'CTCCTCG-GCGGG-CACGTAG' and the five older MOD-E-RNA patents. Susceptibility to coronavirus disease 2019 and K26R ACE2 gene polymorphism.

The main post starts under the divider bar below, first some updates, remotely related to the topic of this post… Sorry for that and THANK YOU.

Update 1/7/2025(time flies!): It’s about the HISTORY of what is happening:

The creation of personalized bioweapons?

Update 7/16/2023: Mr. R.F. Kennedy Jr. is the first politician admitting the BITTER TRUTH of the issue touched in the topic of this post. Here a link to his statements in an article with not the right title putting the doubt of the fact by adding the word ‘may’: “RFK Jr. says COVID may have been ‘ethnically targeted’ to spare Jews“

https://nemosnewsnetwork.com/rfk-jr-says-covid-may-have-been-ethnically-targeted-to-spare-jews/

Update 11/21/2022: An insider about biotechnology: https://expose-news.com/2022/11/21/those-involved-in-project-to-inject-populations-are-guilty/ an article titled:”Those involved in Project to Inject World with Experimental Biotechnology are GUILTY of Crimes against Humanity”

Update 11/19/2022: quotes from Dr. David Martin’s interview with Patrick Gentempo from his current series at: https://endgameseries.com/viewing/ Episode 9. :

-“the vast majority of our economy in the developed world runs into existential no-go zone, we’ll run out of Social Security money in 2028…, right now somewhere between 30-40% of all the expenditure of every $ spend,.. goes to supporting the PHARMACEUTICAL-INDUSTRIAL COMPLEX“

-”criminals are gonna tell you what they are gonna do because they love part of their fantasy of being criminal. They will tell you what the crime is before they do it or while they are doing it” => my view, criminals love to FEAR/torture the victim, at all times, first, before deciding about the future. The very same applies to official science, patents industry, in which frequently you are getting MONEY for highly questionable research and topics.

-“There is NO FELONY in which IGNORANCE is a defense”

-”The tragedy is we’ve been seduced into justifying an immoral act”

-”in 1961 we’ve been told beware military-industrial complex, we should have been told the PHARMACEUTICAL-industrial complex, which is running the entire ..world since 1604…”

-”is an economy based on drug dealing economy, a pro-HUMAN economy?”

-”between NOW and 2028 (that’s when SS will run out of money) I’m gonna look at my entire world view, how I’m going to save for my future, and how much I’m spending for my life insurance and what am I doing with health insurance, … and say I’m only going to put my capital where it is aligned to my life AND NOT ALIGNED TO MY DEATH!!…The average person would actually change ~70% of their total assets holdings with that one question. We’d step away from the system which is killing us!”

-’when my E-vallet melts from the EMP, do I have a gold mine? If the answer is yes, then I haven’t solved my problem’

The begin of that interview explains the LIFE INSURANCE issue ever since the seventeen hundreds when it was introduced first in GB and later on it became the principle of one of the top economic drivers of United States. Dr. Martin states that the story of America is based on a facade of insidious narrative, to build it on a hegemony of financial industry aligned to the DEATH of humanity, NOT to its life... Proof? 1905 presidential inauguration with 5 life insurance representatives standing next to Roosevelt. Another global example, from Canada, just posted by ‘‘Exposing The Darkness: Dr. William Makis 93 Dead Doctors After Vaccine Rollout at: https://rumble.com/v1vbzju-dr.-william-makis-93-dead-doctors-after-vaccine-rollout.html ==»»»»» If indeed every canadian doctor is covid jabbed 4-5 times, it is TOO LATE for every sngle one of them, assuming they all got the ‘real stuff’ injected into their veins!

David, I’d only add to the last point, your Iphone, it aligns with your death too, if it beams with not the right frequency…

Another amazing docu series at: https://go2.propaganda-exposed.com/docuseries/episode-9/

Update 11/14/2022 : Now the furin site is linked to a “novel nuclear localization signal (NLS) “PRRARSV”, from a post** linking to the article describing that research at: https://www.biorxiv.org/content/10.1101/2022.09.27.509633v1.full.pdf

Just wonder, what comes first, cutting the Spike in 2 pieces or sending it directly to the nucleus… But wait, shouldn’t it be also bound to the membranes of the cells expressing the synthetic genetic material, injected into billions of arms? More comments on this new pre-print at the end of this post.

