However, despite its endorsement by the U.S. National Institutes of Health’s National Library of Medicine, the disturbing study has been heavily suppressed by mainstream media and across social media platforms.
Earlier this week, eminent cardiologist Dr. Peter McCullough took to X with a video dissecting the study’s revelations.
Genomic Integration: Top Target for mRNA Censorship
— Peter A. McCullough, MD, MPH® (@P_McCulloughMD) May 23, 2024
Review of Alden et al has been a top target for instant censorship. Just had huge number of views/likes/reposts on @LinkedIn before it was vaporized. Reverse transcription of mRNA, inserting the foreign code into human DNA… pic.twitter.com/CI7qDmUcrm
In the video, McCullough delves into the widespread censorship of the study across social media platform LinkedIn, despite its endorsement by the NIH’s National Library of Medicine.
The study itself paints a chilling tableau, revealing that mRNA gene therapy vaccines, including those rolled out for Covid, imprint an enduring mark on the genetic fabric of their recipients.
What’s more disconcerting is the notion that this genetic interference extends beyond the immediate host, impacting generations to come through the integration of mRNA into human DNA.
As McCullough explains, the genetic blueprint from Pfizer and Moderna vaccines remains etched within the human genome indefinitely, as per the unsettling findings of the study.
“So as we sit here today we have to reconcile that Pfizer and Moderna potentially could have permanently changed the human genome.”
“What if eggs and sperm took up the Pfizer and Moderna Covid [vaccines] and it’s permanently installed, then they would pass it on to the baby,” he said. “That’s the great concern.”
In the “Discussion” section of the study, the authors explain:
In this study, we present evidence that COVID-19 mRNA vaccine BNT162b2 is able to enter the human liver cell line Huh7 in vitro.
“BNT162b2 mRNA is reverse-transcribed intracellularly into DNA as fast as 6 h after BNT162b2 exposure.
“A possible mechanism for reverse transcription is through endogenous reverse transcriptase LINE-1, and the nucleus protein distribution of LINE-1 is elevated by BNT162b2.”
(Article by Baxter Dmitry republished from ThePeoplesVoice.tv)