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Disease Info Card
Muscular Atrophy
Information about Muscular Atrophy: 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 Muscular Atrophy
Most recent studies have shown that Muscular Atrophy shares some biological mechanisms with amyotrophic-lateral-sclerosis, atrophy, charcot-marie-tooth-disease, dystrophy, hypertrophy, malignant-neoplasms, motor-neuron-disease, muscle-weakness, muscular-dystrophy, myopathy, nerve-degeneration, neuromuscular-diseases, pain, primary-lateral-sclerosis, sclerosis, spinal-muscular-atrophies-of-childhood, spinal-muscular-atrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Muscular Atrophy, and have been seen in publications frequently: Aging, Autophagy, Cell Death, Cell Proliferation, Excretion, Flight, Inflammatory Response, Innervation, Localization, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Pathogenesis, Proteolysis, Reflex, Regeneration, Secretion, Skeletal Muscle Atrophy, Translation, Transport
Quite a number of genes have been found to play important roles in Muscular Atrophy, such as AKR1B1, AKT1, AR, AREG, DMD, FBXO32, FDXR, IGF1, IGFALS, IL6, INS, MSTN, NAIP, SMN1, SNRPN, SOD1, STMN1, TNF, TRIM63. 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.