mRNA Vaccines that Breach the Nucleus and Change the Genome – What are the Chances?

Ask yourself a simple question. Why should the very first examples of mRNA vaccines for humans violate the most important safety standard of the mRNA platform? Why would the vaccines do exactly what they PROMISED US the vaccines would not do?


TL;DR –

They didn’t just lie to us about the spike mRNA not going into the nucleus and not changing human DNA – the whole purpose was very likely to do exactly what they did – to open the cell nucleus and keep it open, so that we as a species can start changing population genomics in a huge way, using a variety of technologies.


The central dogma of molecular biology. They shilled the blue arrows to the masses as lies about safety, while hiding the special red arrow and actually working to open it up for business.


Show-Time (Introduction)

I have finally realized that I need to spell out, in as many ways as needed, what is really going on with SARS-CoV-2 and these derived mRNA vaccines.

I had hoped that people would see the implications of the science which is now open to us, with the publication of first the Jaenish paper, then the De Marinis paper, and finally the Mehedi paper. I have commented extensively on each one of these papers, including very recently on the Mehedi paper, which really makes things obvious. I had thought that somebody more notable than me would try to make the point I am about to make. Sadly, nobody has, so it looks like I’m going to have to do it.

These vaccines are designed to BEGIN to change us on a fundamental level which is not exactly the same as the “transhumanism” that constitutes most of the “clickbait” against the vaccines. It’s similar, but it’s not the same. What we see in the clickbait is a distraction from the actual danger, which is not strange and distant and unbelievable, but is in fact right here, and right now, and very believable, once you understand it.

The truth is a lot more like GATTACA, and a lot less like Transcendence.

It’s already starting, and the infrastructure is being set up. The first step has actually been accomplished, and it was in many ways a HUGE success.

Humans ARE being engineered right in front of our eyes. I hope that you can see this point by the end of this article.

They (meaning WEF and its backers) hacked the human cell nucleus on a population genome level. They created a “Trojan” virus that appears to have “zero-dayed” the human cell nucleus. Artfully, the hack is a lot like state-level “APT” (advanced persistent threat) computer hacks, in that it gets in and holds the door open. Of course, better models can be created, but the self-replicating crowbar for the cell nucleus has obviously arrived, and its imperial version of SPQR is PRRARSV.

THAT is the fundamental advance that was achieved here.

I have to say, it was ingenious and “admirable”, in several senses – scientific, military, and criminal. Of course, your mileage may vary on “admirable”. Many will consider it “diabolical”.

What we are facing is the immediate REAL danger of biological engineering and eugenics, which was employed in a fantasy way, as a technical MacGuffin, in various episodes and productions in the Star Trek universe.

This is a scene from Star Trek II: The Wrath of Khan. These two people are “superhumans” who (according to the story) proved to be disastrous for Earth, during our current century (more or less). The one on the right is “Khan” – obviously in homage to Genghis Khan and his relatives, who ruled much of Asia for centuries.

Don’t get lost in the fantasy stuff. THAT is not the big danger. Stick around for an explanation of the reality which is actually upon us.

Here is how Wikipedia describes Khan, but more importantly, where he CAME FROM.


Khan Noonien Singh is a fictional character in the Star Trek science fiction franchise, who first appeared as the main antagonist in the Star Trek: The Original Series episode “Space Seed” (1967), and was portrayed by Ricardo Montalbán, who reprised his role in the 1982 film Star Trek II: The Wrath of Khan. In the 2013 film Star Trek Into Darkness, he is portrayed by Benedict Cumberbatch.

Khan had controlled more than a quarter of the Earth during the Eugenics Wars of the 1990s.[1] After being revived from suspended animation in 2267 by the crew of the Starship Enterprise, Khan attempts to capture the starship but is thwarted by James T. Kirk and exiled to Ceti Alpha V, where he has the chance to create a new society with his people. In Star Trek II: The Wrath of Khan, set fifteen years after “Space Seed”, Khan escapes his exile and sets out to exact revenge upon Kirk.

In Star Trek Into Darkness, set in the alternate continuity established in Star Trek (2009), Khan is awakened almost a decade before the events of “Space Seed“. Khan is given the false identity John Harrison and coerced by Admiral Marcus into building weapons for Section 31 and Starfleet in exchange for the lives of Khan’s crew. He ultimately rebels and comes into conflict with the crew of Enterprise.


OK – so what are the “Eugenics Wars”?

Back to Wikipedia…..


When the original series of Star Trek was produced, the 1990s were several decades away, and so various elements of the backstory to Star Trek are set in that era, particularly the Eugenics Wars. The references to the Eugenics Wars and to a nuclear war in the 21st century are somewhat contradictory.

The episode “Space Seed” establishes the Eugenics Wars, and has them lasting from 1992 to 1996. The Eugenics Wars are described as a global conflict in which the progeny of a human genetic engineering project, most notably Khan Noonien Singh, established themselves as supermen and attempted world domination. Spock calls them “the last of your so-called World Wars”, and McCoy identifies this with the Eugenics Wars.


OK – don’t get me wrong. I’m not saying it’s EXACTLY like Star Trek, although I do subscribe to the folk notion that Star Trek is a VERY good predictor of things that are likely to happen.

What I AM saying is that genetic engineering of humanity has already started, and now I’m going to explain why this is so.

We will take a brief tour into the PAST, before we return to the future. If a light bulb comes on, keep it lit!


You cannot uninvent the genetic Tommy-gun, nor the gun moll who knows how to code.

Bonnie & Clyde of the Nucleus

BANKS make a really great analogy of the cell nucleus.

  • they’re common and everywhere
  • they contain valuable stuff that needs to be protected yet dispersed
  • they have high security
  • things need to traffic securely in and out of them

Breaking into a bank with very high security is a lot like what the spike protein does. But the spike protein doesn’t do it alone. THAT is an important point from the three papers I keep mentioning. The spike protein has a PARTNER who has all the plans.

OK – just for the record – this is going to deviate a little bit from the ACTUAL story of Bonnie and Clyde. Just warning you – it will get weird.

The spike protein and the spike protein mRNA are a PAIR, and together, they are able to not only break into the bank, but to totally take it over, and keep it taken over. And then to take over more banks.

Here is how it works.

The spike protein is Clyde. He’s got a gun, and he causes all kinds of trouble with it. He’s the “action” guy. He knows how to break into banks, mostly because he has a phony ID that always gets him in. The phony ID says PRRARSV in big letters on it, which makes all the bank guards at Cell Nucleus Bank and Trust say “Why, welcome, Mr. Barrow! We’re pleased to see you at the bank today! Come right on in!”

Or, to use a different analogy…..

These bank guards are such chumps, but it works every time.

Well, here is the problem for the bank. When Clyde goes in, he always brings his partner Bonnie. And SHE is trouble. She’s not so good with a gun or a fake ID, but she is a real scam artist, who knows how to get into the bank and embezzle the hell out of it.