The main post starts behind the divider bar below:) THANK You for reading.

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The number of articles/posts about ‘CTCCTCGGCGGGCACGTAG‘ nucleotide sequence can be found all over, for example at:

CTCCTCGGCGGGCACGTAG

, meaning this post comes very late in the discussion, ever since the first publication describing the presence of this 19-nucleotides string in the SARS-CoV-2 Spike (called Spike2020 in my posts) genome. Then there are articles like: https://healthfeedback.org/claimreview/short-identical-gene-sequence-sars-cov-2-and-gene-sequence-patented-moderna-found-in-other-organisms-not-evidence-virus-engineered-daily-mail/

which says:”Moreover, if we translate the sequence using a tool like ExPASy translate, we notice that the short sequence does not encode for PRRAR in this protein, but rather YVPAE (which is not a furin cleavage site). The translation is from 5' to 3' in frame 1. 5/ pic.twitter.com/ARqQmIY0Yj— Moreno Colaiacovo” <=bioinformatician!?

Moreno, please go to https://web.expasy.org/translate/ and type in the sequence, you will get 6 choices, and the 4th frame shifted 5'3' Frame 3 , encodes the: PRRAR.

Claims, that this genetic insert from the now patented SARS-CoV-2 Spike sequence exists ONLY in one Moderna patent 9,587,003” are NOT true either. That 2017 patent is not the only one having the reverse complementary sequence identical to the one in Spike2020. This nucleotide code section describing the furin insertion site was originally published in the Front. Virol., 21 February 2022 by Balamurali K. Ambati et al.^1 with the title: “MSH3 Homology and Potential Recombination Link to SARS-CoV-2 Furin Cleavage Site.” A simplified explanation of it is at: https://drjessesantiano.com/the-moderna-patented-genetic-sequence-in-sars-cov-2-makes-it-more-infectious/

But the furin cleavage site in Spike2020 was not a new topic, it was proceeded among others, by an article by chinese scientists Li-Meng Yan et al. titled “Unusual Features of the SARS-CoV-2 Genome Suggesting Sophisticated Laboratory Modification Rather Than Natural Evolution and Delineation of Its Probable Synthetic Route“ published in Sep 2020 at: https://www.researchgate.net/publication/344240007_Unusual_Features_of_the_SARS-CoV-2_Genome_Suggesting_Sophisticated_Laboratory_Modification_Rather_Than_Natural_Evolution_and_Delineation_of_Its_Probable_Synthetic_Route

This researchgate article pointed out that the 5’-gcggg-3’ section is actually the so called FauI restriction site (how similar to Fau©I…), embedded in the coding sequence of the ‘PRRAR’ furin site. “The unique FauI restriction-modification system: cloning and comparative analysis of protein structure”^7 describing it in 2003 is in Russian, unfortunately…

In an example section of ~200 nucleotides of the Spike genome these authors showed 2 more cutting sites by other commercial enzymes, implying the cut+paste strategy in the ‘viral research’. The last 3 nucleotides of the insertion, just the ‘TAG’ alone, represents a stop codon, that’s how important every single nucleotide is. For anyone wanting to learn some bioinformatics, one the best first sources describing the origin of SARS-CoV-2, including the furin site was written in Apr 2020, by Juri Deigin at: https://yurideigin.medium.com/lab-made-cov2-genealogy-through-the-lens-of-gain-of-function-research-f96dd7413748

It was astonishing though that Deigin, never mentioned another significant feature of SARS-CoV-2 Spike, the RGD=Arg-Gly-Asp amino acid motif, investigated by yet another A. Deigin, a Prof. from Moscow, many years back. And it was all about blood clotting (bat independent).. There is an entire post about this issue at:

The untold story of Dr. Bret Weinstein, Yuri Deigin and 'RGD' motif in SARS-CoV-2 Spike protein, essential in SYNTHETIC biology

