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Subject It's NOT a VACCINE ! mRNA natural coding errors lead to a wide variety of Human Diseases. Alzheimer’s, Parkinson’s and Cancer
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Original Message As you may know by now, many threads have discussed the proposed "Fast TracK' vaccine and its use of artificial DNA components. Injected into the nucleus of the cell, effectively hijacking the RNA transcription process to produce protein based antibodies to Covid ... however most human disease processes are based in the RNA transcription process. What could go WRONG !

What You Should Know - mRNA natural coding errors lead to a wide variety of Human Diseases - including Alzheimer’s, Parkinson’s and Cancer.

RNA and Disease [link to www.ncbi.nlm.nih.gov (secure)]
“As there are numerous RNAs and a very large number of RNA-binding proteins, the biogenesis of RNPs must be orchestrated with great fidelity. Mutations that disrupt any of the components of RNPs, either RNAs or proteins, or the factors required for their assembly can be deleterious to cells and cause disease (Lukong et al., 2008; Wang and Cooper, 2007).

Table 1 list of RNA diseases, origins and effects on the Body (click to show Table)  
Trans-acting mutations affecting RNA-dependent functions that cause disease [link to www.ncbi.nlm.nih.gov (secure)]

Targeting mRNA translation in Parkinson's disease   [link to www.ncbi.nlm.nih.gov (secure)]
The exact cause(s) of PD is not well understood, although genetic mutations are associated with some forms of the disease. Many of these mutations, in particular those that are found in LRRK2, DJ-1, PINK1, and Parkin, are linked to the deregulation of mRNA translation, suggesting that this process is important for the onset of PD.

mRNA metabolism and neuronal disease [link to www.sciencedirect.com (secure)]
Recent studies have shown that mutations in components acting in trans on mRNAs are frequent causes of a large variety of different human disorders. The etiology of most of these diseases is, however, only poorly understood, mostly because the consequences for mRNA-metabolism are unclear. Here we discuss three prominent genetic diseases that fall into this category, namely spinal muscular atrophy (SMA), retinitis pigmentosa (RP) and X-linked syndromic mental retardation (XLMR).

Dyskeratosis congenita mRNA Disease   
[link to ghr.nlm.nih.gov (secure)]  

The hTR component is an RNA molecule, a chemical cousin of DNA. It provides a template for creating the repeated sequence of DNA that telomerase adds to the ends of chromosomes. The function of the hTERT component is to add the new DNA segment to chromosome ends. Cells that divide rapidly are especially vulnerable to the effects of shortened telomeres. As a result, people with dyskeratosis congenita may experience a variety of problems affecting quickly dividing cells in the body such as cells of the nail beds, hair follicles, skin, lining of the mouth (oral mucosa), and bone marrow.

Breakage and instability of chromosomes resulting from inadequate telomere maintenance may lead to genetic changes that allow cells to divide in an uncontrolled way, resulting in the development of cancer in people with dyskeratosis congenita.

More info at [link to essenceproject.net]
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