 U.S. Code Section 46-C created an exemption. And the exemption said, that if you were a prisoner, if you were an orphan, if you were in the military service, or in any part of the federal service (yes that includes NIH scientists, participating in the very genocide), you actually did not have to receive informed consent.“ Does that mean, all the dead scientists participating in gov projects, can be killed/experimented with, without informed consent…???
And the ALA as an mitochondrial nutrient, important antioxidant, free radical scavenger, was even tested with CoQ10 in the first ‘22 study^8 for the efficacy in chronic Covid syndrome. The study concluded, that the primary and secondary outcomes were met. In 2021 scientists already ‘expected’ that ALA ‘might be of some use’ against viral infections, including covid19. Not only that, it positively influenced toxic situations connected with gp-120 from HIV, the glycoprotein so similar to the toxic Spike protein, encoded in genes applied in every Mod-eRNA/Pfizer genetically modifying injection.  Quick look how simplified ALA looks like in the 2 modes of its actions:
According to another^9 study, ALA similar to NAC, ascorbic acid, and vitamin E in form of intravenous injections was inhibiting viral replication and inflammation both in various cell lines models and in the mice. ^9 mentions further 10 publications with positive effects of ALA in covid19 and it also points to ever since 1991 countless publications describing positive outcomes of ALA affecting HIV infections. In Aug ‘21 another ALA study^10 pointed out its application against Cardiovascular Diseases during COVID-19 Infection, indicating following involved pathways:
A quote from that Aug ‘21 study :”In this context, a compound such as the alpha-lipoic acid (ALA), which is a potent antioxidant and an inhibitor of NF-κB activation [8,9], may boost human host defense against SARS-CoV-2 and could play a vital role in the treatment of patients.” Well, NIH/CDC/FDA et al. knew too good that ‘environmental hazard’ named ALA, in order not to allow that nutrient to be used, as a cure, in the ‘covid19 emergency’.
A summary of all the ALA biological features was given recently in in yet another article ^10a titled “Molecular and Therapeutic Insights of Alpha‑Lipoic Acid as a Potential Molecule for Disease Prevention“.  
In the early days of 19th century the biological sciences were busy with finding out how different organisms survive, i.e. what ‘food’/chemicals/biological substances they need in order to thrive, or die. That knowledge of being on the verge of life and death, depending on so many nutrients/chemical substances, all deeply controlled by the Rockefellers, is having an effect to this very day. An example, an average official daily dose of VitC for an adult male is ~90mg, a plasma infusion for a cancer patient starts with ~100g, that’s about 1000 times more then the ‘recommended’ amounts…
In case of ALA, its history goes way back to 1941, when Dr. Virginia C. Dewey showed that Tetrahymena, the unicellular eukaryote needed three factors I,II,III to grow. In addition to the growth required vitamin B complexes, casein growth medium (Factor III, source of amino acids) was replaced by pyrimidine (has derivatives in form of 3 nucleic acids C, T, U), the other natural growth material (Factor I) was replaced by purine and folic acid. The last Factor II assuring growth, was supplying the thioctic acid, i.e. the lipoic acid (ALA). The many parallel studies on ALA and its function related to metabolic energy within the TCA cycle, ended up with few equivalent names for one and the same substance, as pointed out by Melvin Calvin in his 1954 paper:  
The extremely high binding affinity of alpha-lipoic acid to pyruvic oxidase and alpha-ketoglutaric oxidase, and other important enzymes, as reported by G. Seaman (from Galvestone Laboratory in Texas in 1954 Federal Proceedings p. 731)^11 was eliminated, i.e. completely removed, by adding just one compound, aluminum… Around the same time the biochemist Fritz Lipmann got his Nobel prize for coenzyme A (CoA, “A” stood for “activation of acetate.”), involved in acetylation of choline, in the synthesis of citrate and acetoacetate, and in pyruvate and fatty acid metabolism. In particular pyruvic acid oxidation was very important for Lipmann, (trained like most scientists in Rockefeller Institute), because the pyruvic acid stage is where respiration branches off from fermentation, the hallmark of cancer. His interest in fluoride inhibiting muscle contraction, was directly related to fluoride inhibiting glycolysis while forming a stable fluoro-methaemoglobin (https://nap.nationalacademies.org/read/11807/chapter/14#249). In his 1929 thesis work Lipman described how fluoride also inhibits another essential enzyme, liver esterase. It becomes clear, that F. Lipmann knew all the possible ways to shut down a living organism, completely. 
Thus no surprise here, Fritz Lipmann proudly received the National Medal of Science from President Lyndon B. Johnson in 1966 for his discoveries and contributions to the conceptual structure of modern biochemistry (https://academic.oup.com/eurheartj/article/41/28/2608/5875675). It was the same Lyndon B. Johnson, who once said “ he who controls the weather will control the world”, archived at https://archive.org/details/he-who-controls-the-weather-will-control-the-world-lyndon-b-johnson . Please, listen to his statements carefully, Congress approved the geoengineering efforts going on for decades by now.. What are the current possible consequences of these findings?? Maybe that’s why aluminum is everywhere, including almost every old style vaccine vial injected into arms of newborns and adults, it is in rainwater, food supply, every breath we take.  
So it is ALA, which depending on the presence of light (opening or closing the cyclic disulfide ring) is capable of influencing the photosynthesis and its inversion, the TCA cycle^12, and that while not even representing a pi-bond system:
 
M. Calvin’s thioctic acid (ALA) dilemma in his work on the photosynthesis was about water splitting,  CO2 conversion into ever growing carbon chains of sugars (food for our brains), all depending on light, a cycle which in the darkness would be set up to go into TCA. The missing link between the two inverted processes was the thioctic acid (ALA), which was processing the energy molecule, pyruvic acid. According to Szent-Gyorgi, the spectroscopic transitions involving the triplet excitations in water/ice are stabilized by SH groups, which is the part of that ALA disulfide linkage, which possibly brings the chlorophyll to its light dependent triplet state affecting the water. 
The gene of the SARS-CoV2 Spike protein used across the globe in all ModErna/Pfizer injections caries FOUR (4!!!) codes for the Cys-Cys dipeptides in its C-terminal portion: “MLCCMTSCCSCLKGCCSCGSCCK“ (entire sequence available at https://www.ncbi.nlm.nih.gov/nuccore/NC_045512 ), that is in a sense, for each of these CC’s a potential sulphur-sulphur bond, something UNPRECEDENTED among protein structures! Have to add this now, I worked on MANY of the 3D protein structures, for 2 decades!) Is this just a coincidence now to see a paper like the one at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8189037/  titled “Discovery of Cyclic Peptide Ligands to the SARS-CoV-2 Spike Protein Using mRNA Display“??? Are these scientists INSANE to even ask that question in exactly the same time when the same, just modified to never die mod mRNA’s are being injected into the clueless covid injection victims, now ILLEGALY genetically modified for the rest of their lives??? All the great MD’s and scientists like Dr. Malone, Dr. Kory, Dr. P. McCullough, Dr. J. Rose, Dr. S. Seneff, Dr. Brian Hooker (CHD), ALL of them are deceiving the humanity by once or maybe twice quickly and silently mentioning ‘gene therapy’ and the rest of 99.9% of their talking time is all about ‘vaccines’, exactly what the FDA told them to do.  It is criminal, and they know it. Every single post of mine is mentioning that issue, and I will never stop to ring the bell around that ‘science game’. 
In regard to ALA, this must be far too much to ask, but worth to try:
Is the by FDA/NIH so much disliked ALA molecule the missing link to the modern global genocide, combining medical/environmental/political sciences et al. in this one goal, limiting human/nature beings of getting their required amount of energy with the help of light?  Maybe we should ask the Department of Energy…
And are there more examples of the protective role of ALA in terms of aluminum toxicity? Yes, here few more citations:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976966/
J Toxicol. 2018; 2018: 2817036. “Synergistic Effect of Quercetin and α-Lipoic Acid on Aluminium Chloride Induced Neurotoxicity in Rats.”
https://pubmed.ncbi.nlm.nih.gov/26912408/ Brain Res Bull.2016 Apr:122:19-28. “Alpha-lipoic acid-mediated activation of muscarinic receptors improves hippocampus- and amygdala-dependent memory.“
https://www.sciencedirect.com/science/article/abs/pii/S0946672X1830748X Journal of Trace Elements in Medicine and Biology Volume 54, July 2019, Pages 226-231
“Heavy metal toxicity: An update of chelating therapeutic strategies.”
closing with the one picture from the last citation, showing how to kill the living cells or rescue them using chelators and antioxidants, the superb ones like ALA:
To close the wonderful biological features of ALA, lets add to everything that 2006 study (https://www.sciencedirect.com/science/article/abs/pii/S0006291X0600057X), which showed in vitro inhibition of formation of β-amyloid fibrils by α-Lipoic acid ..
When looking into some 3D structures in the PDB Data Bank one gets even deeper insight into what ALA is involved with:
1HPC: H-protein, a 14 kDa lipoic acid-containing protein is a component of the glycine decarboxylase complex. This complex which consists of four protein components (P-, H-, T- and L-protein) catalyzes the oxidative decarboxylation of glycine. (https://www.rcsb.org/structure/1HPC). The mechanistic heart of the complex is provided by the lipoic acid attached to a lysine residue of the H-protein. It undergoes a cycle of transformations, i.e. reductive methylamination, methylamine transfer, and electron transfer.
2IQD: Reduced alpha-lipoic acid, an anti-oxidant and therapeutic for diabetic complications, was shown to bind aldose reductase with a binding constant of 1 microM. (https://www.rcsb.org/structure/2IQD)
and much more.
Glycine (processed via the first 1HPC structure) the smallest from all amino acids has this peculiar feature in vertebrate heme synthesis, which requires three substrates: succinyl-CoA, which regenerates in the tricarboxylic acid cycle, iron and glycine. For each heme molecule synthesized, one atom of iron and eight molecules of glycine are needed. Thus we get back to the human blood when talking ALA…., and we get even back to the begin which mentioned glyphosate (N-phosphonomethyl-GLYCINE). 
Due to an email length limit on sub-stack, will close this post with hope for few readers with some input;) 
And please note, things surely will be added in case new information flows in. The updates will be attached at the begin of the post, as usual. 
THANK YOU in advance for your time, reading and some comments. And now, Robin (not the bird..) Williams XBOX:
on Obama, Bush, Clinton, the French and others … And the second is to show how the aging works:  
Literature.
"Saving Your Liver" Episode 1 - Video One Dr. Burt Berkson, Jessica Miner & Denise Otten. (https://stopfattyliver.com/remedies/)
B M Berkson “A conservative triple antioxidant approach to the treatment of hepatitis C. Combination of alpha lipoic acid (thioctic acid), silymarin, and selenium: three case histories”. Med Klin (Munich). 1999 Oct 15:94 Suppl 3:84-9.
 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824456/ and also https://diabetesjournals.org/diabetes/article/46/Supplement_2/S62/9708/Lipoic-Acid-in-the-Treatment-of-Diabetic 
https://journals.lww.com/cardioplus/Fulltext/2020/07000/Cardioprotective_Effect_of_Alpha_lipoic_Acid_and.2.aspx and wishy-washy but still at least something at https://pubmed.ncbi.nlm.nih.gov/14608040/
Xiajun Guo et al. “The effects of lipoic acid on respiratory diseases” Int Immunopharmacol. 2023 Mar; 116: 109713. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933494/
 Burton M Berkson et al.“The long-term survival of a patient with pancreatic cancer with metastases to the liver after treatment with the intravenous alpha-lipoic acid/low-dose naltrexone protocol“ Integr Cancer Ther. 2006 Mar;5(1):83-9. https://pubmed.ncbi.nlm.nih.gov/16484716/
Berkson BM & Calvo Riera F. “The Long-Term Survival of a Patient With Stage IV Renal Cell Carcinoma Following an Integrative Treatment Approach Including the Intravenous α-Lipoic Acid/Low-Dose Naltrexone Protocol.” Integr Cancer Ther. 2018 Sep;17(3):986-993. 
Maria Angela Barletta et al. “Coenzyme Q10 + alpha lipoic acid for chronic COVID syndrome“  Clin Exp Med. 2022 Aug 22 : 1–12. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395797/
Stela Dragomanova et al. “Therapeutic Potential of Alpha-Lipoic Acid in Viral Infections, including COVID-19“ Antioxidants 2021, 10, 1294. https://doi.org/10.3390/antiox10081294  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389191/pdf/antioxidants-10-01294.pdf
Luc Rochette and Steliana Ghibu “Mechanics Insights of Alpha-Lipoic Acid against Cardiovascular Diseases during COVID-19 Infection.” Int J Mol Sci. 2021 Aug; 22(15): 7979. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348748/
10a. Amit Kumar Tripathi et al.  Brasileira de Farmacognosia (2023) 33:272–287.
https://archive.org/details/sim_federation-of-american-soc-experimental-biology_march-december-1954_13_1-4/page/731/mode/1up NOTE: Galvestone Lab in Texas was the main source of SARS-CoV-2 viral samples supplied to all scientists across the globe, doing experiments on covid19 disease….
Melvin Calvin at https://archive.org/details/sim_federation-of-american-soc-experimental-biology_march-december-1954_13_1-4/page/698/mode/1up also at https://www.osti.gov/servlets/purl/915447 “Chemical and Photochemical reactions of thioctic acid and related disulfides“
https://archive.org/details/sim_federation-of-american-soc-experimental-biology_march-december-1954_13_1-4/page/715/mode/1up “Oxidative and Transfer Reactions of Lipoic Acid”.



What does the X possibly stand for? Will Bill Gates et al. succeed?
mejbcart — Wed, 17 Jan 2024 22:36:31 GMT
The main post is behind the divider bar, first some updates:
2/4/2024 : If there is any connection between DiseaseX and any old vaccine or not even talking about genetic modifications, by this MD who finally admits some of the truth: 
https://forbiddenknowledgetv.net/dr-dan-neides-gives-tearful-apology-for-pushing-vaccines/
1/30/2024: the ‘symptoms’ of a targeted person: https://www.brighteon.com/8d023fa5-ff19-452b-b740-cff118da3681
1/21/2024: What does the ‘modern medicine’ has in bag for us humans? At the very end.
1/19/2024: Update on live Ebola ‘vaccines’ applied in Denver (CO), in the middle of the post. 
1/17/2024: Updates with Davos ‘24 videos at the end of this post.
We do not know, unless every single one of US says NO, to any/every-thing connected with the next ‘p(l)andemic’, be it X or Y or Z. Unfortunately too many have listened to the authorities and followed their contradictory instructions in the first covid19-I trial, whether by putting that suffocating mask on or worse, allowing to be injected with genetically modifying biological weapons agents. 
Can now a single letter be the cause of the next fear pandemic? 
First, X is everywhere, as the 24th letter in the alphabet, anything UNKNOWN gets the label x, but then, we also got the films, just recently from Mr. Len Blavatnik’s A24 group:
 
and another one coming up in 2024, with 3xX:
yes, the same old Len Blavatnik^1 who sold his stake in Russian aluminum producer United Co. Rusal International PJSC, the world's second largest aluminium (Al) company by primary production output (as of 2016). It was the largest until overtaken by China Hongqiao Group in 2015 (wiki source, sorry). Where does all this aluminum go? Just wonder, how much of it is being used in geoengineering efforts, with X’s invasion on our skies, almost every day, for decades:
 
And surely the HAARP facility connected with the above, is like a degenerated X-mushroom collection in a futuristic forest on many acres of a cold/hot (depending on emission energy) Alaska land:
and this looks like a tiny miniature of the above, on every cell of the human bodies, a self polymerizing laminin, giving you the smooth texture of YOUR HUMAN BODY, including the BRAIN^10 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358660/)    
 
Going back, how much of the overall Al production is in vaccines or in the new genetically modifying mod mRNA concoctions, in daily products, all ending up in many brains of Alzheimer patients? Sorry for this sidetrack, the amount of X-events just strangely accumulates, and hopefully it does not come out of the light cone linking past, presence and future:
First we got SpaceX (why not Space A, or I, no, it had to be X), thousands of them, spinning like Locusta migratoria giving the ‘vital connections’ to so many:
then it got even worse, Twitter turned into X too:
 We already got the X chromosome, one of the two (female and male) sex chromosomes:
not only linked to autoimmune diseases (https://www.nature.com/articles/d41586-024-00267-6), but equally with that so attacked ACE2, positioned exactly on that X-chromosome at location, Xp22.2…^6 , and so heavily involved in covid19^9. And now, on top of it we got the Disease-X everywhere in news, including the latest discussion with the worlds health minister and impossible burger addict Mr. Gates, who explains the details at https://forbiddenknowledgetv.net/disease-x-is-scheduled-for-discussion-on-january-17-at-davos/ . 
The mysterious Disease X can’t be the impossible chromosomal transformation X→Y, and Y→X since ~half of the members of WHO’s Transgender-Health-Committee are not MD’s but rather political LBGT activists^2, all knowing, that once you annihilate your ORIGINAL reproductive organs, the new ‘replacement’ not only does not work, but ignites a plethora of psychological issues, including suicides. A German Prof. Ulrich Kutschera dissects this topic^3 while mentioning the name of  Prof. John William Money from John Hopkins University’s (the same JHU with its ‘Event 201’ in covid19-I plan) and implying a JHU’s role in ‘scientific justification’ of pedophilia^4…. 
Some of the participants of the lastest JHU Oct 2022 prediction for the ‘Catastrophic Contagion’ https://centerforhealthsecurity.org/our-work/tabletop-exercises  are the same old faces: Anita Cicero, Bill Gates (as always), Johanna Hanefeld, K. Vijay Raghavan, Dr. Mike Ryan, Dr. Mark Dybul (Fauci’s ‘scientific offspring’), Dr. Muhammad Ali Pate (Harvard T.H Chan School of Public Health=Trust and Community-based Zuckerberg’s family Leadership Network), Tom Frieden (CDC and CFR affiliated), Tom Inglesby (JHU, CDC, White House COVID-19 Response Team and Biden-Harris transition team), which indicate a ‘continuation’ of the agenda. 
Even here, wasn’t there again a prediction, long time ago, straight out of Hollywood, named Contagion (2011), in the same year the AI purchased Warner Music Group for $3.3 billion and acquired Atlantic, Warner Bros. Records, Rhino, and Warner Music Nashville? The AI stands for “Access Industries” mentioned in: https://www.businessinsider.in/smallbusiness/finance/the-rise-of-billionaire-len-blavatnik-one-of-wall-streets-greatest-dealmakers/slidelist/51143940.cms#slideid=51143944
Right at the begin of Covid19 injections genocide, senate assured that BARDA was awarded $2 billions over four years to prepare against new threats, with the ‘Disease X Act’ in May 2021 at https://www.baldwin.senate.gov/news/press-releases/baldwin-introduces-disease-x-act-to-respond-to-future-viral-outbreaks. 
And today, strangesounds.substack.com writer posted a link to newer ‘Disease X Act of 2023’ introduced in Congress (June ‘23) at : https://www.congress.gov/bill/118th-congress/house-bill/3832/text, which wants: “To establish a program at BARDA for developing medical countermeasures for viral threats with pandemic potential.“ 
So the threats crystallized out, for Senate and Congress now these are: viral threats, again, with reference to the Committee on Energy and Commerce. No ‘health’ institution involved? Others predict that it is going to be a bacterial infection, since the Bifidobacterium modulation in covid19 treatments is a given fact^8. 
The fact that nobody until this day is talking consistently about genetic modifications of HUMANS, means that the entire science, health care, MSM, ALL are preventing vulnerable simple people from finding out the truth. AND when you see the BARDA, now approved members of the top ‘health’ HHS agency, with for example, members Renee Wegrzyn’s (https://forward.darpa.mil/presenters/Dr_Renee_Wegrzyn) activities like: 
“At DARPA, Wegrzyn leveraged the tools of synthetic biology and gene editing to enhance biosecurity, support the domestic bioeconomy, and thwart biothreats. Wegrzyn received the Superior Public Service Medal for her work and contributions at DARPA”
you need to ask, is that above, the top priority for HHS?? Are the human genes so bad that without gene editing the bio-security would collapse?? There is ONLY SYNTHETIC BIOLOGY path, BIO-security and BIO_economy, there is NOTHING ABOUT NATURAL HUMAN HEALTH HERE in that ironically called ‘HEALTH and HUMAN Services‘ department, being literally the left hand of FDA. Try to search their fiscal budget file for ‘bacteri’ and ‘virus’ at:
https://www.hhs.gov/sites/default/files/fy-2023-phssef-cj.pdf  
and check 3 tables on p.188 titled “FY 2023 BARDA ARD Estimate“, “FY 2023 BARDA PBS Estimate” and “Emerging Infectious Diseases”, you will see that the largest amounts of research spending go actually for Rad/Nuc, DRIVe and MCIP and filoviruses (among others, Marburgvirus, Ebolavirus). 
Dr. Richard Bartlett just warned (1/19/24) everyone (https://forbiddenknowledgetv.net/americans-being-infected-with-live-ebola-by-secret-bill-gates-project/) that the first Denver Health care workers got vaccinated with the live ERVEBO Ebola vaccine, genetically engineered from VSV stitched with surface glycoprotein of the Zaire strain of Ebola. The package of the FDA 2019 approved injection states: ”The duration of shedding is not known” (https://www.fda.gov/media/133748/download). Among the proudly injected ‘heroic’ shedders of the first live Ebola GMO’s SEEDS in DENVER are Dr. Maria Frank, Capt. Elizabeth Lenz. (https://www.9news.com/article/news/health/denver-health-medical-team-first-ebola-vaccine/73-b3d8f0fd-35a4-4dff-b67b-19e566cb6d6f). The FDA description sheet points to the still not finished clinical trials of the ERVEBO product, which can be found at: https://classic.clinicaltrials.gov/ct2/show/results/NCT02876328. Among the 4789 participants were 15 deaths, so far, 5 in placebo goups(!!), with 3 of them being CHILDREN above 1 year of age, 10 deaths in control goups. The CIMINAL INSANITY of this all is reaching indeed the tip. When searching for patents related to Q05320 the envelope glycoprotein with furin site (sounds similar?) from the EBOV (ebola virus), lot of repeating organizations are popping up: US 6630144-A 2 07-OCT-2003 (Secretary of the Army), US 10849975-B2 (DHHS), US 9597388-B2 2017 (The Trustees of the University of Pennslyvania, location of Biden’s Center), US 9097713-B2 2015 (SECRETARY OF THE ARMY ON BEHALF OF USAMRMC), US 10160795-B2 15 25-DEC-2018 (DHHS+Secretary of the Army and Humabs BioMed SA). And countless more, almost all for vaccines, neutralizing anti-bodies or monoclonal anti-bodies. What an amazing collection of military applications, all based on molecular biology... Just wonder if the Denver airport will be the first one to screen for Ebola right next to its colorful murals? Strange Sounds pointed today to this OLD Ebola outbreak prediction in 2014 by a very well informed journalist, Harry Vox: 
Harry pointed in his interview to the 2012 CDC Ebola virus patent  for “Human Ebola Virus Species and Compositions and Methods Thereof“ https://patents.google.com/patent/US20120251502A1/en
To close this part here, if there is one person to ask more about viruses, it would be not Dr. Fauci, but the founder of METABIOTA, Dr. Nathan D. Wolfe, currently at Stanford and other places, including the famous Edge.org club (now without Jeffrey Epstein). A good piece of this story was covered by another s-s writer:  
2nd Smartest Guy in the World
Did Epstein Create the C19 Pandemic? 
The below is an excellent companion piece to last week’s article which alluded to the fact that Epstein & Co. were involved in the PSYOP-19 “pandemic,” and associated slow kill bioweapon “vaccines…
Read more
3 years ago · 196 likes · 48 comments · 2nd Smartest Guy in the World
who also pointed to this original old article at: https://expose-news.com/2022/04/13/who-is-the-virus-hunter-dr-nathan-wolfe/
"Disease X" Is Scheduled for Discussion (January 17th) at Davos. This needs to be watched, carefully. But not everything, that can be left out, for now:
https://twitter.com/JackStr42679640/status/1747562775415792120
Internet is and was full of speculations, ever since the covid19 ‘PLAN’demic’ start, for example, one of it was analyzed already 1.5 years ago:
The current agenda announcement: “Davos 2024: Who's coming and what to expect“ at https://www.weforum.org/agenda/2023/12/davos-2024-what-to-expect-and-whos-coming/ , indicates again, the presence of the same cabal: https://www.weforum.org/agenda/2024/01/how-to-follow-the-annual-meeting-2024/ and only proves that in the last 4 YEARS most people DID NOTHING to stop globally the real CRIMINALS even after the obvious covid19 crimes. Imagine billions would do this: 
https://twitter.com/damonimani/status/1747388354587463766
Dr. David Martin^5 always points to the political arena and its importance in the preparations for the future. His newest revelation, no votes for: Vivek Ramaswamy the 24’ presidential candidate “America First 2.0.” who bought out substantial parts of the Arbutus company developing nanomaterials, later on used in the Mod_E-RNA covid19 injections production (https://endpts.com/vivek-ramaswamy-is-diving-into-rna-launching-a-new-biotech-with-arbutus-and-a-team-of-vets/). It is known that Mod-E-RNA prepares for new mod mRNA revolution connected with everything related to side effects of covid-19 genetically modifying injections, so is there any ‘priming’ of the new Diesease X by the old coronaviruses, with their new SYNTHETIC parts coming all but from one source, the covid19 genetic material injections? It appears, that the most recent Disease-X MSM campaign is grounding the new fear on ONE recent publication, mentioned by John Campbell, the widely known nurse educator in his short talk : “Disease X” Has a 100% Fatality Rate in Humanized Mice” at  https://forbiddenknowledgetv.net/disease-x-has-a-100-fatality-rate-in-humanized-mice/ 
It is about a new chinese study titled “Lethal Infection of Human ACE2-Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)“ ( https://www.biorxiv.org/content/10.1101/2024.01.03.574008v1.full ).
What does its abstract say? Quote: “We found that the GX_P2V(short_3UTR)23 clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection.“ 
That’s the ONLY study saying this, the end of this short article points to: “Our findings are evidently inconsistent with those of Zhengli Shi et al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models.” In addition, the authors say: 
“our hACE2 mouse model may be relatively unique.“
this hACE2 mouse model highly expresses the hACE2 in the mouse brain
hACE2 mice have abnormal physiology, with relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice.
Despite of all of this, the chinese scientists conclude “their study offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses.“  
If you have a genetically modified abnormal mouse already and apply on it apparent viruses binding exactly to the vital for their survival tissues, but engineered in a way to bind these ‘foreign invaders’, what would you expect?  That 100% mortality of the ‘humanized mice’, expressing human ACE2 (hACE2) in just 7-8 days after the injection, was proceeded by up to 10% decrease in body weight, piloerection, hunched posture, sluggish movements, and their eyes turned white. 
How all the researchers can even look into the eyes of the tortured mice? Now, they CAN’T! A mice without BARDA wellness testing such as lipids, hormones and metabolics provided by their DRIVe and the Medical Countermeasures Innovation Partner (MCIP), should be eliminated from experimentation. Why not testing on healthy mice, with its own unmodified ACE2 receptors? To get into the RT-qPCR tests performed on the hemogenized mix of infected tissue is another issue but then searching for the N gene copy numbers (the one most common for all corona viruses) while using 40 cycles (15 sec at 95°C and 1 min at 60°C) is just ridiculous, the same fraud as during covid19.. Last but not least, doesn’t pentobarbital, used in this experiment before infection on all animals, affect their brains too? 
Let’s see how the most infectious part of this ‘new threat’ compares with the old one, Spike2020, from the covid19 genetically modifying injections.
Below is the bioinformatics based BLAST (NIH software) Spike comparison of SARS-CoV-2 with the Spike from the studied pangolin coronavirus GX_P2V (https://www.ncbi.nlm.nih.gov/nuccore/2044015426), both sharing 92.3% IDENTITY in their amino acid sequence, with their C-terminal S2 domains being 100% IDENTICAL. The largest difference is the furin site which is entirely MISSING in the pangolin version of the Spike(QVT76606.1) in Query line, and SARS-CoV2 Spike in Sbjct:
Query 1 MFVFLFVLPLVSSQCVNLTTRTGIPPGYTNSSTRGVYYPDKVFRSSILHLTQDLFLPFFS 60
        MFVFL +LPLVSSQCVNLTTRT +PP YTNS TRGVYYPDKVFRSS+LH TQDLFLPFFS
Sbjct 1 MFVFLVLLPLVSSQCVNLTTRTQLPPAYTNSFTRGVYYPDKVFRSSVLHSTQDLFLPFFS 60

Query 61 NVTWFNTIHLNYQGGFKKFDNPVLPFNDGVYFASTEKSNIIRGWIFGTTLDARTQSLLIV
         NVTWF+ IH++   G K+FDNPVLPFNDGVYFASTEKSNIIRGWIFGTTLD++TQSLLIV
Sbjct 61 NVTWFHAIHVSGTNGTKRFDNPVLPFNDGVYFASTEKSNIIRGWIFGTTLDSKTQSLLIV  

Query121 NNATNVVIKVCEFQFCTDPFLGVYYHNNNKTWVENEFRVYSSANNCTFEYISQPFLMDLE  
         NNATNVVIKVCEFQFC DPFLGVYYH NNK+W+E+EFRVYSSANNCTFEY+SQPFLMDLE
Sbjct121 NNATNVVIKVCEFQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLE

Query181 GKQGNFKNLREFVFKNVDGYFKIYSKHTPIDLVRDLPRGFAALEPLVDLPIGINITRFQT  
         GKQGNFKNLREFVFKN+DGYFKIYSKHTPI+LVRDLP+GF+ALEPLVDLPIGINITRFQT
Sbjct181 GKQGNFKNLREFVFKNIDGYFKIYSKHTPINLVRDLPQGFSALEPLVDLPIGINITRFQT  

Query241 LLALHRSYLTPGKLESGWTTGAAAYYVGYLQQRTFLLSYNQNGTITDAVDCSLDPLSETK 
         LLALHRSYLTPG   SGWT GAAAYYVGYLQ RTFLL YN+NGTITDAVDC+LDPLSETK
Sbjct241 LLALHRSYLTPGDSSSGWTAGAAAYYVGYLQPRTFLLKYNENGTITDAVDCALDPLSETK  

Query301 CTLKSLTVEKGIYQTSNFRVQPTISIVRFPNITNLCPFGEVFNASKFASVYAWNRKRISN  
         CTLKS TVEKGIYQTSNFRVQPT SIVRFPNITNLCPFGEVFNA++FASVYAWNRKRISN
Sbjct301 CTLKSFTVEKGIYQTSNFRVQPTESIVRFPNITNLCPFGEVFNATRFASVYAWNRKRISN

Query361 CVADYSVLYNSTSFSTFKCYGVSPTKLNDLCFTNVYADSFVVKGDEVRQIAPGQTGVIAD  
         CVADYSVLYNS SFSTFKCYGVSPTKLNDLCFTNVYADSFV++GDEVRQIAPGQTG IAD
Sbjct361 CVADYSVLYNSASFSTFKCYGVSPTKLNDLCFTNVYADSFVIRGDEVRQIAPGQTGKIAD 

Query421 YNYKLPDDFTGCVIAWNSVKQDALTGGNYGYLYRLFRKSKLKPFERDISTEIYQAGSTPC 
         YNYKLPDDFTGCVIAWNS   D+  GGNY YLYRLFRKS LKPFERDISTEIYQAGSTPC
Sbjct421 YNYKLPDDFTGCVIAWNSNNLDSKVGGNYNYLYRLFRKSNLKPFERDISTEIYQAGSTPC  

Query481 NGQVGLNCYYPLERYGFHPTTGVNYQPFRVVVLSFELLNGPATVCGPKLSTTLVKDKCVN  
         NG  G NCY+PL+ YGF PT GV YQP+RVVVLSFELL+ PATVCGPK ST LVK+KCVN
Sbjct481 NGVEGFNCYFPLQSYGFQPTNGVGYQPYRVVVLSFELLHAPATVCGPKKSTNLVKNKCVN  

Query541 FNFNGLTGTGVLTTSKKQFLPFQQFGRDISDTTDAVRDPQTLEILDITPCSFGGVSVITP 
         FNFNGLTGTGVLT S K+FLPFQQFGRDI+DTTDAVRDPQTLEILDITPCSFGGVSVITP
Sbjct541 FNFNGLTGTGVLTESNKKFLPFQQFGRDIADTTDAVRDPQTLEILDITPCSFGGVSVITP 

Query601 GTNTSNQVAVLYQDVNCTEVPMAIHAEQLTPAWRVYSAGANVFQTRAGCLVGAEHVNNSY  
         GTNTSNQVAVLYQDVNCTEVP+AIHA+QLTP WRVYS G+NVFQTRAGCL+GAEHVNNSY
Sbjct601 GTNTSNQVAVLYQDVNCTEVPVAIHADQLTPTWRVYSTGSNVFQTRAGCLIGAEHVNNSY 

Query661 ECDIPVGAGICASYHSMSS----FRSVNQRSIIAYTMSLGAENSVAYSNNSIAIPTNFTI 
         ECDIP+GAGICASY + ++     RSV  +SIIAYTMSLGAENSVAYSNNSIAIPTNFTI
Sbjct661 ECDIPIGAGICASYQTQTNSPRRARSVASQSIIAYTMSLGAENSVAYSNNSIAIPTNFTI 720
After 4 years of exposure to all sorts of Spikes, is there one person who wouldn’t have a single protecting antibody against the Goliath, no matter to which section of the above or of the not even shown IDENTICAL C-terminal section with additional ~400 residues?  Last but not least, what do we have in common with the genetically modified hACE2 mice??
What is known about the ACE2 gene situated on the SEX X-chromosome at Xp22.2 ^7 and expressing ACE2 receptor? People surely know this, if not all, so here small piece from the abstract^6:
 “Cardiovascular diseases are predicted to be the most common cause of death worldwide by 2020. Here we show that angiotensin-converting enzyme 2 (ace2) maps to a defined quantitative trait locus (QTL) on the X chromosome in three different rat models of hypertension. In all hypertensive rat strains, ACE2 messenger RNA and protein expression were markedly reduced, suggesting that ace2 is a candidate gene for this QTL.“
further:
“Targeted disruption of ACE2 in mice results in a severe cardiac contractility defect, increased angiotensin II levels, and upregulation of hypoxia-induced genes in the heart. Genetic ablation of ACE on an ACE2 mutant background completely rescues the cardiac phenotype. But disruption of ACER, a Drosophila ACE2 homologue, results in a severe defect of heart morphogenesis. These genetic data for ACE2 show that it is an essential regulator of heart function in vivo.“
Every single covid19 injection caring the genetic sequence of the Spike, which then binds ACE2, will end up with disregulating that entire pathway, not even talking about the genetic effects on that X22.2 gene.  
Thus STOP TAKING, PRODUCING, SPREADING of the GENETICALLY MODIFYING contents of covid19 injections, STOP the FEAR and do something against it all, the driving cabal in particular.
Thank You for your attention, reading and hopefully some comments;))
The update for 1/21/24 is in regard to big news:”A brain-dead man was attached to a gene-edited pig liver for three days” to read at : https://www.technologyreview.com/2024/01/18/1086791/brain-dead-man-gene-edited-pig-liver/ Few citations from the article, quote: “During the experiment, the pig liver was mounted into a device from the company OrganOx that is normally used to keep donated human organs warm and perfused with blood so they will be available for transplant longer.“ and “According to eGenesis, its liver, which came from a genetically modified Yucatan minipig, was still healthy even after three days.“ No mentions what happened after, did the man wake up??? The picture of the pig opening the pathway to the merger of animals with humans can be seen at the end of that article and it looks as dehumanzing as possible, to take your last piece of HUMAN DIGNITY away. In the meantime, the next post will be about a ‘drug’, straight out of the human body, which regenerates the livers, within an astonishingly short period of time. Stay tuned;))
More Davos ‘24 video’s:
https://rumble.com/v47jp20-dr.-tedros-von-der-who-wird-in-davos-mit-krankheit-x-covid-lockdowns-und-im.html
Strange Sounds posted links to couple of sessions, including the ‘new pandemic’:
Strange Sounds
This is where we are at...
Our society has been dumbed down and endoctrinated so much, they assume that every critical thinker is a conspiracy theorist…
Read more
3 years ago · 17 likes · 2 comments · Strange Sounds
Literature.
source https://report24.news/mehr-als-die-haelfte-im-who-transgender-komitee-sind-woke-aktivisten-statt-aerzte/
https://report24.news/dieser-professor-erklaert-weshalb-gendertheorie-irrlehre-eines-paedophilen-ist/  The ‘gender identity’ issue is solved in the moment of CONCEPTION, and puberty only fine tunes that ‘moment of origin’.
Janssen, Diederik (2017). "John Money's "Chronophilia": Untimely Sex between Philias and Phylisms". Sexual Offender Treatment. 12 (1).
https://forbiddenknowledgetv.net/did-dr-david-martin-just-end-vivek-ramaswamys-presidential-campaign/
Michael A Crackower et al. “Angiotensin-converting enzyme 2 is an essential regulator of heart function“ Nature. 2002 Jun 20;417(6891):822-8. https://pubmed.ncbi.nlm.nih.gov/12075344/ with quote from abstract: 
Ekta Shirbhate et al. “Understanding the role of ACE-2 receptor in pathogenesis of COVID-19 disease: a potential approach for therapeutic intervention“ Pharmacol Rep. 2021; 73(6): 1539–1550. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236094/
Clarissa Reginato Taufer & Pabulo Henrique Rampelotto “The Role of Bifidobacterium in COVID-19: A Systematic Review“  Life 2023, 13, 1847. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532519/pdf/life-13-01847.pdf
Evangelos Tsiambas et al. “Chromosome X riddle in SARS-CoV-2 (COVID-19) - related lung pathology”. Pathol Oncol Res. 2020 Oct; 26(4): 2839–2841. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370877/ with a quote:  “According to the latest published epidemiologic data, SARS-CoV-2-mediated COVID-19 pandemic demonstrates aggressive clinic-pathological profiles in significant subsets of the infected patients –especially in males- and for this reason the role of chromosome X that hosts the hACE2 gene (band Xp22.2) seem to be critical.“
The link was provided by the kind reader Papillon (in the comments section):
Sebok K. Halder et al. “The importance of laminin at the blood-brain barrier“ Neural Regen Res. 2023 Dec; 18(12): 2557–2563. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358660/