But lets get to the search for that 19-nucleotides piece in todays’ NIH BLAST linked data bases. When you take that nucleotide ‘CTCCTCGGCGGGCACGTAG’ and paste it into the NIH bioinformatics tool at: https://blast.ncbi.nlm.nih.gov/Blast.cgi and enter the search set for using only patented sequences with the ‘megablast’ settings, you will get now 72 patents containing 100% IDENTICAL complementary sequence match. Most of these entries are related to new SYNTHETIC SARS-CoV-2 vaccine compositions, antibodies production, iRNA (complementary s.c. interference sequences, sticking together), detection, prevention, all AFTER 2020, in connection with SARS-CoV-2. There are these not quite SARS-CoV-2 related newer patents for:

1. “Non-integrating HIV-1 comprising mutant RT/IN proteins and the SARS-CoV-2 spike protein” Patent: US 11129890-B1 61 28-SEP-2021 by Vigene Biosciences

2. “USE OF ARGINASE FOR TREATMENT OF CORONAVIRUS INFECTION“Patent: WO 2021202957-A1 4 07-OCT-2021; AEGLEA BIOTHERAPEUTICS INC [US]

3. “Measles virus vaccine expressing SARS-COV-2 protein(s)” Patent: US 11103576-B1 22 31-AUG-2021 < < < NEVER EVER GET ANY OF THOSE, please.

4. “COMPOSITIONS, METHODS AND KITS FOR BIOLOGICAL SAMPLE AND RNA STABILIZATION”. Patent: WO 2021072035-A1 1 15-APR-2021; LIQUID BIOPSY RES LLC [KN], MODLIN IRVIN MARK [US]

And there is this already widely known OLDER 2017 Mod-E-RNA patent for “Modified polynucleotides for the production of oncology-related proteins and peptides“, Patent: US 9587003-B2 11652 07-MAR-2017; ModernaTX, Inc.

AND there are also 4 more, even older ones, all containing 100% IDENTICAL match:

1. “Modified polynucleotides encoding septin-4.” Patent: US 9149506-B2 11652 06-OCT-2015; Moderna Therapeutics, Inc. FILED ON Dec 16, 2013

2. “Modified polynucleotides encoding granulysin.” Patent: US 9216205-B2 11652 22-DEC-2015, Moderna Therapeutics, Inc. FILED ON Dec 16, 2013

3. “Modified polynucleotides encoding apoptosis inducing factor 1.“ Patent: US 9301993-B2 11665 05-APR-2016; Moderna Therapeutics, Inc. FILED ON Dec 16, 2013

4. “Modified polynucleotides encoding SIAH E3 ubiquitin protein ligase 1“ Patent: US 9255129-B2 11652 09-FEB-2016; MODERNA THERAPEUTICS, INC. FILED ON DEC 16, 2013.

The sequences of these 4 by BLAST found matches are: HL457179.1 (in granulysin patent), HL613055.1(SIAH E3 patent), HL240350.1 (septin-4 patent), KH007089.1 (apoptosis inducing factor 1 patent). When translating these nucleotide codes into amino acid code, it appears all 4 entries represent the same protein with the ncbi code KAI4021861.1 and its name is mutS homolog 3 [Homo sapiens] with location at https://www.ncbi.nlm.nih.gov/protein/KAI4021861.1 , the one from the paper ^1, the topic of this post. So when that paper states, quote:”SEQ ID11652 is transcribed to a MSH3 mRNA that appears to be codon optimized for humans.” and that sequence matches with KAI4021861.1 with the title of the first reference for that entry:

TITLE     Assembly and Annotation of an Ashkenazi Human Reference Genome

does that indicate a codon optimization for Ashkenazi Human?? Do I get it right???

The bio-sample of that sequence is named: ‘NIST HG002 NA24385’ and it comes from: Package Human; version 1.0

all can be found at: https://www.ncbi.nlm.nih.gov/biosample/SAMN03283347

The bio-project name for that KAI4021861.1 (mutS homolog 3) entry:

Homo sapiens (human)

Ashkenazi Human Reference Genome

It was submitted with ‘SubmissionRegistration date: 2-Mar-2020’ by
- Johns Hopkins University
- Genome-in-a-Bottle

The Genome-in-a-bottle is a Consortium hosted by NIST (not even NIH!!) with details at: https://www.nist.gov/programs-projects/genome-bottle

