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Disease Info Card
Muscle Weakness
Information about Muscle Weakness: 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 Muscle Weakness
Most recent studies have shown that Muscle Weakness shares some biological mechanisms with atrophy, autoimmune-reaction, dermatomyositis, dystrophy, malignant-neoplasms, muscle-hypotonia, muscular-atrophy, muscular-dystrophy, myasthenia-gravis, myasthenias, myopathy, myositis, neoplasms, neuromuscular-diseases, pain, polymyositis, sclerosis, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Muscle Weakness, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Death, Excretion, Fatty Acid Oxidation, Immune Response, Inflammatory Response, Innervation, Lipid Storage, Localization, Locomotion, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Pathogenesis, Proprioception, Reflex, Regeneration, Secretion, Transport
Quite a number of genes have been found to play important roles in Muscle Weakness, such as ACHE, AR, CHKA, CHKB, CSF2, DMD, DMPK, GAA, GRIP1, IGFALS, INS, LAMC2, PIK3C2A, POMC, PTH, SMN1, SOD1, TNF. 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.