Mod-E-RNA's FOIA file drop and the next synthetic mod mRNA relaxin gene-based 'rescue' for the damaged human hearts, and pregnancies.
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:
and the most recent post from Dr. Makis:
Adding this interview of a victimized nurse after 3 Mod_E_RNA shots:
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:
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+ <<IDENTITIES!!
Sbjct 1 PKKKRKV 7 NLS from SV40
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 <IDENTITIES
Sbjct CASYQTQTNSPR-RARSVASQSIIAY SPIKE YP_009724390.1
******** <= PABPN1-binding in H1N1
Query 209 NGR---PP-LTPKQKREM-AGTIRSEV 230 NS1 Influenza H1N1 PABPN1
NG PP LT EM A + S +
Sbjct 856 NGLTVLPPLLT----DEMIAQYT-SALLAGTITSGWTF Spike SARS-CoV-2
Query 207 NEDGRPPLPPKQKRKM-ARTIESEV 230 NS1 Influenza H5N1 PABPN1
N LPP M A S +
Sbjct 856 NGL--TVLPPLLTDEMIAQYT-SALLAGTITSGWTF Spike SARS-CoV-2
********** <= IFDRLETLIL (NES signal)
Query 130 LKANF----SVIFDRLETLIL 146 H1N1 NS1 nuclear export signal
L +NF SV+ D L L
Sbjct 966 LSSNFGAISSVLNDILSRLDK 986 2020 Spike
********** <nuclear export
Query 132 ANFSVIFDRLETLILLRAFTEEGAI-VGEISPLPSLP 167 1918 H1N1 NS1
N +F ++ + + G +I P PS P
Sbjct 776 KNTQEVFAQVKQIYKTPPIKDFGGFNFSQILPDPSKP 812 2020 Spike
* **** <= 'DRLRR' nuclear localization
Query 17 HVRKRFADQELGDAPFLD-RLRRDQKS 42 1918 H1N1 NS1
V + + + + PFL +++ KS
Sbjct 125 NVVIKVCEFQFCNDPFLGVYYHKNNKS 151 2020 Spike
or the same above 1918 NSL with with different Spike section, its furin site:
***** <= nuclear localization (import)
Query 17 HVRKRFADQELGDAPFLDRLRRDQKS 42 1918 H1N1 NS1
+ + Q +P R R S
C-ASYQTQTN--SP---RRARSVASQS <<2020 SPike furin site
Influenza HOSTS:
H1N1 birds, human, pigs
H5N1 birds, cats, human, pigs
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:
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:
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 (
) 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:
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 V1A (AVPR1a), V1B (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, V1A, V1B and V2 receptors. * marks residues that are conserved among all the receptors. # marks residues that are conserved among OT, V1A and V1B 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; V1A, V1B 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.
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Erythema Multiforme as a result of shedding from exposure to individuals that took the shots occurs, as well as in individuals that have taken the shots. It's anecdotal as far as I know, no one is studying it (not enough funding or too institutionally embarrassing🤨🤦♀️😉), but deeply concerning.
Re the oxytocin/relaxin interference- deeply, deeply concerning as disturbance here, destroys any chance of maternal/neonate connections and psychological relationship- but that aside, physically doesn't this create a potential change to how humans reproduce- "human eggs" if you will. Unable to be traditionally carried internally, but instead incubated externally. Certainly inline with the new biobaby incubation technology currently developing, due for release well before 2050, when it becomes the norm.🤔🤔😐😐😐😤🤐🤦♀️🤦♀️🤦♀️🤦♀️🤦♀️
💝happy giving thanks day to you💝