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Non-genetically modified models exhibit TARDBP mRNA increase due to perturbed TDP-43 autoregulation

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Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by accumulation of fragmented insoluble TDP-43 and loss of TDP-43 from the nucleus. Increased expression of exogenous TARDBP (encoding TDP-43) induces TDP-43 pathology and cytotoxicity. suggesting the involvement of aberrant expression of TDP-43 in the pathogenesis of ALS. In normal conditions. https://trendingcustomes.shop/product-category/sleeve-printed-sweatshirt/
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