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Disease Info Card
Adrenomyeloneuropathy
Information about Adrenomyeloneuropathy: 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 Adrenomyeloneuropathy
Most recent studies have shown that Adrenomyeloneuropathy shares some biological mechanisms with addison-disease, adrenal-gland-hypofunction, adrenoleukodystrophy, atrophy, demyelinating-diseases, demyelination, diffuse-cerebral-sclerosis-of-schilder, multiple-sclerosis, muscle-spasticity, nervous-system-disorder, nervousness, paraparesis, paraparesis-spastic, paraplegia, peripheral-neuropathy, peroxisomal-disorders, sclerosis, spinal-cord-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Adrenomyeloneuropathy, and have been seen in publications frequently: Brain Development, Cell Death, Cognition, Cytokine Production, Hypersensitivity, Inflammatory Response, Localization, Muscle Contraction, Myelination, Oxidative Phosphorylation, Pathogenesis, Peroxisomal Membrane Transport, Pigmentation, Platelet Activation, Reflex, Response To Oxidative Stress, Spermatogenesis, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Adrenomyeloneuropathy, such as ABCB6, ABCD1, ABCD3, ABR, ACSBG1, CD1A, CD1B, CD1C, CD55, CSF2, IL6, LAMC2, MMEL1, PLXNB1, POMC, SELP, SLC27A2, 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.