ShinagawaShiroRenga

Dr. Janci Chunn Lindsay https://www.toxicologysupport.com/abo... Syncytin gene https://pubmed.ncbi.nlm.nih.gov/10693... シンシチン遺伝子 https://www.a.u-tokyo.ac.jp/topics/20... (Script) https://www.lewrockwell.com/2021/05/n..., hi. My name is Dr. Janci Chunn Lindsay. I hold a doctorate in biochemistry and molecular biology from the University of Texas and have over 30 years of scientific experience, primarily in toxicology and mechanistic biology. In the mid 1990's, I aided the development of a temporary human contraceptive vaccine, which ended up causing unintended autoimmune ovarian destruction and sterility in animal test models despite efforts against this and sequence analyses that did not predict this. I strongly feel that all the gene therapy vaccines must be halted immediately due to safety concerns on several fronts. First, there is credible reason to believe that the GTs will cross-react with the synthetic and reproductive proteins in sperm, ova, and placenta and lead to impaired fertility and reproductive outcomes. Respected neurologist Bill Gallagher has made excellent arguments as to why you would expect cross reaction due to beta sheet confirmation similarities between spike protein and sin one and two. I have yet to see a single immunological study which disproves this, despite the fact that it would literally take the manufacturers a single day to do these Sufit and ELISA studies to ascertain this. It's been over a year since the assertions were first made that this could occur. We have seen 100 pregnancy losses reported in VAERS as of April 9. And there have been reports of impaired spermatogenesis and placental findings from both the natural infection, vaccinated, and siM siT knockout animal models that have similar placental pathology, implicating that siM siT-en mediated role in these outcomes. Additionally, we have heard multiple reports of menses irregularities in those vaccinated. Those must be investigated. We simply cannot put these GTs in our children who are at 0.002 risk for COVID mortalities infected or any more of the childbearing age population without thoroughly investigating this matter. We could potentially sterilize an entire generation. Speculation that this will not occur and a few anecdotal reports of pregnancies in the trials are not sufficient proof that this is not impacting on a population-wide scale. Secondly, all of the gene therapies are causing coagulopathies. This is not isolated to one manufacturer and this is not isolated to one age group. We are seeing coagulopathy deaths in healthy young adults with no secondary comorbidities. There have been 795 reports related to blood clotting disorder as of April 9 in the VAERS reporting system, 338 of these being due to thrombocytopenia." There There are forward and backward mechanistic principles for why this is happening. The natural infection is known to cause coagulopathy due to the spike protein All gene therapy vaccines direct the body to make the spike protein. Zhang et al in [a scientific paper published in the Journal of Hematology & Oncology] in September 2020 showed that if you infuse spike protein into mice that have humanized ACE-2 receptors on blood platelets that you also get disseminated thrombosis. Spike protein incubated with human blood in vitro also caused blood clot development which was resistant to fibrinolysis. [Fibrinolysis is the body’s process of breaking down blood clots]. The spike protein is causing thrombolytic events, which cannot be resolved through natural means. And all vaccines must be halted in the hope that they can be reformulated to guard against this adverse effect. Third, there is strong evidence for immune escape— At this point in her oral testimony, Dr. Janci Chunn Lindsay was interrupted by a man’s voice: “Thank you for your comment, your time has expired.”