Bonnie gets into the cell nucleus bank, and with some help from Clyde, she gets a permanent job there. Bonnie and Clyde are set for life. None of this “grab the cash, run out, get caught, and die in a hail of bullets” shit. No sir! THIS Bonnie and Clyde are smart.

Bonnie trains many of the new girls at the bank – and like the pod people in “Invasion of the Body Snatchers”, she turns every last one of them into exact copies of HERSELF. NASTY! So all these fresh Bonnies are trained by the bank and sent out to get into new banks.

But wait! Bonnie can’t get into banks. Bonnie doesn’t have a gun or a fake ID! How can she get into more banks?

Easy! Bonnie and all her Bonnie clones have the power of multiplication – not just to make more copies of each one herself, but to make more Clydes. Bonnie makes more copies of herself while she’s IN the bank, and she makes copies of Clyde while she’s OUT of the bank.

So every Bonnie that leaves the bank, creates hundreds of new Clydes on the outside. The next time Bonnie wanders near a bank, there are bound to be dozens of Clydes just hanging around, ready to escort her, and maybe even other gals [important], into the bank. If no Bonnie is already working there, she gets a job, and the process starts over.

The KEY POINT is that BONNIE makes the CLYDES who can get her, or women like her, into the next bank.

Bonnie can’t get into the bank, and Clyde can’t get a job in the bank, but together, they can make a living by embezzling banks.

Side Note: This is a beautiful example of a contradiction in the Marxist sense. Proteins and nucleic acids can’t do certain things alone, and thus NEED EACH OTHER.

Once Bonnie is on the payroll, this fact introduces a permanent security problem in the bank, and for all other banks.

And why is that?

Once Bonnie is on the payroll, you can’t get rid of her.

She will just create more Bonnies and more Clydes, and they will scam more banks.

In terms of banks, banks can resist just Clyde or just Bonnie, but they can’t resist the pair.

In terms of the cell nucleus, it can resist the spike protein or the spike mRNA, but it cannot resist both of them together.

Which pair, oddly, is exactly what the vaccines create.

WHAT ARE THE CHANCES?


We can use other analogies, using banks, which emphasize the spike protein more.

Imagine a bank that was convinced to crank out KEYS TO THE BANK, and to send out these keys. Imagine thousands of keys to the bank being sent out by the bank into the community, perhaps in a really stupid PR stunt.

God knows WHO is going to get into the bank now.

God knows WHAT is going to get into the genome now.

Are you starting to see what they did?


Fact Checking the Fact Checkers on DNA Change

The absolute best way for me to convince you that they really said these vaccines could not do what they are now proven to be doing, is to simply play back the words of the “fact checkers”.

See if you can spot how many LIES are told in this video.

If you’re not spotting the lies, read THIS ARTICLE.

AND – by the way – this video is a GREAT explanation of the way things NORMALLY work. It’s totally out to lunch on the way things ACTUALLY work.

Did you spot the lies? Tell me what you found in the comments.

This video is not alone – there are HUNDREDS OF THEM.

There are also hundreds if not thousands of articles of a similar nature. I’m just going to pick one of them – the one that happened to have the graphic I used above. That article is dated from MARCH of 2021 – right when the authorities were hard-selling the “vaccines”.


mRNA Covid-19 vaccines: Facts vs Fiction

MARCH 10, 2021

By: Maria Elisa Almeida Goes
Editing: Offspring Magazine Editorial Team
Images: Nina Lautenschläger.

LINK: https://www.phdnet.mpg.de/offspring/Covid-19_vaccines

ARCHIVE: https://archive.fo/irZec


Interestingly, this archive was made only 5 months ago. It was very likely archived by Wikipedia or somebody else who is shilling the false explanation, when faced with the emerging science showing nuclear translocation and genomic incorporation. But it’s perfect for me to preserve evidence.

As an aside, I find it terribly sad that this particular lover of “Max Planck” era scientific history, lived to see one of Planck’s namesake organizations lying about science on a grand scale, but yet here we are.

Let me just pull out the most relevant section. I was planning on highlighting ALL of the lies, fibs, evasions, etc., but there are so many, I decided to only highlight or [comment on] the most horrible and ironic.


mRNA vaccines will not alter your DNA, this is why:

Concerns about the effects mRNA vaccines over the integrity of our DNA also exist. Thankfully, you do not need to worry about this. Such an event would challenge everything scientists know about basic cell biology, and is so improbable, that one can actually call it impossible.

The main reason for that is that, besides being chemically and structurally different from DNA, mRNA is located in a different cellular compartment. While DNA is enclosed in the nucleus, mRNA is produced in the nucleus, but is quickly exported to the cytoplasm with a one-way ticket: it does not come back. In fact, only specific proteins carrying “nuclear localization signals” are able to migrate from the cytoplasm into the nucleus, and mRNA vaccines definitely do not include such molecular instruction. Thus, because mRNA cannot spontaneously be trafficked to the nucleus, it cannot modify your DNA sequence.  Additionally, the RNA molecule is charged and carries the same charge as the nucleus, so as our 6th grade physics taught us, like charges repel, and hence the RNA molecule is physically repelled by the nucleus. [Note added by Wolf – WHAT THE HELL???]

One might also argue [HA! You TOADS! Yes, one “might”!] that there are mechanisms through which RNA can be integrated into the genome – HIV viruses being the classic example. The key differences here are that such viruses (1) express special enzymes which are able to code DNA back into RNA and (2) can associate with proteins that can traffic them into the nucleus. Neither scenario is applicable to the mRNA vaccines. [OH, THE IRONY]

For the same reasons, mRNA vaccines cannot affect your unborn children. This would require genomic mutations [oh, really!] in the reproductive cells – sperm and egg – since only these could potentially be transmitted to the next generation. [AND???!!!]

Speaking of children, you might have heard that Covid-19 vaccines would cause infertility in women [why don’t you just stop there, and not go on to one bad hypothesis?] because antibodies against the spike protein could mistakenly attack placenta cells, due to an alleged similarity with a placental protein called syncytin-1. There is no scientific evidence supporting this claim – and, in fact, the two proteins are barely similar, sharing only 4 sequential amino acids out of 538. [This did seem to be a bit of a miss. Nevertheless, what new hypothesis explains all the pregnancy problems?]

Still, you might want to ask why pregnant women are excluded from the vaccination campaigns [wait a minute….not in the US], and why, during clinical trials, women are asked to use contraceptive methods that will avoid pregnancy [because there might be a problem?]. Again, this is not a red flag. Any clinical trial for a potential vaccine or drug will exclude children, pregnant women, old people and people with specific underlying conditions. Initially, trials are designed to obtain major insights whether the developed pharmaceutical product works at all, in healthy adults. Once safety and efficacy are determined [read what you just said before that, where you excluded safety as a motive], tests are expanded to smaller groups that at first were set aside. Excluding pregnant women from trials only shows that trials are being done systematically and following standard protocols. [I’m sorry, but this sounds like happy horseshit, lady.]