The 20 years of 'genomic medicine'. JP Morgan, is it about money or health?
mejbcart — Thu, 11 Jan 2024 08:33:24 GMT
Update: 1/29/2024 The title “Cell-free DNA and RNA—measurement and applications in clinical diagnostics with focus on metabolic disorders” in Physiol Genomics 53: 33–46, 2021, implies, to what extend the medial cartel planned their future, while forcing the genetically modifying covid injections on billions of clueless citizens, ever since the end of 2020, the begin of that universal therapy, which started with changing the RNA pools of the human genome. The medical genocide goes that far, that SATNFORD, sorry Stanford, publishes proudly an article titled ‘The beat goes on’, in which since 2022 cardiothoracic surgeries are being performed with still beating hearts form cardiac arrest patients (the ones caused by the covid injections?) with astonishing success!!! A new field of ‘morpholome’ was invented, also in Satnford, sorry, stanford, which refers to variety of cell shapes taken on by an organism. Euan Ashley, Maddison Masaeli and Mahyar Salek (google AI expert) while analyzing the HEART CELL MORPHOLOME, want to differentiate deceased cells from others that have been ‘cured’(????) by gene-editing technology (Stanford Medicine, Issue 3, 2023). Between Apr 2023 and the print out date of that Stanford magazine (begin of ‘24), the amount of this sort of heart transplants, more than DOUBLED (https://med.stanford.edu/news/all-news/2023/04/beating-heart-transplant.html) 
Another Stanford hero, https://profiles.stanford.edu/michael-ma, published in ‘22 statistics on infants heart transplants, https://pubmed.ncbi.nlm.nih.gov/35835207/, strangely covering the years 1994 to Sep 2019, and avoiding anything AFTER 2020 (WHY????), together 2552 infant heart transplants reported to UNOS.. If there is anyone who could help the embalmers to decipher the terrible clot issues, it would be this person specializing on multilevel obstruction of systemic and pulmonic arterial systems… Straight from Chemical Engineering to medicine, what an ideal transformation, unfortunately with ZERO input for the embalmers struggling with dead bodies of covid injected victims!!!
The main post is behind the divider bar below. THANK You for reading and SHARING.
Who took over our world, made of genes, by Patrick Wood, incredibly good talk: https://rumble.com/v2dhgmh-the-evil-twins-of-technocracy-and-transhumanism-patrick-wood.html
How many educated people, the young ones in particular, do know what ‘genomic medicine’ is? The annual 42nd JP Morgan Healthcare Conference in San Francisco this year https://www.genomeweb.com/business-news/jp-morgan-healthcare-conference-day-1-bruker-exact-sciences-qiagen-neogenomics indicates an industrial trend shift of some of the big companies. For example Brucker; its CEO defines the era we live now, as ‘postgenomic era’, here his quote: 
"The last 20 years were dominated by genomics," he said. "But proteomics and related fields like glycomics, lipidomics, metabolomics, epiproteomics … is going to be at least equally important as genomic medicine, and in many areas will be able to go far beyond what genomic medicine was able to do."
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Truly stunning, because once again, how many people know that we got the ‘genomic medicine’ for 20 years already? Some call it ‘precision medicine’, but why precision? To cover up the involvement of every 100% INDIVIDUAL, personal GENE? Bret Weinstein and all MD’s on sub-stack until this very day have extreme difficulties to even mention GENE THERAPY consistently when talking about covid injections, including the alternative ‘officially punished’ MD’s. On the other hand, substack writer Eric Topol (erictopol.substack.com), the notorious NIH award recipient, first in 2016 for US$207 million for the Precision Medicine Initiative, and then just recently renewed for further $282 million over five years, and that in addition to Clinical and Translational Science Awards (CTSA) who threw into the basket another $46.8 million for 7 years, mainly writes about genes and their applications, but is seldom combining it with the word ‘vaccines’ or gene therapies in case of covid19 injections. The newsletter Ground Truths has the same loopholes as all the posts of the alternative good MD’s, unfortunately, the truths are missing. There are many more ‘truths’ here on sub-stack, for example ‘Unreported Truths’, equally filled with PART-truths completely missing the essence, or straight misinforming, again.. It looks like if you have a family member working for the establishment, for example the medical cartel, you do not won’t to get into a ‘bad spotlight’, including NOT ALLOWING to comment under own posts, here on this ‘liberal’ platform. 
So the NIH page at https://www.genome.gov/health/Genomics-and-Medicine/accomplishments, lists accomplishments of that ‘genomic medicine’ discipline all the way back to 2011, with posted reviews/publications for each year between 2011-2023. So there is about one decade of information missing, but nevertheless very much worth browsing and looking at some of them, at least...
The very first registered Jan 2011 publication comes from Welcome Trust with the title “Massive genomic rearrangement acquired in a single catastrophic event during cancer development”^1. It almost sounds like the 2020 catastrophic PLANdemic with exactly the very frequent issue of covid19 injected individuals who are fighting with horrifying cancers, right now.  
The very first entry in Feb 2012 was titled “Truncations of Titin Causing Dilated Cardiomyopathy“ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660031/#SD1). 
BLAST comparison of that largest muscle protein titin with SARS-CoV-2 Spike (done already in 2022 in my older posts), results in thousands of fragments with very high homologies to the Spike, clearly indicating disturbances of the natural production of titin during the same time of the Spike production, not even talking about the mutual interactions of all these products. Table 14 summarizes mutations within titin which correlate with specific human diseases. Here the amino acid section similar in titin (query line) (https://www.uniprot.org/uniprotkb/Q8WZ42/entry) and Spike (Sbjc line), with the lysine 33915 whose mutation is involved in Congenital Myopathy, according to that 2012 publication: 
Query 966  LSSNFGAISSVLNDILSRLDKVEAE---VQIDRLITGRLQS LQTYVTQQLIRAAEIRAS
           + ++ G++SS     +  +   EA+    Q    IT + ++ +Q  ++Q+ +R+ EI+ S
Sbjc 33853 VKNSAGSVSSSCKLTIKAIKDTEAQKVSTQKTSEITPQKKAVVQEEISQKALRSEEIKMS  
Query1022  ANLAATKMS  1030  human titin
              +  K++
Sbjc 33913 EAKSQEKLA  33921 SARS-CoV-2 Spike
             K33915<<= mutation causing the myopathy
to produce that section of titin, one needs 7 positively charged amino acids (R,K), to produce this Spike section requires 13 of those, in the same time!
Lets take more series of the NIH ‘Genomic medicine’ program, for example publication from Aug 2012 Vemurafenib: a new treatment for BRAF-V600 mutated advanced melanoma seems to be applicable to covid19 in 2020 too, according to https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114699, quote “the findings suggest that vemurafenib can be used for the treatment of COVID-19 (84).“
July 03, 2014 - Loss-of-function Mutations in APOC3, Triglycerides and Coronary Disease by Broad Institute (BI at MIT), with George Church^1, the covid19 national response co-coordinator, being also part of that genomes super sequencing center. This is a BLAST output on APOC3 (one of many) special section, covering BOTH mentioned mutations R19 and A43: 
* rarely mutated residues causing lower plasma triglyceride levels
                  *                               *
Query  13   ALLASARASE----AEDASL-LSF-MQGYM--KHATKTAKD  45 APOC3 human
            ALLA + +S     A  A L + F MQ  M  +
Sbjct  876  ALLAGTITSGWTFGAGAA-LQIPFAMQ--MAYRFNGIGVTQ  913 Spike2020
and the above Spike 2020 amino acid sequence string, now in billions of human bodies, comes up, again and again, maybe because of the physical importance arranged below???
In the same year, the entry from Jul 2014 - Spread of Artemisinin Resistance in Plasmodium falciparum Malaria^2 is special, because it points to the perpetrators of covid19  single catastrophic event, and here they are, in acknowledgments:
Supported by grants from the U.K. Department for International Development, the Worldwide Antimalarial Resistance Network, the Intramural Research Program of the National Institute of Allergy and Infectious Diseases of the National Institutes of Health, and the Bill and Melinda Gates Foundation. The Mahidol-University Oxford Tropical Medicine Research Programme is funded by the Wellcome Trust of Great Britain.
It is about parasite P. falciparum’s (malaria agent) toxic protein known as kelch13 (https://www.uniprot.org/uniprotkb/Q8IDQ2/entry) and artemisinin-based remedies and the resistance to these drugs. For those who forgot :”Nobel prize for the artemisinin and ivermectin discoveries: a great boost towards elimination of the global infectious diseases of poverty”^2. And here a BLAST between Spike and the kelch13 protein, some of which are just stunning indeed:
Query  372  KDSFIEKLLSGRHHVTRDKQGRI  394  Kelch protein K13
            K SFIE LL     VT    G I
Sbjct  814  KRSFIEDLLFNK--VTLADAGFI  834  Spike 2020
THE MOST known KRSFIEDL  section of Spike, and more:
Query  438  KFLPFPLVF--CIGG-FDGVEYLNSMELLDISQ  467 Kelch protein K13
            KFLPF   F   ++   D V    ++E+LDI+  
Sbjct  558  KFLPFQQ-FGRDIADTTDAVRDPQTLEILDITP  589
ACE2 binding domain:
Query  496  GGN-NYDYKALFE-TEV--YDRLRDV  517 Kelch protein K13
            GGN NY Y+ LF  + +  ++  RD+
Sbjct  446  GGNYNYLYR-LFRKSNLKPFE--RDI  468 ACE2 RBD in Spike
               the piece with  C580Y mutation of Kelch13 (in pub)
                               *
Query  562   MKAWVEVAPLNTPRSSAMCVAFDNK-------IYVIGGTN  594 K13
                 V     N     A C   D K       ++V  GT 
Sbjct  1066  --TYVPAQEKNFTTAPAIC--HDGKAHFPREGVFVSNGTH  1101 Spike
It looks like the Spike, despite of having nothing to do with parasites must have some of its features somewhat similar to that parasitic protein Kelch13, to a level, where they both bind to the same drug, artemisin related ivermectin….. The Single Point Mutation C580Y is important, quote: In this large study, multiple kelch13 SNPs (single-nucleotide polymorphisms) were highly predictive of slow parasite clearance and were associated with more than double the parasite clearance half-life. Some SNPs (notably C580Y) predominated. The very controversial Spike and IVERMECTIN issue, ends in this article with one quote^4:”Our experimental data on the docking of ivermectin on SARS-CoV-2 spike protein (in native form) revealed a strong binding of the compound with an energy value of -261.74 and -287, respectively, for B1a and B1b homologs.” And the conclusion:”Our study enlightens the candidature of ivermectin as an effective drug for treating COVID-19.” 
April 01, 2015 - “Cell-free DNA Analysis for Noninvasive Examination of Trisomy” publication is describing Down's syndrome detection based on cell-free DNA (cfDNA) fragments representing all or part of a third copy of chromosome 21. Just one question, what’s in that chromosome and how many similar/homologs of its fragments are inside of every vial of the covid19 gene based treatments contaminated with billions of cDNA fragments? 
April 07, 2016 - Near real-time monitoring of HIV transmission hotspots from routine HIV genotyping: an implementation case study at https://www.thelancet.com/journals/lanhiv/article/PIIS2352-3018(16)00046-1/fulltext indicates, genotyping was done then and now even more so. Everyone knows the first Spike variant mutation D614G^5. Is that residue conserved in HIV gp160 protein, to which spike is so similar? Here the BLAST output of ~160 amino acid long continuous string, with Query being HIV gp-160, Sbjct the Spike, placing at the position of that aspartic acid (D) the ’ * ‘ sign:
Query  129  DLSTLRNATDNSSTTEGGEIKKCSFN----ITTSIKTKVKDYALFYKYDV------VQID  
            D++   +A  +  T E  +I  CSF     IT  + T     A+ Y  DV      V I 
Sbjct  568  DIADTTDAVRDPQTLEILDITPCSFGGVSVITPGTNTS-NQVAVLYQ-DVNCTEVPVAIH 
 in LYQ>D, the CONSERVED D614 in HIV and in the Spike>>>>*
Query  179  ND--TAKYRLINCNTSVI-TQACPKVSFEPIPIHYCAPAGFAILKCNDEKFNGAGKCKNV  
             D  T  +R+    + V  T A   +  E +   Y          C+     GAG C   
Sbjct  626  ADQLTPTWRVYSTGSNVFQTRAGCLIGAEHVNNSY---------ECDIPI--GAGICASY  
Query  236  SAVQCT-HGIRPVVSTQLLLNG-SLAEEEVIIRSSNFTNNAKIIIVQLN--ESV  285
             +   + +  R V+S  ++    SL  E     S  ++NN+ I I   N   SV
Sbjct  675  QTQTNSPRRARSVASQSIIAYTMSLGAEN----SVAYSNNS-IAIPT-NFTISV  722

and using different BLAST search parameter:        *
Query  377  NTTPLFSSIWNADGTWNGTTGGGNITLPCRIKQIVNMWQEV-----GKAMYAPPIEGQIR
            + TP       + G  + +T G N++      Q+  ++Q+V     + A++A  +    R
Sbjct  586  DITPC------SFGGVSVITPGTNTS-----NQVAVLYQDVNCTEVPVAIHADQLTPTWR  
Does this has anything to do with the long HIV-like covid19??? Dr. Fauci, please confirm, over. Oh, there is a memory blackout on the other side, right now. A substitution comes right on time with the title “NEW - Dr. Deborah Birx Says 'Long COVID' is Similar to HIV”: 
https://twitter.com/thechiefnerd/status/1745568361537216766
Little more patience, few more years of genetic medicine, with continuously increasing number of publications, many mentioning LOSS OF FUNCTION in animals/humans being studied, and that, while the viruses seem to gain more and more of their functions...
May 24, 2017 - Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease (https://www.nejm.org/doi/full/10.1056/NEJMoa1701329)
So this study claims (nejm, be careful) when affecting the genes of angiopoietin-like 3 (ANGPTL3) and in ANGPTL4 via application of ANTI-sense oligonucleoties (mRNA, the real ones) the result in REDUCTION of production of those proteins (=LOSS OF FUNCTION), will change the plasma LDL cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides.  The study concludes: no serious adverse events, and how strange, exactly like in their published covid19 injections studies, the identical amount of controls and placebos, reported the same side effects, dizziness. No wonder, brain without cholesterol does not exist.
August 10, 2017 - Analysis of plasma Epstein-Barr virus DNA to screen for nasopharyngeal cancer (https://www.nejm.org/doi/full/10.1056/NEJMoa1701717) 
Nejm again, this time saying EBV DNA in plasma specimens is a biomarker for nasopharyngeal carcinoma. The complete genome of EBV virus is at https://www.ncbi.nlm.nih.gov/nuccore/NC_007605.1  There is that one special nuclear antigen EBNA-LP protein code for YP_401636.1 of EBV virus with the following amino acid sequence, mentioned one of the first posts of mine:
 >YP_401636.1 nuclear antigen EBNA-LP [Human gammaherpesvirus 4] MGDRSEGPGPTRPGPPGIGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPRGDRSEGPGPTRPGPPGIGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPRGDRSEGPGPTRPGPPGIGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPRGDRSEGPGPTRPGPPGIGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPRGDRSEGPGPTRPGPPGGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPRGDRSEGPGPTRPGPPGIGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPRGDRSEGPGPTRPGPPGIGPEGPLGQLLRRHRSPSPTRGGQEPRRVRRRVLVQQEEEVVSGSPSGPLRPRPRPPARSLREWLLRIRDHFEPPTVTTQRQSVYIEEEEDED
do you see the six ‘RGD’ motifs, special hallmark of all integrins, including Spike? Do you see the seven ‘PRRVR’ motifs, homologs of furin ‘PRRAR’ sites, like the one in Spike? Do you recognize the SPSP motif, responsible for phosphorylation and possible role in cancer initiation or progression^6? That ‘RGD’ motif, also in Spike2020, these simple THREE AMINO ACIDS Arg-Gly-Asp, has to do with cancers. And it looks as if somebody programmed almost intentionally the killer series of ‘RGD's into EBV. The article “Every step of the way: integrins in cancer progression and metastasis“ at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629548/  describes more the details of the process. Why was the Spike designed with RGD motif, to disregulate all the others?? 
The genomic medicine in 2019 starts with the publication - Integrating Genomics into Healthcare: A Global Responsibility by Stark Z. (https://pubmed.ncbi.nlm.nih.gov/30609404/)
That publication summarizing who and how much was spend for the endeavor to hack the HUMAN GENOME ends with quote: “We have a global responsibility to accelerate the implementation of genomic medicine and enable the timely realization of the benefits of genomics for individual patients, families, and healthcare systems.” 
At the end of 2019 MIT and its entire crew, which started the hacking in 2011, no must be much earlier than that(!) NIH page admits, knew already that “Rare Genetic Variants Associated with Sudden Cardiac Death in Adults“ are related with, for example the mentioned above gene encoding titin (TTN), with apolipoprotein B (APOB) and tyrosine-protein phosphatase (DSP2) ^7.  
The science met the practice with the covid19 injections clinical studies in 2020 and the global injection campaign in 2021, until now, while slowly incorporating the health care providers into the genomic medicine, which ended with Aug ‘23 publication: “An Introductory Tutorial on Cardiovascular Pharmacogenetics for Healthcare Providers“ (https://pubmed.ncbi.nlm.nih.gov/37303270/). 
The abstract ends with the positive view of the authors, quote “Ultimately, improved education among healthcare providers on cardiovascular pharmacogenetics will lead to a greater understanding for its potential in improving outcomes for a leading cause of morbidity and mortality.“ The choice on bold characters of the last sentence is mine.
Today the ‘health care’ professionals can get training in this new discipline, of which many still do not know, that it exists: https://www.genome.gov/careers-training/Modules-in-Genomic-Medicine-for-Healthcare-Professionals, and that only, because once again, ALL MD’s are silent about the covid genetically modifying injections and continue talking about ‘vaccines’. Sorry for repeating the same x^x^x-times, like MSM.
The most recent and last publication of NIH+Welcome Trust ‘genomic medicine’ is the first one mentioning the word CRISP:
”October 31, 2023 - CRISPR-Cas9 Editing of the HBG1 and HBG2 Promoters to Treat Sickle Cell Disease (https://pubmed.ncbi.nlm.nih.gov/37646679/)
Without any further analysis of the above, the last thing, today’s personal information status on covid19 genetically modifying injections: one family’s good friend died suddenly last week, one cousin got cancer, and had to undergo extensive surgery, after the 4th covid jab.  
Who is going to help all the victims of misinformation? The now ‘genetic medicine’ trained MD’s, who won’t tell any patient that they got genetically modified because of their advice to get ‘vaccinated’??? Maybe that is part of the training, to keep it secret…
And the horror of synthetic biology grows exponentially with every day:  https://dornsife.usc.edu/news/stories/synthetic-chromosomes-faster-cheaper/
rising completely out of proportions, while literally taking over in an absolute arrogant way the entire nature, laughing in the face of those who appreciate the real Creator, with their new “CReATiNG (Cloning Reprogramming and Assembling Tiled Natural Genomic DNA)“ synthetic nonsense.
How much the TOP American MD’s involved in covid injections ‘truth movement’, are INFLUENCED by the ‘genomic medicine’ can be clearly heard when listening to Dr. Cole in UK:
Pierre Kory’s Medical Musings
UK Parliament Testimony Videos From MP Andrew Bridgen's Historic Meeting - Dr. Ryan Cole, Dr. Angus Dalgleish, Steve Kirsch
Earlier this week, I posted Part 1 of this series which was an overview of all the events and government actions leading up to, during, and after MP Andrew Bridgen’s historic meeting in the UK Parliament titled, “For Truth, Democracy, and Freedom.” I included the testimony videos for the first three speakers at the meeting, that of Drs. David Martin, Pi…
Read more
3 years ago · 193 likes · 47 comments · Pierre Kory, MD, MPA
and NOW IN USA, (spare yourself of listening to Dr. McCullough…) just start at ~35:00 when Dr. Cole is speaking:
COVID Intel - by Dr.William Makis
VIDEO - Dr.Peter McCullough testifies at Rep. Marjorie Taylor Greene's Hearing on COVID-19 Vaccine Injuries (7 min)(Jan.12, 2024)
VIDEO - Dr.Peter McCullough testifies at Rep. Marjorie Taylor Greene's Hearing on COVID-19 Vaccine Injuries (7 min)(Jan.12, 2024…
Listen now
3 years ago · 109 likes · 39 comments · Dr. William Makis MD
Literature.
Philip J Stephens “Massive genomic rearrangement acquired in a single catastrophic event during cancer development.“ Cell 2011 Jan 7;144(1):27-40. https://pubmed.ncbi.nlm.nih.gov/21215367/
https://biophysics.fas.harvard.edu/people/george-m-church also covered in 
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143591/#SD1
E. Tambo et al. “Nobel prize for the artemisinin and ivermectin discoveries: a great boost towards elimination of the global infectious diseases of poverty“  Infectious Diseases of Poverty volume 4, Article number: 58 (2015) https://idpjournal.biomedcentral.com/articles/10.1186/s40249-015-0091-8
Abhigyan Choudhury et al. “Exploring the binding efficacy of ivermectin against the key proteins of SARS-CoV-2 pathogenesis: an in silico approach” Future Virol. 2021 Mar : 10.2217/fvl-2020-0342. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996102/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184998/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570649/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067308/
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Mod-E-RNA, cancers and Programmed cell Death Protein 1 pathway (PD-1/PD-L1). And who is Len Blavatnik?
mejbcart — Sun, 07 Jan 2024 05:54:24 GMT
Thank You for reading and your attention. For readers who unsubscribe, please, let me know why? Or maybe it is Sub-stack, who regulates the number of ‘allowable’ subscribers for writers who do not request MONEY for their work… ? Cor-por-at-I-on.
Updates first, the main post is under the divider bar.
Update 6/26/2026: The importance of Len Blavatnik can’t be understated, this is just one document out of many, showing who belongs to his circles: https://www.justice.gov/epstein/files/DataSet%2010/EFTA01924576.pdf
Update 4/4/2024: What are the PD-1 inhibitors which block the receptors on tumor cells? Flavonoids, as simple as cabbage in a daily diet….
Update: 3/17/2024: despite of their crimes, Mod-E-RNA expands: https://expose-news.com/2024/03/17/why-is-moderna-substantially-expanding-manufacturing-capacity-despite-current-low-demand-for-their-poison/ . Who is paying for this global universal annihilation of the human genome?? US???
Update 3/3/2024: reminder of an old issue, in 2012 filed Moderna patent for “METHODS AND COMPOSITIONS FOR TARGETING AGENTS INTO AND ACROSS THE BLOOD-BRAIN BARRIER“ at  https://patents.justia.com/patent/20150030576 specifically states, that  “modified mRNAs that are capable of penetrating the blood-brain barrier (BBB) for delivery to the central nervous system (CNS)” and “The modified nucleic acids or mmRNA of the invention may include a first region of linked nucleosides encoding a polypeptide of interest, a first flanking region located at the 5′ terminus of the first region, and a second flanking region located at the 3′ terminus of the first region.” and that mmRNA can be a modified uridine, like N1-methyl-pseudouridine, the one from covid genetically modifying injections. That means, COVID INJECTIONS WERE DESIGNED ON PURPOSE TO CROSS BBB!!! Incorporation can happen via 2 ways, electrical currents or soundwaves.
Update 2/29/2024: Anti cancer treatments with IV of liposomal p53 gene, IVs of VITC, blood ozone treatments, propolis applications, all of which have direct killing effect on cancer cells, according to Dr. Akiyama from Tokyo (TTAC info). Other example from Japan to use plain water fasting, for 12 days, in order to get rid of cancer.
Update 1/7/2024: new links to more generous support of Mr. Blavatnik, DARPA related (thanks to https://forbiddenknowledgetv.net/leave-the-world-behind-sonic-weapon-explained/), at the end of this post.
Update 1/9/24: Blavatnik School Of Government https://www.bsg.ox.ac.uk/research/covid-19-government-response-tracker 
The physical feeling of an empty space, like a desert, or a food store in a communist land, with nothing in it but the sales person, is just a moment of surprise, or not even that, when you look at the faces of those who wanted democracy, wrong, freedom (Tiananmen square, 1989, video on Ytube lXJ6gHFME0w):
A missing person in ones life, generates a different empty space around, no matter how full, or empty it is… That space is in the heart. And a smile on a humans face, suddenly can fill up that space again. A good healthy soul and spirit always fills that space, in a time independent way. That’s the ‘forever thing’ in which the death of something much bigger than matter, has no place. That physical death is feared most, and that’s what CIA lives from, fear. And it propagates into all ‘intelligence’, in particular science. 
The ‘modern science’ claims that the Cell Death on a molecular level is associated with few major proteins, among others, one is called PD-L1, which stands for Programmed cell Death Ligand 1,  a protein with features summarized at https://www.uniprot.org/uniprotkb/Q9NZQ7/entry . And the other is called PD-1, Programmed cell Death protein 1, with more details on it at https://www.uniprot.org/uniprotkb/Q15116/entry. Both proteins play an important role in apoptosis, cell death and thus in cancer cure (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136921/). Few of those examples from uniprot data base:
PD-1 is inhibiting immune responses and promoting self-tolerance through modulating the activity of T-cells.  
Delivers inhibitory signals upon binding to ligands CD274/CD273
PD-1 associates with CD3-TCR in the immunological synapse and directly inhibits T-cell activation
Blocking the PD-1/PD-L1 pathway will affect the immune response. Anti–PD-1/PD-L1 treatments, according to the recent Mod-E-RNA clinical trials of their new NEO-anti-gen anti-cancer vaccines https://s29.q4cdn.com/435878511/files/doc_presentations/2023/Apr/16/aacr-23_ct001-mrna4157_april-16.pdf , will need monitoring of just one factor (p. 13), the PD-L1 status:
“mRNA-4157 (V940) and pembrolizumab combination treatment demonstrated an improvement in RFS irrespective of PD-L1 status”, where RFS stands for relapse-free survival. The PD-1/PD-L1 pathway as a target in Mod-E-RNA cancer treatment, https://investors.modernatx.com/news/news-details/2023/Merck-and-Moderna-Initiate-Phase-3-Study-Evaluating-V940-mRNA-4157-in-Combination-with-KEYTRUDA-pembrolizumab-for-Adjuvant-Treatment-of-Patients-with-Resected-High-Risk-Stage-IIB-IV-Melanoma/default.aspx  was very predictable, given that PD-1, an inhibitory receptor on antigen activated T-cells, plays a critical role in induction and maintenance of immune tolerance to self. Following T-cell receptor (TCR) engagement, PD-1 directly inhibits T-cell activation. It suppresses T-cell activation through the recruitment of PTPN11/SHP-2: following ligand-binding, PD-1 is phosphorylated within the ITSM motif, leading to the recruitment of the tyrosine phosphatase PTPN11/SHP-2 that mediates dephosphorylation of key TCR proximal signaling molecules, such as ZAP70, PRKCQ/PKCtheta and CD247/CD3zeta. With one word, tolerance and autoimmunity are connected^1 and T-cells are essential in this process^2. 
The VAERS system, tracing side effects of covid genetically modifying injections, as of 11-18-2022  has stopped putting free text field information in the public data for Europe/UK (https://www.openvaers.com/covid-data). So based on what’s left there, Moderna COVID-19 (mRNA-1273) injections and their bivalent followers caused, according to VAERS (run in expert mode) 779 cases of all sorts of autoimmune conditions including 10 deaths. That, despite of the global suppression or straight prohibition (like in Kaiser Permanente facilities, surely just one out of many) to enter the covid injections injuries into VAERS, by the ‘oversight’. It does not include a family member, who suddenly got ‘citric acid’ allergy, yes, the same from the TCA cycle of every human of earth..!??
It gets even stranger, because the cancer/carcinoma cases AFTER Mod-E-RNA injections registered in VAERS are: 
“Found 28 cases where Vaccine is COVID19 or COVID19-2 and Manufacturer is MODERNA and Symptom is Cancer fatigue or Cancer gene carrier or Cancer in remission or Cancer pain or Cancer screening or Cancer screening normal or Cancer staging or Cancer surgery”, with NOT A ONE DEATH. 
I personally have a neighbor, who died after the 3-rd Mod-E-RNA shot due to super fast growing liver/lung cancer, another friend who died Jan ‘23 after the 4th, due to heart issues, another one, just 2 weeks ago, and countless others who developed cancers or suffered re-emissions shortly after… And I’m just one out here, seeing the damage, VAERS can’t see… 
So now, Mod-E-RNA, which managed to inject billions(?) with the highest (~3x the amount in Pfizer’s  BNT162b2 ) concentration of synthetic genetic material of NON-HUMAN, patented origin, has their new computer based construct stitched out of ~34 mod mRNA Neo-Antigen pieces as a personalized anti-cancer mod mRNA GENETIC MODIFICATION TREATMENT, which ‘they’ still call ‘vaccine’. That one method, out of 5 others,  mRNA-4157 PCV (Merck)  has the following mode of action:
whereby the application of a specific drug called pembrolizumab, according to: https://s29.q4cdn.com/435878511/files/doc_presentations/2023/Apr/16/aacr-23_ct001-mrna4157_april-16.pdf , results in a ‘great outcome’, quote from p.14: “mRNA-4157, a personalized cancer vaccine, in combination with pembrolizumab, demonstrates trend for improved recurrence free survival compared to pembrolizumab alone in adjuvant melanoma patients across tumor mutational burden subgroups”. Never mind the table from p.11, listing 104 cases of significant adverse events in 104 tested patients… 
What is pembrolizumab? It is human IgG4 (mutant S228P) anti-PD1 antibody with a 3D structure known for almost a decade: https://www.rcsb.org/structure/5DK3. 
Surely everyone remembers the headlines from last year:
”IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein” https://pubmed.ncbi.nlm.nih.gov/37243095/
“IgG4-related Disease Emerging after COVID-19 mRNA Vaccination” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258086/
“Post-COVID mRNA-vaccine IgG4 shift: worrisome?” https://pubmed.ncbi.nlm.nih.gov/37191589/
Sounds like that’s the same human IGg4 in Moderna’s new drug ‘wonder’ and the one associated with the Spike gene based treatments.… What if we take the heavy chain from IGg4 of that 5DK3 pembrolizumab structure and compare it to the Spike bound to ‘UT28K-RD Fab heavy chain|Homo sapiens’ from the 8K5H Pdb data bank in the “Structure of the SARS-CoV-2 BA.1 spike with UT28-RD”? BLAST gives even in the default mode, no twitching, 92% sequence coverage with 77% IDENTITY. Here the major one, with query being part of Spike anti-body, and Sbjct the ‘anti-cancer-antibody’ PD-1:
292 bits(748) 3e-102 Compositional matrix adjust. 171/223(77%) 188/223(84%) 2/223(0%)
Query  1    QMQLVQSGPEVKKPGTSVKVSCKASGFRFSISAVQWVRQARGQRLEWIGWIVVGSGDTNY  
            Q+QLVQSG EVKKPG SVKVSCKASG+ F+   + WVRQA GQ LEW+G I   +G TN+
Sbjct  1    QVQLVQSGVEVKKPGASVKVSCKASGYTFTNYYMYWVRQAPGQGLEWMGGINPSNGGTNF  

Query  61   AQKFQERVTITRDMSTSTAYMELSSLRFEDTAVYYCAAPYCGGDCSDGFDIWGQGTMVTV  
             +KF+ RVT+T D ST+TAYMEL SL+F+DTAVYYCA      D   GFD WGQGT VTV
Sbjct  61   NEKFKNRVTLTTDSSTTTAYMELKSLQFDDTAVYYCARRDYRFDM--GFDYWGQGTTVTV  

Query  121  SSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ  
            SSASTKGPSVFPLAP S+STS  TAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ
Sbjct  119  SSASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ  

Query  181  SSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPK  223
            SSGLYSLSSVVTVPSSSLGT+TY CNV+HKPSNTKVDK+VE K
Sbjct  179  SSGLYSLSSVVTVPSSSLGTKTYTCNVDHKPSNTKVDKRVESK  221

an for the light chain of anti-Spike and human IgG4 (mutant S228P) anti-PD1 antibody, it looks even better:

390 bits(1001) 	2e-144 	Compositional matrix adjust. 	195/218(89%) 	200/218(91%) 	3/218(1%)

Query  21   EIVLTQSPGTLSLSPGERATLSCRASQSVSSS---YLAWYQQKPGQAPRLLIYGASSRAT  
            EIVLTQSP TLSLSPGERATLSCRAS+ VS+S   YL WYQQKPGQAPRLLIY AS   +
Sbjct  1    EIVLTQSPATLSLSPGERATLSCRASKGVSTSGYSYLHWYQQKPGQAPRLLIYLASYLES  

Query  78   GIPDRFSGSGSGTDFTLTISRLEPEDFAVYYCQQYGNSPWTFGQGTKVEIKRTVAAPSVF  
            G+P RFSGSGSGTDFTLTIS LEPEDFAVYYCQ   + P TFG GTKVEIKRTVAAPSVF
Sbjct  61   GVPARFSGSGSGTDFTLTISSLEPEDFAVYYCQHSRDLPLTFGGGTKVEIKRTVAAPSVF  

Query  138  IFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLS  
            IFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLS
Sbjct  121  IFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLS  

Query  198  STLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC  235
            STLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Sbjct  181  STLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC  218
Doesn’t it look like the Moderna ‘Spike vaccines’ prepared the victims for their ‘anti-cancer’ new ‘wonder’ treatment with 100% significant adverse events, similarly to what the covid injections did? Anyone, who reads this and is familiar with immune ‘therapies’, please help out here, I’m just looking at the amino acid sequences… 
Thus clearly Spike must be somewhat related to the Programmable Death Proteins and their ligands, that PD-1/PD-L1 pathway. According to uniprot, PD-1 has 2 conserved negatively charged motifs (just few amino acids long!!):
PD-1’s immunoreceptor tyrosine-based inhibitory motif (ITIM):  VDYGEL  (221-226)
PD-1’s immunoreceptor tyrosine-based switch motif (ITSM)    :        EYATI  (247-251)
inside of the full length PD-1 protein with the sequence code Q15116.3 (PD-1 in Query line). The comparison with SARS-CoV-2 Spike (also called Spike2020 for the first version of it) shows ~27% of identities (SARS-CoV-2 Spike code YP_009724390.1), among others the following homologous sections, including the above ITIM and ITSM motifs:Query  18   GWRPGWFLDSPDRPWNPPTFSPALLVVTEGDNATF-TCSFSNTSESFVLNWY 68 PD1
            GW  G  LDS          + +LL+V    N     C F   ++ F+  +Y
Sbjct  103  GWIFGTTLDSK---------TQSLLIVNNATNVVIKVCEFQFCNDPFLGVYY 145 

Query  56   FSNT-SESFVL--NWYRMSPSNQTDKLAAF----PED  85 PD-1
            F+N  ++SFV+  +  R     QT K+A +    P+D
Sbjct  392  FTNVYADSFVIRGDEVRQIAPGQTGKIADYNYKLPDD  428 Spike2020

Query  26   DSPDRPWNPPTFSPALLVVTEGDNATFTCSFSNTSES  62 PD-1
            D+P  P+N   +       TE  N      F  T +S
Sbjct  80   DNPVLPFNDGVY----FASTEKSNIIRGWIFGTTLDS  112 Spike2020
by hand the section which 
                        >>VDYGEL<<=ITIM motif !!!
Query  207  QPLKEDPSAVPVFSVDYGELDFQWREKTPEPPVP  PD-1 
            Q +K+   + P+   D+G   F++ +  P+P  P
Sbjct  784  Q-VKQIYKTPPIK--DFGG--FNFSQILPDPSKP  Spike2020
           Tyr789 * <YATI':

Query  246  TEYAT-IVFPSGMGTS  260 PD-1
            ++Y++ ++   G  TS
Sbjct  871  AQYTSALLA--GTITS  885 Spike2020

Query  238  PVPCVPEQTEYATIVF  251 PD-1
            +  C     +Y++  F
Sbjct  746  STECSNLLLQYGS--FCT  759 Spike2020

Query  247  EYATIVFPSGMG  258 PD-1
            EY +  F   + 
Sbjct  169  EYVSQPFLMDLE  180 Spike2020

Query  221   VDYGELDFQWREKTPEPPVPCVPEQTEYA  249 PD-1
             VD+   +++       +P   V  +  Y 
Sbjct  1040  VDFCGKGYHLMSFPQSAPHGVVFLHVTYV  1068 Spike2020

Query  247  EYATIV  252 PD-1
            +++  V
Sbjct  428  DFTGCV  433 Spike2020

Query  241  CV-PEQTEYATIVFP  251 PD-1
            C  P Q+ Y+
Sbjct  488  CYFPLQS-YG---FQPTN  496 Spike2020
BLAST cant find that one, so by hand, FULL COVERAGE
CVPEQTEYATIVFPSG-M PD-1
CV   ++Y+ +++ S  +
CV---ADYS-VLYNSASF Spike2020

CVPEQ----TE-YATIVFPS-GM-GT PD-1
K-PFERDISTEIYQAGSTPCNGVEGF Spike2020 - ACE2 receptor binding domain

Also the richest Trp section, as conserved in the HIV gp160 protein is here:

      QA-PWPV-VWAVLQLGWRPGWFLD PD-1
      QYIKWPWYIWLGFIAGLIAIVMVT Spike2020
All of the above, does not look random, to me.
According to this summary titled “Clinical and Recent Patents Applications of PD-1/PD-L1 Targeting Immunotherapy in Cancer Treatment—Current Progress, Strategy, and Future Perspective “  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358377/ the number of patents related to PD-1/PD-L1 pathway started to explode around 2015, despite of the Nobel-prize winning discovery of PD-1 in 1992:
and the top FDA ‘approved’ were:
 from which the mentioned pembrolizumab has the application for the widest range of all sorts of cancers (Table 4). That’s where Mod-E-RNA comes in. In 2015 it signed agreement with MERCK to develop mRNA-based anti-viral vaccines, after it developed the synthetic mod mRNA doing even better job than the natural mRNA version. It was with 2013 DARPA’s financial support when the RNA ‘therapeutics’ started its progress (https://www.flagshippioneering.com/timelines/moderna-timeline The ModERNA collaboration with Harvard however, was way before the official admission, that on September 26th, 2019 Harvard University establishes mRNA immunotherapy research collaboration with Moderna. 
The 2 big names in the CRISP/RNA genetics/PD-1/PD-L1 arena, all going back to Moderna, are linked to the Blavatnik Institute (BI). The Blavatnik Family Foundation has made sizable investments into Harvard University, the New York Academy of Sciences, Oxford University, and other institutions, in total ~$900 million. Much of Harvard’s Office of Technology Development success has come from the life sciences, where commercially promising research can get an extra boost from the Blavatnik Biomedical Accelerator, and where emerging companies benefit from Boston’s robust early-stage venture ecosystem. These 2 mentioned BI members are:
Dr. George Church, covid19 national response team
Dr. Arlene Sharpe, The Blavatnik Biomedical Accelerator Advisory Committee (https://otd.harvard.edu/accelerators/blavatnik-biomedical-accelerator/), holder of every Harvard patent for PD-1 related molecules.
Blavatnik, Ukrainian-born British-American businessman and philanthropist., with apparently no ties to Russia any more, pays for the TOP geneticist George Church, for lot of work at MIT, for others in Yale (https://medicine.yale.edu/news-article/blavatnik-family-foundation-to-provide-10-million-grant-for-immunobiology-research-at-yale/ , https://ventures.yale.edu/news/blavatnik-fund-innovation-yale-awards-25-million-11-yale-faculty-led-projects-developing-new) , Columbia (https://www.engineering.columbia.edu/news/blavatnik-gift), for scientists from all over (https://www.eurekalert.org/news-releases/709174), who are lucky to be supported by such a generous rich source, to a level, where even CNN gets concerned, since when equally, LOT of politicians, including the honorable EDGE member Bill, everyone knows (picture from https://edition.cnn.com/2022/05/11/us/russian-oligarchs-philanthropy-ukraine-war-invs/index.html), 
all are getting lot of money, the question is, where it comes from and is its purpose really a pure philanthropy? Certainly, politics does not belong to that category, by definition. The https://hms.harvard.edu/research/blavatnik-institute with a special department at https://sysbio.med.harvard.edu/about-our-faculty and research areas at: http://be.mit.edu/research-areas/systems-biology has one more special member of the EDGE.org society:
http://be.mit.edu/directory/laurie-a-boyer, a MODERNA Consultant 2016-2020 and then in 2018, just on time, received a grant in: “Regenerative medicine holds great promise for treating heart failure, but that promise is unrealized, in part, due to a lack of sufficient understanding of heart development at the mechanistic level. Boyer’s research aims to achieve a deep, mechanistic understanding of the gene control switches that coordinate normal heart development. She then aims to leverage this knowledge and design effective strategies for rewiring faulty circuits in aging and disease.” (https://news.mit.edu/2018/advancing-knowledge-medical-genetic-sciences-mathers-foundation-grants-0626). It could be just coincidence, after all each human has just one heart, which can get sick, for many reasons. Just the timing is strange…
The official list of money spend by Blavatnik for BOTH political 2-party system in USA at:
https://www.opensecrets.org/donor-lookup/results?name=blavatnik&order=desc&sort=A
and his company with countless biotechnology investments:
https://www.accessindustries.com/
smells like insider trader on almost all the issues which the covid gene based therapies are causing, from blood related heme synthesis modulation (https://www.discmedicine.com/our-pipeline/), to cancer treatments, in particular children ( https://www.dayonebio.com/), iron storage, including the PD-1/PD-L1 pathway. Blavatnik’s influence on science, politics, economy (https://www.thedailybeast.com/len-blavatnik-and-his-access-industries-are-shareholders-of-calpine-which-helped-kill-clean-energy-in-maine) but science in particular (https://sysbio.med.harvard.edu/about-our-faculty) is indeed stunning!
Only few people in this world get that far as Len Blavatnik did, the position of a https://en.wikipedia.org/wiki/Knight_Bachelor in 2017, which maybe ended with https://www.royal.uk/the-order-of-the-garter, all this after opening in 2010, the Blavatnik School of Government at Oxford University. That all in turn proceeded the big money flow for MIT (~200mln$ in 2018).
Len Blavatnik also extensively supports research done in Israel, in particular one of the top scientific research centers in the world, the Weizman Institute established by Chaim Azriel Weizmann (https://en.wikipedia.org/wiki/Chaim_Weizmann, the Russian-born biochemist, Zionist leader and Israeli statesman who served as a president of the Zionist Organization and later became the first president of Israel): 
https://www.weizmann-usa.org/news-media/in-the-news/three-exceptional-scientists-receive-2019-blavatnik-awards
https://www.weizmann.ac.il/WeizmannCompass/sections/briefs/blavatnik-award-to-three-weizmann-scientists
https://www.weizmann-usa.org/news-media/news-releases/prestigious-blavatnik-awards-for-young-scientists-in-israel-announces-its-2022-laureates/
https://www.weizmann-usa.org/news-media/feature-stories/prestigious-blavatnik-awards-for-young-scientists-in-israel-announces-2023-laureates/ 
In fact, the entire scientific-advisory-council of Blavatnik’s Institute gives awards to only 3 nations, US, UK and Israel:
http://blavatnikawards.org/awards/national-awards/
http://blavatnikawards.org/awards/united-kingdom-awards/
http://blavatnikawards.org/awards/israel-awards/scientific-advisory-council/
The amount of money involved in private sectors and general research in genetics can be found here:
https://frontlinegenomics.com/world-of-genomics-usa/
https://frontlinegenomics.com/world-of-genomics-israel/
and some of the planned future here:
https://d4-pharma.com/the-festival-of-genomics-biodata-in-london-2024/
Last thought:
Is the Russiagate ‘scandal’ a programmed cell death from very begin? Who knows:
https://qz.com/1521847/major-gop-donor-len-blavatnik-had-business-ties-to-a-russian-official
I’m very sorry for citing wiki too often. Looks like wiki-leaks has quite a lot on Blavatnik too: https://search.wikileaks.org/?q=Len+Blavatnik
Now the newest, related to financing different areas of Mr. Blavatnik interests.
An ultrasonic analysis of the new B+M Obama’s movie called ‘Leave the world behind’ presented by Bonnie and John Mitchell of AwakenVideo^3 points to an applications of DARPA’s technology developed under a project within the Brain Initiative (https://www.darpa.mil/program/our-research/darpa-and-the-brain-initiative). The project’s name is Electrical Prescriptions (ElectRx). Two researchers involved in ElectRx who are mentioned at https://www.darpa.mil//news-events/2015-10-05 were also financially supported by Blavatnik:
Dr. Elisa Konofagou (Columbia) (https://www.engineering.columbia.edu/news/latest%20blavatnik%20fellows%20announced)
Polina Anikeeva, PhD (MIT) (http://blavatnikawards.org/news/items/announcing-finalists-2020-blavatnik-national-awards-young-scientists/)
It looks like the ‘Self-Healing of Body and Mind’ as advertised by DARPA in its project, was used in Obama’s movie (!!) in an extremely evil way, to actually harm the viewers^3. It is hard to imagine the involved scientists know about who and how is using their work. The Michell family mentions in their presentation a very new science field, the s.c. sonogenetics, which when combined with optogenetics, can remotely stimulate the human body in an unprecedented way.
And lastly, this post is NOT to condemn science, which lives from finances, and maybe that’s why it is so limited, but rather to point to the fact, that every work everyone is doing is paid by somebody with special interests, and those can be good, or bad. Always keeping an eye on who is doing what with ones own work, should be kept in mind, while judging upon anyone but oneself..
Thank you for the attention, and
Belated Happy New Year Wishes!
Literature. 
Ian R Mackay “Tolerance and autoimmunity”.  West J Med. 2001 Feb; 174(2): 118–123. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1071274/
Prabhakaran Kumar et al. “Restoring self-tolerance in autoimmune diseases by enhancing regulatory T-cells“ Cell Immunol. 2019 May:339:41-49. https://pubmed.ncbi.nlm.nih.gov/30482489/
https://forbiddenknowledgetv.net/leave-the-world-behind-sonic-weapon-explained/



