This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Machado-joseph Disease
Information about Machado-joseph Disease: 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 Machado-joseph Disease
Most recent studies have shown that Machado-joseph Disease shares some biological mechanisms with ataxia, ataxia-spinocerebellar, atrophy, cerebellar-ataxia, dentatorubral-pallidoluysian-atrophy, dystonia-disorders, huntington-disease, multiple-system-atrophy, muscular-atrophy, nerve-degeneration, nervousness, neurodegenerative-disorders, nystagmus, olivopontocerebellar-atrophies, opca-menzel-type, parkinson-disease, spinocerebellar-degeneration, trinucleotide-repeat-expansion.
Among the many pathways, these few ones have gauged particular interests from scientists studying Machado-joseph Disease, and have been seen in publications frequently: Aging, Autophagy, Cell Cycle, Cell Death, Cognition, Dna Repair, Gene Conversion, Histone Acetylation, Localization, Meiosis, Muscle Atrophy, Neuroprotection, Nuclear Export, Pathogenesis, Protein Folding, Proteolysis, Reflex, Rna Interference, Segmentation, Transport
Quite a number of genes have been found to play important roles in Machado-joseph Disease, such as AR, ATN1, ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, CREBBP, HSPB1, HTT, LY6E, MAPT, PDYN, SCD, SLC6A4, SQSTM1, TBP, 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.