At this point one has to go back to Dr. Lee Merritts’ interview at for example: https://rumble.com/v193dl3-dr.-lee-merritt-targeted-dna-harvesting-and-damage-de-population-globalists.html

and start searching for the K26R genotype, which is basically the mutation at the 26th N-terminal amino acid switching Lysine with Arginine in the ACE2 receptor, which makes the above population IMMUNE or less prone to the SARS-CoV-2 infection due to the decreased electrostatic attraction between the Spike and the ACE2 receptor. What is comes down to is, that delivering the Spike/SARS-CoV-2 virus to populations like: East Asian, South Asian, African and African American, European, European and South Asian populations, will make them sick, while the Ashkenazi Jewish population is protected. A scientific article on this topic was published in Biochem Biophys Rep. 2020 Dec; 24: 100798, its title:”ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity” accessible at: https://pubmed.ncbi.nlm.nih.gov/32844124/. That topic was also covered at: https://www.jebms.org/full-text/30 in yet another 2020 article titled:”Effects of Human Genetic Factors (Ethnicity and Race) on Clinical Severity of SARS-CoV-2 (COVID-19” and in the 2021 Nature article at: https://www.nature.com/articles/s42003-021-02030-3 with an article titled:”Human ACE2 receptor polymorphisms and altered susceptibility to SARS-CoV-2”. Strangely, according to great page with lot of details at:

https://www.biblaridion.info/blog/cjd-amyloid-and-k26r/

the Nature paper claims the opposite to what the first 2 papers state, there must be a reason there… The following paper uncovered even more details on the ethnical connection to SARS-CoV-2:”ACE2 and FURIN variants are potential predictors of SARS-CoV-2 outcome: A time to implement precision medicine against COVID-19” at https://www.sciencedirect.com/science/article/pii/S2405844021002383 . That study was done with 1378 participants. These are not the only studies on this topic which now seems hard to combine with ‘BAT viral PREFERENCES’ for specific racial groups. A 2022 review on the entire issue can be found in an article titled “Polymorphisms and mutations of ACE2 and TMPRSS2 genes are associated with COVID-19: a systematic review“ at: https://eurjmedres.biomedcentral.com/articles/10.1186/s40001-022-00647-6 .

Usually wouldn’t cite this page, but one can learn something there too: https://geneticliteracyproject.org/2021/11/09/a-lucky-segment-of-the-population-is-genetically-immune-from-the-covid-virus-what-can-we-learn-from-them/

Last but not least, a K26R mutation with a special Lys26 seems to be not only in SARS-COV-2, reports on other unrelated viruses pop up, for example:

- “NS5A-ISGylation via Lysine 26 Has a Critical Role for Efficient Propagation of Hepatitis C Virus Genotype 2a” https://www.med.kobe-u.ac.jp/journal/contents/67/E38.pdf

-”Biochemical and HIV-1 coreceptor properties of K26R, a new CCR5 Variant in China's Sichuan population” J Acquir Immune Defic Syndr. 2005 May 1;39(1):38-43. at https://pubmed.ncbi.nlm.nih.gov/15851912/

According to Dr. Merritt, the BioNTech CEO Dr. Ugur Sahin who DESIGNED the Pfizer genetic sequence of the Spike delivered exactly around the same time, is possibly associated with the Kazharian Empire. Delivering a sequence which is targeting ONLY specific populations, across the entire world, while knowing that fact, can be called a premeditated MASS murder. Stew Peters covering sometimes controversial topics, also presented it at: https://forbiddenknowledgetv.net/horrifying-russian-report-ukrainian-biolabs-creating-special-bioweapons-for-ethnic-cleansing/

linking that work to apparently the ukrainian countless biolabs.

Also isn’t it strange that the human version 1.0, is in series of Mod-E-RNA patents which use the services of the Silicon Valley Company called DNA2.0, ‘designing’ their genetic sequences, according to their patents?

So why one and the same protein mutS homolog 3 is described by 4 different names each representing identical string of nucleotides? Intentional confusion? So if 4 different patents for 4 different proteins, whose sequence ID’s are not even mentioned in these patents, are ‘somehow’ connected to the same mutS homolog 3, what is this all about? Maybe the function of all 5 of them for ‘future explorations’?