The CHRISTMAS, the 'Cys-His-Arg-Ile-Ser-Thr' (C-H-R-I-S-T) amino acid sequence and the SARS-CoV-2 Spike.
mejbcart — Mon, 25 Dec 2023 10:37:04 GMT
Merry Christmas to everyone, also to those who celebrate, enjoy, believe and remember traditions. This post was written on December 24-th, the Christmas Eve, the day of the year, many believe, including myself, Jesus was born.
Updates:
12/28/2025: this is why things are the way they are: 
”Kitten’s Secret Garden”
Now the Government Can Legally Kill Christians 
Read more
10 months ago · 10 likes · 17 comments
4/16/2025: The content of this post is directly connected with this post titled “ERASING CHRIST THE QUIET REMOVAL OF JESUS FROM OUR TIMELINE“ by Ron:
Ron’s Substack
ERASING CHRIST THE QUIET REMOVAL OF JESUS FROM OUR TIMELINE
Major academic publishers tacitly update style guides…
Read more
2 years ago · 1 like · Ron Chapman
12/25/2023 The bioinformatics analysis presented here will be continued, so checking occasionally for those who are interested would make sense. The post might become huge… Thank you for reading and not-unsubscribing;))
1/1/2024: HAPPY NEW YEAR WITH NEW HOPES for more JUSTICE, PEACE and LOVE and appreciation for our Creator, on this planet. An incredible scientist will REVOLUTIONIZE the world with new truths, FACTS:  https://expose-news.com/2024/01/01/let-a-scientist-speak-presentation-goes-viral-because-its-true/ and music, can support our battled souls on a different level:
There is only one word which relates to the night today and that is the word CHRIST.
It means a lot to many, special birth, love, wonders, devotion, forgiveness, peace, special death, but also the highest power. 
This short post will relate molecular biology and religion, via this one word CHRIST. For people who read bible the meaning of WORD is very important. In todays world where religion is attacked on every level, where values are destroyed, and creation is being overwritten via GENETICS, one has to realize the level of hidden complexity by those who have the power to know and to decide what others know, and become. As usual, all will be based on bioinformatics, assumed as a known tool for the reader.
Natural proteins contain 20 amino acids described by a single letter code covering the entire alphabet except for the letters : B, J, O, U, Z, X. These missing letters in protein codes already exclude the existence of the short pentapeptide, like for example ‘J-E-S-U-S’. As a side note, there is one special artificial amino acid ‘hybrid’ called glyphosate. It represents a mix of glycine (the human inhibiting neurotransmitter) and a phosphono-group, together called N-phosphonomethylglycine. Wi-ki calls it broad-spectrum systemic herbicide and crop desiccant… And there are more, but will be left out for now.
One can start with opening the NIH BLAST page at https://blast.ncbi.nlm.nih.gov/Blast.cg (with ‘PROTEIN’ analysis option) and type into the search window the fasta code ‘CHRIST’ which is equivalent to ‘Cys-His-Arg-Ile-Ser-Thr’=’Cysteine-Histidine-aRginine-Isoleucine-Serine-Threonine’ or the string of letters ‘C-H-R-I-S-T’. Now search for ‘Reference Proteins’ with blastp algorithm and just hit BLAST button. Enough to choose the default first 100 hits, one can go much higher and deepen the analysis.
If the amino acid sequence ‘CHRIST’ (from now on it will be called ‘CHRIST section’ because in this search it represents a short peptide as defined by molecular biologists, an amino acid sequence) had no meaning in all the found proteins, their relation for example to SARS-CoV-2 Spike (its amino acid sequence is at https://www.ncbi.nlm.nih.gov/protein/YP_009724390.1) should be zero, but it is not. 
The result shows proteins with 100% hit for the word ‘CHRIST’ from all possible organisms sorted after amino acids length, i.e. molecular weight. Let’s take the first one, non-ribosomal peptide synthetase with the NIH code WP_052438536.1, and compare it with the SARS-CoV-2 Spike (BLAST search with 2 entries in which Spike will be the line with query in all the examples below), one gets 78% coverage with 47% identities, using special parameters. Here just 3 hits, chosen according their importance in Spike features, among countless others:
Query  663   DIPIGAGICASYQTQTNSPRRAR  685 Spike's FURIN Site
             + P  AG+ A  ++ T + ++AR
Sbjct  6346  EAPTVAGVAARIESLTTTKKKAR  6368  WP_052438536.1
Query  460   NLKPFERDISTEIYQAGST  478 Spike's ACE2 binding site
             +L P  RD+S+  Y A +T
Sbjct  3323  SLAPLARDVSAA-YAARTT  3340 WP_052438536.1
Query  704   TMSLGAENSVAYSNNSIAIPTNFTISVTTEILPVSMTKTSVDCTMYICGDST  747
               +     S  +++ ++ +P+    +   E+     ++T  D T  + GD T
Sbjct  2581  DVAECHRISTEWNDTAVDLPA----ATLPELFAAQAARTP-DATALVFGDET  2619
Note the last line with the CHRIST sequence, Spike doesn’t have it. Let’s take the IgGFc-binding protein XP_030268704.1, which comes up for many organisms in this search. The first is the section containing the ‘ALLAG-TITS-G-WTF-GAGAA‘, it was mentioned many times in my posts, here it really looks like it was added into Spike with the conserved ‘TSGW’ tetrapeptide… Spike sequence is in query line, IgGFc sequence in Sbjct line:
Query  844  IAARDLICAQKFNG-LTVLPPLLTDEMIAQYTSALLAGTITSGWTFGAGAALQIPFAMQM  
            + ++D   A   NG L+ LP +L +  I  Y         TSGW     A ++  F +++
Sbjct  409  VISKDNPGAVVINGELSNLPMMLNNNTIHLY---------TSGWF----AVIETDFGVKL 
Query 1034  LGQSKRVDFCGKGYHLMSFPQSAPHGVVFLHVTYVPAQEKNFTTAPAICHDGKAHFPREG 
            +GQS   D C    H  S  Q A   VV  ++T  P +          C+  +      G
Sbjct  1067 VGQSIITDDC----HRISTCQ-ASGVVVSQNMTCDPNESCLVKNGVMGCYIQQCFLDSNG
The last line with the divided CHRIST sequence is not present in Spike, except for the C, H and S residues. Is IgG-Fc somewhat related with covid19? Just one citation^1 showing how important it is, with no further analysis. The next one,  transmembrane channel-like protein 3  XP_049638825.1, with over 30% identities:
Query  1    MFVFLVLLPLVSSQCVNLTTRTQLPPAYTNS  31 Spike 
            M  F+V+  L++ Q    T+R ++PP +  S
Sbjct  154  MGAFVVIPELIAGQPFGSTARKRVPPEHVAS  184  XP_049638825.1

Query  1082  CHDGKAHFPREGVFVSNGTH  1101 Spike 
             CH   +  P+     +  TH
Sbjct  746   CHRISTCSPKGRCSRAPSTH  765 XP_049638825.1
The word ‘CHRIST’ disappears in Spike, except for the first CH and last T residues. despite of many similar sections. Try to run similarities with the transmembrane channel-like protein 3 and nsp3 from SARS-CoV-2, 67% sequence coverage and ~40% identities including section showing their direct electrostatic relationship:
Query  842  EEEGEEE  848 
            EEE EE+
Sbjct  154  EEEQEED  160
Next protein, XP_007803561.1, P-type cation-transporting ATPase, this time the ‘CHRIST’ section in the first hit is not conserved, but other fragments are, the special perverse one, even for this totally different protein, comes up, again:
Query  91   YFASTEKSNIIRGWIFGTTLDSK  113 Spike2020
            Y A T      R    G +LD +
Sbjct  141  YIAKTTGFTCHRISTHGQSLDIR  163 XP_007803561.1
Query  880  GTITSG-------------WTFGAGAALQI------PFAMQMAYRFNGIGVTQNVLYENQ  
            GT+T G              +  A  AL +      P +  +A      GV + VL EN 
Sbjct  581  GTLTKGELSVLAEDHFSESQSVAASIALGLTMNSKHPVSAALAAHLQARGV-EPVLIENM  
Cation transporting ATP-ase is involved in binding Mg, a process affected by SARS-CoV-2^2. 
Next protein eukaryotic translation initiation factor 2-alpha (code XP_048641134.1), almost 38% identical with Spike:
Query  452  LYRLFRKSNLKPF-ERDISTE  471 Spike ACE2 binding domain
            ++  F     KPF E DI  +
Sbjct  277  IFAEFTSEKEKPFGECDIENQ  297 TIF2A
Query  485  GFNCYFPLQ-SYGFQP  489 SPIKE
            G  C      S    P
Sbjct  397  GHYCHRISTLSGQVCP  401      XP_048641134.1 = TIF2A
The ‘CHRIST’ section is gone again, except fot the first Cys residue.
Next protein reverse transcriptase/maturase family WP_087017951.1 with 71% identities(!!!) over 50% sequence coverage:
Query  446  GGNYNYLYRLFRKSNLKP  463 Spike 
            GG    +  L RKS   P
Sbjct  252  GGICHRISTLHRKSKNNP  269 WP_087017951.1 reverse transcriptase
Query 668 AGICASYQT-QTNSPRRARSVASQSIIAYTMSLGAEN---SVAYSNNS 711 FURINsite
           GIC    T    S     S   +  IA  + L  +     V   NN 
Sbjct 252 GGICHRISTLHRKSKNNPDSPDREKWIAEEVELKRQRVKIPVYQDNNK  299
Query  1246  GCCSCGSCCKFDEDDSEPVL  1265 Spike 
             G C    C      DSEPV+
Sbjct  541   GICELCGC------DSEPVV  554 WP_087017951.1
Query  1098  NGTHWFV  1104 Spike
             NGT+WF+
Sbjct  150   NGTKWFI  156 WP_087017951.1
In the above example 2 different Spike sections match the ‘CHRIST’ section from the reverse transcriptase. The high homology between Spike and reverse transcriptase is troubling, and like above, it does not contain the ‘CHRIST’ sections, except for one or two residues conservation. 
The next protein chromatin modification-related protein EAF7-like XP_048006383.1 with less homology but still many highly homologous sections, just one as example:
Query  40   DKVFRSS--------VLHSTQDLFLPFFSNVTWFHAIHVSGTNGT  76
            D VFR+S        + H+T++     F  V   +    SG N +
Sbjct  406  DLVFRTSDSFENLEPIAHTTENFDNEEFEPVEEMREAQGSGANES  450
And when you see Nature articles title like this one:”SARS-CoV-2 restructures host chromatin architecture”, you might ask WTH (what the hell) is going on here? Have to put this new link to an interview with an incredibly suffering nurse:
COVID Intel - by Dr.William Makis
VIDEO - Florida ER Nurse (Dawn) diagnosed with Alveolar Rhabdomyosarcoma (Turbo Cancer), 5 months after COVID-19 booster. She had 3 Moderna vaccines in total.
VIDEO - Florida ER Nurse (Dawn) diagnosed with Alveolar Rhabdomyosarcoma (Turbo Cancer), 5 months after 2nd COVID-19 booster. She had 3 Moderna vaccines…
Listen now
3 years ago · 85 likes · 32 comments · Dr. William Makis MD
Dawn is mentioning a Forkhead protein related possibly to her cancers. The chromatin remodeling proteins do interact with forkheads in order to rearrange DNA strands. That’s why Forkheads do contains DNA binding domains (FOX-DBD) with known motifs, summary of which is accessible at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501956/ . Table 1 of that pub lists the determined structures of these motifs, among others, one of those ‘GTAAACA’. Is it in the Spike? Sure it is (sorry for the increasing irony), right at the position 25091-25097 of the entire SARS-CoV-2 genome with 21563-25384 range covering the Spike (https://www.ncbi.nlm.nih.gov/nuccore/NC_045512). Pdb Data Bank entry at https://www.rcsb.org/fasta/entry/7CBY/display shows how that piece of HUMAN DNA (now in synthetic Spike genome) binds the human Forkhead box protein G1.
A large family of serine incorporator 4 proteins with example XP_045305889.1 contains the very unique cysteine rich section, very homologous to the Spike and very rare among proteins:
Query  1235  CCMTSCCSCLKGCC  1248 Spike
             CC  + C+C   CC
Sbjct  41    CCGPAPCTC---CC  51 serine incorporator 4
or by hand:
 CM-TSCCSCLKGCCSCGSCCK Spike
  +  SCC      C+C  CC+
 FYQVSCCGPAP--CTC--CCH Serine incorporator 4
 
Query  356  KRISN  360 Spike
             RIS 
Sbjct  510  HRIST  514 Serine incorporator 4
extention of the above by hand adding the C-terminal section
Query  356  YAWNRKRISNCV  360 Spike
            +    +RIS     <<< the highest homology with 'CHRIST' section
Sbjct  510  FRRQCHRISTAR  514 serine incorporator 4
The  ‘CHRIST’ section in all Serine Incorporator Protein Families is located at the very C-terminal end and in case of this protein from  Leopardus geoffroyi (Geoffroy's cat) (https://www.ncbi.nlm.nih.gov/protein/XP_045305889.1), it actually ends with almost the biblical inter-twinned words ‘CHRISTAR‘=CHRIST-STAR. Also in this case the serine incorporator 4 protein containing the sequence ‘CHRIST’ is connected with SARS-CoV-2^3. 
Next WD-40 repeat protein located at https://www.ncbi.nlm.nih.gov/protein/PNY03708.1 . Here its few BLAST alignments with Spike:
Query 1109  FYEPQIITTDNTFVSGNCDVVIGIVNNTVYDPLQPE-----LDSFKEELD-KYFKNHTSP
            FY+P+++T +N+   G     +G   +TV  P+  E     +   ++ L+ +Y  +H   
Sbjct 733   FYQPEVLTNENSIDFGTTQ--LGGKLDTVKLPVWAENPIDFIHKHRKALESEYVSSHLHE 
here the ACE2 receptor bindinding domain:
Query  438  SNNLDSKVGGNYN--YLYR-LFRKSNLKPFERDISTEIYQAGST  478 Spike
            SN   +   G Y   +LYR L R+S L+ F  D S   +  GS+ <CHRISTGIHA------WR  291 WD-40 'CHRIST' section

and now the only best conserved 'CHRIST' section in Spike:
Query  354  NRKRISNCVADYSVLYNSASFSTFKC  379 Spike 
              +RI+  V +YS   ++ +   +KC
Sbjct  471  TSRRINFIVDNYSNETSATTDGVYKC  496 WD-40
Is there anything in common between WD-40 repeat like proteins with the WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly, and Spike??? Sure there is, the recent research, just published in the most prestigious journal, available at https://www.nature.com/articles/s41467-023-44076-3 ^4. This it the first time when the scientists talk about ‘genetic vaccines’, for a change… Here one sentence from their abstract, quote: “Because this C-terminal residue is the key determinant of SARS-CoV-2 assembly and fusogenicity our work provides a framework for the export of S protein encoded in genetic vaccines for surface display and immune activation“. 
One more, this huge one, >5000 resides, its name MIDASIN (could be mid-a-SIN) with ~90% sequence coverage and ~40% IDENTITIES(!!) with Spike. It is s.c. AAA ATPase with vWA domain (i.e. Von Willebrand factor type A domain), involved in ribosome maturation (Translation, ribosomal structure and biogenesis):
Query  737   DCTMYICGDSTECSNLLLQYGSFCTQLNRALTG  769 Spike 
             D + Y CGDST  S+L+     F + L R + G
Sbjct  4956  DSSDYKCGDSTHSSSLM-----FYSNLKRIVMG  4983 Midasin
Query  132   EFQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLEGKQGNFKN
             E   C   F  +   + N++W     RV S      F       +MD + K+GN+K 
Sbjct  1208  ERDLCVASFFVLVERQRNEAW---RARVKSIIEKWCF-------MMDRDDKKGNWKE
Query  1244  LKGCCSCG--SCCKFD-EDDSEP  1263 Spike 
             LK  C+ G     K D EDD E 
Sbjct  5140  LKRVCTVGVDRVLKLDSEDDQEN  5162 Mid-a-SIN

two Spike sections align with the 'CHRIST' motif in Mid-A-SIN

Query  1001 LQSLQTYVTQQLIRAAEIRA  1020 Spike
               + TYV+Q  I  + +RA
Sbjct  178  CHRISTYVSQHDIILSPVRA  197 Mid-A-SIN 'CHRIST-1'section
Query  354  NRKRISNCVADYSVLYNSASFSTFKCYGVSPTKLNDLCFTNVY  396 Spike
              +RIS  V+ + ++ +       K +     K++     N+Y
Sbjct  180  FCHRISTYVSQHDIILSPVRADDVKVFCDGIEKISTEIRKNLY  219 Mid-A-SIN
=> the 'KRIS'section of Spike shows the highest homology found by BLAST
And is that Mid-A-SIN with its Von Willebrand factor type A domain somewhat related to covid19?? Of course it is, a big time, here only two citations ^5,^6, out of countless more…
This one is also special, CRISPR/Cas system-associated protein Cas3, taken out of human oral metagenome with sequence in https://www.ncbi.nlm.nih.gov/protein/PIE47861.1. Here just few alignments, including the ‘CHRIST’ section in comparison with Spike:
Query  451  YLYRLFRKSNLKPFERDISTEIYQAGSTPCNGVEGFNCYFPLQS  494 Spike RBD
            ++Y  F  +N KP   DIS  I +      +     N  F + S
Sbjct  948  FIYPGFETNNFKPHSYDISELITENQLARIDAQARINNNFAMDS  991 Cas3
Query  134  QFCNDPFLGV-----YYHKNNKS  151 Spike
            Q CND   GV      YHK +KS
Sbjct  762  QLCNDLMQGVIQLHQRYHKLDKS  784 Cas3

and now THREE(!!!) Spike pieces aligned with 'CHRIST' section in Cas3:

Query  365  YSVLYNSASFST-FKCYGVSPTKL-------------NDLCFTNV  395 Spike
            Y +L +SAS ST   C  +S  KL             N+L +  V
Sbjct  46   YQLLKDSASRSTAVSCHRISTRKLTKLVWIVGNKRKFNELGYVAV  90 Cas3
Query  669  GICASYQTQTNSPRRARSVASQSIIAY  695       Spike FURIN site!!!
            G+ + YQ   +S  R+ +V+   I +
Sbjct  41   GLRTVYQLLKDSASRSTAVSCHRISTR  67        Cas3
Query  347  FASVYAWNRKRISNCVADYSVLYNSASFST-FKCYGVSPTKLNDLCF  392
              +V              Y +L +SAS ST   C+ +S  KL  L +
Sbjct  42   LRTV--------------YQLLKDSASRSTAVSCHRISTRKLTKLVW  74
For this one that’s not even a question to relate it to SARS-CoV-2, this time, to its detection^7,^8…
And few more examples:
DNA endonuclease rbbp8      KAI8505736.1 
Query  1069  PAQEKNFTTAPAICHDGKA 1086 Spike
             PA +      PA CH   +
Sbjct  43    PAADGAEPDTPAPCHRIST  60 rbb8

Toll/interleukin-1 receptor domain-containing protein [Oscillospiraceae bacterium] MBR4036625.1
Query  229  LPIGINITRFQTLLALHRSYL  246 Spike 
            L +GI    F   +  HR
Sbjct  538  LVMGIVENPFNWYVDCHRIST  555 Toll receptor

Pseudomonas phosphoenolpyruvate--protein phosphotransferase (PtsA)
Query  10   LVSSQCVNLTTRT-QLPPAYTNSFTRGVYYP  39
            L ++QC  ++T    LP A         ++P
Sbjct  805  LDAAQCHRISTDLLNLPSAAAVRQACHQHWP  835
A special addition, because of its importance in governmental interests (DOE, LBNL,  Los Alamos National Laboratory), it is a fungal protein from HET-R family. A review from 2000^9 describes that cell fusions in fungi can lead to cells with different nuclear types forming s.c. heterokaryons, genetically controlled by specific loci termed het loci (for heterokaryon incompatibility). From that 2000 abstract: “Heterokaryotic cells formed between individuals of unlike het genotypes undergo a characteristic cell death reaction or else are severely inhibited in their growth.” Here some of the alignment of HET-R protein with Spike (this time in Sbjct line):
Query  79   PVRVVVYS  86  HET-R  
            P RVVV S
Sbjct  507  PYRVVVLS  514 SARS-CoV-2 Spike
Query  640   DVSGLNS  646 HET-R  
             D+SG+N+
Sbjct  1168  DISGINA  1174  SARS-CoV-2 Spike
Query  259  QIFSGSSDGTLRVWDVQSGTCRHTISGHGDNVNCVA  294  HET-R  
            ++F+ +   ++  W+      R  IS      NCVA
Sbjct  340  EVFNATRFASVYAWN------RKRIS------NCVA  363 SARS-CoV-2 Spike
Query  167  VYSPKGDQVASGCADSSVRLWNVASG  HET-R    
            VY+    ++++  AD SV L+N AS  
Sbjct  349  VYAWNRKRISNCVADYSV-LYNSASF  SARS-CoV-2 Spike
Query  391   YDGTMRLWDVDTGTCHRISTGHTS  414  HET-R  
             YD      D       +    HTS
Sbjct  1138  YDPLQPELDSFKEELDKYFKNHTS  1161 SARS-CoV-2 Spike
and last with manual adition:
              SPRRARSVASQ  >>SARS-CoV-2 Spike Furin Site
              SP+   VAS
Query  168  VYSPKGDQVASGCADSSVRLWNVASGECSHIF    HET-R  
            VY+    ++++  AD SV L+N AS      +
Sbjct  350  VYAWNRKRISNCVADYSV-LYNSASFSTFKCY    SARS-CoV-2 Spike
  
There are so many, many more proteins with the above features. But that above implies to me already, that Spike was build from relevant proteins which contain the amino acids sequence, that short peptide ‘CHRIST’, which during the incorporation was overwritten with different amino acids (code) in highly homologous sections.  All those proteins carrying the word related to CHRISTmas are also closely related with specific SARS-CoV-2 characteristics. It is as if one can take all the proteins containing the special sequence ‘CHRIST’ (without even concentrating on species), and their functions will be related to Spike, while not having that sequence anymore in Spike.
On the other hand that highest homology tripeptide ‘RIS’ from the last BLAST output above, in the Spike and the ‘Serine Incorporator 4’has its short homolog in protein called luciferase (NIH data location at https://www.ncbi.nlm.nih.gov/protein/UUA44467.1 ). BLAST finds one hit with the Spike ‘RIS’ section, the second was found by human eyes:
Query  386  QRGELCV  392 Luciferase
         GVNQRGELCVRGPM
            +R   CV
         WNRKRISNCVADYS
Sbjct  356  KRISNCV  362 Spike
now by hand, a different part of Luciferase overlaps better with Spike:
GLNTNHRIVVCS Luciferase 
     ++I  C
YAWNRKRISNCV Spike2020
or when adding gaps:
GLNTNH-RIVVCS Luciferase 
    N+ RI  C
YAW-NRKRISNCV Spike2020
We know SARS-CoV-2, its Spike in particular, was designed over a period of many years, ending with countless patents. Current bioinformatics search for anything related to Spike, ends up with many, many thousands of Spike closely related ‘variants’, to a level where in fact one can’t find anything, but the Spike. A digital bio-invasion, in my opinion. If the ‘Spike origin idea’ presented here, has nevertheless some meaning in reality, if it is indeed true (it looks to me like it is), then imagine the amount of HATE that ‘somebody’ (who pays for all this ‘modern science’) must have against the ORIGINAL CREATOR, GOD. That hate must be immense, based on incredible jealousy, resulting in overwriting the original genetic code, with the one, which does not carry the word ‘CHRIST’ any more.
Dr. Fauci (Jesuit) and his connection with this special day was mentioned exactly a year ago, in a post at, with quite few non-existing links any more:
Thank you for your attention.
Literature:
David G Alleva et al. “Development of an IgG-Fc fusion COVID-19 subunit vaccine, AKS-452“ Vaccine 2021 Oct 29;39(45):6601-6613. https://pubmed.ncbi.nlm.nih.gov/34642088/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955571/
Shaofen Xu et al. “The Emerging Role of the Serine Incorporator Protein Family in Regulating Viral Infection“ Front Cell Dev Biol. 2022; 10: 856468. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010877/
Debajit Dey et al. “A single C-terminal residue controls SARS-CoV-2 spike trafficking and incorporation into VLPs” Nature Communications | (2023)14:8358 https://www.nature.com/articles/s41467-023-44076-3
Yoshihiro Fujimura^#¹, Linda Z Holland“COVID-19 microthrombosis: unusually large VWF multimers are a platform for activation of the alternative complement pathway under cytokine storm“ Int J Hematol. 2022 Apr;115(4):457-469.https://pubmed.ncbi.nlm.nih.gov/35316498/ 
Kan Li et al. “SARS-CoV-2 Spike protein promotes vWF secretion and thrombosis via endothelial cytoskeleton-associated protein 4 (CKAP4)“ Signal Transduction and Targeted Therapy volume 7, Article number: 332 (2022).  https://www.nature.com/articles/s41392-022-01183-9
Pallavi Deol et al. “CRISPR use in diagnosis and therapy for COVID-19“ Methods in Microbiology. 2022; 50: 123–150. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073596/
Kazuto Yoshimi e tal. “CRISPR-Cas3-based diagnostics for SARS-CoV-2 and influenza virus“ iScience. 2022 Feb 18; 25(2): 103830. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801231/
Sven J. Saupe “Molecular Genetics of Heterokaryon Incompatibility in Filamentous Ascomycetes” Microbiol Mol Biol Rev. 2000 Sep; 64(3): 489–502. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC99001/ 


A call to ditch Face-book or Me(e)t-A(i) and the "Game Over 2 – Attack on the Microbiome" 
mejbcart — Thu, 21 Dec 2023 02:50:26 GMT
Update 10/23/2024: Who runs META at https://mronline.org/2022/07/14/meet-the-ex-cia-agents-deciding-facebooks-content-policy/
Update 5/13/2024: The RFK Jr. video Meta doesn't want you to see, but recommended to see by Elon Musk, at: https://www.kennedy24.com/who-is-bobby-video-donate
Update 1/12/2024: despite of the global war on all farmers some of the cows on our planet will finally enjoy real american humane welfare standards, and Mark ZuckerBerg takes the lead on it, with beer and macademia nuts, in Hawaii, many sources report, one in german:  https://report24.news/das-volk-soll-laborfleisch-und-insekten-essen-waehrend-zuckerberg-die-teuersten-rinder-zuechtet/ Will all the farmers follow? Kobe beef should get cheaper ;)) And what about the noxious methane burps and farts? Oh here ArkeaBio come in, with the help of Gates (of hell..). And will the Zucker-cows ‘get vaccinated’???
 
His ambitious plans to improve the world and its inhabitants grow, exponentially: https://t.me/uncut_news/64188
Update 12/22/2023: Synthetic biology Hub of three: Allen Institute, the Chan Zuckerberg Initiative and the University of Washington launches a plan to build a ‘genomic smart watch’ with more links and explanation added below.
Update 12/21/2023: A great video, a MUST WATCH, featuring a connection of many big names to Jeffrey Epstein’s money giving gestures, available at: https://forbiddenknowledgetv.net/epsteins-eugenics/ The completely sick plan of these young rich elites starts ~37:00. The involvement of the top American scientists, politicians, industrial leaders is equally sickening.
Update 1/2/2024: One more Edge member, brother from the great Dr. Fauci protector, Dr. Ezekiel Jonathan "Zeke" Emanuel.
In 2016^1 the Face-book and now Met-A ‘family’ established the Chan Zuckerberg Biohub (CZB or also called CZI ), which started to be extremely active in covid19 times from the very begin in 2020. Sorry actually in 2019, when the pandemic was already predicted in the legendary Event 201 organized by the Open Philanthropy Project, OPP (Dustin Moscovitz, one of the face-book founders). OPP is one of the leading investors in Sherlock Biosciences (SB), which got EUA from FDA for its gene-editing technology products. Other leading investors in SB are ( https://sherlock.bio/about/ ): Bill&MelindaGatesFoundation, Catalio Capital, ALBANY Capital, Baidu, Illumina and Nortpond Ventures, and NOVALIS Life Sciences. With the latter giving certificates to ‘health care providers’ for sticking to ‘standarts’ in health! Looks like this closes in part the circle of evil, implying that ‘they are all in this together’. A fairer statement would be actually ‘we are all in this together’, since it is the USERS (face-book, health insurances, etc.) who enrich that entire money making crime. Unless, you ditch them all, your face-book, health insurance, etc..   
Thank you, the very kind reader ‘The BarefootHealer’ for that important Dust-in Moscov-vitz reminder! Dr. David Martins’ investigations^8 of the covid crimes are priceless!! The fact that Dust-in Moscov-vits was covered in this post from Jun 2022: 
makes me really worry, about the amount of memory loss..
The picture below shows Zuckerberg among members of the very influential Edge club (https://www.edge.org/people) featured in the epsteins-eugenics video mentioned above:
 The EDGE members include top of the entire science world with countless Nobel Price winners, to mention just two, the CRISP star https://www.edge.org/memberbio/jennifer_a_doudna and there was the RIP Kary Mullis, there is the very well known Israeli speaker https://www.edge.org/memberbio/yuval_noah_harari  (lives with his husband in moshav Mesilat Zion near Jerusalem), all of the participants in the above video, Bret Weinstein (the one who interviewed the mRNA injections guru Dr. R. Malone and the optical mouse inventor S. Kirsch at https://childrenshealthdefense.org/defender/censored-dark-horse-podcast-bret-weinstein-robert-malone-inventor-mrna-vaccine-technology/), the so beloved TV star Dr. Oz, not so well known author of ‘The Society Without God’ Phil Zuckerman, and lastly a special part of the society:  https://www.edge.org/memberbio/marina_abramovic, known for her ‘Spirit Cooking dinners’… Elon Musk is a member of the Edge society too, the one who wants everyone to have a brain chip and be remotely controlled: https://forbiddenknowledgetv.net/whitney-webb-why-did-elon-musk-actually-buy-twitter/, also via his close relationships with the government… Given that Musk’s choice for Au10tix stationed in TelAviv to verify identity of every X user for money, indicate his preferences for a collaboration.. The EDGE.org lists the name of Ariel Zev Emanuel, the CEO of the second-largest agency in Hollywood. His father, Jerusalem-born Benjamin M. Emanuel, was a pediatrician who was active in the Irgun, a Zionist paramilitary group, that operated in Mandatory Palestine during the 1930s and 1940s. Ari’s brother Dr. Ezekiel J. Emanuel is the no 1 figure of the covid19 crime scene, which includes: 
membership in the COVID-19 Advisory Board****, thanks to the President-elect Joe Biden, having a https://global.upenn.edu/penn-biden-center in the same place Dr. Emanuel is working for https://global.upenn.edu/global-initiatives/person/ezekiel-j-emanuel-md-phd (on 4/14/2025 click on these upenn links about ezekiel-j-emanuel-md-phd do not work). Dr. Emanuel’s links are now at: https://global.upenn.edu/people/ezekiel-j-emanuel-m-d-phd/ Dr. Emanuel was/is a member of the s.c. ‘Covid Crisis Group’ (https://covidcrisisgroup.org/members) which published “Lessons from the Covid War: An Investigative Report“ under the lead of PHILIP ZELIKOW (https://www.hoover.org/research/lessons-covid-war-investigative-report), the same person who ‘came up with’ : ‘The 9/11 Commission Report: Final Report of the National Commission on Terrorist Attacks Upon the United States (9/11 Report)’. Strange, that terrorists wars and health crisis issues are being investigated by the very same essential people… Tucker Carlson interviews 9/11 whistleblower: 
https://www.brighteon.com/7650dac6-8863-43ee-a3fb-7765c9c6efe7 
calls for mandatory vaccinations (https://www.acpjournals.org/doi/10.7326/M21-3150) and claims that mandatory vaccinations (in case of covid products ILLEGAL GENE THERAPIES!!!) do not violate the Nuremberg code (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127050/pdf/main.pdf ) while claiming huge ‘Declaration of Competing Interest’*****.
letter of support for Dr. Fauci https://www.cspinet.org/resource/letter-support-dr-anthony-fauci-and-his-role-us-covid-19-response
In 2019 Zuckerberg’s wealth was ~$65.6 billion (https://money.com/mark-zuckerberg-net-worth-2019/), it went up to 100 bln in 2020 (https://www.cnn.com/2020/08/07/tech/mark-zuckerberg-net-worth-intl-hnk/index.html) and in 2023 it increased apparently to ‘just’ 118.6 bln, according to https://www.forbes.com/sites/chasewithorn/2023/12/19/the-10-billionaires-who-gained-the-most-wealth-in-2023 . Whether these numbers are true indeed, would be a matter for the tax collectors, in any case, the frightening popularity of using facebook by BILLIONS of people (some covid injected, some not) and being affected by this ‘media hype’ was THE CRITICAL POINT of influencing the plandemic fear. The sneaky way to step into governmental affairs by ‘building bridges’ between the ‘users’ and their rulers is another issue one should be aware of (https://www.facebook.com/gpa/best-practices/government-organization/). 
And it could be great, if it all was with good intentions, for example, having that opportunity of saying officially to CDC how many family members died after covid19 genetically modifying injections and try to warn others, BUT with face-book, that was/is not the case. Why people are still using that platform, despite of such censorship?
The genocide of the covid genetically modifying injections can’t be the reason why this is happening right now: 
https://expose-news.com/2023/12/17/facebook-ceo-mark-zuckerberg-is-building-a-massive-doomsday-bunker/. 
Or maybe it is? Imagine all the billions of people ‘on face-book’, would finally STOP using that programming utility, and start using simple email, or postal services for the exchange of PERSONAL information! That ‘PERSONAL’ is the biggest threat of all, because it taught facebook, ever since 2004 and now it teaches Met-A (maybe that stands for MEet Ai…) AI’s how to think, exchange, react, act as a HUMAN. That Giving Away your HUMAN features to AI’s via digital technology which uses only specific frequency ranges, is a HUGE issue, in my opinion. Zuckerbergs’ outrageous and brazen AI action pays off, as seen on his accounts and new actions related to automatization of everything: 
https://www.technologyreview.com/2023/11/14/1083336/how-facebook-went-all-in-on-ai/
https://about.fb.com/news/2021/03/building-ai-that-works-better-for-everyone/
https://ai.meta.com/blog/pytorch-builds-the-future-of-ai-and-machine-learning-at-facebook/
Theoretically, face-book (change the name and do not degrade human face to a book!) could be a great gift (gift means poison in german language…) to humanity, if it was not for the initial US$500,000 Zuckerberg received from Peter Thiel^3, the CEO of ‘Palantir Technology’="products for human-driven analysis of real-world data"^4 established in 2003 (after 9/11…) with the "CIA seed money".  The video at: https://forbiddenknowledgetv.net/they-wont-be-able-to-walk-down-the-street-2023-edition shows Burla (Pfizer CEO) in front of Palantir (Pal-an-tir, how about ‘Pal an animal’ in german…) building while arrogantly ignoring every serious question from the reporter! ‘They’ do not need to answer us, the gentiles, with no rights to be a HUMAN… What Thiel/CIA et al. have for everyone? Just few titles, chrono-logically:
Palantir begin: https://finance.yahoo.com/news/what-is-palantir-everything-you-need-to-know-about-the-supersecretive-20-billion-tech-firm-set-to-ipo-164310444.html Founded in 2004 with funding from the CIA’s not-for-profit venture capital arm In-Q-Tel.. and this from Aug 2020 https://www.cnet.com/culture/palantir-co-founded-by-facebook-board-member-peter-thiel-files-to-go-public/ claiming the soldiers will be safe.. 
“Palantir to Help U.S. Track Covid-19 Vaccines“ https://www.wsj.com/articles/palantir-to-help-u-s-track-covid-19-vaccines-11603367276 , Oct 2020, BEFORE the massive injection genocide and around the same time all merges together at https://www.cnbc.com/2020/09/30/facebooks-billions-behind-palantir-and-asana-direct-listings.html with the three major facts, Palantir and Asana are pursuing direct listings, following the path of Spotify and Slack; Peter Thiel, an early Facebook investor and board member, co-founded Palantir and invested early in Asana; Dustin Moskovitz made billions of dollars as a Facebook co-founder and used some of it to start Asana in 2008.
midden in the covid injections genocide “CDC Partners with Palantir to Bolster the Fight Against COVID-19“ leading builder of operating systems, in news on February 22, 2022
”Palantir Is Rapidly Expanding Its Presence In Healthcare” https://www.forbes.com/sites/saibala/2023/06/23/palantir-is-rapidly-expanding-its-presence-in-healthcare/ from Jun 2023, AFTER and still during the injection genocide.
Will the PALANTIR AI endeavor merge at some point with MEeTAi?? Time will tell… Going through some of the Zuckerbergs et al. and CZB special covid19 related endeavors/publications might be useful in giving some insight of what’s behind the plandemic, and possibly what to expect in the future.   
Preparing for the pandemic https://www.researchgate.net/publication/340236453_The_Event_201
https://finance.yahoo.com/news/mark-zuckerberg-launches-facebook-covid-162229626.html (March 15, 2021 Zuckerberg launches COVID19 vaccination initiative)
https://news.stanford.edu/press-releases/2021/01/05/nanoparticle-vaccine-covid-19/ ( Stanford single-dose nanoparticle vaccine for COVID-19 with CZB involved)
https://med.stanford.edu/news/all-news/2021/09/covid-19-autoantibodies.html (CZB with others monitors increase in self-attacking antibodies claiming it is due to severe COVID-19, while still promoting covid19 injections) 
https://www.kennedy.ox.ac.uk/news/single-cell-ancestry-vaccine-research-funded-by-the-chan-zuckerberg-initiative (Single-cell ancestry vaccine research funded by the Chan Zuckerberg Initiative=>monitoring the genetic aspect of the gene therapies falsely calling the very same gene therapies ‘vaccines’..)
https://pubmed.ncbi.nlm.nih.gov/33482248/ (May ‘21 “SARS-CoV-2 vaccines in advanced clinical trials: Where do we stand?“ ( C. Venter^5, the ‘creator’ of the 1.08 million base pair Mycoplasma mycoides genome, the first artificial GMO bacterium, now together with CZB is involved in research of ALL covid injections; this ‘21 work reviewed the Spike ‘stabilization’ features, in red text below
)
and here the same Dr. Craig Venter (who participated in covid19 governmental programs) with some of his friends, many recognize the NMRIP Jeffrey^12… The NM stands for ‘never maybe’. So far, there is only ONE political 24’ candidate who wants Epstein files to be released, Mr. RF Kennedy^13!
From very begin of the covid injections PLAN, Dr. C. Venter knew what will happen with all the covid injected victims, here his own words :
 “It’s pretty stunning when you just replace the DNA software in the cell, and the cell instantly starts reading that new software, starts making a whole different set of proteins. And within a short while, all the characteristics of the first species disappear. And a new species emerges from this software that controls that cell going forward.” I posted that 1.5 years ago, substack writers saw it and wouldn’t react ( including the optical mouse inventor, just wonder WHY???) , the link is at at:
 
https://catalyst.nejm.org/doi/full/10.1056/CAT.21.0340 ( AFTER the above, in Jan ‘22 ‘The Evolution of a Hospital-Based Covid-19 Vaccination Program for Inpatients’ doubled down on injections strangely using mainly the Pfizer/Mod-E-RNA synthetic genetic countermeasures in that IP Program. Could that IP also stand for Internet Protocol?)
https://pubmed.ncbi.nlm.nih.gov/31831639/ (little back, in Dec. 2019, genes of Clostridium pieces were ‘knocked out’ via CRISPR-Cas9–based genetic system which affected branched short-chain fatty acids production and THEN caused immunoglobulin A-modulatory activity in mice colonized by Clostridium)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933713/ (Feb ‘23 investigation of Clostridioides difficile infection, a real burden in covid19 disease, yet covid19 is not mentioned in a single word in this study, instead ‘countermeasures’ in form of nutritional butyrate are discussed!!!)
On 12/21/2023 The Seattle Hub for Synthetic Biology, which includes CZB, will build new technologies that let scientists measure changes in single cells in real time, with the goal of using the tech to research, diagnose and treat disease. More details can be found at: https://www.fiercebiotech.com/research/new-seattle-hub-synthetic-biology-launches-build-genomic-smart-watch
Is ‘their’ plan now finally more visible? Just wonder, what is going to do the ticking in their ‘genomic smart watch’? The Cs133 with its 9,192,631,770 vibrations per second, i.e. ~9.1GHz, the 5G range so much forced upon the entire world?? Are people going to be turned into global GPS network, with ChatGPS making the ‘talking’??? Or is it going to be the Cs137 isotope, Todd Callender is talking about, with the 30.17 years to go in elementary particles, photons emission all the way to the final mass ‘stability’ of 133??? A newest update on this topic was just posted by Dr. Mercola linking to:
https://rumble.com/v3nh3ad-dig-it-202-space-the-new-frontier-for-the-control-grid-special-report.html
For the tech-enthusiasts the industry has already their first product: https://www.techspot.com/news/56372-the-cesium-133-is-the-worlds-first-true-atomic-wristwatch.html
To change humanity on genetic level first, and now to pretend to try to fix it?? It is most probably much worse than that. These individuals should be prosecuted, NOW!
If you take into account, that Zuckerberg et al. was also involved into collecting PCR tests (carrying genetic information of the tested person) already very early in the 2020  reported at: 
https://www.ucsf.edu/news/2020/06/417881/inequality-fueled-covid-19-transmission-san-franciscos-mission-district-says 
while owning the s.c. ‘Zuckerberg San Francisco General Hospital and Trauma Center (ZSFG).’ with link at https://zuckerbergsanfranciscogeneral.org/
you should be really worried when looking into that ‘ancestry vaccine research’ the CZB is pursuing^6. 
The head of science at CZB (or CZI) was Rockefeller’s Cori Bargmann, a neuroscientist who was also a co-chair of another grand science adventure, the Obama’s Brain Initiative from the NIH, all summarized at https://www.nature.com/articles/s41587-020-0685-y 
The list of interests of the CZB foundation, with the original pledge to “prevent or manage all diseases by the end of the century“ is HUGE, almost like the 158,000 Recorded Side Effects — A World Record in the list of side effects of the Pfizer injections, available at: https://peckford42.wordpress.com/2022/03/03/pfizer-adverse-events/ . The link comes from EXPOSE at: https://expose-news.com/2022/05/18/pfizer-guilty-committing-fraud-in-covid-vaccine-trials/
Whoever went through ‘covid19 disease’/shedding, frequently, if not always, had immense gut issues, confirmed by countless main resources and alternative doctors, just 2 of those for example:
“COVID-19 disrupts gut microbiome” https://www.nih.gov/news-events/nih-research-matters/covid-19-disrupts-gut-microbiome
“Gut microbiota in COVID-19: key microbial changes, potential mechanisms and clinical applications” (https://www.nature.com/articles/s41575-022-00698-4)
Thus there must be some kind of predictive programming when you see the 2018 article about CZB titled: “Chan Zuckerberg Biohub funds new research efforts, microbiome initiative” announced at: https://www.med.stanford.edu/news/all-news/2018/10/biohub-funds-new-research-efforts-microbiome-initiative.html
and years earlier, NIH in 2012, shows the same interest “Human Microbiome Project (HMP)” https://commonfund.nih.gov/hmp
Given all that, why were we not prepared for the gut issues which were swallowing tax money starting already almost decade earlier? And why CDC didn’t have probiotics on its list of covid19 ‘countermeasures’?
And why CBZ didn’t come out with their 2019 butyrate story in Nov ‘22 when Nature just stated in their next COVID-19 story, quote: “Ranking all bacterial family trajectories by their estimated changes over time in infected mice showed that this increase in Akkermansiaceae was accompanied by significant losses of Clostridiaceae 1, a family of obligate anaerobe bacteria, and of Erysipelotrichiaceae“.
There are SO MANY bugs in human gut, but CBZ knew in advance what to concentrate on, and how to CRISP the mice in order to see the metabolic consequences of it. It’s almost like CBZ is some kind of palm readers office where the crystal ball is spinning into the next future… Will it end with Zuckerberg et al. in their underground bunkers? Time will tell.
And now it gets even more serious, because there is a new book coming, NOW, with the already huge credibility to what Dr. Heiko Schoening together with RF Kennedy and others did in Aug 2020. Namely, they warned the world about the 2020 introduction of fearmongering covid19 protocols and vaccines (while not talking yet about the genetically modified injections at that time***):
 
also in this legendary speech in Berlin Aug 2020**** :
So the new book, announced on 12/19/2023 by Dr. Schoening in his interview, is warning everyone about the new coming BACTERIAL bio-plandemic. The interview is unfortunately in German, but can be translated into English with the right app: https://auf1.tv/das-grosse-interview/heiko-schoening-sagt-voraus-angriff-aufs-mikrobiom-das-wird-groesser-als-corona
Dr. Schoenings first 2022 book, ‘Game Over’ presented some of the material described in few of my old posts, and also recently again in: 
In this latest interview Dr. Schoening is talking about the same bacterial genus Clostridium, in particular the family of Clostridioides difficile, which plays the crucial role in covid19.. He also mentions his friend David Rogers Webb, who just recently produced a must see documentary “The Great Taking’:
https://live.childrenshealthdefense.org/chd-tv/events/the-great-taking-film-premiere/great-taking-film-premiere-event/
It is about ‘You will own nothing, and you will be happy’.  
This short post is not to make anyone afraid though, but free! In particular in adding to dumping face-book, by also dumping the universal spying devices called IPhones:
 
Be NOT afraid, just be prepared and active in protecting yourself! That would include learning how to make own sauerkraut, grow own veggies and support healthy gut microbiome;) A wonderful example of it can be found here at:
Gavin’s Newsletter
30 Reasons To Make Your Own Sauerkraut and Include a Daily Forkful In Your Diet (and a basic recipe from my book to make your own at home).
Preserved cabbage looks simple (and the process to make raw cabbage i…
Read more
3 years ago · 28 likes · 25 comments · Gavin Mounsey
Thank you for reading, if you do indeed..
Literature and links:
https://www.universityofcalifornia.edu/news/600m-chan-zuckerberg-biohub-led-ucsf-uc-berkeley-announced
Jeffrey M. Schaub, et al. “Expression and characterization of SARS-CoV-2 spike proteins“ Nature Protocols volume 16, pages 5339–5356 (2021). https://www.nature.com/articles/s41596-021-00623-0
https://www.washingtonpost.com/technology/2022/06/19/peter-thiel-facebook-new-right/
https://www.newsweek.com/what-palantir-never-profitable-company-born-help-cia-seed-money-makes-market-debut-1535509
https://www.jcvi.org/research/first-self-replicating-synthetic-bacterial-cell
https://www.chg.ox.ac.uk/news/legacy-network-receives-2million-in-funding-from-the-chan-zuckerberg-initiative-for-single-cell-ancestry-vaccine-research
“Gut microbiome dysbiosis in antibiotic-treated COVID-19 patients is associated with microbial translocation and bacteremia“ https://www.nature.com/articles/s41467-022-33395-6#Fig1
https://www.jamesjpn.net/conspiracy/dr-david-martin-who-they-are-the-names-and-faces-behind-the-criminal-coronavirus-conspiracy/
*** these videos are thing of the PAST, having nothing to do with current political situation of RFK (support of cruel Israel war)…. Still, strangely the consequence of using few special words, can be immense https://nemosnewsnetwork.com/watch-cnn-caught-editing-rfk-jr-speech-to-mislead-viewers/
**** https://www.cnn.com/2020/11/09/health/members-of-biden-covid-19-advisory-board/index.html
***** Declaration of Competing Interest, list of Dr. Emanuel activities from “Learning from five bad arguments against mandatory vaccination“ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127050/pdf/main.pdf :
UNESCO Global Conference uncompensated speaker;
School of Pharmaceutical & Biotech Business uncompensated
speaker; NIH Demystifying Medicine Series uncompensated
speaker; ASPO 45th Annual Meeting uncompensated speaker; Blue
Cross Blue Shield uncompensated speaker; National Health Equity
Summit uncompensated speaker; The Galien Foundation uncom-
pensated speaker; Temple Shalom Chicago speaker series uncom-
pensated speaker; AIFA Italian Medical Agency uncompensated
speaker; Rainbow Push Coalition/CEF uncompensated speaker;
IDSA uncompensated speaker, personal fees from Rise Health, travel
fees from The Galien Foundation; Vin Future uncompensated
speaker; personal fees from Well Sky; personal fees from Rightway;
Brown University uncompensated speaker; personal fees from Sig-
nature Healthcare Foundation; Organisation for Economic Coopera-
tion & Development uncompensated speaker, personal fees from
Healthcare Leaders of New York; 21st Population Health Collo-
quium uncompensated speaker; personal fees from Medimpact;
American Academy of Arts & Sciences uncompensated speaker; Vil-
lage MD uncompensated speaker; The Galien Foundation uncom-
pensated speaker; University of Sydney Australia uncompensated
speaker; personal fees from Massachusetts Association of Health
Plans; Virtahealth uncompensated speaker; Tel Aviv University
uncompensated speaker; American Philosophical Society uncom-
pensated speaker; personal fees from Princeton University; per-
sonal fees from Philadelphia Committee on Foreign Relations;
Health Action Alliance uncompensated speaker; personal fees from
Yale University Grand Rounds; personal fees from Hartford Medical
Society; UCSF uncompensated speaker; Ichan School of Medicine
uncompensated speaker; University of Minnesota uncompensated
speaker; IPHS Addis Conference uncompensated speaker; personal
fees from AAHC Global Innovation Forum; personal fees from HMSA
& Queens Health System; Faith Health Alliance Project uncompen-
sated speaker; travel fees from Macalester College; CDC Learning
event uncompensated speaker; travel fees from Oak CEO Summit;
American Academy of Political & Social Science uncompensated
speaker; Primary Care Transformation Summit uncompensated
speaker; 16th World Congress of Bioethics uncompensated speaker;
Blue Cross Blue Shield Research Health Alliance uncompensated
speaker; personal fees from Advocate Aurora Health Summit, travel
fees from DPharm Conference; personal fees from UPMC Shadyside
Medical Center; ASCO Quality Care Symposium uncompensated
speaker; travel fees from UCSF Department of Urology Grand
Rounds; personal fees from Advocate Aurora Health; personal fees
from Cain Brothers Conference; personal fees from Bowdoin Col-
lege; Brookings Institution uncompensated moderator; travel fees
from Galien Jerusalem Ethics Forum; non-financial support from
HLTH 2022 Las Vegas; National Academies Forum on Microbial
Threats uncompensated speaker; National University of Singapore
uncompensated speaker; Williams College uncompensated speaker; NIH Grand Rounds uncompensated discussant, travel fees
from HMSA; Stanford Graduate School of Business uncompensated
speaker; World Bank uncompensated panelist; travel fees from Tel
Aviv University; Serving on the following boards: Board of Advisors
Cellares; Advisor Clarify Health; Unpaid External Advisory Board
Member Village MD; Occasional Advisor Notable; Advisory Board
Member JSL Health; Advisory Board Member Peterson Center on
Healthcare; Special Advisor to Director General WHO; Expert Advi-
sory Member WHO COVID-19 Ethics & Governance Working Group;
Advisory Board Member Biden’s Transition COVID-19 Committee;
Advisory Board Member HIEx Health Innovation Exchange Partner-
ship sponsored by the UN Geneva.
 
