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Disease Info Card
Hereditary Motor Neurone Disease
Information about Hereditary Motor Neurone 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 Hereditary Motor Neurone Disease
Most recent studies have shown that Hereditary Motor Neurone Disease shares some biological mechanisms with amyotrophic-lateral-sclerosis, atrophy, dementia, edema, motor-neuron-disease, muscular-atrophy, muscular-fasciculation, nerve-degeneration, nervousness, neurodegenerative-disorders, neurofibrillary-tangles, neuromuscular-diseases, parkinson-disease, primary-lateral-sclerosis, sclerosis, spinal-and-bulbar-muscular-atrophy-x-linked-1, spinal-muscular-atrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Motor Neurone Disease, and have been seen in publications frequently: Aging, Cell Cycle, Cell Morphogenesis, Cell Proliferation, Lipid Oxidation, Lipid Transport, Muscle Atrophy, Neuroprotection, Pathogenesis, Proteolysis, Regulation Of Lipid Transport, Rna Processing, Schwann Cell Proliferation, Transport
Quite a number of genes have been found to play important roles in Hereditary Motor Neurone Disease, such as AKR1B1, AR, AREG, BDNF, FDXR, HNRNPR, IGFALS, MAP1B, NEFH, OSBP, SLC1A2, SMN1, SNRPN, SOD1, STMN1, SYNCRIP, TARDBP, VAPA. 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.