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- Table of Contents
Information about Mucopolysaccharidosis Type Iiib: 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.
Most recent studies have shown that Mucopolysaccharidosis Type Iiib shares some biological mechanisms with atrophy, dementia, lysosomal-storage-diseases, mps-iii-a, mucopolysaccharidoses, mucopolysaccharidosis-i, mucopolysaccharidosis-ii, mucopolysaccharidosis-iii, mucopolysaccharidosis-mps-iv-a, mucopolysaccharidosis-type-iiic, mucopolysaccharidosis-type-ivb, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders, neuropathology-disease, pfaundler-hurler-syndrome, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mucopolysaccharidosis Type Iiib, and have been seen in publications frequently: Aging, Autophagy, Cell Death, Cell Migration, Cell Proliferation, Cholesterol Efflux, Cholesterol Storage, Circadian Rhythm, Excretion, Glycosylation, Habituation, Localization, Myelination, Neurogenesis, Pathogenesis, Phagocytosis, Pinocytosis, Protein Oxidation, Response To Pain, Secretion
Quite a number of genes have been found to play important roles in Mucopolysaccharidosis Type Iiib, such as BDNF, FGFR1, GLB1, GOLGA2, GUSB, HGSNAT, LAMP1, LYZ, MAP3K14, MAPT, NAGLU, NAGPA, NBAS, QPCT, SCN7A, SGSH, TLR2, TLR4. 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.