Quote from TeamKennedy release:
In his interview with FOX News correspondent Jesse Watters, Robert F. Kennedy, Jr. called for the total and complete release of the Epstein Files. RFK Jr. asked the question, “Why are we hiding this from the American people?” If there were prominent politicians and other government officials and US businessmen on the list and involved in Epstein’s nefarious activities, U.S. citizens should know about it.


The rise of Adrenochrome and the fall of the Oxytocin, not only among the rulers.. Any SARS-CoV-2 Spike connection? 
mejbcart — Mon, 18 Dec 2023 07:43:26 GMT
Update 1/25/2025: https://rumble.com/v6bs8ty-child-trafficking-horrors-former-cia-officer-along-with-eyewitness-testimon.html “CHILD TRAFFICKING HORRORS: Former CIA Officer along with eyewitness testimony confirms the horrors“
Update 1/19/2024:  https://www.brighteon.com/4cdaa696-4098-41c5-9695-ab3fd28d780b “British MP Blows Whistle: 'My Colleagues Are Elite Pedophiles Who Drink Babies' Blood'“
Update 9/14/2024: True adrenochrome stories by a true hero Jim Caviezel at https://rumble.com/v2vgq3u-steve-bannons-warroom-a-sit-down-with-jim-caviezel-full-interview.html
Update 9/3/2024: Ukraine ‘business’ “Adrenochrome Taskforce Rescues Hundreds of Kids Trafficked by Marina Abramovic” at https://rumble.com/v5dh9gt-adrenochrome-taskforce-rescues-hundreds-of-kids-trafficked-by-marina-abramo.html
Update 3/1/2024: Dr. Nehls in a discussion with Mike Adams, explains many things regarding neurogenesis and why the great die off during ‘covid protocols’: https://www.brighteon.com/c2491ae2-4a28-4e74-97a5-d94894a3f56f
“Dr. Michael Nehls, author of The Indoctrinated Brain, reveals terrifying blueprint for the globalist assault on your neurology”.
Update 1/3/2024: Added info on hepcidin drug produced by company financed by Len Blavatnik, an Ukrainian-born British-American billionaire, who Nov 2018 donated ~200mln$ to HMS https://news.harvard.edu/gazette/story/2018/11/a-gift-to-harvard-to-turn-medical-discoveries-into-treatments/ , for enormous opportunity for medical science from organ transplants to polio vaccines to gene therapy! That must have been an inside trader move, just on time, for the covid19 gene based injections, with now the same man harvesting on the side effects of these genetic modifications of suffering humans!!!
Update 12/18/2023: Please read all the way to the end and start thinking about the consequences of the presented analysis. Any critical views here are welcome.. It is about rescuing our world, expressed in different language, by this piece of music, before going into the real post below the video: 
 
Dr. David Martin in his Oct 2023 talk at https://www.bitchute.com/video/MMXfRHgFybqK/ 
points to a Sep 2019 document at: https://www.gpmb.org/reports/m/item/2019-a-world-at-risk
Thanks for reading mejbcart’s Newsletter! Subscribe for free to receive new posts and support my work.
in which the ‘Global Preparedness Monitoring Board’ in its Progress indicator(s) planned by September 2020 (page 8) for:
“WHO and its Member States develop options for standard procedures and timelines for sharing of sequence data, specimens, and medical countermeasures for pathogens other than influenza.” Also: “Distributed manufacturing of vaccines (including nucleic acid types) begins within days of obtaining the new sequences and effective vaccines are pre-tested and approved for use within weeks.“ And lastly: ”Finally, we are grateful for the financial support provided to the GPMB Secretariat from the Government of Germany, the Bill and Melinda Gates Foundation, the Wellcome Trust, and Resolve to Save Lives.”
The most recent CHD Dec 10th 2023 interview of a Kaiser Permanente(KP) nurse at: https://childrenshealthdefense.org/defender/gail-macrae-california-icu-nurse-covid-protocols-vaccine-injuries/
and the same nurse Gail Macrae, in another interview by Steve Kirsch at:
Steve Kirsch's newsletter
The single most important interview I've ever done: former Kaiser nurse Gail Macrae
Executive summary My interview with former Kaiser Permanente Santa Rosa nurse Gail Macrae is the single most devastating interview I’ve done since I first started speaking out against the COVID vaccine in May 2021. Key points of the interview include…
Read more
3 years ago · 321 likes · 143 comments · Steve Kirsch
exposes covid crimes, lies about the 2020 ‘emergency’, about the covid protocols, NOT allowed reporting of injuries after the covid injections, EPIC computer system set up exactly in a way to never give any statistics about side effects in the covid injected victims, etc, etc.. It is shocking to listen to what the hospital staff and administration in this >1.5 year of her work was and still is capable of. KP is one of the largest (and cheapest) health care providers in CA, including their entire system of hospitals and research facilities, which follow the health progress of every member from begin to an end, and sometimes beyond (by inspecting the dead bodies). A publication titled: “Surveillance for Adverse Events After COVID-19 mRNA Vaccination” (https://pubmed.ncbi.nlm.nih.gov/34477808/) in which multiple KP facilities contributed to that overall ‘safety profile’ under the direction of CDC’s coworkers, including Tom T Shimabukuro, would need to be completely questioned, given the testimony of this witness. Given my own family experience, and now these testimonies, one can say with 100% certainty, ALL of the publications claiming safety of gene therapies are flat out LIES! That publication is just one out of many covid injection ‘safety’ studies in which KP almost always participates, using their own patients, with cases paid by the injection providers, like Pfizer. On the 12/14 another nurse came forward: 
COVID Intel - by Dr.William Makis
VIDEO - ICU Nurse - what she witnessed in the ICU during COVID-19 pandemic, hospital protocols (Children's Health Defense) (Nov.19, 2023)
VIDEO - ICU Nurse (Children's Health Defense) (Nov.19, 2023…
Listen now
3 years ago · 94 likes · 39 comments · Dr. William Makis MD
with similar, ICU insider secrets. When you hear the words ‘they all died’ AFTER applying the ‘covid protocols’, any human heart should cry out loud. More of great nurses are coming with more truth about covid protocols, at the end of this post.
If there is one ingredient missing by everyone involved in the covid19 genocide, that would be the beauty/love/cuddle hormone, oxytocin. On the other hand, fear in a threatening situation (loss of job when trying to stand against criminal covid policies, in particular loss of a prestigious job and the ‘ego’ accompanied with it) where coercion plays a role, is connected with adrenaline, which when oxidized, produces adrenochrome, a superb free radical with cardiotoxic properties (https://pubmed.ncbi.nlm.nih.gov/11799843/). Studies in 50- and 60ies were reporting a connection between adrenochrome and thought disorder, derealization, and schizophrenia. The antidote to the toxicity of adrenochrome, was a superdose of Vit C and niacin (Vit B3) with other antioxidative nutrients, all described at http://orthomolecular.org/library/jom/1994/pdf/1994-v09n04-p205.pdf . National Institute of Health (NIMH) has been the leading critic and opponent to the adrenochrome hypothesis since 1954, and because of that, the adrenochrome hypothesis disappeared, together with the antidotes. This is a great pity, because oxytocin production is heavily dependent on the presence of the same compound, ascorbic acid (https://pubmed.ncbi.nlm.nih.gov/3668432/), and that in turn, does effect the outcome of covid19 disease, as we will see below.  Try to ask for VitC injection in Kaiser Permanent-e facility, you won’t get it, ever. Parallel to this post, EXPOSE is publishing their article about adrenochrome topic too:  https://expose-news.com/2023/12/13/the-truth-about-adrenochrome/ , with more references on it. It is worth checking out;)
The previous relaxin post (inspired by the Mod-E-RNA newest patents list) identified its connections to oxytocin, it also defined multiple probable nuclear localization signals in Spike sequence, next to the known furin site and pointed to its old homolog present in Non-Structural protein from 1918 H1N1 influenza virus.
Further bioinformatics of Spike sequence indicated that SARS-CoV-2 Spike ‘design’ intended its crossing of nuclear membrane in both directions. And this is the strangest thing with covid redefinitions and the illegal and thus criminal covid injections, the foreign objects now come not from the outside world causing immune response, the cause for apparent immunity comes now from inside, the human himself… Moderna new planned synthetic mod mRNA injection materials were discussed, in particular the relaxin, human hormone involved in pathophysiology of covid19, and also closely related to the mentioned for longest known human hormone, oxytocin with the amino acid sequence and the cyclic loop structure shown below: Cys – Tyr – Ile – Gln – Asn – Cys – Pro – Leu – Gly – NH₂, or CYIQNCPLG-NH₂..
So not only adrenochrome and oxytocin are effected by Vit C, but so is the IL-6 plasma level, one of the biggest markers of covid19 in high- and low-risk patients (https://www.sciencedirect.com/science/article/pii/S2667268521000358) and so is the CRP level, and the fasting blood glucose (FBG), all vitamin C dependent. The official daily dose of VitC of ~80mg/day, is 2x10 times lower than a study like this one: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492638/, which suggests 2x~1000mg/day for the positive outcome in all the above mentioned markers. Dr. Paul E. Marik’s study, suggested even larger dose (6–24 g/day) of intravenous vitamin C to reduce mortality, intensive care unit (ICU) and hospital stays in case of sepsis and COVID-19 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762433/).
A 2010 study found an elevated IL-6 plasma levels under a psychological stress, with neurons of the hypothalamo-neurohypophyseal system (HNS) expressing not only IL-6 but also vasopressin while providing a neural link between stress and inflammatory responses (https://journals.physiology.org/doi/pdf/10.1152/ajpregu.00131.2010). Thousands of covid19 studies point to the involvement of IL-6 in this new condition (2 examples,  https://pubmed.ncbi.nlm.nih.gov/37095536/, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727200/ ), including the long version of it. This publication (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2603556/) closes the oxytocin importance with one statement, quote:  ‘oxytocin attenuates vascular oxidative stress and inflammation, two important pathophysiological processes in atherosclerosis.’ The positive oxytocin outcome was affecting the measured IL-6 secretion, indicating their mutual dependence in the inflammatory process.  
An IL-6 specialist, the MIT researcher Rahul Kakkar, with history of biopharma experience (https://polarispartners.com/partner/rahul-kakkar/) is currently enjoying a CEO position at Tome Biosciences, whose technology, "represents the maturation of editing technologies, breaking current barriers in genomic medicines discovery": https://www.genomeweb.com/business-news/gene-editing-startup-tome-biosciences-launches-213m-financing
Here a statement of Mr. Kakkar :”"We can finally reprogram the human genome with an elegance and efficiency previously unimaginable.” The company employs John Finn, formerly of Intellia Therapeutics, and Matt Barrows, who led the scale-up for Moderna's COVID-19 mRNA vaccine. Other source mentions at https://www.biopharmadive.com/news/tome-biosciences-gene-editing-startup-programmable/702092/ the plan within the title “Tome Biosciences debuts with $213M and a new way to edit the genome“ (the human genome..). The plan is to use  “programmable genomic integration,” or PGI, to “create gene therapies for liver disorders and cell therapies for autoimmune disease, ..” The Tomes Biosciences web page at: https://tome.bio/wp-content/uploads/2023/12/pr-2023-12-12_Tome-Biosciences-Launches-with-Over-200-Million-in-Funding.pdf discloses who pays and participates in this erasing procedure of the original human genome using insertions with the size of genetic code equal to the entire official size of the SARS-CoV-2 virus (~30 kb). 
It is no surprise, that Mr. Kakkar owns quite few patents (https://patents.justia.com/inventor/rahul-kakkar) related exactly to what is troubling the covid injected victims:
METHODS FOR TREATING CARDIOVASCULAR DISEASE
METHODS FOR TREATING IL-6 MEDIATED INFLAMMATION WITHOUT IMMUNOSUPPRESSION
Treatment of existing left ventricular heart failure
METHODS FOR TREATING HEPCIDIN-MEDIATED DISORDERS
The last oldest of these patents (all after 2020) states, quote: “Typically, the patient has elevated pre-treatment serum levels of IL-6. In some embodiments, the patient has elevated pre-treatment serum levels of CRP.“ Well these are the plasma markers of covid19, among others. And what is the solution? A chemical factory, with countless IL-6 synthetic antagonists… Image below from https://www.universityofcalifornia.edu/news/blocking-love-hormone illustrates the strategy of the pharma based educational system taking over the most precious, the human heart:
 
In regard to IL-6 the post from 2022 at: 
was touching exactly the iron and liver/hepcidin issue. Kakkar’s last patent states that hepcidin expression is known to be influenced by the product of the TMPRSS6 gene, a matriptase-2, a type II transmembrane serine protease. All we know about covid is, that Transmembrane protease serine 2 , TMPRSS2 (https://www.uniprot.org/uniprotkb/O15393/entry) is involved but not  TMPRSS6 (https://www.uniprot.org/uniprotkb/Q8IU80/entry). But these are both serine proteases with rather high sequence homology, yet one is only known to affect covid infection and the other is only known for influencing the iron absorption-regulating liver hormone hepicidin, which in turn is affected by IL-6. There is even a polymorphism involved, in which some people will have higher predisposition than others, to cardio diseases, for example (https://patents.justia.com/patent/20170029499). The uniprot entry details about these two serine proteases : 
for TMPRSS6 at https://www.uniprot.org/uniprotkb/Q8IU80/entry  :
Cellular Component: extracellular space , plasma membrane
Molecular Function: metalloendopeptidase activity , serine-type endopeptidase activity
Biological Process: BMP signaling pathway , collagen catabolic process , extracellular matrix disassembly  intracellular iron ion homeostasis , membrane protein proteolysis , multicellular organismal-level iron ion homeostasis , negative regulation of BMP signaling pathway , negative regulation of DNA-templated transcription , negative regulation of transcription by RNA polymerase II , positive regulation of transcription by RNA polymerase II , self proteolysis
for TMPRSS2 at https://www.uniprot.org/uniprotkb/O15393/entry 
Cellular Component: extracellular exosome , extracellular region , nucleoplasm , plasma membrane
Molecular Function: serine-type endopeptidase activity , serine-type peptidase activity
Biological Process: positive regulation of viral entry into host cell , protein autoprocessing , proteolysis , viral translation
Their transmembrane peptidase domains share ~40% identity over 250 residue section with LDL receptor domains sharing mainly the cysteine backbone pattern, for the 492 residues long TMPRSS2 and 811 residues long TMPRSS6. Despite of all these similarities the smaller TMPRSS2 (involved in Spike cleavage) interacts with 343 other proteins (https://thebiogrid.org/112968) and the much larger TMPRSS6, so important for iron homeostasis and DNA and RNA functions, interacts apparently with just TWO proteins (https://thebiogrid.org/127898). Hepcidin level modulation via inhibition of TMPRSS6, is equivalent with affecting iron levels, an issue in hematologic diseases. A company named Discmedicine https://www.discmedicine.com/our-pipeline/mat-2-inhibitor/ just got a fast-tracked FDA approval in Sep 2023 for that TMPRSS6 inhibition (via monoclonal antibodies) for polycythemia vera (PV), hereditary hemochromatosis, myelodysplastic syndromes (MDS) and β-thalassemia, all blood related. Is it strange that all these symptoms are also related with covid19, or let say, with the aftermath effects of the genetically modifying covid injections?? Isn’t it strange, that this company is financed by Len Blavatnik, the same who finances the MIT Blavatnik Institute, the home of Dr. George Church (the one also paid by Jeffrey Epstein), the super RNA-world geneticist, who oversaw the governmental covid19 operations?? Len is known for infinite amounts of money going to science, government, politics, it is as if Russia had the right hand in the heart of American science, Harvard, so it is no wonder one can see this kind of close cooperation:
:
Oxytocin/Vasopressin are parts of neurophysin I/II, which after proteolytic cleavage are released as hormonal neuropeptides, then binding to the G protein–coupled receptors (GPCRs), the oldest ‘attractive drug targets’ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439316/pdf/abb5419.pdf). Try to find which proteases cut these oldest known essential human hormones out of the neurophysins I/II, thus regulating their release and your life…. Good luck, it is hard to find. Even the WELCOME TRUST MEROPS data base (https://pubmed.ncbi.nlm.nih.gov/19892822/) recognizes the oxytocin sequence LTSA→CYIQNCPLG←GKR as a part of neurophysin, yet for the first cut it only says: XS26.001: signal peptidase complex (animal) and when you go to the link, you get serine type catalytic activity. For the PLG←GKR cut  the ‘search retrieved no data’.. At least this MEROPS entry for the human gene 1p36, apparently deleted from the human genome as a  ‘side effect’ by Pfizer BNT162B2 injections, connects some dots:
AA A28 A28.003 DNA-damage inducible protein 2 MER0030188 DDI2 84301 1p36.21
CA C19 C19.068 ubiquitin-specific peptidase 48 MER0064620 USP48 84196 1p36.12
CA C85 C85.003 OTUD3 peptidase (Homo sapiens) MER0122467 OTUD3 23252 1p36.13
CD C14 C14.010 caspase-9 MER0002707 CASP9 842 1p36.1-p36.3
MA M10 M10.022 matrix metallopeptidase-23B MER0004766 MMP23B 8510 1p36.3
MA M13 M13.002 endothelin-converting enzyme 1 MER0001057 ECE1 1889 1p36.1
MA M13 M13.008 neprilysin-2 MER0013406 MMEL1 79258 1p36
PA S1 S01.154 pancreatic endopeptidase E MER0000149 CELA3A 10136 1p36.12 
PA S1 S01.155 pancreatic elastase II MER0000146 CELA2A 63036 1p36.21
PA S1 S01.157 chymotrypsin C MER0000761 CTRC 11330 1p36.21
PA S1 S01.205 pancreatic endopeptidase E form B MER0000150 CELA3B 23436 1p36.12
PA S1 S01.229 mannan-binding lectin-associated serine peptidase 2 MER0002758 MASP2 10747 1p36.3-p36.2
PA S1 S01.933 brain-rescue-factor-1 (Homo sapiens) MER0098873 MST1P9 11223 1p36.13
PC C56 C56.002 DJ-1 putative peptidase MER0003390 PARK7 11315 1p36.2-p36.3
SC S9 S09.025 lysophospholipase II (Homo sapiens) MER0209507 LYPLA2 11313 1p36.11
Part of the side effects’ list can be found at https://expose-news.com/2022/05/18/pfizer-guilty-committing-fraud-in-covid-vaccine-trials/). The above 1p36 deletions list points to one oxytocin related enzyme: Neprilysin, which according to wiki: “is a zinc-dependent metalloprotease that cleaves peptides at the amino side of hydrophobic residues and inactivates several peptide hormones including glucagon, enkephalins, substance P, neurotensin, oxytocin, and bradykinin.^[5] It also degrades the amyloid beta peptide whose abnormal folding and aggregation in neural tissue has been implicated as a cause of Alzheimer's disease.”
So now all that is gone, potentially… Also, please note the importance of all the essential human biomolecules, frequently given the names by the d-is-tin-guis-hed molecular biologists, ending with the word ‘SIN’.
Oxytocin results in more pro-social behavior, it also affects our memory and thinking (https://www.psychologytoday.com/us/blog/the-savvy-psychologist/202002/the-power-oxytocin ). Oxytocin with all its good features plays also a role in covid19, and the number of publications about it is growing:
AM Barchi-Ferreira % FL Osorio “Associations between oxytocin and empathy in humans: A systematic literature review.” https://www.sciencedirect.com/science/article/abs/pii/S0306453021001426
Keerthi Thirtamara Rajamani et al. “Oxytocin activity in the paraventricular and supramammillary nuclei of the hypothalamus is essential for social recognition memory in rats.” https://www.nature.com/articles/s41380-023-02336-0
“Oxytocin as a Potential Adjuvant Against COVID-19 Infection
Author(s):Pratibha Thakur*, Renu Shrivastava and Vinoy K. Shrivastava
Volume 21, Issue 7, 2021, Published on: 10 September, 2020, https://pubmed.ncbi.nlm.nih.gov/32914732/
“Oxytocin's anti-inflammatory and proimmune functions in COVID-19: a transcriptomic signature-based approach” Physiol Genomics. 2020 Sep 1;52(9):401-407.  doi: 10.1152/physiolgenomics.00095.2020. Epub 2020 Aug 18.
https://pubmed.ncbi.nlm.nih.gov/32809918/
“Could oxytocin reduce autoimmune disease in COVID-19?“ Autoimmun Rev. 2022 Feb; 21(2): 102994. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592845/
“Potential of Endogenous Oxytocin in Endocrine Treatment and Prevention of COVID-19“ Front Endocrinol (Lausanne). 2022 May 3:13:799521. https://pubmed.ncbi.nlm.nih.gov/35592777/
“Cardiovascular protective properties of oxytocin against COVID-19“ Life Sci. 2021 Apr 1:270:119130. https://pubmed.ncbi.nlm.nih.gov/33513400/
“Oxytocin’s anti-inflammatory and proimmune functions in COVID-19:
a transcriptomic signature-based approach“ Physiol Genomics 52: 401–407, 2020. https://journals.physiology.org/doi/pdf/10.1152/physiolgenomics.00095.2020
“Hypothesis: Oxytocin is a direct COVID-19 antiviral” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7528823/
“Oxytocin, A Possible Treatment for Covid-19? Everything to Gain, Nothing to Lose“ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629037/
“Endogenous Opiates: 1993“ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7124241/pdf/main.pdf
Already in the 60’s there was enough indication, that RNA molecules participate in ‘transfer’ of memories:
McConnell JV (1962) Memory transfer through cannibalism in planarians. J Neuropsychiatry 3 [Suppl 1]:S42.
Albert DJ (1966) Memory in mammals: evidence for a system involving nuclear ribonucleic acid. Neuropsychologia 4:79 –92. 
McGaugh JL (1967) Analysis of memory transfer and enhancement. Proc Am Phil Soc 111:347–351.
Luttges M, Johnson T, Buck C, Holland J, McGaugh J (1966) An examination of transfer of learning by nucleic acid. Science 151:834 –837.
Jacobson AL, Babich FR, Bubash S, Jacobson A (1965) Differential approach tendencies produced by injection of RNA from trained rats. Science 150:636 –637.
Lack of consistent reproducibility, due to short life time of RNA, resulted in questioning this ‘memory theory’ for example in:
Gross CG, Carey FM (1965) Transfer of learned response by RNA injection: failure of attempts to replicate. Science 150:1749.
But a recent study confirms that theory again:
“RNA from Trained Aplysia Can Induce an Epigenetic Engram for Long-Term Sensitization in Untrained Aplysia.” May/June 2018, 5(3) e0038-18.2018 1–11 https://www.eneuro.org/content/eneuro/5/3/ENEURO.0038-18.2018.full.pdf
This topic is surfacing up again and again, also around 2001 (https://www.sciencedirect.com/science/article/abs/pii/S0166223600017392 ) which concluded, quote:”RNA-mediated modulation of neural function” and the possibility that “RNAi might be one of the physiologic mechanisms that regulate long-term gene expression in the brain.” or another conclusion “inhibitors of RNA and protein synthesis block formation of long-term memory when administered at the appropriate time (5,6)“. 
Now let’s look at the by the SYNTHETIC mod mRNA expressed C-terminal Spike part, the most cysteine rich section of all and how these cysteines align with oxytocin CYIQNCPLG (https://www.ncbi.nlm.nih.gov/protein/NP_000906.1) or vasopressin Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly =CYFQNCPRG, with only the latter increasing blood pressure but not the former, a result of a difference of 2 amino acids, I→F and L→R:
       Sbjct  1  CYIQNCPLG  9  << oxytocin 1-9
                 CYGVSPTKLN    <YFPLQSYGF    <YFPLQSYG     << SPIKE  488-496
       Sbjct  1  CYFQNCPRG  9  << vasopresSIN 1-9
       Sbjct  1  CYFQNC---PRG  << vasopresSIN 1-9
                 C    C    +G  <CYIQNCPLGGKRAAPDLD---VRKC neurophysin 1
     M    L CC     + L   C    C    K    + D   V K   
     MVTIML-CCMTSCCSCLKGCCSCGSCC---KF--DEDDSEPVLKG Spike
     M    L C       L   C    C    K    + D   V K
     MVTIMLCCMTSCCSCLKGCCSCGSCC---KF--DEDDSEPVLKG Spike
In case the body produces too little vasopres-sin a condition develops called diabetes insipidus (large urin production and thirst). One has to realize, that the dipeptide Tyr-Phe YF part of vasopresSIN is so important, that it can mitigate high-fat and high-fructose corn syrup diet-induced metabolic-associated fatty liver disease via upregulation of Nrf2/HO-1 expressions in C57BL/6J mice (https://www.sciencedirect.com/science/article/pii/S0753332223015226). And yet, the human body wastes FOUR of the Tyr-Phe (YF) dipeptides for every Spike protein synthesised after the Pfizer/Mod-E-RNA injection!!!
 Since we got one integrated neuronal system in our human bodies, there is also a connection between oxytocin and and the small molecule adrenochrome:
 just few publications and interesting links:
“Effect of adrenalin and propranolol on progesterone and oxytocin secretion in vivo during the caprine estrous cycle“ The riogenology 1998 Mar;49(4):837-44.
 doi: 10.1016/S0093-691X(98)00033-8. https://pubmed.ncbi.nlm.nih.gov/10732092/
“Effects of arterial infusions of adrenalin and acetylcholine on luteal secretion of progesterone and oxytocin in goats“ https://pubmed.ncbi.nlm.nih.gov/10734492/
https://www.nienjabrouwer.nl/adrenalin-versus-oxytocin/
https://www.drugs.com/drug-interactions/adrenalin-with-oxytocin-989-4184-1777-0.html
“Inhibitory effect of adrenaline on oxytocin release in the ewe during the milk-ejection reflex“ J Dairy Res. 1979 Jan;46(1):41-6. https://pubmed.ncbi.nlm.nih.gov/438400/
Oxytocin became a frequent target in OPTOGENETICS, a method of remote controlled expression of chosen proteins. Few examples of those reports: 
“Wireless Optogenetic Stimulation of Oxytocin Neurons in a Semi-natural Setup Dynamically Elevates Both Pro-social and Agonistic Behaviors.” Neuron. 2020 Aug 19;107(4):644-655.e7 https://www.cell.com/neuron/pdfExtended/S0896-6273(20)30397-4
What’s the frequency of the stimulation? The citation from the above points to very low frequencies: 
Dine J., Genewsky A., Hladky F., Wotjak C.T., Deussing J.M., Zieglgänsberger W., Chen A., Eder M. Local optogenetic induction of fast (20–40 Hz) pyramidal-interneuron network Oscillations in the in vitro and in vivo CA1 hippocampus: Modulation by CRF and enforcement of perirhinal theta activity. Front. Cell. Neurosci. 2016;10:1–11.
Recently a viral gene delivery in oxytocin neurons of rats was used to monitor the oxytoxin production:
STAR Protoc. 2021 Dec 14;3(1):101032. doi: 10.1016/j.xpro.2021.101032. “Viral vectors for opto-electrode recording and photometry-based imaging of oxytocin neurons in anesthetized and socially interacting rats“ https://pubmed.ncbi.nlm.nih.gov/34977678/
 To control the oxytocin peptide levels with high spatiotemporal precision in vivo, a new method was just recently introduced, without application of gene manipulations, or viral expression vectors. Replacing just the TWO amino acids in the oxytocin, the first Cys and the following Tyrosin with photo-caged unnatural amino acids will impede cyclization through disulfide formation and get activated by UV light of 365 nm subsequently releasing the natural oxytocin while controlling its signalling and binding to its receptor.
“Optopharmacological tools for precise spatiotemporal control of oxytocin signaling in the central nervous system and periphery”.  https://ncbi.nlm.nih.gov/pmc/articles/PMC10081362/
The field of Optogenetics on many top universities in particular the Weizmann Institute established in 1934 by Chaim Azriel Weizmann, a Russian-born biochemist, Zionist leader and Israeli statesman who served as president of the Zionist Organization and later as the first president of Israel, couldn’t thrive better, without the proper funding (https://en.wikipedia.org/wiki/Chaim_Weizmann). Studies on plain illumination of presynaptic neuronal tissues were known to silence the neurotraansmitter release via the optogenetic silencing (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611984/pdf/EMS138041.pdf). An extensive data base of human genes, including the one for oxytocin, can be found at: https://www.genecards.org/cgi-bin/carddisp.pl?gene=OXT. 
With the details about the receptors binding the neuropeptides of interest here:
https://www.uniprot.org/uniprotkb/P30559/entry.  Oxytocin receptor Gene OXTR
https://www.uniprot.org/uniprotkb/P37288/entry. Vasopressin V1a receptor AVPR1A
one could ask, if oxytocin is good against covid, according to check of ~2700 compounds tested for inhibition of Spike-Ace2 interface formation (https://pubmed.ncbi.nlm.nih.gov/34194331/), how about the sequence similarity of the oxytocin receptor and Spike? Here BLAST result showing ~80% sequence coverge with ~40% sequence identities assuming coverage by smaller fragments:
Query  297   VLAFIVCWTPFFFVQM-WSVWDAN-APKEASAFIIVMLLASLNSCCN  325
             +    +     + + + W +W    A+  A  ++ ++L  +  SCC
Sbjct  1214  IDLQELGKYEQY-IKWPWYIWLGFIAGLIAIVMVTIML-CCMTSCCS  1242
Query  292  FIIVLAFIVCWTPFFFVQMWSVWDANAPKEASAFIIVMLLA  319
            ++   A     +PF   QM   ++     +   +    L+A
Sbjct  898  WTF-GAGAALQIPF-AMQMAYRFNGIGVTQNVLYENQKLIA  925
Query  219  CYGLISFKIWQN-LRLKTAAAAAA------EAPEGAAAGDGGRVA  256
            CYG+   K+  N L   T   A +      E    A  G  G++A
Sbjct  379  CYGVSPTKL--NDLCF-TNVYADSFVIRGDEVRQIA-PGQTGKIA  419
Query  124  FASTYLLLLMSLDRCLA  140
            FAS Y      +  C+A
Sbjct  347  FASVYAWNRKRISNCVA  363
Query  122  GMFASTYLLLLMSLDRCLA---ICQPLRS  147
            G+    Y ++++S +   A   +C P +S
Sbjct  502  GVGYQPYRVVVLSFELLHAPATVCGPKKS  530
Query  297   WSVWDANAPKEASAFIIVMLLASLNSCCN  325
             W +W        +  ++ ++L  + SCC+
Sbjct  1214  WYIWLGFIAGLIAIVMVTIMLCCMTSCCS  1242
Query  195   WGPKAYITWITLAVYIVPVIVLAAC  219
             W    ++ +I   + IV V ++  C
Sbjct  1212  WPWYIWLGFIAGLIAIVMVTIMLCC  1236
Query  326   PW-IYMLF-TGHLFHELVQRFLCCSAS  350
             PW I++ F  G +   +V   LCC  S
Sbjct  1213  PWYIWLGFIAGLIAIVMVTIMLCCMTS  1239
Query  171   QVHIFSLREVADGVFDCWAVFIQPWGPKAYITW  203
             Q  I  L EVA  + +    + +    + YI W
Sbjct  1180  QKEIDRLNEVAKNLNESLIDLQELGKYEQYIKW  1212
Query  311  FIIVMLLASLNSCC  324
            F+ ++LL  ++S C
Sbjct  2    FVFLVLLPLVSSQC  15
Query  157  VLATWLGCLVASAPQVHIFSLREVADGVFDCWAVFIQPWGPK  198
            V+ T  GCL+  A +V+     ++  G   C +   Q   P+
Sbjct  642  VFQTRAGCLIG-AEHVNNSYECDIPIGAGICASYQTQTNSPR  682
Query  290  PFFFVQMW  297 OXTR, F291 and F292 bind to OXYTOCIN!!!
            PFF    W
Sbjct  57   PFFSNVTW  64  Spike
Query  59  CVLLALRT  66
           CV L  RT
Sbjct  15  CVNLTTRT  22
Query  235  TAAAAA  240
            TA AAA
Sbjct  259  TAGAAA  264
Query  321  NSCCNPWIYM-LFTGHLFH-ELVQRFLCCSASYLK-GRRLGETSAS  363
            N C N + +  L TG     E   +FL     +   GR + +T+ +
Sbjct  536  NKCVN-FNFNGL-TGTGVLTESNKKFL----PFQQFGRDIADTTDA  575
Query  171   QVHIFSLREVADGVFDCWAVFIQPWGPKA--YITW  203
             Q  I  L EVA ++ +   + +Q  G K   YI W
Sbjct  1180  QKEIDRLNEVAKNLNESL-IDLQELG-KYEQYIKW  1212

ACE2 binding Spike fragment aligns with OTX too:

Query  70   KHS---RLFF---------FMKH-------LSIADLVVAV-FQ---VLPQLLWD  100
            K+S    L F         F K        ++  DL+ A  F+   VLP LL D
Sbjct  814  KRSFIEDLLFNKVTLADAGFIKQYGDCLGDIAARDLICAQKFNGLTVLPPLLTD  867
Detailed interaction motifs of OTR (oxytocin receptor) and OT (oxytocin) at https://www.nature.com/articles/s41467-022-31325-0 describes the ‘PFFF’ motif as a part of the binding interface:
“OT interacts with residues F291^6.51 and F292^6.52 at the bottom of the binding pocket. This interaction induces a rearrangement of F291^6.51, initiating the large outward movement of helix VI through a series of side-chain reorientations in conserved microswitches, including W288^6.48 (CWxP motif), F284^6.44 (PIF motif) and Y329^7.53 (NPxxY motif) (Fig. 3c, d).”
That small part of the PFFF motif above was aligned with the Spike, here a try to expand it, by hand:
287 CWTPFFF-VQMWSVWDAN 297 OXTR
     + PFF  V ++ +
 54 LFLPFFSNVTWFHAIHV 70  Spike

    RTVKMTFIIVLAFIVCWTPFFFVQMWSVWDANAPKEASAFI  OXT receptor
    SVLHST--QDL-FL----PFFSNVTWFHAIHVSGTNGTKRFD  SPike 

and here the Trp-rich Spike section homolog with gp-160 in HIV:

    FIIVMLLASLNSCCNPWIYML-FTGHLFHELVQRFLCCS      OXT receptor
           KYEQYIKWPWYIWLGFIAGLIA-IVMVTIML       Spike
Now assuming Spike has a similar capability as the oxytocin receptor, while binding the oxytocin, what would be the result? It’s regulation, regulation of one of the most important human neurohormone involved in countless physiological pathways from birth to memory to love, and healing. Even without that speculative possibility, the drive of countless single amino acids by the new synthetic genetic code will affect the production of that simple cyclic peptide ‘CYIQNCPLG’ = ‘CxxxxCPLG‘ part of which, the ‘CxxxxC’, is patented by Fauci, for HIV treatment…
The recently deceased H. Kissinger apparently once said the following about GENETICS (2009 WHO council meeting) : https://www.brighteon.com/b220af6f-1a5f-466c-812f-70a88d71db16
“once the herd accepts mandatory magic potions it is game over. They will accept anything. Forcible blood or organ donation for the greater good. We can genetically modify children and sterilize them for the greater good. Control the sheep’s minds and you control the herd. Magic potion makers stand to make billions and many of you in this room are investors. It’ a big win-win. We thin up the earth and the herd pays us for extermination services.”
This text is available on youtube: 
Since this statement had to be ‘fact-checked’:
https://www.politifact.com/factchecks/2019/jun/25/facebook-posts/henry-kissinger-never-said-once-herd-accepts-manda/
one can assume it was true and we are dealing with a total lack of EMPATHY here, something, what on a molecular level, is related to the missing OXYTOCIN. Many American presidents: https://www.kla.tv/index.php?a=showlanguage&lang=en&id=26158&date=2023-11-30 were seriously affected by it, including global world wide affairs...  The tip of the covid crime was perpetuated by those, who forced GENE THERAPIES on clueless citizens, HUMANS:
https://forbiddenknowledgetv.net/pure-lies-pure-fraud-pure-evil/
This crime should never be forgotten.
On the other hand the adrenochrome issue intensifies:
https://www.brighteon.com/28203abb-5d44-4131-aaac-77daac14334c
Let’s hope people will come together, like in this little gathering just recently, and start telling the truth:
https://www.conservativewoman.co.uk/dr-david-martin-and-the-origins-of-the-coronavirus-plot/
https://expose-news.com/2023/12/16/doctor-exposes-the-biggest-hoax-in-medicine-outside-of-covid/
COVID Intel - by Dr.William Makis
VIDEO - Nurse Anesthetist (Christina Morris who now works for FLCCC) - what she witnessed (CHD Dec.15, 2023)
VIDEO - Nurse Anesthetist (Christina Morris who now works for FLCCC…
Listen now
3 years ago · 93 likes · 21 comments · Dr. William Makis MD
Thank you in advance for reading and comments.
Thanks for reading mejbcart’s Newsletter! Subscribe for free to receive new posts and support my work.



