Synthetic mRNA Vaccines and Transcriptomic Dysregulation: Evidence from New-Onset Adverse Events and Cancers Post-Vaccination
sauce/
archive
Using high-resolution RNA sequencing on blood samples, researchers discovered that COVID-19 "vaccines" SEVERELY disrupt expression of THOUSANDS of genes - triggering mitochondrial failure, immune reprogramming, and oncogenic activation that can persist for long years post-injection, potentially permanently up to premature death
Differential gene expression analysis compared mRNA-injured patients (cancer, adverse events) to 803 healthy controls - revealing widespread transcriptomic chaos:
Mitochondrial failure - Complex I breakdown, oxidative stress, energy collapse
Immune reprogramming - chronic inflammation, ACE2 suppression, TLR hyperactivation
Oncogenic activation - MYC up, p53/KRAS down, DNA repair suppression
Cellular stress - ribosome overload, misfolded protein buildup, proteasome activation
Epigenetic remodeling - chromatin shifts, methylation changes, nucleosome displacement
Reverse transcription - patterns consistent with LINE-1 activity and persistent plasmid DNA, raising concern for potential genomic integration or sustained foreign gene expression
The landmark study was conducted by scientists from Neo7Bioscience gen-lab (Dr. John Catanzaro, Dr. Natalia von Ranke, Dr. Wei Zhang, Dr. Philipp Anokin), the University of North Texas (Dr. Danyang Shao, Dr. Ahmad Bereimipour, Minh Vu) and Medicinal Genomics (Kevin McKernan). Funded by the McCullough Foundation