Digital Inbreeding (3)

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Moronic theorists and liberals who tout AI and “De novo design of peptide binders to conformationally diverse targets with contrastive language modeling” 1/22/25 may argue to no avail against established facts from model organisms that link Trump’s 4/23/20 claim to biophysically constrained viral latency across kingdoms via God’s Creation of sunlight and humidity at the origin of life, and the overwhelming complexity of “Rapid and Non-Targeted Qualitative and Quantitative Detection of miRNA in Complex Biological Samples Using Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry with a 3-Aminoquinoline and 2′,4′,6′-Trihydroxyacetophenone Ionic Liquid Matrix” 1/30/25

Claims that link miRNAs from laser light detection of the overwhelming complexity of life to claims that people mathemagically evolved from pond scum after energy automagically emerged from the cosmic void. Simply put, “You are what you eat!” links food energy to the Creation of miRNAs, and the metabolism of food to pheromones linked to the physiology of reproduction in Biblical Genesis. The pheromone regulated physiology of reproduction of species from E. coli to cancer-free African elephants went missing from stupid theories since the time that Jacques Monod famously said: “What is true for E. coli is true for the elephant.”

See for examples wysocki c and preti g 13 results
The Effect of Ethnicity on Human Axillary Odorant Production. 2016
Ethnic/racial and genetic influences on cerumen odorant profiles. 2014

Analyses of volatile organic compounds from human skin. 2008
Biological basis of the third-cousin crush. 2008
Preference for human body odors is influenced by gender and sexual orientation. 2005
Male axillary extracts contain pheromones that affect pulsatile secretion of luteinizing hormone and mood in women recipients. 2003

LH promotes the proliferation of porcine primordial germ cell-like cells (pPGCLCs) by regulating the ceRNA network related to the TGF-β signaling pathway 9/24/24

“LH promoted pPGCLCs proliferation by affecting the interactions of lncRNAs, miRNAs, and mRNAs that were related to the TGF-β signaling pathway.”

See also: The temporal scaling of Caenorhabditis elegans ageing 1/27/16

My group published on this in Hormones and Behavior. See: From Fertilization to Adult Sexual Behavior (1996).

Our claims were linked to: “…an organismal ageing dynamics that is invariant across genetic and environmental contexts provides the basis for a new, quantitative framework for evaluating the manner and extent to which specific molecular processes contribute to the aspect of ageing that determines lifespan.”

AND to all biodiversity across kingdoms via the 2024 Nobel Prizes in Physics, Chemistry and Medicine “for the discovery of microRNA and its role in post-transcriptional gene regulation”

Having learned about the intricate levels of virus-driven disease prevention and healthy longevity before publishing my third peer-reviewed journal article in 2013, I became more concerned when the facts led to the unnecessary suffering and premature deaths of my loved ones and friends during the past decade.

Trump-hating moronic liberals and Artificial Intelligence will continue to cause the unnecessary suffering and premature deaths.

See: What is the origin of the “Regulatory T cells found to safeguard brain health and memory formation” 1/28/25

The origin of the news regarding “Regulatory T cells found to safeguard brain health and memory formation” can be traced back to research findings published by Harvard University. According to posts found on X and related web results, this research was highlighted by Harvard Gazette on January 28, 2025. The study identifies a unique compartment of regulatory T cells residing in the meninges surrounding the brain, which play a crucial role in protecting brain health and aiding memory formation by acting as guardians against inflammation and supporting nerve cell regeneration. This research underscores the broader function of regulatory T cells beyond their traditional immune-regulatory roles, positioning them as key players in maintaining brain health and cognitive functions.

See also: Is there a third generation sequencing panel that links skin cancer to brain cancer? 1/30/25

There doesn’t appear to be a specific third-generation sequencing panel dedicated to linking skin cancer directly to brain cancer. However, several comprehensive cancer panels include genes associated with both skin and brain cancers among other types. Here are some details from existing panels:

Invitae Multi-Cancer + RNA Panel examines genes associated with hereditary cancers across various organ systems, including skin (melanoma, basal cell carcinoma) and brain/nervous system cancers. This panel uses next-generation sequencing technology (NGS) but does not specify it as third-generation sequencing. It also includes RNA testing to aid in variant interpretation. CleanPlex® Comprehensive Hereditary Cancer Panel by Paragon Genomics targets 88 genes linked to hereditary cancers, including those for skin cancer (melanoma) and brain cancer, using amplicon-based targeted sequencing, which falls under next-generation sequencing rather than third-generation. UCSF Expanded Hereditary Cancer Panel targets 88 genes associated with hereditary cancer, covering major organ systems like skin and brain/nervous system. This panel uses Illumina sequencing systems with targeted enrichment, again, part of NGS but not explicitly third-generation sequencing. Illumina’s Cancer Panels provide various NGS panels for cancer research, including panels that might cover gene variants relevant to both skin and brain cancers in a broad pan-cancer context. However, these are not specifically third-generation sequencing panels either. Scientific research has utilized NGS panels to study cancers like melanoma, which can sometimes be linked to genetic predispositions that might also affect brain cancer risk, but these studies focus more on individual cancer types rather than direct links between them.

While these panels do not focus on a direct link between skin and brain cancers, they do include genes relevant to both types of cancers, which might help in understanding shared genetic pathways or predispositions. However, third-generation sequencing, which often refers to technologies like single-molecule real-time sequencing or nanopore sequencing, isn’t explicitly mentioned in these panels for such specific links.

If your interest lies in third-generation sequencing specifically, you might need to look for studies or panels that apply these technologies to cancer research, but as of now, there isn’t a well-documented panel with that specific focus.

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