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Disease Info Card
Neurocutaneous Syndromes
Information about Neurocutaneous Syndromes: 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 Neurocutaneous Syndromes
Most recent studies have shown that Neurocutaneous Syndromes shares some biological mechanisms with angiomatosis, brain-neoplasms, dermatologic-disorders, dysplasia, epilepsy, hamartoma, hemangioma, malignant-paraganglionic-neoplasm, melanocytic-nevus, melanosis, neoplasms, nervousness, neurofibromatoses, neurofibromatosis-1, sclerosis, skin-neoplasms, sturge-weber-syndrome, tuberous-sclerosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neurocutaneous Syndromes, and have been seen in publications frequently: Angiogenesis, Brain Development, Cell Cycle, Cell Growth, Cell Migration, Cell Proliferation, Coagulation, Dna Repair, Enucleation, Excretion, Innervation, Localization, Mitotic Recombination, Myelination, Oncogenesis, Pathogenesis, Pigmentation, Translation, Vasculogenesis, Vasoconstriction
Quite a number of genes have been found to play important roles in Neurocutaneous Syndromes, such as ADH5, AKT1, ALDH3A2, CSF2, IKBKG, LAMC2, MTOR, NF1, NF2, NLRP3, PNPLA6, POMC, SLC12A3, SS18L1, TESC, TSC1, TSC2. 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.