Let’s concentrate on the lies most relevant to this discussion. I’ll isolate them and respond to each one.


In fact, only specific proteins carrying “nuclear localization signals” are able to migrate from the cytoplasm into the nucleus, and mRNA vaccines definitely do not include such molecular instruction.

This is EXACTLY what was found with the spike protein that was produced by the full spike mRNA. What a coincidence! See De Marinis for proof that it happens, and Mehedi for WHY. OH – because there’s a nuclear location signal! Was it a “known” one, and if so, who knew it and who didn’t? If some people knew, and others didn’t, wouldn’t that make it like a “zero day” on the nucleus?

Thus, because mRNA cannot spontaneously be trafficked to the nucleus, it cannot modify your DNA sequence.

OH! But isn’t that SO STRANGE that the Mehedi work shows that the spike protein LITERALLY “traffics” the spike protein mRNA into the nucleus? WELL AHHHHH’LLLLL BE! So maybe this explains the nuclear DNA modification that is seen in the De Marinis results. Yes? Maybe? Come on, girl – you’re a scientist at a prestigious institute. Put on your big girl pants and hypothesize with me! You can do it! This is undergraduate, “smart-alec guy in the back of introductory class raises his hand” stuff! And when you were in that class, you thought the same sorts of things but didn’t raise your hand. Maybe it’s time to be brave!

One might also argue that there are mechanisms through which RNA can be integrated into the genome – HIV viruses being the classic example.

This should have been your really big hint, girl. Our local accountant named cthulhu realized that Fauci’s HIV interests and his bat virus interests had remarkable similarities, both in what he himself did, and in what he was studying. “This isn’t Fauci’s first rodeo.” Ask yourself – why was Fauci interested in this? Could it have been the same reason that Doudna was so interested in CRISPR-Cas9? The desire for WRITE PERMISSIONS on the genome?

The key differences here are that such viruses (1) express special enzymes which are able to code DNA back into RNA and (2) can associate with proteins that can traffic them into the nucleus. Neither scenario is applicable to the mRNA vaccines.

Thank you, my lying lady. You have just provided me with a huge clue, by the process of “liar subtraction” – a form of deductive reasoning. We know from De Marinis that genomic incorporation and modification is a fact. We know from Mehedi that “nuclear trafficking” (your point 2) is a fact. This means that it is almost certain that the spike protein ALSO acts as a promoter of reverse transcription (your point 1). You said it – not me. That sure seems convenient, doesn’t it? My question is now – DID YOU KNOW THIS? Were you part of the plot? Or was the person who reminded you of these things part of the plot? Or were we all part of the plot, when I, too, mindlessly parroted the “central dogma” as a defense of mRNA vaccines?

I’m willing to confess that I was wrong. I will admit to my part in promoting the conspiracy. Will you?


But their defenses get worse.

There are now MSM “fact checks” which specifically try to walk back the implications of both the Jaenisch and De Marinis papers, and you can bet there will be similar fact checks on Mehedi’s paper. There has likewise been pressure on those authors to DOWNPLAY the significance of their own works. To me, this is the height of bullshit.


Jaenisch Paper Downplay

Fact Check-Controversial MIT study does not show that mRNA vaccines alter DNA

LINK: https://www.reuters.com/article/factcheck-coronavirus-vaccines-idUSL1N2PK1DC

ARCHIVE: https://archive.fo/vJwBk


De Marinis Paper Downplay:

Swedish study on COVID vaccines and DNA misinterpreted

LINK: https://apnews.com/article/Fact-Check-COVID-Vaccine-Sweden-Study-986569377766

ARCHIVE: https://archive.fo/vJwBk


Rather than take these arguments apart myself, I ask you all to take a first crack at the different techniques used, by clicking the links and observing the UNETHICAL SKEPTICISM. Much of this does not require a science background.

In particular, knowing what we know now, after the Mehedi work, I think it should be very clear how much the media went to bat for the vaccines without honestly questioning the “authorities”.

I will confirm your findings in the comments, and catch any straggler sins of science.

To me, this media mendacity is all simple, stupid, and predictable.

“Nothing to see here!”

Frankly, it changes nothing for me, if any of these authors get talked into walking back their own work, because push-back on critical work is a common phenomenon in the history of science. Not all scientists are capable of weathering the storm. Here are TWO that did. Both got Nobel prizes, by the way.


A classic case, emphasizing a field aversion among an establishment group to a field solution emerging from deductive reasoning, was Van’t Hoff and tetrahedral carbon. Basically, a doctoral candidate in an applied science school had the temerity to take an old hypothesis and revive it as the solution to a very significant current problem. The guy was good – he went on to win a Nobel prize for other work. However, many chemists, especially older ones, rejected the idea, in my opinion by not prioritizing explanatory power over their own abstract philosophical preconceptions. The fact that important people rejected an elegant solution of remarkable utility and truth shows how bad group-think problems can be in science.

Another case was Rick Smalley and C60 (buckminsterfullerene). The linked article accurately describes the initial skepticism that people had for “soccer ball carbon” or “bucky balls”.

The Nature letter describing C60 was attractive and logical, but seeing a line in a mass spectrum did not convince all scientists of the discovery of a new allotrope of carbon. During the period 1985-1990, the Curl/Smalley team at Rice and Kroto at Sussex managed to amass a wide range of circumstantial evidence to support the fullerene structure proposal. Full acceptance came when Wolfgang Krätschmer of the Max Planck Institute for Nuclear Physics in Heidelberg, Germany, and Donald Huffman of the University of Arizona, with their students Konstantinos Fostiropoulos and Lowell Lamb, succeeded in synthesizing C60 in sufficient quantities to allow structural characterization.

I personally remember colleagues assuring me that Smalley was loony, demented, senile, past his prime, or at best something along the lines of “a nice guy, but clearly deluded and obsessed with an error.” The doubt about C60 as reality – particularly as a stable reality – ran thick. And that doubt was WRONG from the very beginning.


Scientists right now are NOT THINKING, and they’re letting the MEDIA push them around.

Scientists are also letting guys like Anthony FAUCI push them around, mainly by the horrible federal grant system, and by the psychology of woke universities, both designed to control science.

And that doesn’t even begin to address other malign interests altering science and medicine in dishonest ways.


Some Actual Speculation – Why Would They Push These Clearly Defective Shots So Hard?

You want some actual “conspiracy theorizing”? Here it is.

Let me go back to my “TLDR” again…..

They didn’t just lie to us about the spike mRNA not going into the nucleus and not changing human DNA – the whole purpose was very likely to do exactly what they did – to open the cell nucleus and keep it open, so that we as a species can start changing population genomics in a huge way, using a variety of technologies.

There are reasons to suspect depopulation as a motive for these vaccines, and both Gail Combs and I have written extensively about this. I continue to believe that this is part of the motivation of the “complex event” we have been undergoing, between virus and vaccine.

Depopulation is very important to these people.