Septin-4 description at https://www.uniprot.org/uniprotkb/O43236/entry , indicates it has countless functions as a filament-forming cytoskeletal GTPase, it plays an important role in male fertility and sperm motility, it is involved in the migration of cortical neurons and the formation of neuron leading processes during embryonic development, it is required for dopaminergic metabolism in presynaptic autoreceptors and as its name states, it is required for the induction of cell death mediated by TGF-beta.

Granulysin with description at https://www.uniprot.org/uniprotkb/P22749/entry indicates it is an antimicrobial protein that kills intracellular pathogens. As always in macromolecular biology the confusion needs to grow, there is another name for it too: T-cell activation protein 519, it participates in a cellular defense response, like killing Mycobacterium tuberculosis.

Apoptosis inducing factor 1 (https://www.uniprot.org/uniprotkb/O95831/entry) from the oldest patent is a NADH oxidoreductase and as regulator of apoptosis, again with countless essential cellular functions.

SIAH E3 ubiquitin protein ligase 1, with the mouthful name ‘‘Seven in absentia homolog 1A’ mediates ubiquitination and degradation of group 1 metabotropic glutamate receptors. It is a ‘developmental’ protein with its role in Apoptosis, Cell cycle, Differentiation, Spermatogenesis and amyloid fibril formation, among others.

From : https://atlasgeneticsoncology.org/gene/457/siah1-(siah-e3-ubiquitin-protein-ligase-1) , quote: Siah1 is the mammalian homolog of Drosophia seven in absentia (SINA) protein (Carthew and Rubin, 1990), required for the correct development of R7 photoreceptor cells in the Drosophila eye (opsin family→previous OPTOGENETICS posts).

A quote from 2018 publication^4 : ”Seven in absentia (SINA) protein is one subgroup of ubiquitin ligases possessing an N-terminal cysteine-rich really interesting new gene (RING) domain, two zinc-finger motifs, and a C-terminal domain responsible for substrate-binding and dimerization.” and from another one^5: ”Seven-in-absentia homolog (SIAH) proteins are evolutionary conserved RING type E3 ubiquitin ligases responsible for the degradation of key molecules regulating DNA damage response, hypoxic adaptation, apoptosis, angiogenesis, and cell proliferation.”

NIH has now a genetic testing for SIAH1 siah E3: https://www.ncbi.nlm.nih.gov/gtr/genes/6477/

The publication about ubiquitin at https://pubmed.ncbi.nlm.nih.gov/35006464/ says, quote:

“Ubiquitin is a 76-amino acid polypeptide (Figure 2). Within vertebrates and higher plants, the amino acid sequence is absolutely conserved and the differences between animal, plant, and fungal ubiquitins are two or three residues (Callis and Vierstra, 1989).“=>meaning, the metabolic labeling for the DEGRADATION across the board is performed by among others, the very same ubiquitin, for many species..

When you want to digest anything, it has to be labelled first (bound to) by ubiquitin, on a molecular level. And now try to find the sequence of 76 aa’s long ubiquitin on uniprot, it is not there, at least not among the first 10 hits…That’s the most deceptive of all scientific discipline, it is called ‘molecular biology’ with many names for one and the same object.. Lets try at PdbDataBank, great, that’s the one at https://www.rcsb.org/fasta/entry/1UBQ/display with the sequence:

MQIFVKTLTGKTITLEVEPSDTIENVKAKIQDKEGIPPDQQRLIFAGKQLEDGRTLSDYNIQKESTLHLVLRLRGG

There are SEVEN ly-sin-es in it. Look how proteins are chopped down by one of the most important digestive enzymes in human body, tryp-sin (https://unipept.ugent.be/clidocs/casestudies/tpa ):

