She would be the only justice on the current court not to have received her law degree from an Ivy League school. The eight current justices all attended either Harvard or Yale.
Most researchers at Harvard and Yale failed to admit, and failed to teach their students, that God’s Creation of UV light and water biophysically constrains viral latency across kingdoms via oxidative phosphorylation.
They are being forced to tell the whole truth and nothing but the truth by articles like this one: Optoribogenetic control of regulatory RNA molecules 9/24/20
Short regulatory RNA molecules such as endogenous micro RNAs (miR) or synthetic short hairpin RNAs (shRNA) are essential mediators of gene expression1,2,3. They interact with defined complementary sites in the untranslated (UTR) or the coding regions of mRNA molecules, upon which translation is either inhibited or the mRNA is hydrolyzed. Regulatory RNAs have become indispensable in the biosciences for the validation of gene or protein function in cells and in vivo4.
“Optoribogenetic” is an obfuscatory term for “UV light-activated.”
Teaching theories about evolution linked to Big Bang cosmology caused the virus-driven suffering and premature deaths that conservatives and many Nobel Laureates have tried to prevent by telling the truth about where energy-as-information came from: “the God of Abraham” with no obfuscation.
SARCASM ALERT: Energy-as-information did not automagically emerge from nothing in the great void.
The synthesis of RNA in isolated thymus nuclei is ATP dependent.
Unless you can link God’s Creation of UV light and water to His ATP-dependent Creation of RNA, you probably cannot understand why Harvard’s George M. Church et al., patented light-activated carbon fixation and RNA interference as the cure for all virus-driven pathology as: RNA-Guided Human Genome Engineering
5. Repetitive elements or endogenous viral elements can be targeted with engineered Cas+gRNA systems in microbes, plants, animals, or human cells to reduce deleterious transposition or to aid in sequencing or other analytic genomic/transcriptomic/proteomic/diagnostic tools (in which nearly identical copies can be problematic).