MALTHUSIANS AND EUGENISTS MAKE A CASE FOR POPULATION CONTROL

DEPOPULATION – NEVER LET A CRISIS GO TO WASTE

The Population Control Shot – Introduction

The Population Control Shot – Understanding the Peoples Climate Temple

Likewise, there are many other motives, ranging from mercenary profits, to promoting gene therapy, to “Covid communism”, and beyond. Many of these roads lead back to WEF – the World Economic Forum. One of those roads may be an actual attempt to commit humanity to a future of genetic engineering as a kind of fait accompli.

Just listen to Yuval Noah Harari talk about changing humanity. A few times he talks about “we”, “I”, “me”, “my”, and “our” programs of genetic engineering of humanity. It’s not just creepy and megalomaniacal – it seems quite self-assured.

WEF’s interest in genetic transformation of humanity cannot be understated. You will note in the above video, the presence of Jennifer Doudna – the Nobel laureate who (IMO) was most responsible for pushing CRISPR gene editing technology forward. Here is the full video.

I have discussed the technology recently here:

Dear KMAG: 20230213 Joe Biden Didn’t Win ❀ Open Topic / Introduction to CRISPR/Cas9 Gene Editing Technology

This is a particularly good explanation for those who want to dig into the science a little.

So how does CRISPR-Cas9 connect to the spike protein?

I have mentioned that the spike not only is proven to have nucleus-opening properties and cell nuclear mRNA-trafficking properties, but it likely has reverse-transcribing properties as well. Thus, it may have utility in facilitating certain varieties of genomic incorporation of genetic material beyond its own spike mRNA. I’m leaving that open very broadly. We don’t really know how far the “nuclear translocation of mRNA” capabilities of the spike protein actually go.

But even just the incorporation of its own instructions into the cellular genome, makes the spike protein highly relevant to CRISPR-Cas9 gene editing technology.

We can’t REALLY be sure what happens if the spike protein code gets into egg or sperm DNA, and goes on to be a “feature” of every human cell of a “spike baby”, but I can say one thing – if that gene can be REMOVED during in vitro fertilization (IVF) by CRISPR-Cas9 technology, to the betterment of the child, then it’s very likely going to be demanded by elite parents, to assure a healthy baby.

So – I ask again – WHAT ARE THE CHANCES?

What are the chances, that people who are gung-ho on the “solution” of genetic modification of humanity – you know – like WEF – would have anything to do with releasing a virus and promoting a vaccine that would almost FORCE us into that future?

I think that this era is a lot like the chemical revolution of the late 1800s, precisely when Van ‘t Hoff was dealing with chemical theory. Figures like Malone and Doudna operate in the time of our own biological revolution. Remember Rockefeller, and what he did to science and medicine back during the chemical revolution. Well, now we have Gates and what HE did to science and medicine during the biological revolution.

Personally, I think it’s high time for us to stop taking shit from the corporate media – and particularly the “fact checkers” like Reuters and the AP – as they LIE to our faces about science – as they deny reality on behalf of the corporate titans behind them.

These mRNA vaccines are DEFECTIVE relative to how they were sold to us – very likely by intention – and the media and media organizations have LIED to us about those vaccines in the most scurrilous ways. The media has defended LIES and defrauded all of us.

You don’t have to be FOR or AGAINST gene editing per se, to be against LYING, DEFRAUDING, and FORCING IT ON THE WORLD by a criminal conspiracy.

We need to demand TRUTH about the vaccines, or the SHUTTERING of these “media” companies and organizations, which have cosigned onto crimes against humanity.

Demand no less. TRUTH or BREAK-UP. Media that lies and conceals is USELESS and a hindrance to REAL SCIENCE.

W

Genomic DNA Incorporation of the SARS-CoV-2 Spike Protein Explained by Unique Hidden Key to Nucleus and Spike’s Surprising Ability to Transport mRNA

This is SO HUGE. I must explain this to you.


TL;DR – The spike protein not only contains a special sequence that allows it into the cell nucleus – it also has an ability to bring its own spike mRNA sequence with it. Both features appear to be unique among coronaviruses. The features explain genomic incorporation found for both the virus and the vaccines. The special key and the mRNA shepherding can be considered to be defects in any spike vaccine that has them.

¡Muy explosivo!


Due to comments by WSB and Valerie Curren, I realized that I had to do this post.

Also, NONE of the “bigs” are talking about this, but it is HUGE, if only people will read the paper.

By sheer luck, I was alerted to this new development ASAP on Twitter.

A follower of mine, who I had followed back, posted on Twitter the link to a paper with this title:

Nuclear translocation of spike mRNA and protein is a novel feature of SARS-CoV-2

I immediately realized what this was about.

It’s about how the SARS-CoV-2 (COVID) virus spike protein and its mRNA get into the cell nucleus – an extremely important point which WSB has been hitting on over and over. It’s very important, because THAT is how “genomic incorporation” happens. And genomic incorporation is what HIV does – what retroviruses do. They “get into” the DNA and leave cookies, so to speak.

Sometimes, they leave enough cookies, that the whole virus comes back out, fully functional, and ready to infect. Sometimes, they only leave enough junk in the DNA to cause some damage. Sometimes, they leave enough to change us – and that is why human DNA is filled with “viral leftovers”.

In principle, mRNA technology should NOT do this. We were TOLD that mRNA technology could not do this. But somebody LIED TO US. And not only that – NOBODY – from Bill Gates on down – ever apologized to us about lying, or even about just “being mistaken”.

We’ll get to that later.

You will recall that there are two papers I love to mention.

One is the “Jaenisch paper”, which describes how the SARS-CoV-2 virus manages to get some of its genetic instructions for the spike protein into the DNA of cells.

LINK: https://www.biorxiv.org/content/10.1101/2020.12.12.422516v1

ARCHIVE: https://archive.fo/XWC52


The other is the “De Marinis paper”, which describes how the Pfizer vaccine did the same thing to human liver cells in vitro – meaning that in an experiment using cells in culture, the Pfizer vaccine got its mRNA sequences into the DNA genetic material of human liver cells, and it did so in a matter of minutes.

McCullough got in a lot of trouble with Twitter for posting this, even though it was utterly true. Now we know that the government was trying to shut it down. They likely used the technicality of McCullough’s very VALID speculation (stated as speculation and concern), which turned out to be correct, IMSO.

LINK: https://www.mdpi.com/1467-3045/44/3/73

LINK: https://portal.research.lu.se/en/publications/intracellular-reverse-transcription-of-pfizer-biontech-covid-19-m


These papers explain ALMOST everything. When I saw the Jaenisch paper, I predicted that we would see the De Marinis paper. MEANING – when I saw that the virus could get mRNA into the DNA, I predicted that the vaccine might get its mRNA into the DNA, too. And yes, I was right. Clearly others thought the same thing, and decided to investigate.

Now, after the De Marinis paper, it seemed very obvious to me that one did not need any kind of special conditions or reverse transcription promoters to get the vaccine mRNA to incorporate.

