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Disease Info Card
Tdp-43 Proteinopathies
Information about Tdp-43 Proteinopathies: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Tdp-43 Proteinopathies
Most recent studies have shown that Tdp-43 Proteinopathies shares some biological mechanisms with alzheimers-disease, amyotrophic-lateral-sclerosis, aphasia, atrophy, dementia, dementia-hereditary-dysphasic-disinhibition, feline-urological-syndrome, frontotemporal-dementia, frontotemporal-lobar-degeneration, motor-neuron-disease, nerve-degeneration, nervousness, neurodegenerative-disorders, neurofibrillary-tangles, neuropathology-disease, parkinson-disease, primary-lateral-sclerosis, sclerosis, secondary-parkinson-disease, tauopathies.
Among the many pathways, these few ones have gauged particular interests from scientists studying Tdp-43 Proteinopathies, and have been seen in publications frequently: Aging, Autophagy, Cell Death, Cell Division, Cognition, Hyperphosphorylation, Localization, Mrna Processing, Mrna Transcription, Nuclear Export, Nuclear Transport, Pathogenesis, Programmed Cell Death, Proteolysis, Regulation Of Autophagy, Regulation Of Gene Expression, Rna Processing, Rna Splicing, Translation, Transport
Quite a number of genes have been found to play important roles in Tdp-43 Proteinopathies, such as ATXN2, CA1, CHMP2B, DCTN4, FUS, GRN, GTF2H1, IGF2BP2, IGFALS, KHDRBS1, MAPT, NUP62, RBM8A, REG1A, SNCA, SOD1, SQSTM1, TARDBP, VCP. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.