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Disease Info Card
Nerve Compression Syndrome
Information about Nerve Compression Syndrome: 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 Nerve Compression Syndrome
Most recent studies have shown that Nerve Compression Syndrome shares some biological mechanisms with back-pain, carpal-tunnel-syndrome, disorder-of-the-optic-nerve, entrapment-neuropathies, fracture, glanders, intervertebral-disk-displacement, neoplasms, nerve-compression, nerve-entrapment, neuralgia, pain, paresthesia, peripheral-neuropathy, radiculopathy, sciatica, stenosis, trigeminal-neuralgia, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Nerve Compression Syndrome, and have been seen in publications frequently: Aging, Bone Resorption, Cell Proliferation, Coagulation, Dehiscence, Enucleation, Hypersensitivity, Innervation, Localization, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Myelination, Ossification, Pathogenesis, Reflex, Regeneration, Sensitization, Transport, Transposition
Quite a number of genes have been found to play important roles in Nerve Compression Syndrome, such as ARNTL, C2, C7, CSF2, CXCL10, GRIP1, HNRNPC, LAMC2, MVD, PMP22, POMC, PSMD1, RPL4, RPL5, SS18L1, 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.