That bothered me, and I suspected, at the time, that MAYBE – just maybe – the spike protein ITSELF was somehow causing genomic incorporation – that it functioned as a kind of reverse transcription promoter.

Well, it sure looks like that is the case.

According to the discoveries revealed in the new paper, which I have taken to calling the “Mehedi paper”, there is a special sequence in the spike protein that acts like a “key to the nucleus” – and this sequence is found in NO other coronavirus spike protein.

LINK: https://www.frontiersin.org/articles/10.3389/fmicb.2023.1073789/full

ARCHIVE: https://archive.fo/kW9Bd

Here is the abstract of the new paper.


Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes severe pathophysiology in vulnerable older populations and appears to be highly pathogenic and more transmissible than other coronaviruses. The spike (S) protein appears to be a major pathogenic factor that contributes to the unique pathogenesis of SARS-CoV-2. 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. S mRNAs also translocate into the nucleus. S mRNA colocalizes with S protein, aiding the nuclear translocation of S mRNA. While nuclear translocation of nucleoprotein (N) has been shown in many coronaviruses, the nuclear translocation of both S mRNA and S protein reveals a novel feature of SARS-CoV-2.


Let me put that in plainer English.


COVID-19 really hurts old people and seems to be both deadlier and easier to catch than other coronaviruses. The spike protein seems to be why. Although the spike protein is a surface protein that normally would not do this, it might be predicted to get into the cell nucleus because it has a special sequence “PRRARSV,” a known key to the nucleus which appears in no other coronavirus. Sure enough, the COVID spike protein gets into the nucleus of infected cells. What’s more, the mRNA for COVID spike protein also gets into the nucleus. What happens is that the spike mRNA collects near the spike protein, which helps it get in. While a different protein called the “nucleoprotein” of many coronaviruses is known to get into the nucleus of cells, the penetration of the cell nucleus by BOTH the spike protein AND the mRNA for it, seems to be a unique new feature of the SARS-CoV-2 virus.


Once you read it in plain English, it’s much more mind-blowing.

Now – I really recommend that you read the rest of the paper, but it’s really just technical details about what was mentioned in the abstract. Those details can help you gauge the expectedness or unexpectedness of things, but I have tried to do that as best as I could in the translation.

At this point, you should have all kinds of questions.

  • could this defect of the vaccines have been predicted?
  • should it have been predicted?
  • did the Chinese know this when they sent us the sequence?
  • did we know it when we got the sequence?
  • would NOT using the full spike protein have prevented this?
  • if so, why did we use the full spike protein anyway?
  • would the “forbidden” Winfried Stöcker RBD vaccine have avoided this?
  • if so, why was his vaccine suppressed by the German government?
  • does this affect the Peter Hotez vaccine, Corbevax?
  • if not, why didn’t his vaccine get promoted through the process quicker?
  • is nuclear penetration a common problem with mRNA technology?
  • how did this “key” get into the sequence? Naturally or not?
  • could “directed evolution” of the spike have yielded this?
  • why wasn’t this clear from the moment we got the sequence?
  • did people know this and hide the information?
  • were key people like Bill Gates (their side) and Robert Malone (our side) aware of this possibility?

The last question is a gift to WSB and her virologist friend. I am by default a defender of Dr. Malone, but WSB and her friend are long-time skeptics of the technology, and thus of Dr. Malone. In all fairness, I think we have to ask EVERYBODY the same questions.

  • Did people KNOW that mRNA technology had this vulnerability?
  • Does this look any more like an engineered bioweapon, designed to get into the nucleus?
  • Was this thing made by nature, by people, or by somebody with more advanced technology?
  • What is the purpose of getting into the nucleus, if it is designed to do that?

That should be enough. I will leave some links to prior comments I have made, in an appendix, hopefully added later.

Thank you.

W

John Fink and James Coburn discuss case in a scene from the film ‘The Carey Treatment’, 1972. (Photo by Metro-Goldwyn-Mayer/Getty Images)

PS – A great interview of our site mascot!

https://thehollywoodinterview.blogspot.com/2008/02/james-coburn-hollywood-interview.html

Dear KMAG: 20220228 Joe Biden Didn’t Win ❀ Open Topic / Microwave Monday / Google Is Now Anti-Science / mRNA Vaccines Really Do Change Your DNA

Joe Biden didn’t win. This is our Real President:

AND our beautiful REALFLOTUS.

Get your rest, Trumpy Bear! You’re needed in WASHINGTON, DC!!!

Vladdy Bear and Winnie The Pooh are making Sleepy Creepy Joe look like a punching bag!



The Business At Hand

This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).

And indeed, it’s Monday…again.

But we’re ON A ROLL.


The Rules

Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.

The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.

Gonna be quick this time.

SO….. [ENGAGE BOILERPLATE…..]

We must endeavor to persevere to love our frenemies – even here.

Those who cannot deal with this easy requirement will be forced to jump the hoops of moderation, so that specific comments impugning other posters and violating the minimal rules can be sorted out and tossed in the trash.

In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”

That includes the life skill of just ignoring certain other posters.

We do have a site – The U Tree – where civility is not a requirement. Interestingly, people don’t really go there much. Nevertheless, if you find yourself in an “argument” that can’t really stay civil, please feel free to “take it to the U Tree”. The U Tree is also a good place to report any technical difficulties, if you’re unable to report them here. Please post your comment there on one of Wolf’s posts, or in reply to one of Wolf’s comments, to make sure he sees it (though it may take a few hours).

We also have a backup site, called The Q Tree as well, which is really The Q Tree 579486807. You might call it “Second Tree”. The URL for that site is https://theqtree579486807.wordpress.com/. If this site (theqtree.com) ever goes down, please reassemble at the Second Tree.

If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.

We also have some “old rules” and important guidelines, outlined here, in a very early post, on our first New Year’s Day, in 2019. The main point is not to make violent threats against people, which then have to be taken seriously by law enforcement, and which can be used as a PRETEXT by enemies of this site.

In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”


A Moment of Prayer

Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.

Thus, please pray for our real President, the one who actually won the election.

After his speech at CPAC, I think it’s quite clear that praying for President Trump’s return to the White House is indeed praying for our enemies, who are too messed up to realize how much better off they would be under a Trump presidency.


MUSICAL INTERLUDE

For your listening enjoyment, and general encouragement, we continue Wheatie’s tradition of fine music videos, shipped fresh from the seas of information by our intrepid authors.

Microwave Monday reminds me of this song from back in the day.

ENJOY!

This right here is the stiffest dose of teased-out 80s chick hair you are EVER going to get.

And if you want to see it with 2008 hair….

And then there’s an outdoorsy 2014 version which has a really great “live” feel…..

But how about a 2021 version with just Susanna Hoffs and a string section?

But if you’re still feeling like it’s all unfamiliar, here’s the original video!

Yeah – that’s more like it!


Call To Battle (H/T Sundance)

Our beloved country is under Occupation by hostile forces.

Daily outrage and epic phuckery abound.

