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Disease Info Card
Neuralgic Amyotrophy
Information about Neuralgic Amyotrophy: 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 Neuralgic Amyotrophy
Most recent studies have shown that Neuralgic Amyotrophy shares some biological mechanisms with atrophy, brachial-plexus-neuritis, brachial-plexus-neuropathies, hereditary-liability-to-pressure-palsies, inherited-neuropathy, muscle-weakness, muscular-atrophy, nerve-compression-syndrome, nervous-system-disorder, nervousness, neuralgia, neuritis, pain, paresis, peripheral-neuropathy, shoulder-pain, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neuralgic Amyotrophy, and have been seen in publications frequently: Cell Division, Cell Migration, Chromosome Segregation, Coagulation, Cytokinesis, Exocytosis, Hypersensitivity, Innervation, Intracellular Transport, Localization, Meiosis, Muscle Atrophy, Muscle Hypertrophy, Parturition, Pathogenesis, Reflex, Regeneration, Spermatogenesis, Translation, Transport
Quite a number of genes have been found to play important roles in Neuralgic Amyotrophy, such as C5, CSF2, GJB1, KIF1B, LAMC2, LIMS1, LMNA, MAD2L1BP, MB, MPZ, PMP22, PSMA7, PXMP2, RPLP0, SEC14L1, SOD1, SRSF2, TIMP2. 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.