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In 1989, researchers from the Salk Institute in California published a paper detailing how they developed an RNA transfection system that could “directly introduce RNA into whole tissues and embryos”.
The concept of using RNA as a drug is first described in this paper, making it the seminal work that formed the foundation for decades of further research in this area.
One of the Salk Institute researchers listed on the paper is Dr Robert W. Malone, a scientist who has recently been censored on social media for warning about the possible dangers of the covid-19 vaccines.
Malone’s research, which resulted in a procedure that could be used to “efficiently transfect RNA into human cells” using a “synthetic cationic lipid” was supported by grants from the American Cancer Society and the National Institute of Health (who currently have a stake in the Moderna mRNA vaccine, showing their allegiance to the technology.
...
Far more interesting is the institution that produced the research in the first place – the Salk Institute.
Pfizer’s infant trials and the Wellcome Leap’s alarming “1kD” project indicate that key to this agenda is the conditioning and control of children from a young age, something that Aldous Huxley detailed extensively in his disturbingly prophetic, eugenicist novel, Brave New World.
mRNA “Vaccines”, Eugenics & the Push for Transhumanism
Moderna, Inc.
☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934, August 6 2020. Pg 70 reads...
Currently, mRNA is considered a gene therapy product by the FDA. Unlike certain gene therapies that irreversibly alter cell DNA and could act as a source of side effects, mRNA-based medicines are designed to not irreversibly change cell DNA; however, side effects observed in gene therapy could negatively impact the perception of mRNA medicines despite the differences in mechanism. In addition, because no product in which mRNA is the primary active ingredient has been approved, the regulatory pathway for approval is uncertain. The number and design of the clinical trials and preclinical studies required for the approval of these types of medicines have not been established, may be different from those required for gene therapy products, or may require safety testing like gene therapy products. Moreover, the length of time necessary to complete clinical trials and to submit an application for marketing approval for a final decision by a regulatory authority varies significantly from one pharmaceutical product to the next, and may be difficult to predict.
originally posted by: Guyfriday
a reply to: EndtheMadnessNow
Well that's a little offensive, but I think it's telling that ATS isn't on there. Google must really hate us.
originally posted by: Thoughtful1
a reply to: EndtheMadnessNow
Out of curiosity do you have coi fish?
originally posted by: Thoughtful1
a reply to: RookQueen
I am not on Telegram. Is there any way I can see? I have seen enough ugliness in the not artwork and the music side has some really, really awful messages especially when tied in with their music videos.