We can give in to despair…or we can be defiant and fight back in any way that we can.

Joe Biden didn’t win.

And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.

…..and now for…..


Microwave Monday

After recent discussion of Havana Syndrome, and the possibility that it involves electromagnetic radiation (and in particular microwaves), I have decided that we all need to LEVEL UP our gut-level understanding of the electromagnetic spectrum – even beyond what Steve has done with his explanation of the science behind it.

This will also help us deal with both the REALITIES and DISINFORMATION of 5G telecom.

I will be doing this by giving you all a bunch of INFOGRAPHICS to get started.

Steve got us started HERE, in his 8th science lesson on LIGHT.

You may remember some of this stuff….. (CLICK TO ENLARGE)

Let’s start breaking up that electromagnetic continuum into REGIONS that have NAMES.

You can see that microwaves lie between RADIO and INFRARED.

Let’s look even more closely at those groups.

We can even start breaking those radio and microwave regions down into BANDS that you are all familiar with.

Here you can start to get a feel for the SIZE OF THE WAVES versus objects and frequencies.

The SIZE OF WAVES and WHAT THEY AFFECT actually matters – although it’s not simple.

Megahertz, gigahertz, teraherz, and petahertz are all there.

You can really see it more easily in the following infographic.

You can easily see how we have made “radio devices” push farther and farther away from the very SAFE “radio” region, through television, mobile phones, and WiFi, closer and closer to the microwave and infrared radiation that constitutes COOKING MICROWAVES and RADIANT HEAT ITSELF.

And as you can see here, many technologies emit electromagnetic radiation – and some more than you may have realized.

So where are the 5G frequencies? Please be aware that there is constant change in this stuff, so that these infographics may be slightly out of date. Do not let that deter you – minor changes don’t NIX any issues of the basic range in which 5G operates, unless specifics of the science are given.

Use COMMON SENSE.

Let’s zoom in a bit.

Note that the above is just the US – other countries use different regions.

Here is more detail on European and US 5G.

Much of this is SQUARELY in the microwave region. From Wikipedia, we’re basically talking 300 MHz to 300 GHz.

Now let’s start looking at ALLEGED but possibly REAL health effects of EMR in the microwave region, which may VARY ACROSS THE REGION.

Remember also that DOSAGE MATTERS – like anything else.

You have to squint to see the next infographic, but look at “Biological Effect”.

It depends strongly on FREQUENCY / WAVELENGTH.

This is a very good listen. This lady is also a climate dupe, but she will get you to realize that your microwave devices may actually be doing to YOUR MEAT what microwaves normally do to YOUR MEAT, albeit at LOWER BUT LONGER DOSAGES.

This is another good one!

More of her schtick. This gal will get you to question the “harmless” narrative, just like vaccines, but try to keep some common sense. Remember – driving is a killer, too. You still want the freedom to drive?

Common sense! How do we get the BEST of both worlds?

Now I’m just going to play a bunch of their infographics. Caveat emptor! But some of this stuff is interesting and counter-intuitive. SIGNAL and NOISE matter. In more ways than one.





SO – maybe you should THINK about how to handle the devices you have!!!

But then talk back to all that stuff HERE.

Be sure to be SKEPTICAL of this SKEPTIC lady – that is an essential part of ETHICAL SKEPTICISM. We don’t want to be panicky about 5G, or believing disinformation, but we do want to treat MICROWAVES as maybe not that awesome for our health, in doses that exceed our individual sensitivity.

So BEWARE of BROAD-BRUSH SKEPTICS who downplay too much in favor of technology.

After all, we just got through a BATTLE ROYALE over disastrous mRNA technology that was advanced too fast for all the wrong reasons.

LINK: https://www.skeptic.com/reading_room/electromagnetic-fields-and-parental-panics/

Finally, a GREAT infographic. It’s MASSIVE. I’m only showing you the small version – you have to click the link for the BIG ONE that’s easy to read down to the details.

MASSIVE EMR Infographic (Thumbnail)

MASSIVE EMR Infographic (Full Version)

LINK: http://www.50northspatial.org/wp-content/uploads/2015/12/EMR_Welch.png

So that’s it. Let’s start investigating 5G, Havana syndrome, spy devices, and microwave crowd control devices, with some intelligent skepticism.

And may be even start thinking about HEADBAND technology.


Google Is Now Anti-Science

Something stinks, and to my nose, it’s the New World Odor.

But first, a disclaimer.

I’m actually ashamed that I wanted to work for Google at one point, but I need to get that out into the open right away, lest somebody, someday, use that “gotcha” against me and think it’s actually damaging.

Heck – I even bought a variety of Google swag, back when they were small and upstarty, just like when Netscape, Firefox, various Linux brands, and other rising tech companies were once “new” and “cool”.

A lot of people once thought that Google’s motto of “Don’t be evil” was a bit of a bass-ackwards under-performer, which should have been a positive, rather than a double-negative. Not me. I realized back then that this paradoxical formulation was exactly why the motto was so ahead of the curve.

“Being good” lacks skepticism – particularly of self. “Being good” as a primary motivator is a guaranteed set-up for the primary sin of PRIDE.

“Not being evil”, in contrast, is automagically skeptical of self. And skepticism isn’t just good for science – it’s good for religion.

Yes – I think it’s clear you need both. This is part of why (IMO) Christianity always refreshes itself by going back to its Jewish roots when there are foundational questions. No matter how you slice it, we need to concern ourselves with the Law, which includes consequential negatives, because we don’t want to get rid of our saving prohibitions.

We need our Peters, but we also need our Pauls.

Thus, when Google ditched “don’t be evil”, I smelled trouble.

And what is happening now, may be evidence that Google has forgotten how to “not be evil”.


Google has made mistake after mistake since they began tampering politically with their search engine, largely during the Obama years, but to an even greater degree during the Trump years. And now, in one short year of Biden – Google has arrived at the point of adopting a policy that conflicts with the most basic principles of science.

Simone Gold, of America’s Frontline Doctors, just tweeted this.

“Nor do we allow content from any site that contradicts or runs contrary to scientific or medical consensus and evidence-based best practices.”

Well THAT’S great. How do you think science is going to advance? YOU CHUMPS!

Let’s just save that tweet, simply to make sure that it doesn’t disappear when Twitter inevitably suspends Dr. Gold.

Note these final words from Dr. Gold.

And we have been proven right, again and again, and again.

Dr. Simone Gold, AFLD

Dr. Gold is not lying. Throughout COVID-19, free and independent doctors and scientists have been LEADING captive science and captive medicine against their BIASED FUNDERS AND CONTROLLERS – which clearly include GOOGLE now.

The “concensus” science has repeatedly and continuously been ABNORMALLY WRONG due to BIAS, and has required continuous correction by – very sadly – OUTSIDERS.

Science does not progress by sticking to consensus. It advances by CHALLENGE TO CONSENSUS. Google is INTERFERING with that process. SHAME!!!


In my opinion, “they” are all scared.

And the reason they’re scared it this.