Sweet deals in viral spikes and in politics..
mejbcart — Tue, 28 Nov 2023 21:21:35 GMT
Update 12/5/2023: NZ covid injections data exposed by COVID whistleblower Barry Young make huge news:  https://www.brighteon.com/8723fded-a3eb-43f9-967c-188ed779971b while almost in the same time the ‘very tiny UK parliament’ invites few very important witnesses of covid crimes: 
Pierre Kory’s Medical Musings
UK Parliament Testimony Videos From MP Andrew Bridgen's Historic Meeting - Martin, Kory, Malone
I am writing in honor of my having been being invited to speak at Andrew Bridgen’s UK Parliament meeting entitled “For Democracy, Truth, and Freedom” on Monday, December 4, 2023. If you want to skip my overview of the events leading up to and at the meeting, the first three testimony videos are at the end of the post (Martin, Kory, Malone). The rest I w…
Read more
3 years ago · 161 likes · 30 comments · Pierre Kory, MD, MPA
Update 12/9/2023: Amazing lecture by Dr. David Martin exposing all the crimes related to covid:  https://www.bitchute.com/video/MMXfRHgFybqK/    Sept 12 2023 Live Stream - Anthroposophical society in Dornach Switzerland at the Eurythmeum“
The financial flow is always shedding some light on specific events, like for example the 2023 alphabetical list of support for the political Green Party in Germany, just published at:
with a source, in German though, at: https://report24.news/festival-der-doppelmoral-pizza-sause-sponsored-by-lufthansa-spott-und-hohn-nach-parteitag-der-gruenen/
The above is a very strange list, in which google, amazon, a non-german companies want to influence the german Green world. But then there is also Abbott Diagnostics with its ID NOW, the first CLIA-waived point-of-care molecular platform, also non-german company. So it is no wonder, that Lufthansa wants also more Green future, and Bayer AG too, and all the high tech companies, but why on earth ‘The Tooth and Mouth-health BW’ (IZZ) gives the highest donation and even worse, the contradicting to that Industrial SUGAR Association also throws in few pennies? Any sweet tooth results in high dental costs, so why the sugars are SO important, health-wise and otherwise? 
It is a wide stretch, but maybe because of the posttranslational modifications of proteins, known as glycosylation??? Clearly in covid times it was extremely important topic^1,2,3,4,5 and tons more on that not only on PubMed, with the first publication showing which sugars actually bind to the covid Spike. The potential of the emerging field of ‘glycomedicine’ is enormous^6 and it becomes truly frightening, to me, to read Bayer’s AG/+Mon-SAN-To patent for their new sweet corn MESSENGER 10194622, for example at  https://patents.google.com/patent/US10194622B1/en describing the changes in that crop, quote:
 “the DNA coding sequences can affect these phenotypes by encoding a non-translatable RNA molecule that causes the targeted inhibition of expression of an endogenous gene, for example via antisense- or cosuppression-mediated mechanisms (see, for example, Bird et al., Biotech. Gen. Engin. Rev., 9:207, 1991). The RNA could also be a catalytic RNA molecule (i.e., a ribozyme) engineered to cleave a desired endogenous mRNA product (see for example, Gibson and Shillito, Mol. Biotech., 7:125, 1997). Thus, any gene which produces a protein or mRNA which expresses a phenotype or morphology change of interest is useful for the practice of the present invention.“ 
The statictics of the old Monsanto GMO sugar beets spread (plants glyphoste resistant, https://patentimages.storage.googleapis.com/05/70/ee/4f6f1a2e5b948e/US7335816.pdf), according to wiki, implied a super fast grow, almost like the Warp Speed 2020, just years back, quote:  “In 2008/2009, 60% of the sugar beets grown in the US were GM. By 2009/2010, the percentage of GM beets had grown to 95%.^[5]^[9]^”That was thanks to the in 2003 filed patent US 7.355.816 B2. (http://www.monsantotechnology.com/content/genuity-traits-sugarbeets.aspx)
Given the ILLEGAL approval of ALL GMO’s, and the quiet approval trend in constantly higher levels of applied chemicals accompanying GMO’s on crop fields, there might be no ‘original versions’ of anything left, after the planned application of the CRISP genetic cuttings..  And that’s not all, GB goes ahead with the first  CRISPed HUMAN, according to https://childrenshealthdefense.org/defender/uk-crispr-therapy-humans/. Btw. what a name, CRISP, just bite into it!
Back to the sweet topic. Which sugars are in sugar beets? Sucrose, a disaccharide with following 2D structure:
with the left non-flat ring-like being glucose, and the right fructose. The five-carbon sugar, s.c. pentose in DNA, the deoxyribose, in RNA ribose, have identical arrangements, with the exception of ONE oxygen atom difference, giving for example, the overall structure of the DNA gene segment (image taken from https://www.genome.gov/genetics-glossary/Phosphate-Backbone):
Table 1 in ^1 at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880561/ shows the types of sugars binding to the SARS-CoV-2 Spike and Tab. 2 shows the ‘The carbohydrate binding preferences of spike protein S1 and S2 subunits’ with an similar result in one of the meta-analysis studies^7 summarizing that issue, quote: “This meta-analysis shows associations between blood groups and SARS-CoV-2 infection and supports the hypothesis that blood type O may have a slightly lower risk of infection, whereas blood type A may have a slightly higher risk of infection.” 
The types of sugars bound to the SARS-CoV-2 Spike^1 are all of the 6-carbon type, (hexoses type) belonging to glucose-, mannose-, fucose-, rhamnose-, lactose(galactose+glucose)-like or combinations thereof. Why there is no ribose or fructose, pentose-type on the Spike?? Is it maybe because it is glucose and not fructose, which stimulates pancreas to produce insulin?? And also maybe because cancer cells crave for glucose while having 15-17 more insulin receptors on their surface? That won’t be answered here, unfortunately, but for everything there is a reason, so more search is required;)
Which sugars are determining the blood types, related to immunologic reactions? N-acetylgalactosamine (A antigen) and D-galactose (B antigen), both hexoses, with the former one, also called GalNAc, playing a role in cancer^8.  And another sugar, so hugely abundant in soy (https://pubmed.ncbi.nlm.nih.gov/12406739/), also in GMO soy, the Galactose-α-1,3-galactose causes equally trouble, rejection of human transplants, and the CDC blames only the poor animals’ meat for that. Here from CDC pages (https://www.cdc.gov/ticks/alpha-gal/index.html):
Alpha-gal (galactose-α-1,3-galactose) is a sugar molecule found in most mammals.
Alpha-gal is not found in fish, reptiles, birds, or people. 
Alpha-gal can be found in meat (pork, beef, rabbit, lamb, venison, etc.) and products made from mammals (including gelatin, cow’s milk, and milk products).
But aren’t baby’s formulas frequently containing soy, stored behind the locked glass doors in every pharmacy, also the one contributing to the explosion of babies IgG’s within the first six months of their life? The Alpha-gal’s 2D structure:
is at least in terms of overall formula somewhat similar to the one of the highest bound sugars on S2 domain of Spike, which is melibiose^1. According to wi-ki:
“Melibiose is a reducing disaccharide formed by an α-1,6 linkage between galactose and glucose. It differs from lactose in the chirality of the carbon ... It can be formed by invertase-mediated hydrolysis of raffinose, which produces melibiose and fructose.”  And its structure is:
In 2002 bacterial gene for alpha-Gal was discovered, which was regulated at the transcriptional level, i.e. induced by melibiose, the melA gene was from Lactobacillus plantarum (https://pubmed.ncbi.nlm.nih.gov/12406739/). Melibiose permease, the protein which binds and transports that sugar through the cell membrane, (https://www.uniprot.org/uniprotkb/P02921/entry ) mediates the transport of also other galactosides by a symport mechanism while using sodium, lithium and protons as coupling cations, depending on the sugar substrate and the cationic environment. Melbiose transport system research goes all the way back to 80-ies, including the 1989 PhD thesis work titled “Structure-Function Correlations of the Melibiose Carrier of Escherichia Coli” by Botfield M.C. at Harvard. No, sorry, melibiose history is much older (search on https://www.ncbi.nlm.nih.gov/pmc for melibiose and sort by pub date and start with the oldest). In 1935 Blank & Arnold from Harvard Uni. published an article titled: “The inhibition of growth of Bacillus Subtilis by Ultra-Violet irradiated carbohydrates” (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC543682/pdf/jbacter00807-0056.pdf)
So once the above sugars added to agarose and agropectin (so called agar plates), or just on their own were irradiated with 253.7nm, serving as the bacterial growing media, their irradiated byproducts completely inhibited the bacterial growth, i.e. duplication with every ~20min… The above table shows that the time of irradiation proportional to the toxic material to prevent the bacterial growth, after seventy-two hours incubation at 30'C, is the highest for mellbiose, raffinose, corn starch but for our luck, exceptional for glycogen. In other words, many good sugars, in particular D-glucose (our brain lives from it!), will be gone first, while many bad ones will still support the growing bacteria, except for the branched polymer of glucose, the glycogen. Question is, which bacteria in addition to this Bacillus species? Years back, I realized, that the only bacteria capable of degrading glyphosate, are the pathogenic ones, not the good ones, again, leaving them thriving, while the good ones are gone... All random or intentional?   
The alpha-gal issue in human transplants is so huge, that in face of the human covid genetically modifying injections, FDA approved even GMO pigs. The first experiments were done in 2003 with knocked out alpha-gal gene (or GaIT-KO) in pigs using the nuclear transfer cloning (https://pubmed.ncbi.nlm.nih.gov/11778012/).
So what about SARS-CoV-2 Spike sugars?? According to uniprot entry for the Spike (https://www.uniprot.org/uniprotkb/P0DTC2/entry ), its following residues are glycosylated: 
a) 17, 61, 74, 122, 149, 165, 234, 282, 331, 343, 603, 616, 657, 709, 717, 801, 1074, 1098, 1134, 1158, 1173, 1194, all on Asparagine (N) residues
b) 323, 676, 678, on Threonine(T) residues
c) 325 on Serine (S)
That’s a sugar-sponge with LOT of sugars, all protecting the Spike which infects and invades. The glycosylation ‘evolution’ between SARS-CoV and SARS-CoV-2 on these 2 examples with Query being the 2002 and Sbjct the 2020 Spike of SARS-CoV-2 virus:
                 *122
Query  114  VIIINNSTNVVIRACNFELCDNPFFAV----SKPMGTQTHTMIFDNAFNCTFEYISDAFS
            ++I+NN+TNVVI+ C F+ C++PF  V    +     ++   ++ +A NCTFEY+S  F 
Sbjct  117  LLIVNNATNVVIKVCEFQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFL
                         3         4        *149            *165
and around the furin site:

Query  643  DTSYECDIPIGAGICASYHTVS----LLRSTSQKSIVAYTMSLGADSSIAYSNNTIAIPT  
             + SYECDIPIGAGICASY T +     RS + +SI+AYTMSLGA++S+AYSNN+IAIPT
Sbjct  657  NNSYECDIPIGAGICASYQTQTNSPRRARSVASQSIIAYTMSLGAENSVAYSNNSIAIPT
            *657         7        *predicted^9                  *709

9. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513636/
indicates that for some sections new glycosylated asparagines were introduced.. A BLAST comparison of the SARS-CoV-2 Spike (Sbjct) with the melibiose permease (Query), gives a potential melibiose binding sites (by homology):
Query  365  ESIAYSVQTMVV  376      Melibiose permease NCBI code P02921.2
             S+AYS  ++ +
Sbjct  703  NSVAYSNNSIAI  714      SARS-CoV-2 Spike YP_009724390.1
                  * glycosyated Spike site

Query  37   VGLSVGLVGTLFLVARIWDAINDPIMGWIVNATRSRWGKFKPWILI------GTLANSV  
            +G+++    TL  + R +    D   GW   A     G  +P   +      GT+ ++V
Sbjct  231  IGINITRFQTLLALHRSYLTPGDSSSGWTAGAAAYYVGYLQPRTFLLKYNENGTITDAV  
               * glycosylated Spike site

Query  80    ILIGTLANSV  89    Melibiose permease (MB)
             ++IG + N+V
Sbjct  1128  VVIGIVNNTV  1137 SARS-CoV-2 Spike
                   * glycosylated Spike site

Query  118   MTYTIMDIPFWSLVPTITLDKR  139         MB
             +TY       ++  P I  D +
Sbjct  1065  VTYVPAQEKNFTTAPAICHDGK  1086        Spike
                      * glycosylated Spike site

Query  102  GTTQIVFVCVTYILWGMTYTIMDIPFWSLVPT  133 MB
            GT     V V Y     T   + I    L PT
Sbjct  601  GTNTSNQVAVLYQDVNCTEVPVAIHADQLTPT  632 Spike
              * glycosylated Spike site

Query  150  FFASLAGF  157                        MB
            FF+++  F
Sbjct  58   FFSNVTWF  65                         Spike
               * glycosylated Spike site

Query  204  VFSSDNQPSAEGSH  217
             ++S+N  S  G +
Sbjct  435  AWNSNNLDSKVGGN  448

and the special Spike and HIV fragment, aligning partly with melbiose

Query  142   EQLVPYPRF--FASLAGFV  158
             EQ + +P +     +AG +
Sbjct  1207  EQYIKWPWYIWLGFIAGLI  1225
This is a short story based just on few older publications, but given the first sentence of the 1935 print, quote: “While investigating the killing of the spores of the anthrax bacillus by sunlight, Roux (1887) came to the conclusion that germination of the spores could be inhibited by materials which were formed as a result of the oxidation of the carbohydrate fraction of the medium. “, there must be way more knowledge out there.
If there is one point here, that would be: limit your sugars intake;), at least not to feed the Spike, also because all is paid for by politicians. 
Last but not least, how many and WHICH sugars are actually measured in case of diabetes tests?? The sweet TASTE of many synthetic compounds in comparison to the taste of refined sugar, the substances, which will never leave the human body, according to Focus issue no 44, are the following:
Synthetic Sugar | Its E-number.  | how many times sweeter than sugar
Acesulfam          |       -                   |   350 
Advantam          |     E969               |  20,000-37,000
Advantam2        |      E962.             |  200  
Cyclamat            |      E952              |   35
Neohesperidin  |       E959              |   400-600
Neotam              |       E961.            |    7,000-13,000
Saccharin          |       E954             |     300-500
Stevia                 |.      E960.            |     200
Thaumatin.       |.       E957.           |    2,000-3,000
Thank you, as always for reading and checking in, without ID NOW tests, passports, etc. Also the sub-stack limit is there…
Literature:
 1. Yung-Kuo Lee et al. “Carbohydrate Ligands for COVID-19 Spike Proteins”  Viruses. 2022 Feb; 14(2): 330. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880561/
Tingting Feng et al. “Glycosylation of viral proteins: Implication in virus–host interaction and virulence“ Virulence. 2022; 13(1): 670–683. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037552/
Amanda E. Dugan et al. “Advances in glycoscience to understand viral infection and colonization.” Nature Methods volume 19, pages 384–387 (2022) https://www.nature.com/articles/s41592-022-01451-0
https://www.nist.gov/news-events/news/2023/09/new-nist-method-can-better-identify-sneaky-sugars-viruses-spiky-weapons
Vijay Kant Pandey et al. “N-glycosylation, a leading role in viral infection and immunity development.” Molecular Biology Reports (2022) 49:8109–8120 https://link.springer.com/article/10.1007/s11033-022-07359-4
Colin Reily et al. “Glycosylation in health and disease.” Nature Reviews Nephrology volume 15, pages 346–366 (2019). https://www.nature.com/articles/s41581-019-0129-4
Federico Banchelli et al. “The Role of ABO Blood Type in Patients with SARS-CoV-2 Infection: A Systematic Review” J Clin Med. 2022 Jun; 11(11): 3029. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9181227/
R. Aguado et al. “Unveiling the Shape of N-Acetylgalactosamine: A Cancer-Associated Sugar Derivative”.  J. Phys. Chem. A 2022, 126, 42, 7621–7626. https://pubs.acs.org/doi/10.1021/acs.jpca.2c04595
Not organized material, an additional literature to consider, related to this post:
Biosynthesis of α-Gal Epitopes (Galα1-3Galβ1-4GlcNAc-R) and Their Unique Potential in Future α-Gal Therapies. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601398/
Beyond Shielding: The Roles of Glycans in the SARS-CoV‑2 SpikeProtein. Lorenzo Casalino at al. https://pubs.acs.org/doi/epdf/10.1021/acscentsci.0c01056
diabetes tests: https://diabetesjournals.org/care/article/26/1/163/22514/Discordance-Between-HbA1c-and-FructosamineEvidence 
“Primary Structure and Characteristicsof the Melibiose Carrier of Klebsiella pneumoniae 1992
Characterization of the melA Locus for -Galactosidase in Lactobacillus plantarum by Aurelio Silvestroni 1992 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC129937/pdf/0938.pdf
Membrane Topology of the Melibiose Carrierof Escherichia coli* by Martyn C. Botfield  at  https://www.jbc.org/article/S0021-9258(18)46019-X/pdf
Glycosylation of viral proteins: Implication in virus–host interaction and virulence.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037552/pdf/KVIR_13_2060464.pdf


Mod-E-RNA's FOIA file drop and the next synthetic mod mRNA relaxin gene-based 'rescue' for the damaged human hearts, and pregnancies. 
mejbcart — Fri, 24 Nov 2023 19:33:31 GMT
For getting faster to the point of that topic, please jump behind the link to Arkmedic post below. Also, updates will be attached at the begin here, with the main text starting below this  divider bar. THANK YOU for subscribing! 
Update 12/23/2023 : Manufacturing facility for Moderna, the National Resiliance company partners with Military https://www.jpeocbrnd.osd.mil/Media/News/Article/3607443/enduring-capability-jpeo-cbrnd-evolves-publicprivate-partnership-with-national/
Updates 12/20/2023: EU ‘prediction’ of the coming pathogenic invasions (can be translated into english): https://report24.news/eu-vaccelerate-programm-prognostiziert-die-erreger-der-naechsten-pandemien/ , with the number 1 Influenza. ANd now please check the seqeuence alignments of the Spike below, with the 1918 H1N1…
Update 12/19/2023: Dr. Heiko Schoening, the author of the ‘Game Over’ book, comes out with a new warning about a planned bacterial plandemic, all summarized in his new book ‘Game Over 2 - Attack on the Microbiome’. The interview abou the details is available in German at:  https://auf1.tv/das-grosse-interview/heiko-schoening-sagt-voraus-angriff-aufs-mikrobiom-das-wird-groesser-als-corona
Update 11/25/2023: Coming from EU conference, a big hope (shared from post by Dr. J. Rose on her substack Unacceptable Jessica), Dr. R. Cole starts with the right title of his talk at:                                                                 https://www.internationalcovidsummit.com/it
Update 12/6/2023: Dr. Ah Kahn Syed (his pseudonym as a medical whistle-blower) summarizes part of this post in much more detail at: https://expose-news.com/2023/12/06/plasmid-dna-in-pfizer-c19vaccine-enters-nucleus-of-cells/ 
Update 12/7/2023: Another bombshell, the synthetic genetic material, most probably due to steric hindrances on the first translated NON-human nucleotides, causes s.c. frameshifting, the ribosome itself is highjacked.. All in Nature paper, published just yesterdy, available at:  https://www.nature.com/articles/s41586-023-06800-3 titled “N¹-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting“. For our luck even ribosomes have limited life span!
Nobody on this planet has the right to deliberately change the human genome without the consent of the willing participants, no geneticist, no scientist, no MD, no politician, no pharma cartel, no government, has the right to REPROGRAM the entire humanity with one and the same mixture of synthetic toxic genetic code, like the one from the universal SARS-COV-2 Spike gene-based treatment, no matter the circumstances. The nightmare is, exactly that is being done on the entire globe while keeping it highly confidential! If you look at the pictures of so many of the covid injected VICTIMS while taking ‘just’ the skin issues for example, you have to admit, something is incredibly wrong, and it looks like humanity is CHANGING:
COVID Intel - by Dr.William Makis
mRNA Injury Series - Erythema Multiforme after Pfizer and Moderna COVID-19 mRNA Vaccines - 14 papers reviewed with photographs of 20 confirmed cases - mRNA Injury to the Immune system
Papers Reviewed: 2023 Jun (Murata et al) - Erythema Multiforme Induced by Zonisamide and Triggered by the First Dose of COVID-19 Vaccine (Pfizer-BioNTech) 2023 Apr (Yousefian et al) - Occurrence of erythema multiforme following COVID-19 vaccination: a review…
Read more
3 years ago · 54 likes · 7 comments · Dr. William Makis MD
and the most recent post from Dr. Makis:
COVID Intel - by Dr.William Makis
mRNA Injury Series - Bullous PEMPHIGOID and PEMPHIGUS VULGARIS: Severe skin injuries caused by Pfizer & Moderna COVID-19 mRNA Vaccines - 22 published photographed cases (Viewer discretion is advised)
2023 Feb (Hsuan-Chi Chen et al) - Pemphigus aggravation following Pfizer-BioNTech vaccination: A case report and review of literature 39M had 1st dose of Pfizer mRNA one week later he developed painful vesicles and erosions that progressed rapidly over his trunk and limbs, involving 30% of total body surface area…
Read more
3 years ago · 41 likes · 9 comments · Dr. William Makis MD
Adding this interview of a victimized nurse after 3 Mod_E_RNA shots:
COVID Intel - by Dr.William Makis
VIDEO - Florida ER Nurse (Dawn) diagnosed with Alveolar Rhabdomyosarcoma (Turbo Cancer), 5 months after COVID-19 booster. She had 3 Moderna vaccines in total.
VIDEO - Florida ER Nurse (Dawn) diagnosed with Alveolar Rhabdomyosarcoma (Turbo Cancer), 5 months after 2nd COVID-19 booster. She had 3 Moderna vaccines…
Listen now
3 years ago · 80 likes · 23 comments · Dr. William Makis MD
One should NOT FORGET, that the first cinical trials of Mod-E-RNA shots started in Kaiser Permanente Washington Health Research Institute (KPWHRI) in Seattle (https://www.niaid.nih.gov/news-events/nih-clinical-trial-investigational-vaccine-covid-19-begins). Were their protocols equal to what we are hearing here or were they at least little bit more truthful? Looking at the first NJEM publication claiming the efficiacy and safety of ModE-RNA shots, I’d say NO, they coudn’t have been honest.  
Repeating myself so many times, but I will do it again, like the MainStreamMed-ia.  Many, if not all MD’s when talking about covid shots are using the word mRNA, like in the above titles, which is scientifically wrong, all Mod-E-RNA and Pfizer injections contain SYNTHETIC modified genetic material mRNA (fact expressed even in the name of Mod-E-RNA), that’s why the name mod mRNA, different genetic material than normal HUMAN mRNA. Strategically, this renaming represents a very deceiving word game, perpetuated unfortunately even by all the good doctors. Most of the official covid PubMed publications today, do exactly the same, never any mention at least the word: covid SYNTHETIC GENE-based products. 
Majority of the previous posts constantly touch that topic, in particular the one among the first ones:
And just recently, Arkmedic reminded everyone that issue, again:
Arkmedic's blog
Genetically Modified Organons
[Note… If you’d like to share this article on twitter please use this link] This week could well have been a defining moment in the unravelling of the burning pyre of lies that we have been plagued with for the last 4 years (actually much longer …
Read more
3 years ago · 624 likes · 204 comments · Dr Ah Kahn Syed
This essential step of overseeing the production of every single protein in the human body by all sorts of natural every subsecond new RNA pools, now taken over by a synthetic NEW pseudo-GENE, having no origin in HUMAN genome, i.e. DNA, is so unprecedented, that it should outrage and horrify anyone who even remotely has a grasp of what DNA/RNA actually is and how it functions, and somehow, the entire digital world, i.e. todays’ ‘news’, stay silent and blind to this, intentionally covering it up. WHY? WHY is the end-product of these for long time planned gene treatments on the entire humanity so deeply confidential?? The topic of genetics involved in covid injections, moves officially little bit more forward though. Here is Dr. Janci Lindsay’s recent testimony in SC Senate Hearing in Sep 2023:
https://www.reddit.com/r/Trumped/comments/16n079p/sc_senate_hearing_dr_janci_lindsay/
It clarifies some details given by the proceeding testimony of Prof. Dr. Phillip Buckhaults before South Carolina Senate Medical Affairs Ad-Hoc Committee on DHEC: https://ugetube.com/watch/dr-phillip-buckhaults-cancer-genomics-expert-dna-contamination-in-vaccines-south-carolina-senate_dMpyKtpEgUft2fg.html
Dr. Lindsay mentioned the SV40 part in the universally injected covid plasmids, carrying in addition to the Spike also a NUCLEAR LOCALIZATION SEQUENCE, NLS, which will transport that plasmid to the nucleus... But have we not been told that all what the ‘covid’ injected genes encode is the Spike with ‘some’ parts necessary for its translation by the ribosomes in the cytoplasm, never reaching the nucleus? NLS is known as a short amino acid sequence that 'tags' a protein for import into the cell nucleus by nuclear transport, usually few positive charged amino acids, lysines, arginies or combinations thereof. The first discovered NLS was the sequence PKKKRKV in the SV40 Large T-antigen (wiki NLS entry), +5 positively charged string of amino acids in a raw. That was reported in 1984 publication^1.
This 1984 reported sequence aligns partly with the ‘new’ furin site within the SARS-CoV2 Spike, and even ~100% in the few of the HIV proteins (HIV genome deposited at https://www.ncbi.nlm.nih.gov/nuccore/AB750369.1 ) :
Query  675  QTQTNSPRRARSVAS  689  SARS-CoV-2 Spike
                  P++ R V
Sbjct  1          PKKKRKV      7  NLS from SV40

Query  61  IRILQQLLFIHFRIGCQHSRIGIIRQRRARNGASRS  96 HIV1-Vpr protein
                                     ++ R  +
Sbjct  1                            PKKKRK-V      7  NLS from SV40

Query  13  PGSQPETACTNCYCKRCSYHCLVCFQTKGLGISYGRKKRRQRRSAPQ 60 HIV-Tat 
                                             ++KKR+    <
In fact, majority of viral spikes sequences, like the example of HIV, Infectious bronchitis virus , EBV (like its nuclear antigen EBNA-LP with YP_401636.1 ), to name just a few, contain patches of positively charged amino acids, in order to cross the negatively charged cellular membranes first and later on the nuclear portion. The fact that SARS-CoV-2 Spike protein and its mRNA has the homolog of the NSL site and that this knowledge came out only in 2023 in NIH published study^2, with the oldest in it cited publication from 1998, which in turn cites the original 1984 finding, is unprecedented. The 2023 NIH publication ^2 mentions only one NLS site, quote: ”Importantly, Spike mRNA colocalized with the S protein in the cytoplasm and nucleus (both inside and outside the surface of the nucleus).”
One has to remember, normally, every single amino acid counts, every dipeptide, tripeptide, etc., all coupled to countless biological processes in every cell in every moment connecting its past to its future, while performing 100,000 reactions simultaneously. There are charges and aromatics in all biological matter, which steer everything in a wonderful end result, being YOU, an INFINITY more of what you can see in a mirror. And that suppose to change.    
NLS motifs within proteins can be found using few available bioinformstics software packages at:
   1.  https://rostlab.org/services/nlsdb/
https://nls-mapper.iab.keio.ac.jp/cgi-bin/NLS_Mapper_y.cgi
Enter the SARS-CoV-2 Spike sequence (https://www.ncbi.nlm.nih.gov/protein/YP_009724390.1?report=fasta)  into 1. and you will get 2 strings, both from the C-terminal section, S2 domain of the SAR-CoV-2 Spike:
LSRLDKVEAEVQIDRLITGRLQSLQTYVTQQLIRAAEIRASANLAATKMSECVLGQSKRVDFCGKGYHLM        P59594  start 963   end 1032   ADDED IN 2017-10-11
and
SEPVLKGVKLHYT             P59594      start 1243  end  1255   ADDED IN 2017-10-11
That protein found by the 1. server, the SPIKE_SARS P59594 (https://www.uniprot.org/uniprotkb/P59594/entry#sequences) is the 2003 Spike from SARS-CoV ~76% identical with the Spike from SARS-CoV-2, with these 2 signaling NLS peptides being IDENTICAL in the old 2002 and the new 2020 Spike of the coronavirus. The server at 2. gives somewhat different result, the most special C-terminal Spike section:
 Predicted bipartite NLS 
Pos. Sequence  1244 LKGCCSCGSCCKFDEDDSEPVLKGVKL   Score 5.9
Since it looks like the servers do not include smaller ‘internal’ protein fragments in their NLS predictions, the apparent Spike furin site does not show up in these results, despite of being listed even in the wiki...What a bad comparison.. But even if one doubts in the results of both these servers, the fact is, that a shorter nuclear localization signal (NLS) ‘DRLRR’ can be found in yet another viral protein NS1 from 1934 Influenza A virus (strain A/Puerto Rico/8/1934 H1N1) with the uniprot code P03496.1. Its alignment with SARS-CoV-2 Spike, is shown below in the first case. Second alignment shows the residues 223-230 in PABPN1-binding section of NS1 and third the residues 137-146 of its nuclear export signal (NES) and how it aligns with the Spike. Last alignment shows the 1918 Influenza NS1 protein (https://www.uniprot.org/uniprotkb/Q99AU3/entry) nuclear export and NLS signals and how they align with 2020 Spike:
Query  24   DQELGDAPFLDRLR-RDQKSLRGRGSTLG  51  NS1 Influenza NLS 34-38
                       R R R   S          
The above 1918 NS1 Influenza protein (https://www.uniprot.org/uniprotkb/Q99AU3) was binding RNA, according to uniprot entry, and here is how part of this 1918 RNA binding section (1-73) aligns with few fragments of the 2020 Spike:
15.5 bits(28) 5.8 Compositional matrix adjust. 13/43(30%) 20/43(46%) 5/43(11%)
Query  20   KRFADQELGDAPFLD--RLRRDQKSLRGRGSTLGLDIETATRA  60   1918 H1N1
            KRF +  L   PF D       +KS   RG   G  +++ T +
Sbjct  77   KRFDNPVL---PFNDGVYFASTEKSNIIRGWIFGTTLDSKTQS  116  2020 Spike

Query  10    QVDCFLWHVRKRFA-----DQELGD  29       1918 H1N1
             ++D+F   + K F      D +LGD
Sbjct  1144  ELDSFKEELDKYFKNHTSPDVDLGD  1168     2020 Spike
Thus the most recent NIH+&Co. findings, claiming the Spike can bind to RNA, cross nuclear membrane in both directions, are not so surprising, given possibly its long history, all the way back to 1918, or is it all just random speculation? Let’s keep the PABPN1-binding section of the NS1 homolog of Spike for hopefully another post and do not forget, that the synthetic nanoLIPIDS, can cross these membranes too..
With these new details about Spike sequence used in covid injections, lets go back to Mod-E-RNA, who now introduces: 
https://www.cnn.com/2023/09/13/health/moderna-mrna-flu-shot/index.html
their new experimental shot, dubbed mRNA-1010. What is it? According to Moderna web page at: https://s29.q4cdn.com/435878511/files/doc_presentations/program-detail/respiratory/Flu-(11-04-21).pdf 
it is quote ‘quadrivalent seasonal flu vaccine, which targets WHO recommendations, such as  H1N1, H3N2 and influenza B Yamagata and Victoria lineages’. What a worldwide collection of flu’s, all at once….
  One can assume, these injection materials, like the covid mod mRNA1273  contain the same SYNTHETIC GENETIC MATERIAL N-1-methylpseudouridine or mod mRNA, just this time encoding more of the toxic, pathogenic proteins, hemagglutinin (HA) glycoproteins of these 4 flu strains…. 
The last page in the document on the above MODERNA link, states: 
“no mRNA drug has been approved in this new potential category of medicines, and may never be approved; mRNA drug development has substantial clinical development and regulatory risks due to the novel and unprecedented nature of this new category of medicines; and those described in Moderna’s most recent Annual Report on Form 10-K filed with the U.S. Securities and Exchange Commission (SEC) and in subsequent filings made by Moderna with SEC, which are available on the SEC's website at www.sec.gov. “
So who approved that non-approvable technology? And who is producing Moderna’s synthetic genetic material? It is the National Resilience (what a telling name..), with details from https://www.businesswire.com/news/home/20210908005677/en/Resilience-to-Manufacture-mRNA-for-Moderna%E2%80%99s-COVID-19-Va , quote:
‘Under the terms of the multi-year agreement, Resilience will produce mRNA for the Moderna COVID-19 vaccine at its facility in Mississauga, Ontario in Canada, for distribution worldwide.’
“Moderna’s COVID-19 vaccine has saved countless lives, and we’re excited to manufacture mRNA for this important vaccine,” said Rahul Singhvi, Sc.D, Chief Executive Officer of Resilience. “This collaboration has the potential to ensure more people are protected around the world from the deadly COVID-19 virus.”
The current VAERS status: From the 9/8/2023 release of VAERS data, for patients injected with Moderna products: Found 10,347 cases where Vaccine is COVID19 and Manufacturer is MODERNA and Patient Died.
Sounds like Rahul Singhvi is a LIAR, and the LIES explode, when listening to the presidential candidate RF Kennedy’s Jr. revelations at https://rumble.com/v21ddeo-rfk-jr-says-150000-reports-disappeared-from-vaers.html
and a literal proof of it can be seen while personally searching the VAERS data base in an expert mode at  https://www.medalerts.org/vaersdb/index.php  and looking for deaths AFTER ANY covid19 injections among people living in HAWAII, for example. Here is what VAERS says:
From the 9/15/2023 release of VAERS data: Found 39 cases where Location is Hawaii and Vaccine is COVID19 and Patient Died. That number didn’t change since Nov 2022. Renewed search on the 11/13/2023 gives: From the 10/27/2023 release of VAERS data: Found 40 cases where Location is Hawaii and Vaccine is COVID19 and Patient Died. 
According to https://census.hawaii.gov/main/2022-state-pe/  on  July 1, 2022 the resident population for the State of Hawaii was 1,440,196 and between 2021 and 2022 there were 37 deaths per day.. The covid injections status of the ‘primary series’ according to: https://health.hawaii.gov/coronavirusdisease2019/tableau_dashboard/21778/  is 79%, meaning, among the 1.1 mln covid injected, there was ONE death in ONE year, according to VAERS…!??? So the 37 dead every day are only from the rest of the population, the ~0.3mln non covid-jabbed, since the jabs a so protective?? Clearly these numbers can’t reflect the presence of the possible deaths among the deceased victims who were annihilated in the 8/8/2023 Lahaina Natives extinction ‘fire’.    
Going back to the members of the provocatively named Resilience company, here we got: former FDA Commissioner, Scott Gottlieb, MD (approval and production goes hand in hand), Susan Desmond-Hellmann, MD, MPH, Former CEO, Bill & Melinda Gates Foundation (advertisement), Rahul Singhvi, ScD (founder), Chris Darby CEO, In-Q-Tel/CIA (final goal of the covid gene therapies), Frances H. Arnold (FHA mastermind ideas), PhD Nobel Prize Laureate, CalTech Professor, specialist in DIRECTED EVOLUTION with knowledge of biological enzymes speeding everything up (just wonder why the cancer grows so fast these days..?), with the entire team at: https://resilience.com/meet/team/ . 
Dr. Arnold’s Nobel prize lecture 
clearly describes FHA’s opinion about natural Creation: it is a MACHINE, a simple algorithm. FHA wants to BUILD ENZYMES, like the nature, which is a PLAYGROUND, with the biggest problem, the space exploration… It is the MUTATIONAL SPACE of PUTTING protein blocks, encoded by DNA together, into something meaningful, what nature used to do via creating life in a breeding process, and now, what Dr. FHA is in charge of, at 9:08…
On the 13th of Sep 2023, I’ve send out the following message (separately) to the main authors of the paper published in June 2023, available at: https://pubmed.ncbi.nlm.nih.gov/37271785/
Dear Dr. Jae-Hwan Nam,
I came across that title of your recent publication:
"Analyzing immune responses to varied mRNA and protein vaccine sequences"
while looking for the real ingredients of the Moderna new seasonal flu injections described at:
https://s29.q4cdn.com/435878511/files/doc_presentations/program-detail/respiratory/Flu-(11-04-21).pdf
What I'm looking for is the sequence of the new products mRNA-1010 and the confirmation of the presence of N1-methylpseudouridine-5′-triphosphate (m1ΨTP; TriLink, CA, USA) in it? Since you write about them, it would be extremely important to know the details. Also, can you please indicate the lifetime of the synthetic above mentioned nucleoside, which if used indeed in these formulations, should absolutely not be called mRNA, but rather mod mRNA.
With a hope for your answer,
….
No answer, yet, in Nov 2023, meaning, there won’t be any answer… For the record, even wiki admits what it is, namely: “synthetic pyrimidine nucleoside used in biochemistry and molecular biology for in vitro transcription”. 
Below you see the genetic ‘construct’, the thousands of the modified N1-methylpseudouridines in the ‘first style’ covid Pfizer BNT162b2 injection:
Also the Pfizer new flu injections will continue with the same synthetic gene-based technolgy: https://t.me/AllesAusserMainstream/38402
The most recent study (https://onlinelibrary.wiley.com/doi/epdf/10.1002/prca.202300048) investigating the indirect ‘lifetime’ of the synthetic mod mRNA, still expressing the Spike, indicated a timeline of ~half a year. That study with its final investigation timeline as of Apr ‘23 and rather small sampling quantity, could possibly detect longer lifetime of the synthetic nucleosides. Indeed Dr. Ralf Tillenburg from Germany who is treating constantly increasing number of patients injured after the covid shots is talking about presence of covid genetic materials in one of his patients 2 years after the shot... These synthetic genetic building blocks have one very special feature, quote from an article at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600071/ : “ Ψ-modified RNAs, coding for four transcription factors (KLF4, c-MYC, OCT4, and SOX2), were successfully used to reprogram human cells to pluripotency with great efficiency (Warren et al., 2010)”. Derrick J Rossi, one of the MODERNA main founders, coauthored another paper in 2013, available at https://www.nature.com/articles/nprot.2013.019.pdf titled “Reprogramming human fibroblasts to pluripotency using modified mRNA“. Here few citations from Rossi’s work, quote:
-”In light of these and other studies, modified mRNAs synthesized with complete substitution of cytidine and uridine with the modified nucleosides pseudouridine and 5-methylcytidine could be introduced repeatedly into cells with minimal activation of innate immune responses and limited cytotoxicity, thereby allowing robust and sustained protein expression.”
-”Combined with medium supplementation of B18R, a Vaccinia virus–encoded neutralizing type I interferon receptor to quell residual interferon-mediated immune responses, daily transfection of modified mRNAs encoding the reprogramming factors (OCT4, SOX2, c-MYC, KLF4 and LIN28A) permitted successful reprogramming of human fibroblasts to pluripotency with high efficiency”
That reprogramming to pluripotent stem cells is connected with self-renewal from an embryonic state, followed by differentiation to all possible cell types. That is substantial, because it implies a ‘rebirth’, something what normally, only DNA can do. 
 Strange Sounds  (another Substack writer) recently posted a link to the Mod-E-RNA proprietary documents retrieved in FOIA request by the ‘Defending The Republic Team’ about their covid mod mRNA-1273 gene injection material:
https://defendingtherepublic.org/moderna/
A short keywords search of the 4 Moderna Clinical Study Reports (files 16.2.7) listing the Adverse Events between Nov 2020 and May 2021 (~0.5 year, whereby around the same time placebo groups got ‘unblinded’ ^1 leaving the question if this documents summarizes 100% of those who received modmRNA1273..) gives the following, sorted according to chosen keywords with the search limit of 1000(!):
Report No (pages).   FATAL      CANCER    INFESTATIONS      ‘NOT RECOVERED’  
1 (11508)                     144/32T          177         >1000 (search limit)   >1000 (search limit….)
2 (218)                          15/12T           20                  66                            51
3 (1650)                          -                     -                   64                            25
4 (312)                            -                     -                  233                           87
Report No 1,2 has entries about two ‘Subject ID’s per page (injected volunteers). Lot of Subject ID’s are repeated multiple times (the first no in the second column), depending on the reported symptoms at specific time. Final table of the report no1 lists 32 deaths in total, it is grouped in 2 sections, each with 16 deceased participants, first one having 15 deaths in placebo group, in which the 16th additional ID 3672203, is not described anywhere in the entire document. The second modmRNA1273 injected group of ALSO 16 (how strange!!) deceased has 5 ID’s which are again, not listed anywhere in the entire document. These ID’s are: 3422244, 3472001, 3512042, 3862141, 3962094.  Also ID3822443 equally deceased, was omitted entirely in that final list, thus also in counting, a black American…  The file 2 “Moderna Clinical Study Report 16.2.7 Adverse Event Listing (May 2021) lists additional 12 deaths, from which one ID is already listed in files 1, thus there are 43 DEATHS in ~0.5 year in total in the entire study, ‘unblinded’ placebo and the control group. There is also that remarkable RACIAL PROFILE of the deceased: 
Listing 16.2.12 : ONE Asian, 3 black Americans, 3 of Indian origin and the entire rest 23 are white, predominantly males. The file 16.2.12.3 lists 8 white deceased (4 females, 4 males), 4 black Americans (2 males and 2 females)... Given the numbers of participants in each of that racial group which were accepted into the study: 
Volunteers                          DEAD after the trial
12,000 whites                =>  23 + 8 =  31
1563 black Americans  =>  3 + 4   =   7
651 Asians                     =>   1     =    1
112 native Indians       =>    3      =     3
32 Hawaiians                =>   1     =    1
2 UNKNOWN (!!!)
The above, implies, that ~3x more of black people, 1.7x more white people, 17x more native Indian people, 20x more Hawaiians are dying after the Mod-E-RNA injections than Asians, after normalization to the total number of participants in each study group… Side note, if the Asians can stand the Spike protein so well, they should stand equally the SARS-CoV-2 virus, which, despite of that, showed up in Wuhan for the first time.. Btw. isn’t that approximate racial profile of the deaths after the Mod-E-RNA injections, the one Mr. Kennedy was talking about in front of the congress and was so heavily censored because of that? A video of it at: https://childrenshealthdefense.org/defender/rfk-jr-house-committee-dystopia-totalitarianism/
Detailed list of Asian ethnic groups can be found at:  https://en.wikipedia.org/wiki/Ethnic_groups_in_Asia, with Israel belonging to West Asia. More on this issue was posted at: 
Every single family who lost a loved one AFTER the covid genetically modifying injections (thanks to the laughing face shown above, and many others..) , is a tragedy on its own, and no statistics can ever replace the loss of life in such a pain!!! Many summaries of those victims are given by that unfortunately not widely known writer: 
https://emc2.substack.com/p/emc2-articles
In the meantime, the synthetic mod mRNA technology is flooding the ‘health industry’, thanks to illegal approval processes and plain scientific fraud and lies in covid era, discussed for example by Prof. Bhakdi at: 
https://www.bitchute.com/video/bDcNw082QOGs/
which includes extremely important new protocol of discovering the synthetic mod mRNA in the blood of the covid injected. 
‘Moderna ESG Day’ publication from November 10th, 2022, at:
https://s29.q4cdn.com/435878511/files/doc_presentations/2022/11/Moderna-Final-ESG-Day-Slides-11.10.22.pdf
presents their goal, which is to: “to create a new generation of transformative medicines for patients“ with a portfolio of “vaccine and therapeutic programs” for: 
respiratory infections covid19-1→mRNA-1273, 
RSV→mRNA-1345,
Flu→mRNA-1010, 
covid19-2, 
hMPV+PIV3, 
covid+Flu+RSV→mRNA-1230, 
HCoV, RSV+hMPV), 
global health infectious diseases (CMV, Zika→mRNA-1893, EBV→mRNA-1189, HIV→mRNA-1574, 1644, Nipah, EBVtherap , VZV, HSV), 
rare diseases (PA, MMA, GSD1a, CFTR, Cn1, PKU, OTC), 
oncology (PCV→mRNA-4157, KRAS→mRNA-5671, IL-12, triplet, checkpoint vaccine), 
autoimmune (PD-L1→mRNA-6981), 
cardiovascular (VEGF-A→AZD8601, Relaxin→mRNA-0184).
The ‘cardiovascular’ application using Relaxin was announced by Mod-E-RNA in Nov 2021, ~one year after begin of covid gene-based experiments:
But Relaxin and its isoforms, belong to insulin family of hormones, are essential in pregnancy, plus there is a  close connection related to the very same ligand for the receptor targeted by Sars-CoV-2 Spike:
“Relaxin requires the angiotensin II type 2 receptor to abrogate renal interstitial fibrosis“ https://www.kidney-international.org/article/S0085-2538(15)30253-2/pdf
“Relaxin treatment reduces angiotensin II-induced vasoconstriction in pregnancy and protects against endothelial dysfunction†” https://pubmed.ncbi.nlm.nih.gov/28379296/
observed ability of relaxin2 to act as a regulator of mRNA expression levels not only LGR7 but also classic angiotensin receptors suggested that renin-angiotensin system and relaxin family peptide system are functionally linked, in “A common effect of angiotensin II and relaxin2 on the PNT1A normal prostate epithelial cell line“ https://pubmed.ncbi.nlm.nih.gov/27119161/
“Interaction between angiotensin II and relaxin 2 in the progress of growth and spread of prostate cancer cells” https://pubmed.ncbi.nlm.nih.gov/27035428/
2021 paper at https://pubmed.ncbi.nlm.nih.gov/33585554/ summarized major pathways involved in SARS-CoV-2 pathophysiology, one was the  HIF-1 (hypoxia-inducible factor 1) signaling and second, the relaxin signaling, in which the viral proteins NSP7 and NSP13 were involved, with the latter blocking the entire relaxin2 pathway. Uniprot entry at: https://www.uniprot.org/uniprotkb/P04090/entry describes the relaxin2 features, including its additional regulatory functions in angiogenesis and gene expression and the fact that its overexpression can cause prostate cancers.   
The direct description of even more products at: https://www.modernatx.com/en-US/research/product-pipeline does not specify any more details. Also in 2021 the planned gene editing became official:
https://www.fiercebiotech.com/biotech/moderna-finally-cracks-into-gene-editing-metagenomi-pact-thanks-irresistible-data titled “Moderna finally cracks into gene editing with Metagenomi pact thanks to 'irresistible' data“.
According to recent MODERNA pages (https://investors.modernatx.com/news/news-details/2022/Moderna-Announces-First-Participant-Dosed-in-Phase-1-Study-of-its-mRNA-Epstein-Barr-Virus-EBV-Vaccine/default.aspx), their recently stopped trial for the EBV (
Unreported Truths
EXCLUSIVE: Moderna has halted a trial of a new mRNA vaccine for young people after a suspected myocarditis case
Investigators for Moderna today halted an early-stage clinical trial for its mRNA Epstein-Barr virus vaccine in adolescents after a participant in the trial developed a suspected case of myocarditis. The case “necessitates an immediate suspension of all dosing for ALL adolescents,” an investigator at the company that is supervising the trial for Moderna …
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3 years ago · 346 likes · 41 comments · Alex Berenson
) contained mRNA-1189 which, quote: “contains four mRNAs that encode EBV envelope glycoproteins (gH, gL, gp42, gp220), which mediate viral entry into B-cells (a type of immune system cells) and epithelial surface cells, the major targets of EBV infection.” 
Combining those four EBV surface proteins into one vector sequence by hand and putting it in BLAST comparison with SARS-CoV-2 Spike, gives as usual, lot of similar fragments, for example (Query line represents the retracted EBV mix, Sbjct the amino acid sequence of the already injected Spike 2020):
18.5 bits(36) 5.1 Compositional matrix adjust. 6/21(29%) 13/21(61%) 0/21(0%)
Query  1630  RYNATTYLPPSTSSKLRPRWT  1650    EBV FOUR glycoproteins mix
             ++N  T LPP  + ++  ++T          IDENTITIES
Sbjct  854   KFNGLTVLPPLLTDEMIAQYT  874     SPIKE 2020

