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- W2934821657 abstract "Through a combination of in silico research and reviews of previous work, mechanisms by which nonsense-mediated mRNA decay (NMD) affects the inheritance and expressivity of Waardenburg syndrome is realized. While expressivity and inheritance both relate to biochemical processes underlying a gene's function, this research explores how alternative splicing and premature termination codons (PTC's) within mRNAs mutated in the disease are either translated into deleterious proteins or decayed to minimize expression of altered proteins. Elucidation of splice variants coupled with NMD perpetuating the various symptoms and inheritance patterns of this disease represent novel findings. By investigating nonsense mutations that lie within and outside the NMD boundary of these transcripts we can evaluate the effects of protein truncation versus minimized protein expression on the variable expressivity found between Type I and Type III Waardenburg syndrome, PAX3, while comparatively evaluating EDN3 and SOX10's role in inheritance of Type IV subtypes of the disease. This review will demonstrate how alternative splicing perpetuates or limits NMD activity by way of PTC positioning, thereby affecting the presentation of Waardenburg syndrome." @default.
- W2934821657 created "2019-04-11" @default.
- W2934821657 creator A5052784998 @default.
- W2934821657 date "2017-10-01" @default.
- W2934821657 modified "2023-10-14" @default.
- W2934821657 title "Waardenburg Syndrome Expression and Penetrance" @default.
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- W2934821657 doi "https://doi.org/10.29245/2572-9411/2017/6.1118" @default.
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