Now – as insurance companies look around to see who picks up the tab for people dying from the ERRORS OF THE CONSENSUS, it sure ain’t gonna be able to pin it on the people who WARNED about the experimental vaccines.

It may indeed be that some of the blame (moral, even if not monetary) will land on those who CENSORED THE SAVING WARNINGS.

Over and over, people like Google censored us because they said that the things WE SAID were not true, and yet it turned out that the things we said WERE true, and that the consensus THEY said was true, was both WRONG and responsible for MANY DEATHS.

And THIS may be the biggest CENSORED TRUTH of all.


mRNA Vaccines Really Do Change Your DNA

You will notice that this tweet no longer exists.

https://twitter.com/P_McCulloughMD/status/1497284602540351491

It was up for a day, and then it disappeared. I was lucky we had copies up in WordPress.

Here is a “tweetstamp”, that proves that it really did exist.

https://tweetstamp.org/1497284602540351491

Here is the text, where Twitter can’t touch it.


Alden et al, Lund University, Sweden, confirms one of our worst fears. The exogenous genetic material coding for the dangerous Spike protein is reverse-transcribed into the human genome; possible long-term constitutive expression/synthesis of disease promoting/lethal Spike. pic.twitter.com/JEzSwSruWM— Peter McCullough, MD MPH (@P_McCulloughMD) February 25, 2022


Here, I saved an image of a copy which was only partially destroyed by Twitter.

And here I saved the actual tweet (in two pieces).

Here is that image within the tweet, in more detail.

So what is McCullough talking about? And what is Twitter hiding?

THIS SCIENTIFIC PAPER.

LINK: https://www.mdpi.com/1467-3045/44/3/73/htm

ARCHIVE: https://archive.fo/TIfnZ

Open Access Article

Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line

by Markus Aldén 1,
Francisko Olofsson Falla 1,
Daowei Yang 1,
Mohammad Barghouth 1,
Cheng Luan 1,
Magnus Rasmussen 2 and
Yang De Marinis 1,*
1Department of Clinical Sciences, Lund University, 20502 Malmö, Sweden
2Infection Medicine, Department of Clinical Sciences, Lund University, 22362 Lund, Sweden
*Author to whom correspondence should be addressed.

Academic Editor: Stephen Malnick
Curr. Issues Mol. Biol. 202244(3), 1115-1126; https://doi.org/10.3390/cimb44030073 (registering DOI)
Received: 18 January 2022 / Revised: 19 February 2022 / Accepted: 23 February 2022 / Published: 25 February 2022
(This article belongs to the Topic Clinical, Translational and Basic Research on Liver Diseases)

Abstract

Preclinical studies of COVID-19 mRNA vaccine BNT162b2, developed by Pfizer and BioNTech, showed reversible hepatic effects in animals that received the BNT162b2 injection. Furthermore, a recent study showed that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of human cells. In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro. Huh7 cells were exposed to BNT162b2, and quantitative PCR was performed on RNA extracted from the cells. We detected high levels of BNT162b2 in Huh7 cells and changes in gene expression of long interspersed nuclear element-1 (LINE-1), which is an endogenous reverse transcriptase. Immunohistochemistry using antibody binding to LINE-1 open reading frame-1 RNA-binding protein (ORFp1) on Huh7 cells treated with BNT162b2 indicated increased nucleus distribution of LINE-1. PCR on genomic DNA of Huh7 cells exposed to BNT162b2 amplified the DNA sequence unique to BNT162b2. Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure.

Keywords: COVID-19 mRNA vaccineBNT162b2liverreverse transcriptionLINE-1Huh7


I am going to call this the De Marinis paper, after the lead author, Yang De Marinis, to whom correspondence is to be addressed.

I do this in analogy to a very important COVID-19 paper I refer to as the Jaenisch paper, which bears heavily on this more recent work.

LINK: https://www.biorxiv.org/content/10.1101/2020.12.12.422516v1.full

ARCHIVE: https://archive.fo/XWC52

I have discussed the Jaenisch paper numerous times since I became aware of it in December of 2020, and more importantly in March of 2021.

In fact, in the following blog post I made in April of 2021, I actually hypothesized a scenario which is basically the findings of the De Marinis paper!!!


Wolf’s Red-Hot Date With Retrotranscriptive Faucipox

Alternate Title: Is Persistent Reverse Transcription a Hidden Virus/Vaccine Objective? Gloating Pre-Preface There are few feelings of satisfaction like opening up the NEWS and knowing one’s theories and understandings are WORKING even better than one thought. Let’s see if they use this one for damage control, and get the “new science” out before the STORY …


See also: https://www.theqtree.com/?s=Jaenisch


Now – let me state, in the simplest possible way, what these papers mean.

The Jaenish paper proves that the SARS-CoV-2 (COVID-19) virus alters human DNA.

The De Marinis paper proves that the Pfizer mRNA vaccine also alters human DNA.

Oh, there are quibbles that I’m “oversimplifying”, but they’re just quibbles, and I will show you WHY they are not just quibbles, but extremely disingenuous ones.

And please note that I am UNDERSTATING when I just say “alters DNA”. The Jaenish paper proves that the viral DNA changes are going into GENOMIC DNA. The De Marinis paper strongly suggests that THE SAME may be happening due to the vaccine.

But before I give you MY take on the De Marinis paper, let me give you the opinions of OTHERS.

Let’s review one first.


Peter McCullough:

Alden et al, Lund University, Sweden, confirms one of our worst fears. The exogenous genetic material coding for the dangerous Spike protein is reverse-transcribed into the human genome; possible long-term constitutive expression/synthesis of disease promoting/lethal Spike.


Translation: The pseudo-mRNA code for the spike protein in the Pfizer vaccine gets into the genomic DNA inside human cells in test tube experiments, and produces both DNA and mRNA coding for what was uniquely in the vaccine. This new cellular DNA and RNA very likely (as a consequence) produces spike protein, causing long-term disease and health issues.

One can legitimately contest the assertion that genomic DNA is being altered (we don’t know this yet – hopefully soon), but any denial of the fact that CELLULAR DNA is being changed, is simply not “fact-based”.

For example, I saw “downplay trolls” on the original McCullough tweet, quibbling about in vivo vs. in vitro – that these results don’t “prove” that the same thing happens in living humans – only in living human cells in a test tube.

The reason this is a hypocritical crock of shit, is that “due to an abundance of caution”, almost every single “carcinogen” and other “bad boy chemical” that is restricted or controlled in the United States, at the cost of trillions of dollars which go into the pockets of the deep state and China, is because of IN VITRO results.

Thus, if it’s OK to have vaccines that do what Pfizer’s vaccine does, then it’s OK to remove the restrictions on benzene, and have benzene everywhere. Likewise for thousands of other chemicals.

Starting to see how this works? Let’s move on.


Alex Berenson:

Hey, remember how they told you the mRNA in the vaccines could NEVER wind up in human DNA? A new study out of Sweden suggests otherwise (at least in lab-grown cells).

