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- Table of Contents
Disease Info Card
Limb Ataxias
Information about Limb Ataxias: 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 Limb Ataxias
Most recent studies have shown that Limb Ataxias shares some biological mechanisms with ataxia, ataxia-spinocerebellar, atrophy, cerebellar-ataxia, cerebellar-diseases, cerebral-infarction, cerebrovascular-accident, dog-diseases, dysarthria, gait-abnormality, gait-ataxia, infarction, neoplasms, nervousness, nystagmus, paresis, truncal-ataxia, vertigo, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Limb Ataxias, and have been seen in publications frequently: Cell Death, Cognition, Electron Transport, Excretion, Immune Response, Lipid Storage, Localization, Locomotion, Muscle Atrophy, Muscle Contraction, Neurogenesis, Neuron Development, Oxidative Phosphorylation, Pathogenesis, Proprioception, Reflex, Righting Reflex, Short-term Memory, Transport
Quite a number of genes have been found to play important roles in Limb Ataxias, such as AFG3L2, ATXN1, ATXN2, ATXN3, CACNA1A, CAT, CRAT, CSF2, FXN, GAA, GJB1, GLYAT, LAMC2, LY6E, NOP56, NTF3, NTRK3, PDYN, PRNP. 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.