Query  1614  TEPTTDYGGDSTTPRPRYNATTYLP-PSTSSK  1644. EBV vector
             T P  D+GG        +N +  LP PS  SK
Sbjct  791   TPPIKDFGG--------FNFSQILPDPSKPSK  814   Spike

Query  1251  LSLPTSAQDSNF--SVKTEMLG---NEIDIECIM  1279 EBV vector
             +++PT     NF  SV TE+L        ++C M
Sbjct  712   IAIPT-----NFTISVTTEILPVSMTKTSVDCTM  740 Spike
Query  1034  HCTYV----SKFSTVP  1045                  EBV vector
             H TYV      F+T P
Sbjct  1064  HVTYVPAQEKNFTTAP  1079                  Spike

Query  955   KGCCF----------YFTKKKHTW-NGCFQACAELYPCTYFYGPTPDILPVVTRNLNAIE  1003
             K C F          Y+ K   +W    F+  +    CT+ Y   P ++ +  +  N  +
Sbjct  129   KVCEFQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLEGKQGN-FK  187

Query  1004  SLWVGVYRVGEGNWTSLDGGTFKVY  1028
             +L   V++       ++D G FK+Y
Sbjct  188   NLREFVFK-------NID-GYFKIY  204

Query  905   NFNKT--AEQEYGDKE--VKLPHW  924  EBV 
             N N++    QE G  E  +K P +
Sbjct  1192  NLNESLIDLQELGKYEQYIKWPWY  1215 Spike with its HIV fragment

Query  725  PTWGNWAYP-CCHVTQLRAQHLLALENISDIYLVSNQTCDGFSLASLNSPKNGSNQLVIS  783
            PTW    Y     V Q RA  L   E + + Y        G   AS     N        
Sbjct  631  PTW--RVYSTGSNVFQTRAGCLIGAEHVNNSYECDIPIGAGIC-ASYQTQTNSPRR---A  684

Query  784  RCANGLNVVSFFISILKRSSSALTGHLRELLTTLETLYGSFSV  826
            R      ++ +  S     S A         T         SV
Sbjct  685  RSVASQSIIAYTMSLGAENSVAYSNNSIAIPTNF-----TISV  722


Query  1224  PYIKW  1228
              YIKW
Sbjct  1208  QYIKW  1212

Query  537  RLDKV---LMIIPLI  548
            RLDKV     I  LI
Sbjct  983  RLDKVEAEVQIDRLI  997

Query  48   PGLSPEALWREANVTEDLASMLNRYKLIYKT  78
              L   A   + N  E  A      K IYKT
Sbjct  765  RALTGIAVEQDKNTQEVFAQV----KQIYKT  791
Query  529  LPAYKCVDRLDKVLMIIPLINV---TFIISSDREVR  561
               +KC       L      NV    F+I  D EVR
Sbjct  374  FSTFKCYGVSPTKLNDLCFTNVYADSFVIRGD-EVR  408
Query  319  AKSFFELTVL-----KDIIGICYGATVKGMQSYG--------LERLAAMLMA  357
            A  F  LTVL      + I     A   G    G        L+   AM MA
Sbjct  852  AQKFNGLTVLPPLLTDEMIAQYTSALLAGTITSGWTFGAGAALQIPFAMQMA  903
The above is a clear proof, that the SARS-Cov-2 spike genetic code shares many identical fragments with the FOUR (not one, like in SARS-CoV-2), chosen EBV virus new synthetic gene components, which this time, hopefully, do not seem to make to the real world, possibly due to the too fast reprogramming of the clueless volunteers in this trial…
The pharmaceutical cartel got the first finger with their covid ‘spiky’ shots and now it goes really viral, according to Dr. Mercola:  
Dr. Mercola's Censored Library (Private Membership)
iDNA Vaccines to Generate Internal Virus Production
STORY AT-A-GLANCE “Immunization DNA” or iDNA is a novel class of gene therapy “vaccines” that encodes for the whole virus iDNA “vaccines” transcribe the full-length genomic RNA of the live-attenuated vaccine virus. The full-length viral RNA then initiates replication of live attenuated virus in the tissues of the vaccine recipient, resulting in an immune …
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3 years ago · 10 likes · 7 comments · Dr. Joseph Mercola
Lets take the relaxin ‘vacc-gene’, at least one, which corresponds to the natural length of that extremely important human hormone (https://www.uniprot.org/uniprotkb/P04090/entry). According to ModERNA document the new ‘vaccgene’ encoding the relaxin is apparently out there to fix cardiovascular issues, BUT according to that uniprot entry, this hormone actually also: ”acts with estrogen to produce dilatation of the birth canal in many mammals. May be involved in remodeling of connective tissues during pregnancy, promoting growth of pubic ligaments and ripening of the cervix.”!! Moderna patent: “Polynucleotides encoding relaxin” Patent: US 10730924-B2 142 04-AUG-2020 describes the delivery via LNP and modified nucleotides, the same used in SARS-COV-2 SPike gene injections. Moderna relaxin paternt at:
  https://patents.google.com/patent/US10730924B2/en
shows the relaxin sequence stitched (via ggggs fusion segments) with the IgG2 sequence (immunoglobulin heavy chain constant region), all deposited at https://www.ncbi.nlm.nih.gov/protein/QPW22159.1
The abstract of that in 2018 filed and in 2020 granted patent states:
“invention relates to mRNA therapy for the treatment of fibrosis and/ or cardiovascular disease .“ and further, quote:
“mRNA therapies of the invention increase and/or restore deficient levels of relaxin expression and/or activity in subjects. mRNA therapies of the invention further decrease levels of toxic metabolites associated with deficient relaxin activity in subjects.” 
Can the injection of Spike synthetic genes in covid injections somehow affect the naturally produced human relaxin, which now needs to be fixed, by Mod-E-RNA? Blast comparison between the sequences of those two gives the following similarities:
21.0 bits(42) 	0.23 	Compositional matrix adjust. 	38/126(30%) 	41/126(32%) 	39/126(30%)
Query  296  GKEYKCAVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQV---------SLT  
            G E   A SN  +  P   TIS T           LP S   MTK  V         S  
Sbjct  700  GAENSVAYSNNSIAIPTNFTISVTTE--------ILPVS---MTKTSVDCTMYICGDSTE
Query  347  C----LVKGFYPS-------DIAVEWESN-----GQPENNYKTTPPMLDSDGSFFLYSKL  
            C    L  G +          IAVE + N      Q    YKT PP  D  G  F +S +
Sbjct  749  CSNLLLQYGSFCTQLNRALTGIAVEQDKNTQEVFAQVKQIYKT-PPIKDFGG--FNFSQI  
Query  391  TVDKSR  396
              D S+
Sbjct  806  LPDPSK  811
  or
Query  353  YPSDIAVEWESNGQP--------ENNYKTTPPML--DSDGSFFLYSKLT  391
            Y S     +E   QP        + N+K     +  + DG F +YSK T
Sbjct  160  YSSANNCTFEYVSQPFLMDLEGKQGNFKNLREFVFKNIDGYFKIYSKHT  208
Query  356  DIAVEWESNGQPENNYKTTPPML  378
            DIA       Q  N     PP+L
Sbjct  843  DIAARDLICAQKFNGLTVLPPLL  865
or
Query  330  TLPPSREEMTKNQVSLTCLVKGF----------YPS----------DIAVEWESN-----  
             LP S   MTK  V  T  + G           Y S           IAVE + N     
Sbjct  726  ILPVS---MTKTSVDCTMYICGDSTECSNLLLQYGSFCTQLNRALTGIAVEQDKNTQEVF  
Query  365  GQPENNYKTTPPMLDSDGSFFLYSKLTVDKSR  396
             Q +  YK TPP+ D  G  F +S++  D S+
Sbjct  783  AQVKQIYK-TPPIKDFGG--FNFSQILPDPSK  811
Query  172   CHVGCTKRSLARFCGGG  188
             C  G +KR    FCG G
Sbjct  1032  CVLGQSKR--VDFCGKG  1046
Query  270  KPREEQFNS  278
            K    QFNS
Sbjct  921  KLIANQFNS  929

Query  294  LNGKEYKCAVSNK-GLP-APIEKTISKTKGQPREPQ  327
            L G     + SNK  LP     + I+ T    R+PQ
Sbjct  546  LTGTGVL-TESNKKFLPFQQFGRDIADTTDAVRDPQ  580
15.1 bits(28) 	18 	Compositional matrix adjust. 	8/30(27%) 	8/30(26%) 	6/30(20%)
Query  9    LLGVCLLLNQFSRAVADSWMEEVIKLCGRE  38
             LGV    N        SWME         
Sbjct  140  FLGVYYHKNN------KSWMESEFRVYSSA  163
or another way this special fragment:
GVCLLLNQFSRAVADSWME-EVIKLCGRELV   relaxin patent
   L +  + +    SWME E  ++
DPFLGV--YYHKNNKSWMESEF-RVYSSA   SARS-CoV-2 Spike
It looks, to me, like it can. The last example above contains this one amino acid fragment ‘SWMESE’ in the Spike, homolog with SWME-E, which reminds me the unusual name of the by Trump honored judge EdWin Meese, who was the 75th United States Attorney General (1985–1988) in that famous year 1986. Nothing is reported on Meese’s role in that ‘’National Childhood Vaccine Injury Act of 1986’, he is known more in connection to his ‘Meese report’ on pornography… The biggest revelation on his involvement in covid19 issues though is described in the book ‘Game Over’ by Heiko Schoening. 
Search for similar patented relaxin fragments which contain this ‘special’ SWMESE section include patents like:
Hood,L. and Lin,B for “Methods for identifying and monitoring drug side effects” Patent: US 7883858-B2 623 08-FEB-2011;  Institute for Systems Biology; Seattle, WA
Kozlowski,A., McManus, Samuel P. and Shen,X. “ Carbohydrate-based drug delivery polymers and conjugates thereof” Patent: US 8680263-B2 239 25-MAR-2014;
“Relaxin fusion polypeptides and uses thereof”, Patent: US 9382305-B2 37 05-JUL-2016; BAYER INTELLECTUAL PROPERTY GMBH; Manheim
“Relaxin-3 chimeric polypeptides and their preparation and use” Patent: US 7893197-B2 81 22-FEB-2011; Janssen Pharmaceutica N.V.; Beerse
“ Fatty acids and their use in conjugation to biomolecules”Patent: US 10588980-B2 24 17-MAR-2020; Novartis AG; Basel
Aren’t all those institutions mentioned above involved in playing the same game, with Dr. Hood L. being a close friend of Dr. FAuCI?
And it is getting worse, there is also a connection between universal OXYTOCIN and RELAXIN: https://pubmed.ncbi.nlm.nih.gov/6727991/    Nature. 1984 May;309(5966):372-4. “Relaxin affects the central control of oxytocin release”. To realize the importance of that short peptide, one has to know, that OXYTOCIN was the very first sequenced human hormone and neuropeptide, together with vasopressin. It was the work of Vincent Du Vigneaud in 1952, who was awarded the Nobel Prize in 1955 for it. He was also the first to synthesize oxytocin in the lab, yes ‘the hormone that among other things plays a role in sexual intimacy and reproduction among people and mammals’, quote from  https://www.nobelprize.org/prizes/chemistry/1955/vigneaud/facts/. Oxytocin amino acid sequence is:
oxytocin: Cys – Tyr – Ile – Gln – Asn – Cys – Pro – Leu – Gly – NH₂, or 
CYIQNCPLG-NH₂ or also in other words: CxxxxCPLG-NH2
But, that’s also the cysteine motif with multiple homologs in Spike sequence, in 3 different places at its C-term and in 2 more places, and in Fauci’s patent: 
CCMTSCCSCLKGCCSCGSCCKFDE
CEFQFCNDPF
DCTMYICGDSTECSN
and now FAUCI's cyclic peptide related to his HIV patent:
CWLDVC=CxxxxC
The latter is described in Oct 2022 post at: 
There are quite few papers describing positive outcome in covid treatment ( in particular covid injections injuries) while applying oxytocin, including this one, titled provocatively “Oxytocin, A Possible Treatment for Covid-19? Everything to Gain, Nothing to Lose“ (https://pubmed.ncbi.nlm.nih.gov/34908992/). The simplest explanation for this could be, too many oxytocin building blocks are lost for building the Spikes..  
The entry on vasopressin at https://en.wikipedia.org/wiki/Vasopressin specifies all the sequences of the entire vasopressin family, including different species:
Vertebrate Vasopressin Family 
Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH₂ Argipressin (AVP, ADH) Most mammals 
Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH₂ Lypressin (LVP) Pigs, hippos, warthogs, some marsupials 
Cys-Phe-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH₂ Phenypressin Some marsupials 
Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Arg-Gly-NH₂ Vasotocin† Non-mammals
Also for vasopressin, the same pattern: CxxxxC.
The most telling story about oxytocin and vasopressin though is a table from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488062/ comparing the human sequences of those two hormones with their receptors:
Fig.1 Amino acid sequences of human oxytocin and vasopressin neuropeptides (a) and their receptors (b). (a) Primary sequence of oxytocin and vasopressin in single letter amino acid code. (b) Primary sequence of human OT receptors (OTR), and V_1A (AVPR1a), V_1B (AVPR1b) and V₂ (AVPR2) receptors. The amino acid residues that have been described to interact with the endogenous ligands vasopressin (AVP) and oxytocin (OT), as well as the co-factors Mg²⁺ and cholesterol (Ct) are highlighted by the dashed rectangles. Amino acids in bold represent residues that are conserved in the OT, V_1A, V_1B and V₂ receptors. * marks residues that are conserved among all the receptors. # marks residues that are conserved among OT, V_1A and V_1B receptors.: marks residues that have same functional groups. Blue represents amino acids with negative charged side chain; magenta represents residues with positive charge; green represents residues with polar uncharged side chain; purple represents residues with hydrophobic side chain. OTR, oxytocin receptor; V_1A, V_1B and V₂, subtypes of vasopressin receptors; TM, transmembrane; EL, extracellular loop; IL, intracellular loop. Sequence obtained from uniport.org
The importance of the above table will be shared in another post, with just that one note, the vasopressin hormone is a potent inhibitor of trypsin, one of the most important essential DIGESTIVE enzymes in human body.. (https://www.sciencedirect.com/science/article/abs/pii/S0022283605003220 and the 3D structure of it at https://www.rcsb.org/structure/1YF4)
Quickly back to relaxin. A specific search for that WMESE relaxin fragment among human patented proteins results in few hits:
immunoglobulin heavy chain junction region [Homo sapiens] 
Query  1   YYHKNNKSWMES  12
                 YY  NNK W +S
Sbjct  6   YYYDNNKGWFDS  17
 2. prostate-specific antigen [Homo sapiens] 
Query  8   SWMESEF  14
                SWMES+F
Sbjct  62  SWMESQF  68
cDNA selection for complete cds sequencing: ReverseProteomics Research Institute 
Query  1    YYHKNNKSWMESE  13
                   YY KNN   ME E
Sbjct  685  YYLKNN---METE  694
All this here is like identifying the bricks in the architecture of a house, while trying to read the mind of the.., patent-holder.
Relaxin isoform3 is essential for pregnancy and development of fetus, connecting mothers womb with the child (https://www.uniprot.org/uniprotkb/Q8WXF3/entry). The same relaxin is also produced in reptile/snake species (https://www.uniprot.org/uniprotkb/A0A8C6YHT2/entry), whereby the difference, for example in that isoform3 is:
Query  18   ELWPGAEARAAPYGVRLCGREFIRAVIFTCGGSRWRRSDILAHEAMGDTFPDADADEDSL  
            E W   EAR   YGV+LCGREFIRAVIFTCGGSRWRR    A E  G  F        +L
Sbjct  42   EKWLVTEARTPHYGVKLCGREFIRAVIFTCGGSRWRR----AGEQRGCWFIFIGVFPRTL  

Query  78   AGELDEAMGSSEWLALTKSPQAFYRGRPSWQGTPGVL-RGSRDVLAGLSSSCCKWGCS 
             G L        W AL  SP+ F          P  L RG+RDV+  LS++CCKWGCS
Sbjct  98   PGYLLGMYDYLFWFALELSPRWFSYALSE---EPWSLDRGARDVMESLSNACCKWGCS  
This comparison is the result of a thought, guided by Dr. Ardis hints in his presentations, which helped me to associate that special C-terminal Cys-rich section of the Spike (which includes the by Fauci patented HIV peptide..) Ardis’ venom theories point to snakes who lay eggs, with fetus developing outside of the animals body, not inside..
The current horror of the synthetic biology reprogramming the human bodies with the first covid Spike carrying the amino acids ‘RGD’ trimer motif, an essential part of gaiming with integrins, may have the following goal (just a speculative thought) planned by Sanofi Pasteur Vaxdesign Corp. long time ago: 
ARTIFICIAL IMMUNE SYSTEM: METHODS FOR MAKING AND USE
US 8,288,159 B2 filed in 2010: 
Synthetic poly(ethylene glycol)-based hydrogels presenting RGD adhesion peptides Supported the attachment, spreading, and growth of FRCs (Fibroblastic Reticular Cells, stromal cells of the T Zone) over several days in culture (FIG. 32C). These cells also grew well on fibronectin, collagen IV, and collagen I-coated Surfaces, but not on laminin (data not shown).
Once CD4+ T cells are activated by DCs (dendritic cells, which were known to represent neuronal cells) , they may migrate to the periphery of the follicles to provide help to activated B cells for proliferation and antibody isotype Switching (Garside, et al., Science 281: 96-99 (1998)).
Within follicles, B cells proliferate and undergo Somatic hypermutation, a process designed to genetically manipulate the antibody specificity of activated cells to find high affinity mutants that can more effectively eliminate pathogens.
8. the use of a digital printing BioAssembly Tool (BAT) capable of precision-manufacturing 3D ETCs (Engineered Tissue Constructs), specifically with fine volumetric control to create 3D constructs;
From “Mechanism and regulation of class switch recombination“
Antibody class switching occurs in mature B cells in response to antigen stimulation and costimulatory signals. It occurs by a unique type of intrachromosomal deletional recombination within special G-rich tandem repeated DNA sequences [called switch, or S, regions located upstream of each of the heavy chain constant (C(H)) region genes, except Cdelta]. The recombination is initiated by the B cell-specific activation-induced cytidine deaminase (AID), which deaminates cytosines in both the donor and acceptor S regions. AID activity converts several dC bases to dU bases in each S region, and the dU bases are then excised by the uracil DNA glycosylase UNG; the resulting abasic sites are nicked by apurinic/apyrimidinic endonuclease (APE).
Is that the reason why uridine nucleotides are being ‘replaced’ by the Nobel prize winning synthetics of Kariko and Weissman??? And doesn’t it all really look like the NEXT HUMAN from the cover of National Geographic in the Apr 2017 issue, a complete overwrite of our HUMAN CREATION?
==>Kawahara M, Ueda H, Morita S et al. 2003 Bypassing antibiotic selection: positive screening of genetically modified cells with an antigen-dependent proliferation switch. Nucleic Acids Research 31, e32
from article “Symposium: Nuclear reprogramming and the control of differentiation in mammalian embryos Transfer of human artificial chromosome vectors into stem cells“   
For anyone who got that far, THANK YOU FOR READING and if possible, maybe even sharing with others. 
Happy Giving Thanks day;)
Literature:
   1. D Kalderon et al. “A short amino acid sequence able to specify nuclear location.”            Cell. 1984 Dec;39(3 Pt 2):499-509. A short quote from its abstract: “A short sequence of amino acids including Lys-128 is required for the normal nuclear accumulation of wild-type and deleted forms of SV40 large T antigen. A cytoplasmic large T mutant that lacks sequences from around Lys-128 localizes to the nucleus if the missing sequence is attached to its amino terminus. The implication that the sequence element around Lys-128 acts as an autonomous signal capable of specifying nuclear location was tested directly by transferring it to the amino termini of beta-galactosidase and of pyruvate kinase, normally a cytoplasmic protein.“
Sarah Sattar et al. “Nuclear translocation of spike mRNA and protein is a novel feature of SARS-CoV-2“  Front. Microbiol. 14:1073789.
doi: 10.3389/fmicb.2023.1073789  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909199/pdf/fmicb-14-1073789.pdf
Quote: “Although the S protein is a surface transmembrane type 1 glycoprotein, it
has been predicted to be translocated into the nucleus due to the novel nuclear
localization signal (NLS) “PRRARSV,” which is absent from the S protein of other
coronaviruses. Indeed, S proteins translocate into the nucleus in SARS-CoV-2-
infected cells.“
Hana M. et al. “Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase“ November 4, 2021 N Engl J Med 2021; 385:1774-1785 https://www.nejm.org/doi/full/10.1056/NEJMoa2113017 
with quote “A total of 32 deaths had occurred by completion of the blinded phase, with 16 deaths each (0.1%) in the placebo and mRNA-1273 groups; no deaths were considered to be related to injections of placebo or vaccine, and 4 were attributed to Covid-19 (3 in the placebo group and 1 in the mRNA-1273 group) (Tables S19 and S26). The Covid-19 death in the mRNA-1273 group occurred in a participant who had received only one dose; Covid-19 was diagnosed 119 days after the first dose, and the participant died of complications 56 days after diagnosis.
-



WHATIF ACE2 scenario and the hell of the infinite VARIANTS. 
mejbcart — Tue, 12 Sep 2023 20:00:12 GMT
The main post starts behind the divider bar, few updates upfront. AND THANK YOU for reading;) 
Update 11/18/2023: Important interview with Dr. Michael Palmer on a planned genocide in regard to gene modifications via covid injections: https://www.bitchute.com/video/z5B7nGKZrEkh/ with a link to his book explaining more details of the new synthetic genes-based technology:  https://doctors4covidethics.org/mrna-vaccine-toxicity/
Update 9/24/2023: Not quite the topic of this post, just some science history from Germany, related to the field of macromolecular biology, hidden behind every ‘variant’ of todays’ covid hell. A link to the 2017 interview with a German scientist: https://archive.embl.org/uploads/r/archive-of-european-molecular-biology-laboratory/1/3/7/137250e31a096f825c420a141e4aa13c842483849ff66f57f26399ca623bc897/2017_11_16_HeinrchStuhrmann_transcript.pdf
 who summarizes all his scientific work achievements using only one name (in addition to his collaborators), his daughters name, despite of having the entire team of other highly qualified PhD students, who actually did all the technical work... The interview touches extremely important ribosomal work done by the Israeli researcher Ada Yonath, who got the Nobel prize for it  https://www.nobelprize.org/womenwhochangedscience/stories/ada-yonath
We are always being told in advance what’s gonna happen, please read the above from the front cover of Time edition on 1/11/1999, in particular the small print. And remember the date, backwards… We are in that future, right now, and the reminder about this Time edition, comes from Dr. Bryan Ardis, whose interview can be found in the previous post 
Update 9/15/2023: each scientist, each politician, health care specialist of all kinds, should be MANDATED to watch ALL the series at:  https://www.bitchute.com/search/?query=sterben%20nach%20den%20impfungen&kind=video which have this one in common: injections of SYNTHETIC genetic material covering ALL the variants, from 0 to X, material is which falsely called ‘vaccine’, including ALL the most prestigious scientific journals out there! All on purpose, all with a goal, which even those participating criminals (scientists), do not seem to grasp.
Update 9/14/2023: Dr. DAVID MARTIN’S speech in EU just yesterday: https://www.brighteon.com/9fe23bf5-7a03-4c38-9305-1ef3c44b8115 title of it: ““Dr. David Martin at EU Parliament in Strasbourg:Expert Panel about WHO's power grab!Wed, Sept. 13th” talking about Barick’s publication analyzed in this post.
New 9/13: VERY IMPORTANT analysis of SARS-CoV-2 ‘variants’ publication from Feb 2022, at the end of this post. 
Everyone remembers the admitted fact that “Pfizer did not know whether Covid vaccine stopped transmission before rollout, executive admits“, still available to watch at: 
https://www.news.com.au/technology/science/human-body/pfizer-did-not-know-whether-covid-vaccine-stopped-transmission-before-rollout-executive-admits/news-story/f307f28f794e173ac017a62784fec414
Months back, Kevin McKernan on his substack, answered the question about distinguishing the natural Spike (KV) from the injected Spike (PP): there is no method to detect the difference (Proline-Proline) between the synthetic injected Spike and the one coming from the natural SARS-CoV-2 infection, carrying the Lys-Val (KV) on the same position. That was hard to imagine, given todays genetic capabilities of producing point mutations in countless proteins and detecting them… That changed recently, in different way, working on proteins only. The consequences of a genetic modification treatments via injections of Spike gene coding for specific Proline-Proline(PP) mutation, were just published by Carlo Brogna et al. (https://doi.org/10.1002/prca.202300048) ”The specific PP-Spike fragment was found in 50% of the biological samples analyzed, and its presence was independent of the SARS-CoV-2 IgG antibody titer. The minimum and maximum time at which PP-Spike was detected after vaccination was 69 and 187 days, respectively.” (https://onlinelibrary.wiley.com/doi/epdf/10.1002/prca.202300048) 
That injected gene and the amount of its produced Spikes (fragments containing the PP mutation in this study) to the resulting antibody independence, indicates many possible reasons, one of which is considered in this post. The extreme importance of that new study is the finding, that none of the covid jabbed study participants had the Spike with the PP mutation, meaning ‘the shedding phenomena’ must be Spike protein independent, including the gene shedding, which would continue producing the PP-mutated Spike. It is possible, it can be a detection limit issue of the MS (mass spectrometry) method though. The question how many of the covid non-jabbed did have the natural ‘KV’ mutation was not addressed in it, a great pity…. 
The main point here is, again, Spike related:
This post considers the possibility of ACE2 having nothing to do with SARS-CoV-2 infection(-rate) but rather, ‘just’ with the universally injected, patented Spike toxin binding that essential human MEMBRANE BOUND ACE2 protein, not even speaking about the integration of the synthetic Spike gene, for now. The consequences of this, are quite essential, because it would explain why the Spike design and its injections, in form of FOREIGN, SYNTHETIC GENETIC MATERIAL, with optimized features of binding to ACE2 via the RBD Spike domain, do nothing to the ‘viral transmission’, as confirmed in EU Parliament by the Pfizer rep. J.Small, but rather to take away from circulation the HUMAN ACE2 protein and its building blocks, while causing illness and death. That assumption would also affect the variants issue.
The VARIANTS.
The SARS-CoV-2 most out-sticking portion, the now by MANY companies PATENTED^1 universally injected Spike toxin (with venom-like sub-compounds..) and its versions, has 1273 amino acid (aa) residues. We are being told, the for decades developed Spike (with the oldest patent of its homolog going back to 1987 Duphar International for ‘new antigenicity active proteins and peptides and Infectious Bronchitis Virus vaccines) binds to the ACE2 receptor, which then leads to a viral entry and infection. Human ACE2 receptor NEVER CHANGES its sequence/folding, it is a zinc metalloprotease MEMBRANE FIXED HUMAN PROTEIN, given to you from your birth. So how something like the Spike on the viral surface, which constantly mutates, still manages to bind to the ALWAYS THE SAME ACE2 SURFACE, which first THEN causes OPENING of the cell membrane following the viral entry and infection??? ACE2 has only few residues participating in its catalytic action, Glutamic acid (proton acceptor) at position 375, that’s the E* in the TAHHE*MGHIQ motif, Hystidine505 (proton donor) in a string (ASLFH*VSNDY) and Histidine345 and arginine Arg273. All E, H and R are charged residues, which participate in cutting at the position of PF (see below) of very small peptides(examples at the end of this post). So how ACE2 suddenly cuts into a 1273 residues Spike monster^5?? ACE2 uniprot entry lists 13 publications which talk about ACE2 which “Acts as a receptor for human coronaviruses SARS-CoV and SARS-CoV-2, as well as human coronavirus NL63/HCoV-NL63.“ Here are the citations in regard how ACE2 participates in SARS-CoV-2 viral entry, from some of the abstracts:
-Collectively, our results in conjunction with those of previous studies indicate that TMPRSS2 and potentially related proteases promote SARS-CoV entry by two separate mechanisms: ACE2 cleavage, which might promote viral uptake, and SARS-S cleavage, which activates the S protein for membrane fusion.” (J. Virol. 88:1293-1307 (2014))
-Here, we demonstrate that SARS-CoV-2 uses the SARS-CoV receptor ACE2 for entry and the serine protease TMPRSS2 for S protein priming. A TMPRSS2 inhibitor approved for clinical use blocked entry and might constitute a treatment option. Finally, we show that the sera from convalescent SARS patients cross-neutralized SARS-2-S- driven entry. (Cell 181:1-10 (2020))
-”We determined cryo-EM structures of the SARS-CoV-2 S ectodomain trimer, providing a blueprint for the design of vaccines and inhibitors of viral entry. Finally, we demonstrate that SARS-CoV S murine polyclonal antibodies potently inhibited SARS-CoV-2 S mediated entry into cells, indicating that cross-neutralizing antibodies targeting conserved S epitopes can be elicited upon vaccination.” (Cell 180:1-12 (2020))
-”Here, using SARS-CoV-2 S protein pseudovirus system, we confirm that human angiotensin converting enzyme 2 (hACE2) is the receptor for SARS-CoV-2, find that SARS-CoV-2 enters 293/hACE2 cells mainly through endocytosis, that PIKfyve, TPC2, and cathepsin L are critical for entry, and that SARS-CoV-2 S protein is less stable than SARS-CoV S.” (Nat. Commun. 11:1620-1620 (2020))
- “crystal structure of the receptor-binding domain (RBD) of the spike protein of SARS-CoV-2 (engineered to facilitate crystallization) in complex with ACE2. In comparison with the SARS-CoV RBD, an ACE2-binding ridge in SARS-CoV-2 RBD has a more compact conformation; moreover, several residue changes in the SARS-CoV-2 RBD stabilize two virus-binding hotspots at the RBD-ACE2 interface.“(Nature 581:221-224 (2020))
- “It is now well‑established that entry of SARS‑CoV‑2 into host cells is facilitated by its spike proteins mainly through binding to the angiotensin‑converting enzyme 2 (ACE‑2). Preclinical studies have suggested that neuropilin‑1 (NRP1), which is a transmembrane receptor that lacks a cytosolic protein kinase domain and exhibits high expression in the respiratory and olfactory epithelium, may also be implicated in COVID‑19 by enhancing the entry of SARS‑CoV‑2 into the brain through the olfactory epithelium. In the present study, we expand on these findings and demonstrate that the NRP1 is also expressed in the CNS, including olfactory‑related regions such as the olfactory tubercles and paraolfactory gyri. This furthers supports the potential role of NRP1 as an additional SARS‑CoV‑2 infection mediator implicated in the neurologic manifestations of COVID‑19. Accordingly, the neurotropism of SARS‑CoV‑2 via NRP1‑expressing cells in the CNS merits further investigation.“(Mol. Med. Report. 22:4221-4226 (2020))
-”Cleavage of S generates a polybasic Arg-Arg-Ala-Arg (RRAR=furin site) carboxyl-terminal sequence on S1, which conforms to a C-end rule (CendR) motif that binds to cell surface neuropilin-1 (NRP1) and NRP2 receptors. We used x-ray crystallography and biochemical approaches to show that the S1 CendR motif directly bound NRP1. Blocking this interaction by RNA interference or selective inhibitors reduced SARS-CoV-2 entry and infectivity in cell culture. NRP1 thus serves as a host factor for SARS-CoV-2 infection and may potentially provide a therapeutic target for COVID-19.”(Science 370:861-865 (2020))
None of these publications describe precisely how the MEMBRANE BOUND whole length ACE2 receptor opens the cell membrane and lets the SARS-CoV-2 viruses in, AFTER binding the Spike. The crystallographic structure at https://www.rcsb.org/fasta/entry/6M0J/display showing the ACE2 and the Spike has only pieces of  both, NOT the two ENTIRE molecules, in particular the cell membrane anchored portions are NOT THERE. To crystallize a membrane protein, just one, is already a huge challenge, like real vaccine, it can take years, and here not even speaking about 2 proteins anchored on different membranes…. So the fact that ACE2 actually really binds Spike is proven by crystallographic data, of fragments, in soluble phase.  
All this leads me to put the ACE2 based viral cell ENTRY, that, what happens AFTER binding to the SARS-CoV-2 Spike, into question. 
Science 2022 Mar 4 edition describes how a chinese team did EM studies: https://pubmed.ncbi.nlm.nih.gov/35133176/
 of many variants with, they say, full length ACE2 with supplemental material at : https://www.science.org/doi/10.1126/science.abn8863#supplementary-materials
in which the description about ACE2 states, quote: “The N-terminal peptidase domain of human ACE2 (residues Ser19–Asp615) with an N-terminal GP67 signal peptide for secretion and a C-terminal 8×His tag for purification was inserted into a modified pFastBac vector (Invitrogen).“
that’s NOT full length ACE2, which has 805 residues!! Further, quote: “The fractions for the peptidase domain of human ACE2 were collected, concentrated to about 2 mg/ml, and stored at− 80 °C until use.“
how the cell membrane was simulated"?? “10 nM ACE2 were attached to streptavidin-coated donor beads, and 10 nM His6-tagged Omicron spike ECD were attached to nickel-chelated acceptor beads.“ 
In the entire materials section there is no mention about the WHOLE length of MEMBRANE BOUND ACE2, yet, the protein data bank data show the ‘modeled’ ALL 805 residues of ACE2, bound to the trimer of Spikes, with NO MEMBRANES around, with coordinates at https://www.rcsb.org/structure/7WPA
while uniprot actually defining the 741-761 region of ACE2 being anchored in the membrane and the 762-805 residues being cytoplasmic portion, in which the section  778-786 ‘ENPYASIDI’ represents the ‘cell entry system’, located INSIDE of the cytoplasm, never reachable by the viral Spike coming from OUTSIDE of the cell, in natural infection. 
That chinese study cites the no 1 source for their MODELS: https://pubmed.ncbi.nlm.nih.gov/33271067/ , Cell Host Microbe. 2020 Dec 9;28(6):867-879.
This 2020 publication in turn states: “Overall, our findings provide structural definition for the binding of up to three ACE2 molecules per SARS-CoV-2 spike trimer and define a key structural transition between pH 5.5 and 4.5, highlighting the crucial role of a refolding region with multiple aspartic acid residues—a pH-dependent switch—that mediates positioning of RBDs, by twisting the relative orientation of disulfide-linked helices and coordinating the interprotomer movement of domains.“
How much of ACE2 was in this ‘models’?? The methods section says, quote:”Human ACE2 proteins were prepared in monomeric form (residues 1-620) and in dimeric form (residues 1-740). The expression plasmids were constructed and the protein purified as described previously (Zhou et al., 2020b).” 
Again, that study does NOT INCLUDE the FULL LENGTH of the entire MEMBRANE ANCHORED ACE2. 
Transmembrane protease serine 2 (TSMPRSS2) which is also said to be involved in pre-proteolytic cleavage of the spike, has the N-terminal 84 residues in the cytoplasm, 85-105=20 residues anchored in the membrane, and 106-492 outside of the cell, with 3 residues 296-345-441 (His-Asp-Ser) representing s.c. CHARGE-RELAY-system, thus performing the proteolytic cuttings outside of the cell, like ACE2. So what the papers describing that feature say? Uniprot on TSMPRSS2 at: https://www.uniprot.org/uniprotkb/O15393/entry#O15393-1 points to 6 publications on it, here just one of them:
-The demonstration of T-ex5 PPMO efficacy in the present study suggests that reducing TMPRSS2 expression by use of an mRNA-directed approach in general and by PPMO in particular is worthy of further consideration. PPMO are highly selective inhibitors of target gene expression. They bind to a complementary sequence in target mRNA and can affect gene expression by steric blockage of translation initiation or pre-mRNA splicing. (TMPRSS2 and furin are both essential for proteolytic activation of SARS- CoV-2 in human airway cells. Life. Sci Alliance 3:1-14 (2020))  => not a proof of enzymatic digestion of ACE2, but rather inhibition of the protease by manipulating its mRNA.
The ACE2 uniprot entry has just one section related to its special membrane features, quote:”In addition, ACE2 C-terminus is homologous to collectrin and is responsible for the trafficking of the neutral amino acid transporter SL6A19 to the plasma membrane of gut epithelial cells via direct interaction, regulating its expression on the cell surface and its catalytic activity (PubMed:18424768, PubMed:19185582).” Both of the here 2 cited publications, indicate that the ACE2 activates the expression of neutral SINGLE amino acid transporter on the cell membrane, and do not indicate opening of the cell membrane by ACE2… 
What would be the advantage of actually proving, that the natural ACE2 (whole length and membrane bound) contributes to viral spread by BINDING the SARS-CoV-2 Spike first (given) and THEN (questionable) opening the cell membrane and allowing the SARS-CoV-2 in? It would justify the application of covid injection materials, reprogramming human bodies so it produces the Spike which then suppose to generate antibodies to it, it would justify the current ‘scenario’. And what if ACE2 does not open the cell walls, and all what the injected Spike is doing is to ‘just’ bind to ACE2? Well, no effect on transmission.. Also every Spike bound ACE2 is a lost ACE2, thus still affecting the blood and circulation system by its very functional properties, but it had little to do with viral load!  Also, will a synthetic gene, mimicking the behavior of a human gene (because it is allowed to express the Spike), suddenly cause the body to reject it?? Not even talking about the mimick while using FOREIGN genetic material here..  
And if the natural, membrane fixed ACE2 is just binding the Spike, will the countless Spike mutations have any effect on infection, determined mainly by the viral load, i.e. number of replicating viruses which CROSSED the cellular membrane, ‘opened’ by ACE2, something what ACE2 does not seem to do?? 
 If the Spikes JUST bind and never release all the ACE2, what consequences that may have? The answer was already proven, in a publication at https://www.nature.com/articles/s41467-020-18880-0 titled “ACE2 mouse models: a toolbox for cardiovascular and pulmonary research”. Table 1 describes what will happen with a mouse not producing ACE2 receptors (equivalent with a situation of releasing ‘just’ the SPIKE with ACE2 binding capacity on all accessible cells, and later penetrating them, a part done by the nanos, in both directions), here just one of the listed 4 models: 
Table 1 Global ACE2 KO (so called knockout mouse) models and associated phenotypes.
Country of origin Canada (Source Life Science Institute, The University of British Columbia)
Phenotypes Source
Cardiovascular: Enhanced susceptibility to Ang-II or pressure overload-induced heart failure23,24, cardiac hypertrophy and myocardial fibrosis14 , myocardial infarction25 , vascular dysfunction and atherosclerosis26,27, abdominal aortic aneurysm28
Metabolic: Lipodystrophy and steatosis29 , obesity-induced epicardial adipose tissue inflammation and insulin resistance31 , diabetic cardiovascular complications 32, reduced intestinal uptake of tryptophan and altered serotonin metabolism37,38
Liver: Hepatic steatosis and fibrosis29,30
Lung: Resistant to SARS-CoV infection39 , exacerbated ALI/ARDS due to acid aspiration, lipopolysaccharide or pseudomonas aeruginosa infection41–43 , impaired inactivation of des-Arg9 -bradykinin43 , exacerbated lung fibrosis with a sex dichotomy44, increased susceptibility to respiratory viral infection45–47
Kidney: Renal fibrosis and inflammation33,34 and diabetes or hypertension associated nephropathy3
The options in molecular biology, which the eyes can’t see, are limitless, it appears there is another peptidase, which can do the ACE2 cutting job, quote: ”The type II transmembrane serine proteases TMPRSS2 and HAT can cleave and activate the spike protein (S) of the severe acute respiratory syndrome coronavirus (SARS-CoV) for membrane fusion. In addition, these proteases cleave the viral receptor, the carboxypeptidase angiotensin-converting enzyme 2 (ACE2), and it was proposed that ACE2 cleavage augments viral infectivity.”
Assume there is no infecting virus around, will TMPRSS2 still cut and destroy ACE2 in a healthy body, when actually both of them are anchored/fixed in cell membranes??? Uniprot lists only one 2011 publication describing this issue only in presence of SARS-CoV. What does it say? Quote (https://journals.asm.org/doi/10.1128/jvi.02062-10):”ACE2 and TMPRSS2 colocalized on cell surfaces and enhanced the cell entry of both SARS S-pseudotyped HIV and authentic SARS-CoV. Enhanced entry correlated with TMPRSS2-mediated proteolysis of both S and ACE2. These findings indicate that a cell surface complex comprising a primary receptor and a separate endoprotease operates as a portal for activation of SARS-CoV cell entry.”  Entry while using HIV??
No, lets’ forget the TMPRSS2 for a moment, and go back to Barick’s in Sep 2015 to PNAS submitted article titled:”SARS-like WIV1-CoV poised for human emergence” with that one sentence, quote: ”The identification of WIV1-CoV and its capacity to use ACE2 orthologs offers a warning for possible reemergence and provides an opportunity to prepare for a future CoV outbreak.” (https://www.pnas.org/doi/10.1073/pnas.1517719113 )
That work didn’t produce new viruses but rather concentrated on ‘production’ of the Human ACE2 Expressing Mice, with consequences described in this quote from that work:”In the context of both the SARS-CoV and MERS-CoV outbreaks, focus had been primarily directed to spike binding as the key component of emergence and pandemic potential. Supported by adaption at Y436H in mouse-adapted SARS spike (10), improved binding to host receptor cannot be discounted as a crucial component in emergence. This fact is supported by improved replication of WIV1-CoV in mice expressing human ACE2 compared with control (Fig. 2D versus Fig. 3B).” One also should ask, is it reversible what Baric says: “we generated a mouse that expresses human ACE2 receptor under control of HFH4, a lung ciliated epithelial cell promoter”?? Improved replication by expressing more ACE2 (in mouse chimera) which then bind the Spikes and affect the titration curves??? 
Just one link more, for everybody to know, that the SYNTHETIC coronavirus was by then, already mostly ready, progress can be seen in Baric’s CurriculumVitae: https://sph.unc.edu/wp-content/uploads/sites/112/2016/09/CV_Ralph_Baric.pdf
 That docking of the viral surface of the 1273 aa large Spike on the viral surface to the ~800 aa large ACE2 MEMBRANE bound receptor happens via the RBD domain, according to NIH data base, which spans residues from a Region  319..541, with a single letter code for all amino acids:
301 ctlksftvek giyqtsnf>>>rv qptesivrfp nitnlcpfge vfnatrfasv yawnrkrisn
361 cvadysvlyn sasfstfkcy gvsptklndl cftnvyadsf virgdevrqi apgqtgkiad
421 ynyklpddft gcviawnsnn ldskvggnyn ylyrlfrksn lkpferdist eiyqagstpc
481 ngvegfncyf plqsygfqpt ngvgyqpyrv vvlsfellha patvcgpkks tnlvknkcvn
541 f<<
Spike original data:   https://www.ncbi.nlm.nih.gov/nuccore/NC_045512 (YP_009724390.1 protein in it)
this gives at least 222 Spike residues, which can mutate.. How many choices that gives? 222!=1.120507558E+426, which is basically infinity, infinity of tests, lockdowns, injections targeting the immune response to every single of these variants.
Again, the ACE2 surface does NOT mutate, it is a FIXED entity, binding to its small ligands and performing PROTEOLYTIC enzymatic actions at fixed positions, outside of cells expressing it, participating in pathways of many essential short peptides:
Angiotensin I DRVYIHPFH→L     P
Angiotensin 1–9 DRVYIHPFH      N
Angiotensin II DRVYIHP→F        C
Angiotensin 1–7 DRVYIHP           N
Angiotensin 1–5 DRVYI.               N
Apelin-13 QRPRLSHKGPMP→F C
Apelin-36 (C terminus shown) . . .QRPRLSHKGPMP→F C
Bradykinin RPPGFSPFR               N
des-Arg9 -bradykinin RPPGFSP->F C
Lys-des-Arg 9 -bradykinin KRPPGFSP→F P
Bradykinin fragment 1–7 RPPGFSP N
beta-Casomorphin           YPFVEP->I C
Neocasomorphin YPVEP→I C
Dynorphin A 1–13 YGGFLRRIRPKL→K C
Ghrelin (C terminus shown) . . .ESKKPPAKLQP→R P
Neurotensin 1–8 pE-LYENKP→R P
i.e. all what ACE2 does, as defined by uniprot data (https://www.uniprot.org/uniprotkb/Q9BYF1/entry), it is producing:
angiotensin II + H2O = angiotensin-(1-7) + L-phenylalanine
vasoconstriction peptide hormone and precursors for neurotransmitters^3, discussed in 2022 post:  
Just few thoughts about how to fit specific facts, like the viral transmission issue and have to digest… If you think otherwise and have 100% proof of the issue in question, please let me know in comments. Last but no least, imagine a huge hole in cell membranes letting in ‘just’ the 1273 Spike amino acids, at once, in the same time where the same membrane regulates every single water molecule…
Thank you for getting that far! This post will be edited, or corrected, like all many other posts, to reflect feedback about new coming FACTS. 
The most important: NEVER FORGET, NEVER GIVE UP, ALWAYS FIGHT FOR YOUR RIGHTS TO STAY HUMAN, NEVER EVER ALLOW TO INJECT YOURSELF with FOREIGN, SYNTHETIC GENETIC MATERIAL produced by those who want to change us via genetic engineering!!!
9/13: Analysis of the publication at https://onlinelibrary.wiley.com/doi/10.1002/jmv.27927 titled “Omicron (BA.1) and sub-variants (BA.1.1, BA.2, and BA.3) of SARS-CoV-2 spike infectivity and pathogenicity: A comparative sequence and structural-based computational assessment“ by Suresh Kumar et al. in Jun 2022. Now check it for yourself. At https://www.rcsb.org/fasta/entry/7T9L/display is the sequence of the Spike and ACE2 used in this publication to predict the PHYSIOLOGICAL parameters, which will set people in quarantaines!!! Take ACE2 first and compare the sequence with NATURAL human ACE2 at https://www.uniprot.org/uniprotkb/Q9BYF1/entry. For ACE2:
missing the entire N-terminal portion ‘MSSSSWLLLSLVAVTAA’ in the model
the residue 616Q in natural ACE2 was changed to CHARGED His! but this was NOT enough!
the ENTIRE C-terminal in MODELLED ACE2 is MISSING: SIKVRISLKSALGDKAYEWNDNEMYLFRSSVAYAMRQYFLKVKNQMILFGEEDVRVANLKPRISFNFFVTAPKNVSDIIPRTEVEKAIRMSRSRINDAFRLNDNSLEFLGIQPTLGPPNQPPVSIWLIVFGVVMGVIVVGIVILIFTGIRDRKKKNKARSGENPYASIDISKGENNPGFQNTDDVQTSF ==»> ONE HUNDRED EIGHTY NINE residiues were ERAZED and instead s.c. Histidine tag attached: HHHHHHH
For the ‘mutated’ Spike VARIANT:
the entire C-terminal section of the wild type SPike is NOT there in the ‘model’ YIKWPWYIWLGFIAGLIAIVMVTIMLCCMTSCCSCLKGCCSCGSCCKFDEDD SEPVLKGVKLHYT
the furin site is MISSING,  BLAST comparison of the model with the natural Spike:
Query  655   NSYECDIPIGAGICASYQTQTKSHGSASSVASQS VARIANT MODEL
             NSYECDIPIGAGICASYQTQT S   A SVASQS
Sbjct  658   NSYECDIPIGAGICASYQTQTNSPRRARSVASQS Natural Spike
the model has 1285 residues, the ‘natural’ 2020 PATENTED Spike only 1273 residues=> the VARIANTS are GROWING and loosing entire sections of their sequences???!!!! And now read the PUBLISHED abstract in THE MOST PRESTIDIOUS JOURNAL of all times ((2022) Science 375: 760-764), for that 3 dimensional VARIANT analysis at https://www.rcsb.org/structure/7t9l , quote:
“The newly reported Omicron variant is poised to replace Delta as the most prevalent SARS-CoV-2 variant across the world. Cryo-EM structural analysis of the Omicron variant spike protein in complex with human ACE2 reveals new salt bridges and hydrogen bonds formed by mutated residues R493, S496 and R498 in the RBD with ACE2. These interactions appear to compensate for other Omicron mutations such as K417N known to reduce ACE2 binding affinity, resulting in similar biochemical ACE2 binding affinities for Delta and Omicron variants. Neutralization assays show that pseudoviruses displaying the Omicron spike protein exhibit increased antibody evasion. The increase in antibody evasion, together with retention of strong interactions at the ACE2 interface, thus represent important molecular features that likely contribute to the rapid spread of the Omicron variant.“
Every single process here is a COMPUTER SIMULATION resulting in The Table 1. Its title: “The predicted effect of Spike protein single mutations of Omicron variants on pathogenicity by using PredictSNP tool.”
Table 2 titled “Docking analysis of single-point mutation of Wuhan-RBM (receptor-binding motif), Omicron (BA.1)-RBD, and sub-variants (BA1.1, BA.2, and BA.3)-RBD residues with ACE2 using HEX software.” lists docking energies WITHOUT units…
Table 3 is interesting, salt bridge formation and hydrogen bond formation between ACE2-RBD predicted for Omicron and sub-variants using PDBePISA (PISA) web-based tool.
Salt bridge formation(ACE2‐RBD) Hydrogen bondformation (ACE2‐RBD)
WTa     ASP 30-Lys417                     Gln24-Asn487 (PDB ID: 6MOJ)                                          Asp30-Lys417
BA.1.1 GLU 57-LYS 478 LYS 31-TYR 450
            GLU 35-ARG 490 LYS 68-TYR 470 
            GLU 35-ARG 493 GLN 42-ALA 481 
           ASP 38-ARG 490 GLN 42-CYS 485
           ASP 30-ARG 495 THR 27-THR 497 
          ASP 30-ARG 498 ASP 30-TYR 446
BA.2 ASP 30-ARG 490 ARG 559-ALA 472 
         ASP 30-ARG 490 GLN 388-ASN 484 
         GLU 35-ARG 495 LYS 68-THR 497 
         ASP 38-HIS 502 ASP 30-ARG 490 
        ASP 38-ARG 400 GLU 35-ARG 495
As you can see there are basically FOUR NEGATIVELY charged amino acids on the ACE2 interface, Asp30, Asp38, Glu34, Glu57, to which the positively charged residues of the Spike mutants attach with the strongest electrostatic forces caused by their total charge of -4. No matter how many positively charged Spike residues are around, that binding will take place if there is no steric hindrance to it. And now the CUT off of the first N-terminal residues in the ACE2 molecule, even if uncharged, will leave ‘lot of space’ for possible ‘new variants’… The official interpretation of the VARIANTS is using AFFINITY of the Spike to the ACE2 receptor, ‘binding strength’ if you will, but since that BINDING was ‘improved by design’ illustrated in the countless patents over decades, one can assume, once The spike binds, it binds, and it DOES NOT MATTER whether it is strong or weak, just my opinion as non-chemist..
The above listed positively charged ACE2 residues, attacked by the Spikes, on a micro-level, can be very easily handled, by adding SINGLE positively charged AMINO ACIDS, L-Lys, L-Arg, L-His to your diet, which will help to neutralize and shield of the ‘however mutated’ spikes… There are some studies confirming exactly that:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264737/ →supplementation with zinc and zinc ionophores; vitamins C, D3 and E; and l-lysine during covis19
https://pubmed.ncbi.nlm.nih.gov/34372507/      →lysine supplementation
https://www.wholefoodsmagazine.com/articles/8667-lysine-reported-to-halt-coronaviruses-an-interview-with-bill-sardi
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619186/  →arginine supplementation
I can only add one, to this CRIMINAL SCAM, the published conclusion, quote:
“In this study, Omicron (BA.1) and sub-variants (BA.1.1, BA.2, and BA.3) are compared and investigated with WT using various computational tools. There are 11 shared common mutations G339D, S373P, S375F, K417N, N440K, S477N, T478K, E484A, Q493R, Q498R, and N501Y in RBD Omicron and sub-variants that may contribute significantly to changing the host spectrum of SARS-CoV-2 in immune evasion and potential transmission. The Omicron sub-variants (BA.1.1, BA.2 and BA.3) are likely more transmissible than omicron (BA.1) and Delta.“ 
puts a HUGE QUESTION MARK to it all, even without the s.c. COOT, a 3D visualization tool for macromolecules, which became unavailable with windows 10… How strange, Gates knew what he was doing years back!!!
Literature.
Please open BLAST at https://blast.ncbi.nlm.nih.gov/Blast.cgi and search for patented sequences similar to YP_009724390.1. You will get: Altimmune Inc.; DEFENCE THERAPEUTICS INC.; NOVAVAX, INC.; Janssen Pharmaceuticals, Inc. and Beth Israel Deaconess Medical Center, Inc.; CUREVAC AG (german company with the highest numbers of patents of Spike); Regeneron Pharmaceuticals, Inc.; Suzhou Abogen Biosciences Co.; University of Pittsburgh now patented the spike inserted into Measles virus vaccine(US 11103576-B1),and many more. Something happened to the NIH data base of the patented sequences, because right now among thousands of entries, you will NOT find Pfizer, Mod-E-RNA patents ANY MORE..
2005 [YEAR:20-4-2005]Li,W., Zhang,C. et al. Receptor and viral determinants of SARS-coronavirus adaptation to human ACE2. EMBO J (20-4-2005) 24, 1634-1643.
John D Fernstrom¹, Madelyn H Fernstrom “Tyrosine, phenylalanine, and catecholamine synthesis and function in the brain“  J Nutr. 2007 Jun;137(6 Suppl 1):1539S-1547S. https://pubmed.ncbi.nlm.nih.gov/17513421/



