Information Wars started by medical professionals (4)

Summary: Schrödinger at 75 – The Future of Biology – September 2018 will link what ages 10+ can learn about cell biology by playing the game, Cytosis to what they will also be able to learn when the game Subatomic becomes available.

The serrulatane diterpenoid natural products RAD288 and RAD289 stimulate properties of olfactory ensheathing cells useful for neural repair therapies (July 6, 2018)

These results indicate that RAD288 and RAD289 stimulate specific but different activities of OECs, and are active on select cell types. These serrulatane diterpenoids are therefore potentially useful for improving glial cell activity in cell transplantation therapies.


… we showed that the serrulatane diterpenoids RAD288 and RAD289 enhanced proliferation and phagocytic ability of mOECs and that only RAD288 stimulated migration of the cells. In contrast, RAD288 and RAD289 had no effect on Schwann cell viability suggesting that they may have cell-type specific effects on OECs. Therefore, these natural products may have high potential for improving the use of OECs for transplantation therapy for neural repair.

Cell-type specific effects on OECs are quantized energy-dependent and RNA-mediated. The effects link DNA repair to healthy longevity and effective treatments for virus-damaged DNA.   Delayed reporting of results like these obfuscates what is known to all serious scientists about how biophysically constrained viral latency is linked to healthy longevity.

Reported on August 13, 2018 as: Could nose cells treat spinal cord injuries?

  1. Researchers used cells supporting the ‘olfactory’ nerve cells, which create our sense of smell.
  2. …humans are more complex. But this research paves the way for clinical trials anticipated to begin in 2020, using nasal cells from spinal cord injury sufferers and giving hope to many that they may walk again.

The complexity of the molecular mechanisms does not vary across species or across kingdoms.

See: Feedback loops link odor and pheromone signaling with reproduction.

See for comparison: 2011 Pheromones and the luteinizing hormone for inducing proliferation of neural stem cells and neurogenesis

Re: Use of a pheromone, a luteinizing hormone (LH) and/or a human chorionic gonadotrophin (hCG) to induce proliferation of neural stem cells and neurogenesis.

The method can be practiced in vivo to obtain more neural stem cells in situ, which can in turn produce more neurons or glial cells to compensate for lost or dysfunctional neural cells. The method can also be practiced in vitro to produce a large number of neural stem cells in culture. The cultured stem cells can be used, for example, for transplantation treatment of patients or animals suffering from or suspected of having neurodegenerative diseases or conditions.

The effective treatment of all neurodegenerative diseases has been put on hold for several years. Biologically uninformed theorists failed to link the creation of anti-entropic virucidal light to biophysically constrained viral latency and healthy longevity in all living genera via the pheromone-controlled physiology of reproduction in species from microbes to humans.

The hold may be explained in the context of attempts to secure the patent on naturally occurring biophysically constrained viral latency in the context of RNA interference.

RNA-Guided Human Genome Engineering (2015)

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).

The fact that the virus-driven degradation of messenger RNA can be targeted with the light activated energy-dependent creation of microRNAs in all cell types of all microbes, plants, and animals was revised for representation. Rather than admit that naturally occurring RNA interference is the key to DNA repair, obfuscation via use of the terms “spacer-repeat units” and “cleavage of nucleic acids” has clearly prevailed.

See: RNA-guided human genome engineering (2016)

…exemplary short RNA/enzyme systems may be identified within bacteria or archaea, such as (CRISPR)/CRISPR-associated (Cas) systems that use short RNA to direct degradation of foreign nucleic acids. CRISPR (“clustered regularly interspaced short palindromic repeats”) defense involves acquisition and integration of new targeting “spacers” from invading virus or plasmid DNA into the CRISPR locus, expression and processing of short guiding CRISPR RNAs (crRNAs) consisting of spacer-repeat units, and cleavage of nucleic acids (most commonly DNA) complementary to the spacer.

Thank God, Schrödinger at 75 – The Future of Biology – September 2018 will link what ages 10+ can learn about cell biology by playing the game, Cytosis to what they will also be able to learn when the game Subatomic becomes available.

Author: James Kohl

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