See first: Pheromones protect us from viruses (7)


When others link God’s Creation of anti-entropic virucidal light to pH-dependent biophysically constrained viral latency via His Creation of water, which is required for the creation of all oxygen-dependent life on Earth, we will see how God’s Creation of Genotypes in all species once protected them, and us, from the virus-driven degradation of messenger RNA.

More than 118,000 indexed published articles mention ‘microRNA.’ It is long past time for theorists to learn how light-activated microRNA biogenesis links microRNAs from food odors and pheromones to biophysically constrained viral latency and healthy longevity across kingdoms via the physiology of pheromone-controlled genetic processes that prevent the virus-driven degradation of messenger RNA in organized genomes.

Only then will biologically uninformed theorists, Communists, and other atheists stop touting pseudoscientific nonsense about self-assembly, like this:

In vivo self-assembled small RNAs as a new generation of RNAi therapeutics 3/29/21

…our strategy induces controllable and predictable self-assembly and delivery of siRNAs in the heterogeneous, dynamic in vivo environment and allows precise control of gene expression in a purpose-driven mode. This state-of-the-art technology has major theoretical significance and translational value because it provides a feasible strategy to overcome the paramount barrier to the therapeutic application of RNAi in vivo, thus representing a new generation of RNAi therapeutics for a variety of diseases ranging from cancers to metabolic diseases.

Nothing self-assembles itself. Their ‘strategy’ is to lie about the fact that light-activated assembly of the microRNA-RNA-peptide nanocomplex biophysically constrains viral latency across kingdoms via pheromone-regulated genetic processes of reproduction.

For comparison, George M. Church et al., patented in vivo RNAi therapeutics. See: 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…(in which nearly identical copies can be problematic).

All intelligent serious scientists have followed the lead of Church et al.  See for instance: The predictive power of the microbiome exceeds that of genome-wide association studies in the discrimination of complex human disease 1/1/20 and Regulation of host and virus genes by neuronal miR-138 favours herpes simplex virus 1 latency 2/8/21. The report on biophysically constrained viral latency involved collaboration with researchers from China. Is George M. Church an atheist, or a Communist sympathizer?

Is there something that he is not telling us? See: The potential of miRNA-based therapeutics in Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection: a review 3/24/21

It attests to the facts that link peptide synthesis at the origin of life to biophysically constrained viral latency across kingdoms via light-activated carbon fixation and Prebiotic synthesis of cysteine peptides that catalyze peptide ligation in neutral water 11/13/20, which was presciently reported as: Life’s biochemical networks could have formed spontaneously on Earth 5/3/19.

If you try to link what could have formed spontaneously to self-assembled small RNAs as a new generation of RNAi therapeutics, you will be ridiculed by all intelligent serious scientists who have linked God’s Creation of sunlight and humidity to Visualizing a protonated RNA state that modulates microRNA-21 maturation 10/26/20.

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