HONOR THE INDIGENOUS PEOPLE of HAWAII, Gov. Green. Latest reports on Lahaina "fires", the "new normal fires"..
mejbcart — Fri, 18 Aug 2023 02:05:08 GMT
Please keep the Lahaina victims who lost their children, families and their own land to live (for now), in your prayers.
Also ALL OFFICIALS involved in anything CRIMINAL related to this TRAGEDY have to know: if you are an IMPORTANT WITNESS WHO PARTICIPATED IN THIS CRIME, please know, the people of this planet can forgive, BUT THOSE WHO LED YOU TO THESE CRIMES, will not. You might be getting more money now, but nobody knows for how many more days. You have your free will to join the forgiving majority OR stay with the annihilating FEW.  
Updates first, the main post starts behind the divider bar, way below. THANK YOU.
Update 2/24/2026: Redacted interview with HI resident who wrote a book about Maui fires, also presenting incredible pictures of dead animals and a human, affected by a DEW, at 1:17:57. Link at: https://rumble.com/v766dlu-price-andrew-arrested-israel-controlled-epsteins-security-w-whitney-webb-re.html
Update 3/15/2024: A substack writer investigating 9/11 events collects incredible amount of data, videos, reports, which hopefully will force the human minds to more open thinking: 
9/11 Revisionist
Where did all the people go on 9/11?
This is a rather tough subject for me to touch on, seeing I’ll be sharing very graphic footage, but we need to revisit the jumpers as well as the people who were never recovered in the rubble of the Twin Towers, post September 11, 2001. We need to get to the bottom of what exactly the people in the towers were experiencing that made them make the decisi…
Read more
3 years ago · 3 likes · 4 comments · 9/11 Revisionist
Update 3/3/2024: RFK is visiting Lahaina and reports on it at: 
RFK Jr.’s Policies + Politics
I Visited Lahaina and Saw First-Hand the Worst Example of Government Inefficiency and Corruption
Last August’s wildfire in Lahaina caused widespread devastation across Maui. It was among the worst natural disasters Hawaii’s ever seen—and the deadliest wildfire in modern U.S. history…
Read more
3 years ago · 138 likes · 44 comments · Robert F. Kennedy, Jr.
Update 11/4/2023: Newest reports from Lahaina, thanks to Greg Reese post at: 
The Reese Report
Lahaina Reopens and New Questions Arise
Watch now (5 mins) | Much like other recent fires such as Paradise, California, there have been several anomalies involving the recent fires in Maui. In the middle of an area untouched by fire, a random car with melted glass, and melted aluminum wheels. NORAD tracked CCP satellites…
Read more
3 years ago · 143 likes · 61 comments · Greg Reese
with many proofs of laser/plasma weapons applied in the Lahaina ‘fire’, for example at 16:50 a metal grid cut almost perfectly into half at 13-th column, parallel to the removed long slice of the concrete/asphalt. On the cut out pathway to the back of the building, which was destroyed, are 2 more of the metal grids. GPS could do it too, but maybe the weapons needed some kind of height calibration by determining the position of the ground? Just a speculation.. All the destroyed smart meters (like in other fires) point to the TARGETED localization of every object which was planned to be destroyed. That solidified frog, similar to the dog posted already in Aug reports, points to the super fast speed (short time laser/plasma burst) of the applied microwave energy. This entire crime WAS PROVEN TO INVOLVE MICROWAVES/plasma from the very begin, all what is needed NOW to act is a testimony of a highly qualified governmental PHYSICIST (NIST/DOE), in addition to a fire specialist… This needs an investigation NOW, just a truthful one and not a crap of lies, like the 9/11 one, done by NIST.. Message to Eric: please check out all the by EPA et al. ‘scrabbed piles of materials’, like the one at 21:23. As if somebody listens, a physicist, specialist on explosives and static of buildings, Prof. Dr. Maximilian Ruppert comes out with an opinion, that 100% of 9/11 job had to be planned for at least 2 years ahead:  
Update 9/15/2023: Citizens fight for investigating the police in an INTENTIONAL genocide: https://www.brighteon.com/86b0d959-8a4b-4bbf-a352-d5eec779f3d3 
also one more witness: https://forbiddenknowledgetv.net/testimony-of-anne-williams-at-maui-county-council-september-14-2023/
There are no words to describe it all. Found out this old show, might help you in those TOO MANY unimaginable tragedies, all the time! In trauma, if possible, it helps to ‘take a break’, maybe listen to some jokes, like this one, showing how to cook. Robin Williams alongside Martha Stewart: 
Update 9/14/2003: First :”O’KEEFE UNDERCOVER IN LAHAINA PART 1” at: https://www.brighteon.com/1f784938-103f-4fd0-8316-eaeb862ac006
and also Greg Reese summarizes recent investigations on Lahaina ‘fires’, just be prepared for a HORROR picture of a HUMAN VICTIM at 4:20 of that video: 
The Reese Report
CCP Satellites Over Maui At Time of Fires
Watch now (5 mins) | Steve Favis is an expert in computer science and advanced robotics. He has been researching the Maui fires and has compiled evidence that the technology exists to have started these fires from a satellite in earth orbit. He has also confirmed that the CCP had satellites capable of doing so above Maui at the time of the fires. His work has been published…
Read more
3 years ago · 121 likes · 85 comments · Greg Reese
on the same day a substack contra post appears, disputing the IR chinese beam theory of Lahain fires. It is about the difference between hot (thermal energy across the entire EMF spectrum by coherently, highly focused beams) and COLD DEWs represented by a plasma/particles beams, all having one would almost need to say anti-matter character. That substack source: 9/11 Revisionist in todays post titled: 9/11 Alchemy - Hollywood and dustification.
Update 9/11/2023: the bad history repeats itself, if we do not root out the causes of the evil. Here some hawaiian history, even wiki source is good enough: https://en.wikipedia.org/wiki/Overthrow_of_the_Hawaiian_Kingdom
Update 9/9/2023: More most recent developments: https://davidicke.com/2023/09/08/update-missing-children-school-bus-mystery-maui-massacre/
Update 9/8/2023: One month anniversary of the crime on Maui/Lahaina ends with the most recent report at:  https://expose-news.com/2023/09/08/royally-screwed-by-government-hawaii-victims-getting-desperate/ and also Peggy Hill continues to investigate, unfortuntely she posted that on youtube…, video no watch? Go to: v=FT2__Tf6Wg4  One more summary at: https://forbiddenknowledgetv.net/so-the-rumors-are-true/ with Mr. RF Kennedy explaining the housing market on Maui and the role of the biggest powers in it.. For anyone new to the DEW technology here is an old documentary: https://www.brighteon.com/c48650f0-0b06-4ea2-a0c7-aa58a27fdbb9  titled “Conspiracy Theory, Jesse Ventura, 2012, Tesla Invents Direct Energy Weapons“. In the meantime https://www.brighteon.com/08c4d139-d154-4ad1-b58e-0908265dbe43  “Paddle Out 9-8-23” and a message from Gov. Green in the ‘era of superstorms and climate change’, with melting cars and glass: https://www.brighteon.com/479eeea7-32ec-43c3-98c9-1a851191d7d6
I’ll be expanding this post with more details on microwaves interaction with biological matter, all at the end of this post.
Update 9/7/2023: There is another way to take away people’s homes, in addition to a plain murder, this time its official: https://expose-news.com/2023/09/07/net-zero-zealots-will-use-the-energy-bill/  PLEASE, NEVER STOP FIGHTING. Also a new analysis of the foreign satellites locations by a programmer who indicates again, a DEW systems, this time with IR source of  GWatt power. Jeffery Prather’s video at: https://forbiddenknowledgetv.net/proof-of-china-satellites-over-maui-at-fire-starts/ 
with lot of facts, in particular at ~22:00 with the 2 very characteristic double focal points of the footprint of the fires in Lahaina and on the higher elevation at Kula and Olinda, could be that the impacting beams are coming from the same source, rotated in space/time..?  The adjustment of the focal point decides about how big area supposed to be destroyed.. I ignored Reese’s report about the chinese green survey lasers over Maui, because, what’s happening here is similar to what was going on in CA fires, and partly on 9/11. Did China blew the Towers?? Why nobody speaks about what Russia is doing, not even Latypova. Sorry, it’s getting political, but what about the zionists running the gov in 2001, all really complicated… If this is a satellites war, then just wonder, what are the COUNTLESS Starlinks doing in the meantime??? And why would Musk ban Steve, the programmer, from his X??? Also how the entire Hawaii gov (lead by Mr. Green) is COLLABORATING with the Chinese on the issue of their plan of UN ‘sustainability’??? 
Update 9/6/2023 A: on the 9/2 I posted an interview with an arborist who very precisely analyzed the Lahaina fires and I additionally mentioned a personal very important event in Santa Rosa which took place BEFORE the devastating fires there. Now Peggy Hill interviews the same arborist while asking him about the fires history, all published now on the very questionable platform (for many reasons, to me) at: https://forbiddenknowledgetv.net/looking-for-clues-in-the-canadian-fires/
The history and character of these fires investigated by Mr. Brame is extremely important though, because he points to that one FACT: ALL THESE FIRES BEHAVED LIKE BURNS CAUSED BY MICROWAVES. All synchrotron facilities, national labs are the SOURCE of all continuous forms of X-rays of super powers, which would not exist without microwaves.. This is the foundation for the entire crystallography and its connection to the fundamental medical research on DRUGS and biological molecules, including the never ending VARIANTS of covid deception (more on it in the hopefully next post). The need for metal presence in the forensic analysis by Robert Brame is connected with the presence of ‘free electrons’ in the conductivity band of metals, which get accelerated with microwaves being absorbed. Dr. D. Klinghardt expresses it this way: metals are the antennas for microwaves, they resonate with them. The trees with burned out interior portion containing lot of water go back to the ‘cooking’ principle of microwave oven, rotational spectrum of water molecules in GHz range. Oh, that the very same range of Starlink and other satellites, based GHz range spectrum…Is that part of the reason why they are out there, in masses?? The most terrifying message of that video comes at ~28:00, where Mr. Brame shows a STERILIZED ground, >1 year after the fire, with NO vegetation growing on it!!! Is it possible, that maybe MONSANTO’s aluminum resistant crops (patented in the past) would grow here??? Btw. CA capitol in recent months was exchanging many wooden electrical poles AND the metal wiring going to home panels, with new ones.. Around the METAL WIRING on the main post, there is a plastic tube all the way to the ground! SMUD, the electrical utility company participates in geoengineering efforts AND in the same time prepares for the fires! How strange, one would need to ask, WHO gives the commando to start the burnout??? 
Update 9/6/2023 B: The strange statistics of 2,207 Lahaina structures damaged or destroyed, with 115 ‘final’ confirmed deaths, implies >2000 homes/buildings middle in a vacation season, along the ENTIRE COAST, were EMPTY? All that with no alarms, text messages, no power or some power??? Somebody will need to answer the question, what is left from the human body when put into high density microwave or IR laser beam? 
Update 9/4/2023: more dots to connect and OPEN YOUR EYES    https://www.brighteon.com/5e2ea0a3-319b-4c60-8510-25de4f14123a
https://expose-news.com/2023/09/02/wildfire-conspiracy-dr-david-martin/
Update 9/3/2023: Eric West, the HERO from Lahaina (now, not a hero, according to Prather) who exposed MANY LIES of the official narrative of what is really going on there, he and his family are now being targeted, according to Eric. Please listen to his today’s message and HELP HIM with the TRUTH which he tried to share with the entire world: https://www.brighteon.com/3fd6bfc5-fdd4-49de-87ae-b7cf1518c7da   
The NO ONE mistake Eric did, in my opinion, is to use the digital gofundme Silicon Valley platform, the very same which in 2022 seized the funds raised for FREEDOM CONVOY of truckers in Canada, it STOPPED THE ENTIRE FREEDOM MOVEMENT IN COVID TYRANNY TIMES of the most courageous people in Canada!!! Gofundme is the fuel of ALL covid19 related scams and CRIMES. Here from https://www.pymnts.com/personnel/2018/instacart-david-hahn-executive-chief-product-officer/ “Instacart Names David Hahn Of GoFundMe Chief Product Officer”, yes, that the Hahn from LinkedIN, Bilderberger group! Eric, who unknowingly exposed the geoengineering crimes which lead to ‘unextinguishable fires’, is being destroyed by the Deep State and not by one individual! Please remember that. If you want to donate, do not give your money to CRIMINALS, send a letter with CASH to those in need!!!
Update 9/2/2023: A personal note about an event which took place in Santa Rosa in Aug 2015 during Sonoma County Harvest Fair. At that time while being very active in anti-GMO movement I learned from Jeffrey Smith’s friend about it. His book “Genetic Roulette” can explain a lot. The speakers in that gathering were extraordinary, Jeffrey, Vandana Shiva, Steven M Druker who just published his 2015 book “Altered Genes, Twisted Truth: How the Venture to Genetically Engineer Our Food Has Subverted Science, Corrupted Government, and Systematically Deceived the Public“ being the first official document describing how Bill Clinton was involved in a complete annihilation of the scientific proof of harm of the first genetically modified crop plants, all done in a collaboration with british Primeminister Blair. It was S.M. Druker who was public interest attorney, who initiated a lawsuit that forced the U.S. Food and Drug Administration (FDA) to divulge its files on genetically engineered foods. Nothing happened of course, and 2 years later, the place he was talking about it all, while being severely shadow-banned by huge group of suddenly young loudly speaking individuals) was in fire….. Must be a coincidence..
Another VERY IMPORTANT video in regard to Lahaina ‘fires’: https://www.brighteon.com/e336da96-dca4-4848-a410-87a18844ce32   Try to take temperature in a microwave oven…. This very much in depth analysis titled “Arborist Of 48 yrs Questions Maui Wildfire - Directed Energy Weapons“ mentions one fact, there are no more cast iron water pipes any more, in any store, all what you get is plastic. WHY? Is that a shortage of metals or in fact long time planning ahead with this current global burn out in which melting of metal pipes underground is prevented by diverting the manufacturing process over the years to plastics? Just a speculation.. The fire specialist suggests to search for the dumped plastic on the island, as an evidence of trying to hide it for a good PROSECUTOR. Another speculative thought, is the current ‘trend’ to prohibit all gas stoves actually with that purpose to avoid fires with open flames facing the air totally saturated with flammable nanoparticles sprayed on us, almost every day???
And a new good video comparing google map images with current status of a Lahaina area in which the entire japanese JODO temple is gone, but the Buddha sculpture:  https://www.brighteon.com/66245e30-805f-4a3d-a33e-d3c112dd343a
Also Eric West in talk with more locals about their experiences during the tragedy on youtube channel  in video number TbJ-41dZtpg with title “Listen to the Cry of Hawaiian People - Ku Kia’i Maui” post from 
Hawaii Real Estate
Update 9/1/2023: Amazing PASTOR about details on DEW weapons in USA. One has to remember the AI tests of the MAUI DEW weapons right at the end of July ‘23, week or so BEFORE the fires:
Also more from Eric West in Lahaina on TikTok, which I won’t post here, but can be found on other substack from EMC2 NEWS BITES on the 9/1/23, and another testimony from a military specialist at
 https://www.bitchute.com/video/00I9fPnOQdlI/
Childrens Health Defence posted another interview from a local Hawaiian Jeremy Loffredo at: https://live.childrenshealthdefense.org/chd-tv/shows/good-morning-chd/how-the-us-govt-failed-the-people-of-maui/
Update 8/31/2023: Battle between electrical utility and county officials from a report at: https://www.staradvertiser.com/2023/08/27/hawaii-news/power-lines-didnt-start-deadly-lahaina-inferno-hawaiian-electric-says/ 
>> “A fire at 6:30 a.m. (the “Morning Fire”) appears to have been caused by power lines that fell in high winds.
>> “The Maui County Fire Department responded to this fire, reported it was ‘100% contained,’ left the scene and later declared it had been ‘extinguished.’
>> “At about 3 p.m., a time when all of Hawaiian Electric’s power lines in West Maui had been de-energized for more than six hours, a second fire (the “Afternoon Fire”) began in the same area.
>> “The cause of the devastating Afternoon Fire has not been determined.”
will need one proof, how the voltage of maybe ~400V, igniting surrounding GRASSES, or maybe even trees,  can cause temperatures of ~3000F…
also Debra Tavares, a long term expert on environmental fires/city plans describes many of the analogies between Lahaina and CA fires which started in 2017:
https://forbiddenknowledgetv.net/death-zones-kill-cities-deborah-tavares/
also a very good capture of lot of the ANOMALIES in Lahaina fire, which seems to have attacked the old buildings but not the 2 years old, with solar panels, as if the fire knew how to JUMPsmartMaui… Oh boy, today 9/1 that section showing that little corner in the SMART area, which first catches fire but then miraculously backs off, is cut out to a substantial degree (YT and AI collaboration on editing videos???)
Update 8/29/2023: The chinese style of dealing with human properties on a private land, by the officials, is becoming obvious, here a report on the latest https://www.thegatewaypundit.com/2023/08/mysterious-black-curtain-special-police-spotted-around-mauis/
Update 8/27/2023: DIRECT PROOF (again) of DIRECTED ENERGY WEAPONS IN LAHAINA at: https://forbiddenknowledgetv.net/another-smoking-gun-maui-fire-breaks-science-as-we-know-it/  The comments section contains good explanations to explain the obvious facts.
Update 8/20/2023: The evil escalates, super fast! What happens RIGHT NOW in Lahaina is continuing to be THE TIP of what one can imagine: https://expose-news.com/2023/08/20/are-maui-survivors-right-to-fear-losing-their-properties/
In addition EXPOSE just published this summary: https://expose-news.com/2023/08/20/uk-governments-nefarious-chemtrail-programme-exposed/
Update 8/23/2023: anyone having doubt about ‘space lasers’ please try to digest that talk I was listening to, almost 8 years ago in the West Photonics exhibition in San Francisco: 
 also from another SubStack writer about the newest from FEMA announcement in Lahaina:  
Strange Sounds
Can someone explain one good reason for this?
That's quite an... unusual... size... for a rodent... First ever Anti-Rat Day of Action held in Harlem to fight "rats the size of Crocs"… When it was Covid, there was nonstop footage publicized of pop-up morgues and bodies bagged on guerneys or laid out for effect. Respect for those who perished didn’t stop them then. They used it to advance the cause… C…
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3 years ago · 4 likes · 3 comments · Strange Sounds
no more pictures of anything from Lahaina, because those 2 shown above, tell more than enough….
This post is not about the universal Spike from covid injections, it is about the victims of the illegally approved, administered and mandated GENETICALLY MODIFYING the entire humanity, Spike injections, precisely gene modifying ‘therapies’ and new undisclosed sources of energy which can turn to ashes 50% of the houses while leaving the other right next to it untouched in this above enclosed area, where you have wide water canal on one side,  wide street on the other side and untouched vegetation from the other 2 sides. There is NO entry point for the fire to come in via ground, except for well, from the air above and the fire source would need to be DIRECTED. Would a wind, blowing from north-east (in the lower picture) at ~70mph be able to do that with such a knife precision destruction, while suddenly stopping at that raw of trees in the lower part of the photo??? That’s something else and that’s a view of many by now. “Forest Fire as a Military Weapon” as pointed by Dane Wigington from geoengineeringwatch.org describes how forest can be ‘prepared’ by chemical sprayings to let the tiniest branches fall, while leaving, quote “practically no hinderance to infrared scanning, laser scanning or other fixed-point, line-of-sight remote sensing techniques.” But Lahaina is NOT a forest, plus the average humidity in HI (middle in the ocean) in Aug is 80-60% and the max moisture for the incendiary operations of military value is 25%, according to that book at  https://www.geoengineeringwatch.org/documents/GeoengineeringWatch%20-%20Vietnam%20War%20Forest%20Fire%20As%20A%20Military%20Weapon.pdf
These moisture values however can be very well manipulated by the geoengineering sprayings of metals (AL, Ba, Sr), binding the water molecules tightly and preparing these complexes for interactions with radiation sources, like RF, wi-fi, 5G or with surfaces they cover, after slow diffusion towards the ground. The most recently shot scientist Zijie Yan from UNC Chapel Hill and his collaborating coworker, the shooter (from Wuhan lab!!) just published a very informing piece with details how to use laser beams to control and manipulate free standing gold nanoparticles always coupled to photonic-plasmonic resonances (https://onlinelibrary.wiley.com/doi/epdf/10.1002/adom.202301158). 
This is the picture taken by somebody flying over Maui on the 8/8, posted by many sources by now, showing a burning ring, almost like a cross-section of a laser beam, blended out in specific mode, impossible to imagine in a ‘wild event’:
And this was posted by Gateway Pundit showing the NASA satellite photo of Lahaina on the 8/8/2023:
The saturation of the ccd cameras (taking these pictures) caused by the intensity of the fires (proportional to the temperature) and by its own spatial resolution is not allowing for inspection of the details, but it seems like the ‘epicenter’ at that moment was the north portion of the city with the approximate circular cross section, strangely almost totally separated from the rest of the burning mid and south area. There are pictures of the fires posted by HIGHWIRE which indicate total saturation of the horizontal lines causing regular streaks along the entire border of straight objects, like trees… All possibly caused by extreme heat which has different characteristics in case of microwaves. 
A very good LOCAL coverage of about what is going on MAUI is done by this reporter pointing to this link: https://mauilfg.org/ (where people can help out the vicitms) and also to this video which was removed just recently:
Past experience from fires on the US mainland are summarized in this report here:
https://forbiddenknowledgetv.net/dews-directed-energy-weapons-in-action/
Alone this Lahaina picture below, from LA times, does it look like a RANDOM wild fire cutting every house the same way, ‘taking’ the roof away, ripping all the glass out (now it appears majority of it is all melted) and leaving just the WHITE walls, all around the same height, perfectly standing??? Only  really blind will accept this as a ‘wild event’. 
The fires started on the 8/8/2023 : https://www.latimes.com/projects/maps-maui-fire-destroyed-lahaina-satellite/
and it is all connected with contents of this old pot at:
with the now in EU viral section of the above video, in German unfortunately:
https://rumble.com/v3duhbe-us-prsidentschaftskandidat-robert-kennedy-jr.-fragt-nach.-was-droht-uns-mit.html
in which Mr. RF Kennedy confirms the airplane he flew with, did the sprayings too.. This, I’d call almost a targeting event! Sorry for being so pessimistic, just my life experience.
As a consequence in Lahaina fires, hundreds if not ~1000 children and adults, literally disappeared, turned into mostly white ashes, which need apparently a DNA identification (which DNA survives 3000F???), all of which, including cleaning up is now the reason to not allow the survivor’s from the affected 12,702 (2020 census) inhabitants of the Lahaina Beach Resort to get back to their mostly EMPTIED land: https://forbiddenknowledgetv.net/hawaii-wildfires-all-victims-are-john-and-jane-does/
The police forces guided by that FBI trained individual, being also the Lahaina’s coroner (https://legiscan.com/HI/text/HB869/id/2659254), already with an important history, apparently blocked the escape of the cars/people trying to run away:
https://rumble.com/v37t3a8-apparently-maui-police-officers-blockaded-the-escape-and-evacuation-routes-.html
And that despite of the announcement of the same police chief John Pelletier: the fire melted metals.., exactly like on 9/11, according to that Maui resident and Hawaii State Senate candidate, Sheila Walker (important witness):
https://forbiddenknowledgetv.net/eye-witness-reveals-mauis-wildfires-exhibit-same-destruction-as-ground-zero/
What Sheila describes as ‘infrastructure failure’ ended up being a TOTAL NEGLIGENCE by ALL KEY OFFICIALS, who were supposed to ACT in EMERGENCY, and didn’t or ‘just were not around’, in that one day on the 8/8 of apparently no electricity, water and then apparent containment of the fire, whereby the real hit happened after the ‘containment’. Any blockage of people running away from fires is absolutely not different from an Auschwitz concentration camp. It is as if all the representatives of Lahaina inhabitants suffered some kind of a cognitive impairment, in particular given that their own life was at risk, unless they knew it was somebodys else’s life... A report from an apparent FEMA substack writer Reinette Senum's Foghorn Express on other ‘natural’ disasters of similar character, with the title “Lahaina, a Modern-Day Pearl Harbor“ is basically pointing out a total deception in all these issues, all run by the government.  
8/21/2023, a FEMA worker confirms 9/11 similarities between Lahaina murder and 9/11:
On the 12/8 ‘The Last American Vagabond‘ published at https://odysee.com/@TLAVagabond:5/TDWU-8-12-23:5
an extensive summary titled: “Were Directed Energy Weapons Used In Maui? Let's Look At What We Can Prove... “  
There are new updates from Ryan about Lahaina/MAUI today on the 17th of Aug. 
A local Hawaiian, Shelby Thompson described what she experienced down there personally, thanks to The Last American Vagabond (who was the first one pointing to the AFRL facility on Maui) :
https://www.bitchute.com/video/reHG2wk9t7CY/
Any laser (IR, VIS, UV, THz) when operating in empty space/vacuum will not interact with anything, BUT that is not the case with our for decades already MODIFIED AIR CONTENTS:
show also in the most recently uncovered movie by the already deceased Michael J Murphy  https://forbiddenknowledgetv.net/unconventional-grey-unfinished-third-geoengineering-film-of-michael-j-murphy/
PLEASE, never forget the crying Hawaiian with the dehumanizing mask on his face talking about forced injections without which he would not be able to keep his job!
The reports about what the government is doing down in Lahaina are similar to what happened in China recently, a wall was erected so that people were not able to watch the flood tragedy, in Lahaina’s case, fire tragedy.  
Here is what the no 1 science paper Nature writes on the 14th Aug ‘23  about Maui’s cause of the  tragedy at https://www.nature.com/articles/d41586-023-02571-z , with the title “Hawaii wildfires: did scientists expect Maui to burn?”, quote:
“Fire’s causes.
The three main ingredients of a wildfire are fuel, dryness and an ignition source. Hawaii’s key fuel is grass, which proliferated in former agricultural areas as the economy shifted from ranching and sugar and pineapple cultivation to tourism. When dry grasses burn, they can carry fire to forested areas, which tend to become grasslands after the fire, in a self-perpetuating cycle.”
That’s NATURE scientific journal, became ‘political’ (wiki source, sorry):  “On 30 October 2008, Nature endorsed an American presidential candidate for the first time when it supported Barack Obama during his campaign in America's 2008 presidential election.” and right now actually unprecedented with this title from today 8/18: “What is an embryo? Scientists say definition needs to change. Lab-grown structures with the potential to develop into fetuses should be defined — and regulated — as embryos, some researchers say.“  Just can’t stop thinking, in a very ironic way, where all the children killed in order to ‘raise the Phoenix stories from the ashes’???
 Since it becomes unbearable, lets jump back to basics. Can grass fire melt metals? And even, can gasoline melt metals?? NIST in their 9/11 ‘investigation’ report, claimed yes. If so, think for a moment, would we get far with every car for a long time, with the combustion steel chambers burning the fuel internally every single cycle?? How many times did your engine melted or explode while driving your car? Yes, the cooling you say, but that can never completely replace the interface between the fuel and the chamber… Well, unless you drive Tesla (not the Nikola Tesla’s car though..) with different type of engine. For a reference, here is a source of melting temperatures of different SOLID metals: https://www.onlinemetals.com/en/melting-points
and here the one for flammable VAPORS:  https://tnb.ca.abb.com/en/pdf-catalogues/hazlux/ignition-temperatures-and-group-classification.pdf and here ignition temperatures for LIQUIDS, including GASOLINE: https://www.tayloredge.com/reference/Science/ignition.html   => The tendency is clear, in simple words, even if you put a deceased body in a cremating oven with 2000F, you will not be able to melt the titanium implants that person had. Titanium needs 3040F in order to melt. 
Where there any other explosives on the island?? Many people down there confirmed hearing explosions. Many of the footages of the ‘burned down’ house complexes show a patch of white color. Isn’t fire ash frequently black or dark grey at least and isn’t a plasma with lot of aluminum in it giving the whitish color seen down there all over? Please, any scientist working for the 5 big gov in nanoscience labs ( https://nsrcportal.sandia.gov/ ) with the amount of their designed products applied everywhere (paint, building materials, textiles, etc, etc.) growing with the light speed in numbers, all paid by taxpayers: come out from your niche and give some explanations here and stop pretending doing something good for the humanity, while doing exactly the opposite!
Adding one more thing to that mentioned Nature paper. To write a piece in the most prestigious ‘scientific source’, not even a week from the start of the tragedy giving an explanation for something what the authorities can’t explain, shows ‘their’ real desperation in counting on their ‘intellectual authority’, while counting on even more idiocy among the already confused citizens.  
The late Szent Gyorgy once said:”doing experiment is different from reading about it”. If you can effort throwing away your microwave oven, which you should not use for many reasons (leakage of the unlicensed 2.4 GHz radiation out of it) anyway, do it now. Put different materials inside until it burns at highest power, put metals at the very last, very carefully, while holding on to the power cable, just in case..
Also Dr. Mercola puts a post summarizing the Lahaina fire’s stories at: https://articles.mercola.com/sites/articles/archive/2023/08/19/maui-wildfires.aspx
while linking to a conversation between RF Kennedy and Ed Dowd: https://rumble.com/v37nh0m-ed-dowd-updates-robert-f.-kennedy-jr.-on-the-wild-fires-in-maui-august-14-2.html
HIGHWIRE with Del Bigtree presented few more extremely important and terrifying interviews from the Lahaina locals: https://www.brighteon.com/e5ddecbb-498c-4a8e-9d0b-09d7cfc5cd65
We’ll leave the tragedy for now, which hopefully has nothing to do with the Green New Deal (Gov. Josh Green..), and go back to 2019 with the post at:
Arkmedic's blog
The Killing Fields of Samoa
Malo Lava! We’re going back in time today… not all the way back to Ingersoll Lockwood times but just a little bit. To 2019. Just before the “COVID-19 pandemic”. Our location? The beautiful islands of Samoa. And you’re asking “What are you talking about? What happened in Samoa…
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4 years ago · 439 likes · 341 comments · Dr Ah Kahn Syed
This is a story explaining a possible ‘origin’ of SARS-CoV-2 ‘outbreak’. This article below describes to what extend Gov. Green, who became the governor of HI in ‘22, participated in that event:
https://forward.com/news/513992/josh-green-doctor-pandemic-hawaii-healthcare-candidate-for-governor/ 
That article’s title is:
“This doctor steered Hawaii through the worst of the pandemic. Now he wants to be governor”
Gov. Josh Green apparently has a development plan for the entire huge CEMENTARY along the burned down coastline of Lahaina. That article describes the details of Greens’ participation in the Samoa case, quote:
“A different epidemic
Six weeks before the coronavirus pandemic began, Green helped stem another deadly epidemic. In 2019, two Samoan children had died from incorrectly prepared measles vaccines, and many Samoans became suspicious of the vaccine. Declining vaccination rates created the perfect conditions for the virus to take hold.  At one point, so many babies died that funeral homes ran out of tiny coffins.
On Dec. 2, 2019, Green was planning a measles vaccination mission to Samoa with a few friends when the Samoan government asked if he could expand the team in order to vaccinate all of Western Samoa. Within 48 hours, Green enlisted 76 medical personnel and got 50,000 vaccines from UNICEF. He convinced Hawaiian Airlines to provide a plane, a local energy company donated fuel, “and I bought the beer,” Green said.
They vaccinated 36,997 people in two days. It was the “experience of a lifetime,” Green recalled. “And then who would have known that we would have an outbreak of coronavirus and COVID would sweep across the globe six weeks later?”
For the analysis of that incident please read Dr. Syed’s post from Nov 2022, which suggests the possible origin of SARS-CoV-2, without any names, but with that comment, quote: 
“Was Samoa the testing ground for a release of a SARS-like coronavirus in November 2019 - via a UNICEF sponsored vaccine - that proved that the population of the world could be intimidated and coerced into accepting mandatory vaccinations?”
What is equally strange is that Dr. Syed talks in his post about the Chinese army performing the mass vaccinations on Samoa, and the Forward magazine talks about Gov. Green and his friends, the Chinese…??? Or maybe they just helped each other, who knows. Here Dr. Syed’s quote: “They mandated measles vaccination and brought in the Chinese army to help (note that any reference to the Chinese army’s presence in Samoa has been scrubbed from the internet2).“
https://archive.ph/IMEW6
Here is a link to the by Dr. Syed suggested measles strain with 100% identical SARS-CoV-2 Spike in it (provided by Dr. Baric), submitted to NIH data base on 09-OCT-2020 by the german Paul-Ehrlich-Institute : 
https://www.ncbi.nlm.nih.gov/nuccore/MW090971.1
That’s a circular RNA with 19800 base pairs, with few RNA editing proteins, in which the universally injected Spike is described as: ‘codon-optimized for Homo sapiens synthetic SARS-CoV-2 spike glycoprotein’.
Viruses do self-assemble (just few titles from PubMed literature search for viral self-assembly with hundreds of hits):
Exploiting Peptide Self-Assembly for the Development of Minimalistic Viral Mimetics. Janković P et al.
Architecture and self-assembly of the jumbo bacteriophage nuclear shell.
Laughlin TG et al.
Viral self-assembly pathway and mechanical stress relaxation. 
Castelnovo M.
Physical virology: From virus self-assembly to particle mechanics.
Buzón P. et al.
etc., etc.
 and yet one has to watch how the geneticists and vaccinologists combine even more different parts, like that measles vaccine with the Spike 2020 (which btw. receives different code name from the original, despite of being identical in amino sequence with the original wild type), and then it is injected into the human veins causing among hundreds of known side effects, also personality changes (https://www.bitchute.com/video/PC5VmjL7VTzC/), which in turn can affect thousands.. Prof. Bhakdi investigating the side effects of the covid19 gene modifying ‘therapies’ in form of the injections mentions even a loss of will power (in german):  https://corona-blog.net/2023/08/07/prof-bhakdi-berichtet-ueber-das-verraeterische-buch-projekt-lightspeed-der-biontech-gruender-2/ and more about personality changes from this source: https://www.brighteon.com/a670eb91-31ad-43a2-9daf-9d8c178f0bd1
That Spike (code QOT47607.1) from the 2020 measles’ vaccine is already patented with 100% identity in countless new products, just few examples:
Altimmune Inc. (US 11382968-B2 410 12-JUL-2022) in yet another Coronavirus immunogenic composition
SARS-CoV-2 surrogate virus neutralization test US 11054429-B1 Singapore
Covalently modified antigens US 11291717-B1 DEFENCE THERAPEUTICS INC.
Vaccine by Novavx Patent: US 10953089-B1
Janssen Pharmaceuticals, Inc. and Beth Israel Deaconess Medical Center, Inc.; Titusville, NJ; US 11384122-B2 71 12-JUL-2022; 
Most probably, there are many if not most of the new products, containing like covid19 injections, synthetic modmRNA, reprogramming the human cells on the genetic level.
The 2024 presidential candidate RF Kennedy was almost banned from participating in the House censorship hearings because of his comments about the DESIGN of the universal Spike toxin for a specific racial profile. RF Kennedy regretted that comment just recently:  https://news.yahoo.com/rfk-jr-denies-being-antisemite-210014870.html
But that comment, was actually backed by science, confirmed by the most recent Mod-E-RNA confidential data drop about the deceased and injured victims of their covid injection product, mod mRNA1273, showing a clear racial profile.
Gov. Green is deeply involved in vaccination program, which now appears it carries a racial profile, something what he struggles with, in particular now, when his MAUI house is strong and standing, while so many others are completely annihilated.
We all, no matter what race, are on this planet because of the most obvious first, our ancestors, who always had a place to live!  The INDIGENOUS PEOPLE of Lahaina need at least their land back, since you, the gov, cannot bring the annihilated children back!!! The big question for anyone reading up to this point: WHY THE CONFISCATION OF THE INDIGENOUS DNA footprint taken from the LIVING LAHAINA SURVIVORS, apparently in order to identify all their deceased relatives, while knwoing 100%, that at ~3000F there is NOTHING LEFT from their DNA???  
Since all the Lahaina-style tragedies (which include CA fires) is clearly connected with the NOT american but rather UN plan for the entire globe (https://sdgs.un.org/2030agenda), one needs to ask, why the United Nations have their Base located exactly on the Holy Land’s Mount Hermon? It is getting more religious…
And here is a message from RF Kennedy, to all Americans, in particular those who do not even have homes and how about who LOST THEIR HOMES? https://www.thegatewaypundit.com/2023/09/robert-kennedy-jr-blackrock-is-robbing-americans-ability/
in an article titled: “Robert Kennedy Jr.: “BlackRock Is Robbing Americans of The Ability to Own Homes” (VIDEO)“
Lastly, from Dr. Lee Merritt, who pointed out that the powers to be, like to write their plans literally in our faces:
 
Not post related, ‘my computer’ is hacked, again, can’t edit the post properly, SORRY!


