Cryptocurrencies, Vaccines and Jumping Bat Genes

Not to preach to the choir, this next video is a shareable link. With just a small amount of Holocaust propaganda, enough to make the forced vaccine problem seem unsolvable, it’s otherwise an intelligent discussion. It’s found on Biological Medicine, a channel I subscribe to on Rumble. Reinette Senum and vaccine expert Dr. Sheri Tenpenny have packed a lot of information into this, but I’ve added quite a bit more.

Dr. Tenpenny explains exactly how the covid vaccines will start working in 3-6 months.


https://rumble.com/ve29jl-how-the-depopulation-covid-vaccines-will-start-working-in-3-6-months.html

This is the point in which a wider circle of targeted people become aware, as the understanding ripples out.

This next video explains the global attack on America being attempted by the IMF and the Federal Reserve. I listened to this several times to get the full impact. It’s important to understand the connection between seemingly unrelated events.


In researching the actual people who created these cryptocurrencies, I came across Stephen Turner and Adam Back. Adam Back is conjectured to be the creator of Bitcoin who is called Satoshi Nakamoto. Adam Back published several papers with Stephen Turner whose computer expertise includes genetics research.

In researching genetic experimentation, I found these interesting bits of information. I’m passing this on so that my readers can learn along with me, as we discover all the different substances that scientists can put into a vaccine and what those substances do. This is all from Wikipedia, therefore not to be trusted entirely, but here are some understandable basics.

Did you know that Bats have the unique quality of having jumping genes? A jumping gene is called a TE.

“A transposable element (TE, transposon, or jumping gene) is a DNA sequence that can change its position within a genome, sometimes creating or reversing mutations and altering the cell’s genetic identity and genome size.[1] Transposition often results in duplication of the same genetic material. Barbara McClintock‘s discovery of them earned her a Nobel Prize in 1983.[2]

Here’s the computer connection:

“Helitrons were the first group of TEs to be discovered by computational analysis of whole genome sequences. In most mammals Helitron’s presence is negligible and limited to remnants of old transposons, with the exception of bat genomes, which are populated by numerous young elements.[7]

“Helitrons seem to have a major role in the evolution of host genomes. They frequently capture diverse host genes, some of which can evolve into novel host genes or become essential for Helitron transposition.[2]

“In 2016, one of the first mechanistic studies of helitron transposition was published in order to shed light on the different steps of transposition.[11] Based on a consensus sequence, it reconstructed the likely ancestor of the Helibat family of helitrons present in the genome of the little brown bat (Myotis Lucifugus), the only group of mammals possessing an important number of helitrons in their genome. This active transposon was inserted into a plasmid acting as the helitron donor. An antibiotic resistance gene was included between the two terminal sequences of the helitron to enable isolation of the cells where transposition occurred.”

The word “therapeutic” is used to describe research that is obviously not therapeutic at all, in practice.

Zinc finger nucleases(ZFNs) offer a way to cause a site-specific double-strand break to the DNA genome and cause homologous recombination. Plasmids encoding ZFN could help deliver a therapeutic gene to a specific site so that cell damage, cancer-causing mutations, or an immune response is avoided.[19]

“Specific zinc-finger motifs were engineered to recognize distinct DNA sequences. The ZFN-encoding mRNA was injected into one-cell embryos and a high percentage of animals carried the desired mutations and phenotypes. Their research work demonstrated that ZFNs can specifically and efficiently create heritable mutant alleles at loci of interest in the germ line, and ZFN-induced alleles can be propagated in subsequent generations.”


The list of Adam Back projects linked and copy/pasted below includes this very, very interesting link:

NSA’s backdoor key from lotus notes — O=MiniTruth CN=Big Brother

“Anyway as clearly inside the application somewhere would be an NSA public key that the NSA had the private key for, I tried reverse engineering it to get the public key.

In doing this I discovered that the NSA public key had an organizational name of “MiniTruth”, and a common name of “Big Brother”. Specifically what I saw in my debugger late one night, which was spooky for a short moment was:O=MiniTruth CN=Big Brother

Literary note: for those who have not read Orwell’s prescient “1984” the Ministry of Truth was the agency who’s job was propaganda and suppression of truths that did not suit the malignant fictional future government in the book, and “Big Brother” was the evil shadowy leader of this government. The whole book is online here.“

The NSA’s Public Key…

—————————————

http://www.cypherspace.org/adam/

Crypto Projects

Bitcoin Related

Publications and Tech Reports

Cryptography

Distributed Systems

  • See also distributed systems publications at the bottom of this page

Crypto Hacks

Breaking weak crypto

Crypto politics

Crypto People

  • People with crypto related pages.

Crypto Mailing lists

Cypherspace Internet Security – Services

Distributed Systems Publications

Related work by Stephen Turner

——————————————————-
Dr. Tenpenny has explained that the vaccines interfere with our natural immune functions. This next research explains the consequences. You can see that logically these adverse reactions would appear slowly over time.

Splicing antibiotic resistant genes into DNA for research purposes dovetails eerily into this research into the effects of infections of the brain’s outer layers, the meningeal layers.

meninges

 [mĕ-nin´jēz] (Gr.) plural of meninx; the three membranes covering the brain and spinal cord: the dura materarachnoid, and pia mater. adj., adjmenin´geal.


Unexpected role of interferon-γ in regulating neuronal connectivity and social behaviour

Abstract

Immune dysfunction is commonly associated with several neurological and mental disorders. Although the mechanisms by which peripheral immunity may influence neuronal function are largely unknown, recent findings implicate meningeal immunity influencing behaviour, such as spatial learning and memory1. Here we show that meningeal immunity is also critical for social behaviour; mice deficient in adaptive immunity exhibit social deficits and hyper-connectivity of fronto-cortical brain regions…”

https://www.nature.com/articles/nature18626

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