Don’t worry, everything is fine.

After all, we have all that long-term placebo-controlled clinical trial data proving the safety of these mRNA shots.*

All that careful preclinical work too.**

*No we don’t.

**Not that either.


Karl Denninger:

LINK: https://market-ticker.org/akcs-www?post=245270

ARCHIVE: https://archive.fo/RpDoE

So About Not Needing Actual Study…[Comments enabled]

Oh, mRNA won’t get taken up into cell lines and thus can’t propagate on a permanent basis in the human body, we were told.

Indeed that’s rather important.  Mutagenic (cancer), cytotoxic (you’re ****ed) and teratogenic (any child you give birth to or sire is ****ed) things that get into cellular DNA can lead to irreversible damage because most cells in the body are replaced on regular basis.

There’s an infamous quote that is in fact wrong: Our body fully replaces itself every seven years.  That’s not true.  It came out of a study that looked at the average age of cells in a human, using Carbon-14 dating.  Anyone who has done any sort of statistical work knows the problem with averages: They are just that, and the statistical outliers are there but unaccounted for with such simplistic tripe.

There are several types of cells that are never replaced.  Certain ones in the cerebellum, for example, that deal with coordination and balance, those in the ocular lenses and the eggs in a woman’s ovaries.

There are also cells that are much more-frequently replaced.  Red blood cells, for example, have a roughly 90 day life cycle.  This is why an A1c test, which measures glycated hemoglobin (that is, red cells that have been damaged by glucose) will tell you what your average blood glucose level has been over the last three months.  The epithelial cells in your intestines last only about five days, and the live (dermal) part of your skin is replaced in about 2 weeks.  Skeletal muscle and the rest of your intestines, on the other hand, are good for around 15 years.

But with few exceptions it is indeed true that most cells are in fact replaced.  This is why you can get cancer; when there is an error in that replication the result can be a cell that has wildly damaged regulatory mechanisms on self-replication.  If that damage kills the cell immediately then there’s no real foul, but if it leads to much more rapid reproduction…… that’s cancer.

We have known for quite a while that viruses can and do in some cases infiltrate into DNA.  We know this because we’ve found pieces of viral RNA in our genome and not a few of them either; they’re literally all over the human genomic code.  It’s wildly improbable that said congruence happened by random alignment of the various codons in our genetic code; ergo, it got in there at some point in evolution and then got into either the eggs of a developing female fetus or the sperm of a male and thus propagated.  We only know, of course, about the integrations that weren’t fatal to offspring or the person in question.  We also know that in general genetic mutation is harmful or fatal nearly all the time, so that we have said evidence in our genome means this sort of thing happens quite frequently and most of the time it screws the person who has it happen to them.

Indeed some cancers are blamed on viral infections where the viral RNA gets transcribed into the DNA of the cells and causes said errors.

mRNA is not really “new” technology; Moderna has been trying to make it work for cancer, for example, for a long time — without success.  The reason for failure has always been dose-related toxicity that has overtaken the benefit when used in sufficient quantity to actually deliver a therapeutic effect.  This is not an uncommon reason for drug and therapy failure; in fact that too happens all the time.

But we didn’t bother doing intermediate and longer-term study on the specifics of using mRNA (or, for that matter, a modified virus as with J&J) to deliver a partial viral payload in this regard before rolling it out.  Instead, we just trusted that there’d be no integration.  Indeed zero epigenic, mutagenic and teratogenic studies were done;they take years to do and we just flat-out didn’t bother.  Where we had original control groups in the summer and fall of 2020 we intentionally destroyed them by giving the placebo arm of the original trials the drug three months later, making analysis on any sort of clean analytical basis impossible.

This was wild arrogance given that we know viruses do indeed integrate via infection.  To presume it won’t happen here, when we cause cells to produce viral proteins, when the very same thing, producing viruses when a cell is infected, sometimes does is ridiculously and wildly-irresponsible arrogance.

Unfortunately now we’re finding out that said arrogance may well screw you and if it has there’s nothing you can do about it — and worse, could screw your offspring.

In the BNT162b2 toxicity report, no genotoxicity nor carcinogenicity studies have been provided [26]. Our study shows that BNT162b2 can be reverse transcribed to DNA in liver cell line Huh7, and this may give rise to the concern if BNT162b2-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects. At this stage, we do not know if DNA reverse transcribed from BNT162b2 is integrated into the cell genome.

This study does not prove that said genetic pollution has occurred, but it raises the distinct possibility as the precursor events required for this to occur are now known to happen with scientific certainty.

We don’t know because we deliberately did not look; the studies were not done prior to use.

MORE: https://market-ticker.org/akcs-www?post=245270


I think I’ve given you enough to chew on for now.

The bottom line is this:

The Jaenisch paper was concerning smoke.

The De Marinis paper is a four-alarm FIRE.

Please warn everybody who is even THINKING about giving an mRNA vaccine to kids.

SET THESE VACCINES ASIDE until we know more. Even spike protein vaccines are too risky, IMO. Set them all aside.

And NEVER, EVER, EVER AGAIN, mandate another vaccine. This was our wake-up call.

Soon, we will talk about the BIG PICTURE of what is going on here.


Wolfie’s Wheatie’s Word of the Day:

genome

noun

In the fields of molecular biology and genetics, a genome is all genetic information of an organism.[1] It consists of nucleotide sequences of DNA (or RNA in RNA viruses). The genome includes both the genes (the coding regions) and the noncoding DNA,[2] as well as mitochondrial DNA[3] and chloroplast DNA. The study of the genome is called genomics. The genomes of several organisms have been sequenced and genes analyzed. The human genome project which sequenced the entire genome for Homo sapiens was successfully completed in April 2003.

genomic DNA

Genomic deoxyribonucleic acid (abbreviated as gDNA[1]) is chromosomal DNA, in contrast to extra-chromosomal DNAs like plasmids. Most organisms have the same genomic DNA in every cell; however, only certain genes are active in each cell to allow for cell function and differentiation within the body.[2]

The genome of an organism (encoded by the genomic DNA) is the (biological) information of heredity which is passed from one generation of organism to the next. That genome is transcribed to produce various RNAs, which are necessary for the function of the organism. Precursor mRNA (pre-mRNA) is transcribed by RNA polymerase II in the nucleus. pre-mRNA is then processed by splicing to remove introns, leaving the exons in the mature messenger RNA (mRNA). Additional processing includes the addition of a 5′ cap and a poly(A) tail to the pre-mRNA. The mature mRNA may then be transported to the cytosol and translated by the ribosome into a protein. Other types of RNA include ribosomal RNA (rRNA) and transfer RNA (tRNA). These types are transcribed by RNA polymerase II and RNA polymerase III, respectively, and are essential for protein synthesis. However 5s rRNA is the only rRNA which is transcribed by RNA Polymerase III.[3]

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While we tend to be more concerned about changes to genomic DNA, changes to any kind of human DNA are potentially problematic.

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