EDTA, the universal covid19 Spike toxin, venoms and some Vit C history. Part 1.
mejbcart — Sat, 12 Aug 2023 08:31:57 GMT
Update 3/3/2024: This type of suppositories is used in Philippines to fight cancer: https://patentimages.storage.googleapis.com/22/91/8c/b1c8307e0aca1a/US6720356.pdf
Update 11/13/2023: Even more amazing research on analysis of all different studies by Dr. Bryan Ardis in regard to snake venoms and EDTA, going back as far as 1902(!!!): https://www.bitchute.com/video/5si4tt2C3x4g/
Update 8/30/2023: Upcoming ‘Healing For the Ages’ by Dr. E. Group, Dr. Bryan Ardis and Dr. H. Ealy at https://rumble.com/v3b182s-venom-in-pharma-medications-and-vaccines-in-transhuman-reptilian-agenda.html 
Interview with title “Venom in Pharma Medications and Vaccines pushing for a transhuman reptilian agenda.“
Update 9/6/2023: RF Kennedy exposes the FRAUD of clinical Pfizer ‘studies’ on X platform, which immediately erases it, here a lucky copy (~4min talk) at:
https://uncutnews.ch/virales-video-von-rfk-jr-von-x-geloescht-hier-ist-was-sie-nicht-wollten-dass-sie-sehen/
do you still think Musk and his new CEO are good??? 
Protein purification in biochemistry almost never happens without the most potent metal chelator, EDTA, which eliminates contaminating divalent cations, hinders protease activity, and inactivates metal ion-requiring enzymes, inactivates venoms, it can be additionally functionalized with graphene oxide to equally remove heavy metals. EDTA is also used for the SARS-CoV-2 ‘universal Spike’ purification^1. 
The amino acid sequence of the toxic, patented Spike protein at: https://www.uniprot.org/uniprotkb/P0DTC2/entry contains the cysteines in its C-terminal section 1235 - 1260, the most intriguing, but also the most conserved  “CCMTSCCSCLKGCCSCGSCCKFDEDD“ portion of the official NIH entry of SARS-CoV-2 at https://www.ncbi.nlm.nih.gov/protein/1796318598. All these 10 C-terminal Spike cytosolic cysteine residues (C in single letter code) are rapidly acylated, i.e. linked to fatty acids within the ER and Golgi^2. That massive lipidation controls spike biogenesis and degradation, among other important functions. In the post at 
analysis of this section was presented, including high homology of its sections with the by A. Fauci patented HIV related cyclic peptide ‘‘CxxxxC”, 2 cysteines separated by any 4 amino acid residues. The post titled “Where did the iron go*, the dopamine and uridine issue with SARS-CoV-2 toxic Spike protein and the mindless science, leading to more thoughts on 'Died Suddenly'. A link to Bing LIU?“ pointed to the fact, that this unusual cysteine rich section is also homologous with part of the crucial liver‐derived anti-microbial peptide hormone, a regulator of systemic iron homeostasis, called ‘hepcidin’, defensin-like peptide, with part of its sequence ‘DTHFPICIFCCGCCHRSKCGMCCKT’. The late Bing Liu pointed out that lipid peroxidation has been recognized as a fundamental part of ferroptosis. The very same name of hepcidin is listed in Table 1 of the article ^3 describing venom peptides, in which hepcidin is described as an ‘antimicrobial cytotoxic peptide’ in animals but not mentioning at all the connection to a human liver hormone, strangely. Questioning of the official documents is always necessary, in particular wiki with its anonymously written entries being cited these days in almost every PhD thesis work, all apparently orchestrated by whom? Intelligence agencies! Here the source https://www.rt.com/news/580735-cia-fbi-edits-wikipedia/ ) For example, in its entry about https://en.wikipedia.org/wiki/Neurotoxin wi-ki defines dopamine as ‘Endogenous neurotoxin source’ (Table 1). That wiki table on the other hand contains also important sources of neurotoxins, bacterial proteins, venoms, metals (Al, Hg, Pb, As) and some organic molecules.  The Forgotten Side of Medicine’s recent post ‘How Did We Know That the COVID-19 Vaccines Would Decimate Global Fertility?‘ mentions a frequent anti-phospholipid syndrome suddenly appearing after the covid injections, which deliver exactly that universal Spike, now so much attracted to the phospholipid containing membranes, via exactly the mentioned C-terminal cysteines.  This apparently autoimmune condition related to ingredients of every single cell in human body manifests itself ‘only’ in thrombosis or pregnancy losses, in hypercoagulation (according to https://dermnetnz.org/topics/antiphospholipid-syndrome). The complement system is involved in this, that’s the systemic ‘director’ of the innate immunity. When human body is exposed to certain venoms^4, components of the same complement system are literally being eaten up. It is as if the venoms give zero time for the prey to develop any immunity. According to ^4, that ‘conversion’ of the victim to the prey via literal digestion which uses metalloproteases can be stopped by EDTA, which inhibits the digestive enzymes. Metalloproteases in venoms need metals in order to do that chop-chop job, and that is extremely well controlled via metal sensors, transporters and stores, in all living organisms, with some ‘variations’ in snakes, which do not digest themselves of course. The level of the no 1 ‘blood metal’, iron, regulated by the liver peptide hormone hepcidine, involves direct iron sensitivity of mRNA. The hepcidin connection to conotoxins^3, sequences of which are listed in a table from a nature article^5, with few examples of their alignment to the Spike cysteine rich section shown below, only indicate, that many of the very small but powerful Spike fragments which are homolog to pieces of the neuronal-specific a-conotoxins, binding to a7 nAChRs receptors, could be also affected by nicotine, which is the ligand (it binds them) for those receptors. It is funny, but only now I found a study: “Editorial: Nicotine and SARS-CoV-2: COVID-19 may be a disease of the nicotinic cholinergic system“ by a greek team from 2020(!!!) in Toxicology Reports Volume 7, 2020, Pages 658-663, available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192087/pdf/main.pdf
The nicotine remedy for ‘Spike envenomation’ as suggested by Dr. Bryan Ardis does actually work for many people struggling with taste/smell loss, including many other ‘long covid’ symptoms. What Dr. Ardis reveals just recently (8/19/23) is extremely important (it shows a clear proof of cause while experimenting with his own treatment protocolls), that what we’ve being attacked with, is a venom.., here his interview: https://www.brighteon.com/85421178-acb8-4b50-b137-3177b4538f75 which includes the REMEDIES for a total healing.
The by Fauci patented anti-HIV cyclic peptide ‘CxxxxC’ is actually a part of the conotoxins defined as quote: “The α-conotoxins are classified based on their cysteine pattern CC-C-C, with a disulfide connectivity of Cys1-Cys3 and Cys2-Cys4.“ There is a specific family of those called CIA (!!!) and CIB with the pattern CCx3Cx5C and CCx4Cx7C, both acting on a neuronal and muscle acetylcholine receptors nAChRs depending on acetylcholine neurotransmission. As innocent as they look, these little peptides with the CIA amino acid pattern ‘NGRCCHPACGKHFSC‘ and CIB ‘GCCSNPVCHLEHSNLC‘, function the following way:
 “Intramuscular injection of α-conotoxin CIA produces a rapid flaccid paralysis of skeletal muscles, as evidenced by a loss of equilibrium of the fish, and ultimately a complete immobilization.“ Below is shown the BLAST (NIH automated alignment software) and by hand performed alignment of two human defensins, hepcidins and other venom toxins, including the CIA and CIB with Spike, at the very end. The first 3 lines show raw amino acid sequence from Beta-defensin 1 and defensin alpha 4 (the 2 lines), both with antimicrobial properties, some overlapping cellular locations, with different functions though but all related to innate immunity.  The NIH BLAST software can’t find any common features between defensins 1 and 2, and yet one can clearly see it below, that these 2 proteins stem from one family. The line 3 represents the full length of hepcidin (also called LEAP-1) discovered by the purification of beta-defensin 1 from human urine. 
      
MRTSYLLLFTLCLLLSEMASGGNFLTGLGHRSDHYNCVSSGGQCLYSACPIFTKIQGTCYRGKAKCCK ->1
MRIIALLAAILLVALQVRAGPLQARGDEAPGQEQRGPEDQDISISFAWDKSSALQVSGSTRGMVCSCR ->2
LVFCRRTELRVGNCLIGGVSFTYCCTRVD ->2
          MALSSQIWAACLLLLLLLASLTSGSVFPQQTGQLAELQPQDRAGARASWMPMFQRRRRRDTHFPICIF ->3
CCGCCHRSKCGMCCKT ->3 (hepcidin or LEAP-1)
MWHLKLCAVLMIFLLLLGQIDGSPIPEVSSAKRRPRRMTPFWRGVSLRPIGASCRDDSECITRLCRKRRC
SLSVAQE -> LEAP-2, another liver antimicrobial peptide described in
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2312392/pdf/0120143.pdf

          DTHFPIC-IFCC----GCCHR-SKCGMCCKT HEPCIDIN 60-84 (1M4F pdb)
           T    C + CC    GCC   S CG CCK <
The NIH entry for the CIA toxin in its full length can be found at: https://www.ncbi.nlm.nih.gov/protein/D4HPD6.1 and its description contains keywords like ‘Acetylcholine receptor inhibiting toxin; Ion channel impairing toxin; Neurotoxin; Postsynaptic neurotoxin;‘ It is astonishing, that the universally injected Spike, has so much in common in its C-terminal section with the human essential liver enzyme hH (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563913/ ) related to inflammation and iron regulation, related to the defensins-like families, that publications like https://pubmed.ncbi.nlm.nih.gov/34206990/ or https://pubmed.ncbi.nlm.nih.gov/33017910/ mention, that the ANTI-MICROBIAL innate immune factors, defensins, are the primary defense against covid19, and despite of all this, the building blocks for the very similar HUMAN defensins homologous sections are now used to produce trillions of toxic NON-HUMAN Spikes in the bodies of the covid jabbed. 
 Defensins homologs in snake kingdom were named disintegrins, which are described little bit in the old post:
The conotoxin name CIA (not explained where it comes from) for part of which Fauci got his patent US 9,896,509 B2 for “USE OF ANTAGONISTS OF THE INTERACTION BETWEEN HIV GP120 AND a4b7 INTEGRIN“, against HIV, could be taken literally, given how much HUMAN suffering one person can cause… And all can be found in NIH data bases, literally written in our faces! It is like with the NIST officials, who told us that the burning gasoline melted all the steel of 9/11 towers which pulverized in the air, and yet we all drive cars for decades with burning gasoline inside of the engine and yet seldom anyone is causing fires with that, unless you drive Tesla, well, not the real Tesla from ~1930, but the X one, you know..! You will say, well there is cooling, BUT that cooling can never touch the surface between gasoline and engine surface!  
Anyway, elevated hepcidin levels are associated with Epstein-Barr Virus Infection (Int J Mol Sci 24 (2), 1630 (2023)), it is also associated with poor prognosis of Patients with Clear Cell Renal Cell Carcinoma (Cancer Invest 41 (1), 84-92 (2023)) and it became a diagnostic tool for covid19 patients (Wiad Lek 76 (1), 65-70 (2023)). Search for PATENTED proteins of snake origin similar to the C-terminal portion of covid19 Spike results in a indian cobra protein (NIH entry CAI46845.1) from patent WO 2005003159-A1 13-JAN-2005, which in its entirety (99% sequence coverage) is ~36% IDENTICAL with Spike amino acid sequence across all its domains, implying a basis for a common drug design. This protein is called Cobra Venom Factor (CVF) consists of multiple domains described at https://www.ncbi.nlm.nih.gov/protein/CAI46845.1 and here some of the BLAST (NIH sites) aligned fragments:
21.9 bits(45) 0.51 Compositional matrix adjust. 14/46(30%) 22/46(47%) 6/46(13%)
Query  681  PRRARSVASQSIIAYTMSLGAEN--SVAYSNNSIA----IPTNFTI  720 Spike
            PR  ++  S + IAY    G+ N   VA ++  I     +P NF +
Sbjct  421  PRERQATKSMTAIAYQTQGGSGNYLHVAITSTEIKPGDNLPVNFNV  466 CVF
Query  439   NNLDSKVGGNYNYLYRLFRK  458. Spike
             N+LDS +    NYL + + K
Sbjct  1146  NSLDSSIKKATNYLLKKYEK  1165 CVF
Query  446  GGNYNYLYRLFRKSNLKP  463     Spike 
            GG+ NYL+     + +KP
Sbjct  439  GGSGNYLHVAITSTEIKP  456 CVF
Query  1236  CMTSCCSCLKGCCS  1249  SPIKE
             C+ + C C    CS
Sbjct  1485  CIGNVCRCAGETCS  1498  CVF
Query  891  GAALQIPFAMQMAYRFNGIGVTQNVLYENQKLIANQFNSAIGKIQDSLSST  941
            GAA++I        R   + V + V   N K   +Q      KI D++  +
Sbjct  560  GAAMKIKLEGDPGARVGLVAVDKAVYVLNDKYKISQ-----AKIWDTIEKS  605
Query  1100  THWFVTQRNFYE  1111
             TH +++QR   E
Sbjct  1560  THQYISQRKCQE  1571
Query  1252  SCCKFDEDDSEPVLKGVK  1269
              CC++        +KGV+
Sbjct  710   ECCRY--------IKGVR  719
ACE2 binding portion
Query  452  LYRLFR-KSNLKPFERDISTEIYQAGSTP------CNGVEGFNCYFP-------------  
            LYR+F    N     + +  E      TP       N V+  N ++P             
Sbjct  144  LYRVFSMDHNTSKMNKTVIVEF----QTPEGILVSSNSVD-LNFFWPYNLPDLVSLGTWR  
Query  492  -LQSYGFQPTNGVGYQPYRVVVL-SFELLHAPA  522
             +  Y   P N   Y   R  VL SFE+   P+
Sbjct  199  IVAKYEHSPENYTAYFDVRKYVLPSFEVRLQPS  231
Query  199  GYFKIYSK--HTPINL-----VRD--LPQGFSALEP  225
            G ++I +K  H+P N      VR   LP     L+P
Sbjct  195  GTWRIVAKYEHSPENYTAYFDVRKYVLPSFEVRLQP  230
Query  66    HAIHVSGTN-------GTKRFD  80
             H  ++ GT+         K+FD
Sbjct  1207  HTHNIEGTSYALLALLKMKKFD  1228
uery  425  LPDDFTGCVIAWNSNNLDSKVGGNYNYL  452
            LP +F    +  N+N+L  K    + YL
Sbjct  460  LPVNFN---VKGNANSL--KQIKYFTYL  482

 CCMTS------CCSCLKGC------CSCGS----CCKF------DED--DSE    Spike
 CCEDVMHENPMGYTCEKRAKYIQEGDACKAAFLECCRYIKGVR-DENQRESELF ANATO domain VCF
with BLAST getting only one fragment on this cysteine rich section:
Query  1253  CCKFDEDDSEPVLKGVK  1269
             CC++        +KGV+
Sbjct  51    CCRY--------IKGVR  59
The last example in the above table compares the Spike with the ANATO domain of the VCF spanning the residues 661..731, including the 666th residue.., and which represents the Anaphylatoxin homologous domain; C3a, C4a and C5a. Anaphylatoxins are protein fragments generated enzymatically in serum during activation of complement molecules C3, C4, and C5, which induce smooth muscle contraction. There is nowhere any entry for a hepcidin-like protein in naja naja species, which do have a liver though.. An example of search in venoms literature (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889763/) based on just visual inspection of the very short toxic sequences in that paper pointed to yet another protein P25668.1 (uniprot code) discovered in 1971, named ‘long neurotoxin’, in fact very short (71aa), which quote: ‘Binds with high affinity to muscular (alpha-1/CHRNA1) and neuronal (alpha-7/CHRNA7) nicotinic acetylcholine receptor (nAChR) and inhibits acetylcholine from binding to the receptor, thereby impairing neuromuscular and neuronal transmission.’ Here its alignment with few pieces of the SARS-CoV-2 Spike: 
Query  28    GFCSIRGKRVDLGCAATCPTVRTGVDIQCCSTDDCDPF  65   neurotoxin (1)
             G  +I    + L C ++C +   G    CCS   C  F
Sbjct  1223  GLIAIVMVTIMLCCMTSCCSCLKG----CCSCGSCCKF  1256  Spike (2)
Query  19   VCYTKTWCDGFCSIRGKRV  37  neurotoxin
            +C+T  + D F  IRG  V
Sbjct  390  LCFTNVYADSFV-IRGDEV  407 Spike 'RGD' motif
Query  33    RGKRVD  38
               KRVD
Sbjct  1036  QSKRVD  1041

The entire c-term of the Spike can be actually overlapped over almost 75% of the entire 1971 toxin, by hand, since BLAST won't do it:
HVCYTKT-WCD--GFCSIRGKRVDLG----CAATCPT-VRTGVDIQCCS------TDDCDPFP-TRK-RP 
   Y+K  W    GF +     V +     C ++C + ++      CCS       D+ D  P  +  +
YEQYIKWPWYIWLGFIAGLIAIVMVTIMLCCMTSCCSCLKG-----CCSCGSCCKFDEDDSEPVLKGVKLHY
If by now, you are still not convinced that the CYSTEINE-pattern in the Spike toxin is special, it’s all coincidence, please go to the complete genome of the Mycobacterium leprae, strain MRHRU-235-G chromosome genome, with ~3.2 millions of base pairs, at: https://www.ncbi.nlm.nih.gov/nuccore/CP029543.1 and do a search for ‘CC’ while searching in the amino acid sequence lines starting with the string ‘/translation=’. Among thousands of entries, you will not find a one which has three of the Cys-Cys dipeptides, not to even speak about 4, like in the universally injected Spike toxin. Or search the Borreliella burgdorferi strain B-17/2013 chromosome, complete genome you will not find a single protein in the entire bacterium (1mln base pairs!!) which has 4 Cyc-Cys dipeptides in a short string like the Spike with ~4000 base pairs = 0.004-th of a milion….
 G-CCSDPRCNYDHPEICX   Pdb Data bank entry 2H8S=alpha-conotoxin Vc1.1
 G CC  P C   H   C    IDENTITIES
NGRCCH-PACG-KHFS-C    CIA conotoxin  
If you go to: https://www.rcsb.org/structure/2H8S and just read the abstract of the publication related to that above entry, you will realize, how much effort goes into finding out the importance of every single amino acid residue in order to make something good out of something really bad, or the opposite, something lethal out of something good. Some call it gain/loss of function, depending on what the SCIENTISTS’ INTENTIONS ARE. 
Among the plant antidotes against naja-naja venoms (listed in that article at  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889763/pdf/tropmed-94-1392.pdf )  are Siris Tree, onions, marshmallow, black mustard, lemon, cumin and many more^6.
The most recent interview with Dr. Bryan Ardis at:
 https://rumble.com/v321i70-keys-2-life-ep53-dr.-bryan-ardis-watch-the-water-2.html
pointed to antidotes for the Spike and its fragments (venoms in his opinion): Glutathione, NAC, Vit C, and EDTA. 
Recent very loud news everywhere about EDTA and VitC clearing the blood of the covid injected AND apparently equally NON-injected people(?), talk not about proteins or even the artificial toxic Spike, but rather about taking apart hydrogels, and graphene by partly exactly the same remedies, EDTA and VitC….. Looks like part of the remedies match both interpretations of the covid story. NIST handbook about graphene applications mentions H2O2, which degrades the 1 atom-thick hexagonal carbon lattice, i.e graphene. 
Lets touch the EDTA, which chelates equally well aluminum^7. FDA approved EDTA for chelation of heavy metals in 1948 used first in lead poisoning of certain workers (https://www.harborcompounding.com/edta-and-heavy-metal-toxicity). Today it is being applied in IV or suppositories form. EDTA also dissolves hydrogels^8, which are for example part of Mod-E-RNA covid injection materials^9. It can be bound to functionalized magnetized graphene oxide for removal of mercury, lead and copper^10.
In the past NIH did perform EDTA chelation therapies, which concluded, quote: ”Post-myocardial infarction patients with diabetes mellitus aged ≥50 demonstrated a marked reduction in cardiovascular events with EDTA chelation.”^11, ^12. One of the presenters in oral health docu series (NaturalHealth365Programs.com), Dr. Thomas Yanossy^13, known for his ORADIX EDTA and glutathione containing suppositories (used for chelation on his own father with Alzheimers), mentioned, that it was Monsanto who carries the 1935 EDTA patent and that the research leading to its discovery was connected with looking for a ‘replacement’ of the well known citric acid chelator. Monsanto did very few, if any good things, so one needs to ask, why to replace the citric acid from the ‘Citric acid cycle’ also known as Szent-Györgyi-Krebs cycle or  TCA or Krebs cycle, which is the A and O of cell metabolism in all species, the delivery of the ENERGY via RESPIRATION through the oxidation of acetyl-CoA derived from carbohydrates, fats, and proteins, the entire food? 
If one thinks to get to basics, time will flow, because Szent-Györgyi got his 1937 Nobel prize for " his discoveries in connection with the biological combustion processes, with special reference to vitamin C and the catalysis of fumaric acid" (https://www.nobelprize.org/prizes/medicine/1937/summary/) and Hans A. Krebs received his for “discovery of the citric acid cycle” (apparently the same cycle from 1937) in 1952 (https://www.nobelprize.org/uploads/2018/06/krebs-lecture.pdf) and didn’t mentioned in a single word the Vitamin C… Thus in 1952  the vitamin C disappeared from the tricarboxylic acid cycle (TCA)… There are other important things which happened in those years, all related to Monsanto’s glyphosate (N-phosphnomethylGLYCINE), an antbiotic and strong metal chelator, like EDTA(..), but that might come later. Here just one thing, EDTA was developed by a german chemist working for IG Farben in early 1930-ies on a ‘replacement’ for a citric acid. 
What’s the difference between citric acid and ascorbic acid, i.e. Vitamin C??  https://www.quirkyscience.com/citric-and-ascorbic-acid/
The highest concentration of vitamin C is in human adrenal glands^9, that’s where Szent-Gyorgyi was looking for it first, later on, he found its source in peppers, and once his work on this topic was done, within 2 years, the chemical industry got its synthetic version C6H8O6, versus what Krebs found 15 years later, C6H8O7. Both Szent-Gyorgi and Krebs enjoyed Rockefellers’ support in their research, which now lead to that difference of one atom of oxygen, that’s huge, optical properties are very different, in UV range in particular. Krebs work cites a malonate which is inhibiting the respiration of all animal tissues, and also mentions that injection of fluoroacetate into the intact organism leads to an accumulation of citrate in animal tissues and represents yet another valuable specific inhibitor of respiration.. A quote from his 1952 lecture about the injection experiment: “fluoroacetate and oxaloacetate appears to prevent competitively the metabolic removal of citrate. “ “The accumulation of citrate in the poisoned organism, by analogy with the accumulation of succinate, may be taken as an indication of its normal intermediary formation.“ in the TCA cycle…
This will be a very stup.. question, to any chemist who might read this. 
The Spike, the acute respiratory syndrome coronavirus 2 (with no 3D structure in any NIH data base) is all about respiration, and yet what brings people back in emergency are VITAMIN C IV injections, in huge amounts, never anything happens when doing it, no deaths, no pain. And yet anyone heard about citric acid IV’s, with one more oxygen in every molecule…? On the contrary, one can read the following titles “Citric Acid in Drug Formulations Causes Pain by Potentiating Acid-Sensing Ion Channel 1“ (https://pubmed.ncbi.nlm.nih.gov/33888605/) or from an abstract “The fastest combination was the injection of 150 g·L−1 citric acid solution in four injection sites (5 mL per site), which killed the starfish in 26.4 ± 4 h.“ (https://www.researchgate.net/publication/311635861_Citric_Acid_Injections_An_Accessible_and_Efficient_Method_for_Controlling_Outbreaks_of_the_Crown-of-Thorns_Starfish_Acanthaster_cf_solaris). Well clearly citric acid is a great metallic ion chelator in antioxidant systems, and not only that, “Citrate is an endogenous inhibitor of snake venom enzymes by metal-ion chelation” (https://pubmed.ncbi.nlm.nih.gov/1440629/), like EDTA(..), and also, while belonging to the s.c. Alpha Hydroxy Acids (AHA, moment…) it removes the top layers of dead skin cells.. When the gene in mice for the Vitamin C transporter protein (SVCT2) is deleted, the animal suffers cerebral hemorrhage and death. Ascorbate protects neurons from oxidative damage, essential in Alzheimer’s, Parkinson’s, and Huntington’s. Dr. Thomas A. Levy has a great resource of what Vitamin C can do in all health situations, it can be found at: http://www.doctoryourself.com/Levy%20Vitamin%20C%20Therapy%20Manila%202017.pdf
or also at: https://www.peakenergy.com/video.php
Szent-Gyorgyi was deriving his detailed conclusions while working with natural tissues and discovering ascorbic acid, and yet Dr. Krebs (in german it means Cancer) discovered different acid, aligning with the newest science confirming, that the human gene for production of ascorbic acid(VitC) is lost. BUT somehow all the receptors binding the VitC are still there??? Why VitC participates in so many processes, it is essential for the CNS system, so many proteins have it as co-factor yet the gene for its production is gone (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145266/), but apparently it is still present in newborns ( https://www.sciencedirect.com/science/article/abs/pii/S0006291X9991272X ) and maybe gone after aluminum exposure?? Just a huge speculation. Dr. Levy attributes it to EPI-genetic changes saying, the gene is there but its translation in cytosol in the process of mRNA-ribosome interaction is impaired... Ironically among the few vertebrates missing the last gene in the ascorbic acid formation from glucose are guinea pigs, and fruit bats! (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725125/). That silenced/lost gene in question, encodes the enzyme L-gulono-1,4-lactone oxidase (EC 1.1.3.8) and the reaction that enzyme performs is the following:
L-gulono-1,4-lactone + O2  = H+   +   H2O2  + L-ascorbate
The official ‘explanation’ for the loss: “Sequence analysis study indicated that the human L-gulono-gamma-lactone oxidase gene has accumulated a large number of mutations since it stopped being active and that it now exists as a pseudogene in the human genome.“ (Am J Clin Nutr 1991 Dec;54(6 Suppl):1203S-1208S. doi: 10.1093/ajcn/54.6.1203s.). So why the mutations only in humans and guinea pigs, or maybe in human guinea pigs(…), like their apparent evolution from apes, few of which are still left over out there until this very day??? Here yet another scientific explanation, from 1966 in journal ‘OXIDATION-REDUCTION AND BIOENERGETICS’ in a study titled “A Kinetic Study of the Mechanism of Action of l-Gulonolactone Oxidase.” (https://www.sciencedirect.com/science/article/pii/S0021925818965506, quote: 
“in the presence of oxygen and 2,6-dichloroindophenol (DCI) the enzyme decreased in activity as the oxygen pressure rose above 4 atm. This is consistent with there being two specific binding sites in close proximity to each other; each site binds only one of the two oxidants, oxygen or DCI, and inhibition occurs when both sites are occupied.“
At least that study showed, that a chemical can inhibit the enzyme, BUT, at 4 atm??? And now a funny little imagination moment, whatif some angels, from far away, where OXYGEN is rare, have fallen down on this planet, and intermingle with HUMANS, who got wonerful lungs dealing with pressures of ~1atm???   
Looks like in the 60ies that Gulonolactone Oxidase enzyme topic was very hot, despite of no global warming at that time…. In 1965, a new study at https://www.jbc.org/article/S0021-9258(18)96626-3/pdf
was published, with the title: “Studies on Microsomal Phospholipids That Inhibit Gulonolactone Oxidase*” announcing, quote: “Complete inhibition of oxidation of L-gulono-y-lactone to ascorbic acid by liver microsomes was observed in tocopherol-deficient rats and rabbits (1, 2). The inhibition is completely prevented or immediately reversed by the addition of tocopherol, Mn++, Co++ cations or ethylenediaminetetraacetate (EDTA) to the enzyme system (3). 
So EDTA can completely reverse the by phospholipis caused inhibition of L-GLO! ??
So how the by the scientists estimated 40 million ( really so long for a mutation which only gets to the humans but not rats, for example???) years long history of disappearing VitC essential enzyme can be fixed? NIH offers the solution at: https://pubmed.ncbi.nlm.nih.gov/14962674/ in an article titled “Functional rescue of vitamin C synthesis deficiency in human cells using adenoviral-based expression of murine l-gulono-gamma-lactone oxidase“ with the quote:
“The cloning of the murine Gulo cDNA and the construction of Gulo-expressing adenoviral vectors are vital steps toward determining the role of vitamin C in basic metabolism and in disease.“
Vitamin C rescue with viruses??? Wait a moment, didn’t Szent-Gyorgi show enough? Do certain genetic mutations happening only to humans and guinea pigs, while everybody else was thriving and happy, full of ascorbig(←intention) acid, make any sense to anyone? 
And there is more fishy stuff when looking into Monsanto’s ‘citric acid issues’ related to the first EDTA patent.  Their patent for “Sorghum aluminum tolerance  gene, SbMATE” (US7582809B2,  https://patents.google.com/patent/US7582809B2/en ), describes a major aluminum tolerance SbMATE gene, which encodes a root citrate efflux transporter that is Al(ALUMINUM)-inducible at the level of gene transcription and is also Al-activated at the level of protein function. In order for the plant to survive the aluminum onslaught, the Monsanto specialists decided to produce more of the ENERGY=>TCA cycle=>citric acid related genes in their new hybrids. 
And all of it must be somehow connected, since how can we have vaccines, for ages, ‘contaminated’ (all well known, approved and mandated by the gov) with the very same metal ALUMINUM, the 13th element in the periodic table (how strange!), out of so many others in that table? The same metal is being sprayed in the skies( https://www.geoengineeringwatch.org/), it is in our water, food supply AND poured into every vaccine batch out there for even NEWBORNS!!!!  We are loosing the MEMORY, partly because of it.
One good thing left by Mon-san-to: EDTA and citric acid, with the latter now used in leprosy.. More info on it can be found in an article “Effects of Citric Acid on the Healing Process of Chronic Wound due to Leprosy“, published ‘just on time’ in Int J Low Extrem Wounds. 2023 Jan 5;15347346221147398.
To add to this topic, covid19 issue is not free from citric acid issues either, since it is all energy, according to the late Dr. Cancer (Krebs in german) here an example:
https://www.nature.com/articles/s41467-021-22166-4#MOESM1
“SARS-CoV-2 infection rewires host cell metabolism and is potentially susceptible to mTORC1 inhibition“.
This post is NOT finished, it is still having lot of issues and many questions, but it became so long that it needs to be ended here, at this late hour.
Thank you for your patience, in case you got that far here;)) Just realized, part of the post shouldn’t even be here. SORRY!
Dr. David Martin with his general critics^16 of the entire modern science, will and should shock every scientist involved in the topic of genetic modifications of our nature/humanity. According to the ex-KGB agent, Y. Bezmenov, only then, you will wake up and STOP DOING SUCH SCIENCE. That shock is not the electrical one, but rather mental.   
Let’s close with a short list of more useful EDTA resources and applications:
https://www.detoxamin.com/references/
https://www.blushield-us.com/products/remedylink-medicardium-edta-chelation-suppositories. ( a seldon Mg-di-potassium EDTA salt, looks to me like the best one…)
https://edta.net/detoxamin-prostate-studies/
https://eartheracademy.com/course/edta-enema-for-heavy-metal-detoxification/
Literature.
Jeffrey M. Schaub et al. “Expression and characterization of SARS-CoV-2 spike proteins“ Nature Protocols volume 16, pages 5339–5356 (2021), https://www.nature.com/articles/s41596-021-00623-0
Francisco S Mesquita et al. “S-acylation controls SARS-CoV-2 membrane lipid organization and enhances infectivity“  Dev Cell. 2021 Oct 25;56(20):2790-2807.e8.
 doi: 10.1016/j.devcel.2021.09.016. Epub 2021 Oct 1. https://pubmed.ncbi.nlm.nih.gov/34599882/
Vidya V et al. “Venom peptides – A comprehensive translational perspective in pain management“ Curr Res Toxicol. 2021; 2: 329–340. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473576/
G. Eggertsen et al. “In vitro studies on complement inactivation by snake venoms”  Toxicon Volume 18, Issue 1, 1980, Pages 87-96. https://www.sciencedirect.com/science/article/abs/pii /0041010180900343
Layla Azam & J Michael McIntosh “Alpha-conotoxins as pharmacological probes of nicotinic acetylcholine receptors“ Acta Pharmacologica Sinica volume 30, pages 771–783 (2009). https://www.nature.com/articles/aps200947/tables/2
https://downloads.hindawi.com/journals/bmri/2014/970540.pdf
A. Fulgenzi et al. “Efficacy of chelation therapy to remove aluminium intoxication“ Journal of Inorganic Biochemistry Volume 152, November 2015, Pages 214-218https://www.sciencedirect.com/science/article/abs/pii/S0162013415300829
Comprehensive Biomaterials 2011 book by Paul Ducheyne, Paul Ducheyne, Kevin Healy, Dietmar W. Hutmacher, David W. Grainger, C. James Kirkpatric.
2018 MODERNA patent US 10,064,959 for “MODIFIED NUCLEOSIDES, NUCLEOTIDES , AND NUCLEIC ACIDS , AND USES THEREOF“ https://assets.modernatx.com/m/6dc651c06fafd781/original/US10064959.pdf
2020 MODENA patent US 10,702,600 for “BETACORONAVIRUS MRNA VACCINE“ https://assets.modernatx.com/m/6fa93a4f95208572/original/US10702600.pdf
L. Ciu et al. “EDTA functionalized magnetic graphene oxide for removal of Pb(II), Hg(II) and Cu(II) in water treatment: Adsorption mechanism and separation property”. Chemical Engineering Journal Volume 281, 1 December 2015, Pages 1-10 https://www.sciencedirect.com/science/article/abs/pii/S1385894715008839
Esteban Escolar et al. “The effect of an EDTA-based chelation regimen on patients with diabetes mellitus and prior myocardial infarction in the Trial to Assess Chelation Therapy (TACT)“ Circ Cardiovasc Qual Outcomes 2014 Jan;7(1):15-24. https://pubmed.ncbi.nlm.nih.gov/24254885/
Clin Chem Lab Med. 2007;45(5):565-76.
 doi: 10.1515/CCLM.2007.110. “The role of ethylenediamine tetraacetic acid (EDTA) as in vitro anticoagulant for diagnostic purposes” Giuseppe Banfi et al. 
https://oradix.com//ninety-percent-reduction-in-cancer-mortality-after-chelation-therapy-with-EDTA-the-famous-swiss-study  
P Patak¹, H S Willenberg, S R Bornstein “Vitamin C is an important cofactor for both adrenal cortex and adrenal medulla“  Endocr Res. 2004 Nov;30(4):871-5. doi: 10.1081/erc-200044126. https://pubmed.ncbi.nlm.nih.gov/15666839/
B. O’Callahan, O. Qafoku, Waters K. et al., “Atomic force microscopy and infrared nanospectroscopy of COVID-19 spike protein for quantification of adhesion to common surfaces.” Langmuir 37, 12089-12097 (2021). [DOI: 10.1021/acs.langmuir.1c01910]  https://www.osti.gov/biblio/1827416
the last video at https://expose-news.com/2023/08/10/there-was-no-sars-cov2-disease-just-a-set-of-symptoms-and-a-branding-campaign-dr-david-martin/

mejbcart’s Newsletter

Oats, memory, the genetically modifying SARS-CoV-2 injections, and the Epstein files.

Evolutionary Dynamics: brought to you by Jeffrey Epstein, with connections to SAR-CoV-2 Spike genetically modifying injections.

HUMANITY in 2025 with prayers for LA=haina2.0, the genetic Spike fallout continues, insulin and H5N1.

How Substack works.. It's about covid19 and HxNy comment.

Insulin sequences within the universally injected Spike? Clock gene, Ozempic, cancer, wars and the last call of the lost Bifidos: STOP ALL RNA-based products, NOW.

`“Stabilized insulinotropic peptides and methods of use”`

The war on human genes, Cholesterol, LNPs and Covid genetically modifying injections, now also in the CRISPED patients.

Stanford, Penn, MIT et al. dream, genetically modified world. More Spike2020 companions, with ADAM33, no EVE yet...

"We've essentially clinically tested the vaccine on billions of people worldwide"

The white clots after the genetically modifying covid injections. Is it the -KV- to -PP- mutation, Fibrin/-ogen, or all of it?

Covid19 and what alpha-lipoic acid (ALA) can do for You?

What does the X possibly stand for? Will Bill Gates et al. succeed?

The 20 years of 'genomic medicine'. JP Morgan, is it about money or health?

Mod-E-RNA, cancers and Programmed cell Death Protein 1 pathway (PD-1/PD-L1). And who is Len Blavatnik?

The CHRISTMAS, the 'Cys-His-Arg-Ile-Ser-Thr' (C-H-R-I-S-T) amino acid sequence and the SARS-CoV-2 Spike.

A call to ditch Face-book or Me(e)t-A(i) and the "Game Over 2 – Attack on the Microbiome"

The rise of Adrenochrome and the fall of the Oxytocin, not only among the rulers.. Any SARS-CoV-2 Spike connection?

METHODS FOR TREATING CARDIOVASCULAR DISEASE

METHODS FOR TREATING IL-6 MEDIATED INFLAMMATION WITHOUT IMMUNOSUPPRESSION

Treatment of existing left ventricular heart failure

METHODS FOR TREATING HEPCIDIN-MEDIATED DISORDERS

Sweet deals in viral spikes and in politics..

Mod-E-RNA's FOIA file drop and the next synthetic mod mRNA relaxin gene-based 'rescue' for the damaged human hearts, and pregnancies.

`Happy Giving Thanks day;)`

WHATIF ACE2 scenario and the hell of the infinite VARIANTS.

HONOR THE INDIGENOUS PEOPLE of HAWAII, Gov. Green. Latest reports on Lahaina "fires", the "new normal fires"..

EDTA, the universal covid19 Spike toxin, venoms and some Vit C history. Part 1.