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Disease Info Card
Niemann-pick Diseases
Information about Niemann-pick Diseases: 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 Diseases
Most recent studies have shown that Niemann-pick Diseases shares some biological mechanisms with aggressive-systemic-mastocytosis, fabry-disease, gangliosidoses, gaucher-disease, inborn-errors-of-metabolism, leukodystrophy-metachromatic, lipoidosis, lysosomal-storage-diseases, metabolic-diseases, mucopolysaccharidoses, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders, niemann-pick-disease-type-a, niemann-pick-disease-type-b, niemann-pick-disease-type-c, sphingolipidoses, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Niemann-pick Diseases, and have been seen in publications frequently: Autophagy, Cell Death, Cholesterol Efflux, Cholesterol Esterification, Cholesterol Homeostasis, Cholesterol Storage, Cholesterol Transport, Endocytosis, Hyperphosphorylation, Intestinal Cholesterol Absorption, Intracellular Cholesterol Transport, Intracellular Transport, Lipid Storage, Lipid Transport, Localization, Myelination, Pathogenesis, Secretion, Sterol Transport, Transport
Quite a number of genes have been found to play important roles in Niemann-pick Diseases, such as ABCA1, APOA1, APP, ARHGAP4, CTLA4, GBA, GFAP, GLB1, HLA-DQA1, HNRNPC, LDLR, MAPT, NOD2, NPC1, NPC1L1, NPC2, PFDN4, SMPD1, 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.