The cuts are always at the positively charged amino acids, ly-sin-es and arginines. It is because most if not all digestive enzymes have the so called charge-relay system of 2 or 3 electrostatically charged amino acids participating in the cuttings. Anyone who ever worked in the filed of protein crystallography knows, that PEG molecules (no matter what their molecular weight) preferentially bind to Ly-SIN-es exposed on surfaces. That’s why lot of those people in that field avoid PEGs in food, cosmetics in the first place! When the ly-sin-es on any to be digested protein are not 3D-accessible, because they are ‘covered’ with PEG’s, you can’t be ‘digested’ properly, literally. Look at the mirror and the bathroom balance, the weight numbers speak for themselves. That’s why some say: ’you are what you eat’ and some ‘you are what you digest’ and the truth is, both are essential, and depend very much on our FOOD. That’s why some of the cancer protocols, like the one from Dr. Matthias Rath in Germany: https://www.drrathresearch.org/research/projects/cancer include plain lysine powder as an essential nutrient, supplement which in my opinion, helps on many levels. One of them would be to divert the synthetic PEG’s in ones body away from the proteins which need to be properly digested and have the ‘stucked’ lysines on protein surfaces freed again.

A publication “SIAH ubiquitin E3 ligases as modulators of inflammatory gene expression”^5 points to the fact that these proteins control how many proinflammatory genes are expressed at a given time.

What is very concerning is, when you check if the above 1UBQ ubiquitin sequence is patented, you see a name like this:

Title: Compositions and methods for control of insect infestations in plants
JOURNAL Patent: US 9238822-B2 23382 19-JAN-2016;
        Monsanto Technology LLC; St. Louis, MO

who basically added the string: "liep slrilamkyn cekmicrkcy arlhpratnc rkkkcghtnn lrpkkklk” to the end of ubiquitin, a piece which reminds me of that extensive positively charged strings from HIV-1 tat protein:”ISYGRKKRRQRRRAHQNS'“. Or the next patent from the next GMO-food producing giant:

TITLE     Ribosomal protein L40 (RPL40) nucleic acid molecules that confer resistance to coleopteran and hemipteran pests
  JOURNAL   Patent: US 10329581-B2 90 25-JUN-2019;
            Dow AgroSciences LLC; Indianapolis, IN

this time with added: “viep tlkilaqkyn cdkmicrkcy arlhpratnc rkkkcghtnn irpkkklk“.

How the by Monsanto and Dow to ubiquitin added sequences align? Almost entirely, without using BLAST..:

liep slrilamkyn cekmicrkcy arlhpratnc rkkkcghtnn lrpkkklk MONSANTO
viep tlkilaqkyn cdkmicrkcy arlhpratnc rkkkcghtnn irpkkklk   DOW

5 amino acids difference, every one of them equivalent, i.e identical with their functional properties.. Just speculating, without a check, different chemicals will attach the same way to each of those sequences… Looks like it is all about our FOOD! Aligned by HAND piece of HIV-1 TAT protein with that C-terminal portion of Monsanto/Dow patented ‘proteins’ (arginine is equivalent with lysine):

  ISYGRKKR-------RQRRRAHQNS  >>> HIV-1 Tat protein
   +  RKK+       R +++ +     >>>> IDENTITIES
PRATNCRKKKCGHTNNLRPKKKLK     >>> Monsanto patent

Monsanto, today Bayer, the very same from Nuernberg processes in WWII, the cancer of humanity, in addition to IG Farben, all with finances from Rockefeller at al.…

Don’t know, but it looks like one needs to investigate patent offices, here another one from Owners: Astrazeneca Uk Limited , Syngenta Limited

TITLE     Human E3 ubiquitin protein ligase
JOURNAL   Patent: US 5976849-A 8 02-NOV-1999;

with the abstract, which tells it all: “A novel human E3 ubiquitin protein ligase is provided as well as a nucleic acid structural region which encodes the polypeptide and the amino acid residue sequence of the human biomolecule. Methods are provided to identify compounds that modulate the biological activity of the molecule and hence regulate cellular and tissue physiology.“

So if the goal of Mod-E-RNA was to ENCODE essential proteins responsible for degradation, cell death, regeneration and defense, by some modified polynucleotides from all their 4 oldest patents, so how now the Spike2020 encoded in the genetic material of all covid injections, could affect all this? Well, the modified Spike genome sequences in Pfizer/Mod-E-RNA ‘covid vaccines’ deliver already the M-methylpseudouridine in billions of bodies, and nobody really knows for how long.

