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Disease Info Card
Peripheral Motor Neuropathy
Information about Peripheral Motor Neuropathy: 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 Peripheral Motor Neuropathy
Most recent studies have shown that Peripheral Motor Neuropathy shares some biological mechanisms with amyotrophic-lateral-sclerosis, atrophy, demyelinating-diseases, demyelinating-polyneuropathy, demyelination, guillain-barre-syndrome, motor-neuron-disease, muscular-atrophy, nervous-system-disorder, nervousness, neuromuscular-diseases, peripheral-neuropathy, polyneuropathy, polyradiculoneuropathy, polyradiculoneuropathy-chronic-inflammatory-demyelinating, primary-lateral-sclerosis, sclerosis, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Peripheral Motor Neuropathy, and have been seen in publications frequently: Aging, Cell Death, Cell Proliferation, Complement Activation, Excretion, Glycosylation, Hypersensitivity, Immune Response, Inflammatory Response, Innervation, Localization, Muscle Atrophy, Muscle Hypertrophy, Myelination, Neuron Death, Neuroprotection, Pathogenesis, Reflex, Regeneration, Transport
Quite a number of genes have been found to play important roles in Peripheral Motor Neuropathy, such as BSCL2, CSF2, CST7, DBNL, GRIP1, HMBS, HSPB1, HSPB8, IGFALS, INS, KIF1B, LAMC2, MAD2L1BP, MAG, SETX, 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.