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Disease Info Card
Niemann-pick Disease, Type A
Information about Niemann-pick Disease, Type A: 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 Niemann-pick Disease, Type A
Most recent studies have shown that Niemann-pick Disease, Type A shares some biological mechanisms with aggressive-systemic-mastocytosis, gangliosidoses, gaucher-disease, globoid-cell-leukodystrophy, hepatomegaly, lipoidosis, lysosomal-storage-diseases, metabolic-diseases, mucopolysaccharidoses, nervousness, neurodegenerative-disorders, niemann-pick-disease-type-b, niemann-pick-disease-type-c, niemann-pick-diseases, ophthalmoplegia, sea-blue-histiocyte-syndrome, sphingolipidoses, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Niemann-pick Disease, Type A, and have been seen in publications frequently: Aging, Cell Death, Cell Development, Cell Differentiation, Cell Proliferation, Cholesterol Efflux, Cholesterol Esterification, Cholesterol Storage, Cholesterol Transport, Exocytosis, Immune Response, Induction Of Apoptosis, Lipid Storage, Localization, Membrane Organization, Myelination, Oligodendrocyte Development, Pathogenesis, Programmed Cell Death, Transport
Quite a number of genes have been found to play important roles in Niemann-pick Disease, Type A, such as ASAH1, CAT, CRAT, FOS, GBA, GLB1, GLYAT, HNRNPC, JUN, LDLR, MAG, MBP, NPB, NPC1, NPC2, PTK2B, SMPD1, SMPD2, 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.