How about REMDESIVIR^6, the 1'-cyano-substituted adenosine nucleotide analogue (strangely produced by Pfizer and send out to Gilead to put the label on it*)??

Here few citations from the septin-4 2015 Mod-E-RNA patent https://patents.google.com/patent/US9149506B2/en containing the ‘cyano’ keyword:

-optionally substituted amino acid, cyano, amidine, optionally substituted aminoalkyl,

-In some embodiments, the modified nucleobase is a modified guanine,…7-cyano-7-deaza-guanosine (preQ0)

-The term “cyano,” as used herein, represents an —CN group….,

- TABLE 177 titled ‘Pseudouridine and N1-methyl-pseudouridine SAR’ one finds: 6-Cyano-pseudo-UTP,.. ,1-Methyl-6-cyano-pseudo-UTP

and here some containing the ‘adenosine’ keyword:

-1-methyladenosine, N6-methyladenosine, N6-isopentenyladenosine,

-all pictures BB-162 - to BB-200 contain examples of a CHEMICAL SLURRY of REPLACEMENTS for HUMAN nucleotides, our GENETIC material!

With one word, Pfizer/Modern covid injections are not only about genetic reprogramming of the HUMAN BODY reusing our own current ‘body parts’, it is also about the replacement of the ORIGINAL HUMAN genetic material with completely new substances, delivered by the covid injections, and possibly all other drugs, pesticides, never being able to get excereted or digested. Do we need to even wonder about the new Materials Genome Initiative at NIST (again) https://www.nist.gov/mgi ???

In 2016 Moderna’s Chief Executive Officer, Stéphane Bancel announced a transition to a ”clinical stage company”, Therapeutics→TX, during a presentation at the J.P. Morgan 34th Annual Healthcare Conference in San Francisco^1! => mon-ey drives it all.

If the 100% identity of the SARS-CoV-2 Spike to the reverse complement of the MSH3 mRNA, described in the first cited here paper, is highly unusual and linked to cancers, then it also looks like there is a connection to a re-DESIGN of the entire human body, via synthetic nucleotides, representing the new bio-logical matter, described in hundreds of pages of ModERNA patents alone. That’s why the name of the silicon valley company DNA2.0 which designed the Spike genes, now floating in billions of clueless victims, into the new age of humanity 2.0.

Are the news like these preparing us all for what is coming?

-”CRISPR cancer trial success paves the way for personalized treatments” Most complicated therapy ever’ tailors bespoke, genome-edited immune cells to attack tumours.” https://www.nature.com/articles/d41586-022-03676-7

-”CRISPR Screens Identify Potential Host Targets to Reverse HIV-1 Latency” https://www.genomeweb.com/gene-editing-gene-silencing-crispr/crispr-screens-identify-potential-host-targets-reverse-hiv-1

-”Enzyme treatment given directly to fetus prevents symptoms of rare genetic disease” First of its kind in utero therapy could treat other genetic disorders https://www.science.org/content/article/enzyme-treatment-given-directly-fetus-prevents-symptoms-rare-genetic-disease

-”Precision Oncology Dx Firm Navignostics Raises CHF 7.5 M in Seed Funding From Bruker, Others” https://www.genomeweb.com/cancer/precision-oncology-dx-firm-navignostics-raises-chf-75-m-seed-funding-bruker-others

-”Number of Appendiceal Cancer Patients Harbor Cancer Predisposition Gene Variants” Nov 15, 2022 on genomeweb.com with a quote:”A portion of appendiceal cancer patients harbor germline cancer predisposition variants, suggesting that patients presenting with the disease should undergo testing for hereditary cancer, a study appearing in JAMA Oncology says.”

-”Germline Testing of Colorectal Cancer Patients Uncovers High Rate of Clinically Actionable Genetic Variants” Nov 15, 2022 on genomeweb.com with a quote: ”Expanding germline multigene panel testing to a broader group of colorectal cancer (CRC) patients could uncover additional individuals with clinically actionable genetic variants, a new study in JCO Precision Oncology has found.”

and more similar ‘solutions’ to current situation caused by the experimental covid gene modification injections, given to billions who got scared or were coerced only in order to keep their financial support for themselves and their families. This above list will be updated DAILY in order to see what the pharma/science drug cartels are reporting on…

Now on the topic touched in the updates at the begin of this post.

The newest co-written by a NIAID paper^8 summarizing the SARS-CoV-2 Spike ‘new features’ says, quote: “While the S protein is an attractive target for therapeutic development [12], the lack of comprehensive information on S protein expression and subcellular translocation hinders the identification of an effective S protein-targeting therapeutic to combat SARS-CoV-2 infection.“ ???? Did Fauci see it?? After ‘Safe and effective infection prevention’ by injecting SPike genome in billions now they start looking into details??? At the very begin the authors say:”The recently emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2…” Almost 3 YEARS is the definition of ‘recently’?? The insanity starts to grow.. Then they say:”translocation of the SARS-CoV-2 S mRNA appeared to be assisted by the S protein which contains an NLS motif that is unique among human pathogenic beta-coronaviruses” and then also “The novel NLS motif “PRRARSV”. And this is THE END, I’d say.

First, millions of researchers saw the furin site, know its sequence in their dreams, and first now ‘they’ say, oh, it will go to the nucleus??

Second, when, ever, the Spike on the viral surface binds to its own properly CUT internal portion from the entire viral genome, binds to this own genetic code and travels with it straight to the nucleus in order to do what? Combine with human genome??? It smells like a try of preparing everyone who had ‘covid19’, including the injection victims, for the bad news. The Spike is now in your genome… Except, NO REAL VIRAL SPIKE during infection ever binds to its own precut genome, released later in process, in order to change the host genome intentionally! Unless it is SARS-CoV-2??? Where did it come from actually? Quote:”SARS-CoV-2 (USA/WA-CDC-WA1/2020 isolate, GenBank accession no. MN985325; kindly provided by CDC)”. Hmmmmm…

But there is some hope, at the end. Here they say:”Although the primer-probe was designed to target S mRNA, the SARS-CoV-2 positive-strand RNA genome (whole or partial) can be targeted by the same probe due to the sequence similarity between S mRNA and the whole or partial genome. Thus, our results lack sufficient detail contributing to the discussion of the controversial scientific topic of whether there is any possibility of SARS-CoV-2 genome integration into the host DNA [47, 48]”

Pity, the experiment was done ONLY with airway epithelium, while ‘covid victims’ or better covid injection victims are dying of heart/blood related issues, nobody wants to talk about..

Literature.

1. https://www.frontiersin.org/articles/10.3389/fviro.2022.884169/full

2. https://investors.modernatx.com/news/news-details/2016/Moderna-Therapeutics-Announces-Transition-to-a-Clinical-Stage-Company-Provides-Business-Update-and-Outlines-2016-Strategic-Priorities/default.aspx

3. “Seven in absentia homolog 1A mediates ubiquitination and degradation of group 1 metabotropic glutamate receptors” https://www.pnas.org/doi/10.1073/pnas.0403042101

4. Wenjie Wang et al. “Functional analysis of the seven in absentia ubiquitin ligase family in tomato“ Plant Cell Environ. 2018 Mar;41(3):689-703. https://pubmed.ncbi.nlm.nih.gov/29320607/

5. M Gordian Adam et al. “SIAH ubiquitin ligases regulate breast cancer cell migration and invasion independent of the oxygen status“ Cell Cycle 2015;14(23):3734-47. https://pubmed.ncbi.nlm.nih.gov/26654769/

6. Egor P Tchesnokov et al. “Mechanism of Inhibition of Ebola Virus RNA-Dependent RNA Polymerase by Remdesivir” Viruses 2019 Apr 4;11(4):326. https://pubmed.ncbi.nlm.nih.gov/30987343/

7. M A Abdurashitov et al. “The unique FauI restriction-modification system: cloning and comparative analysis of protein structure“ Mol Biol (Mosk) 2003 Jul-Aug;37(4):619-24. https://pubmed.ncbi.nlm.nih.gov/12942634/

8. https://www.biorxiv.org/content/10.1101/2022.09.27.509633v1.full.pdf

   *https://rumble.com/v1rumnm-melissa-mcatee-pfizer-whistleblower-the-mark-of-the-beast.html

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   NIH confirms SARS-2 mRNA and S protein translocate to cell nucleus