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Disease Info Card
Lysosomal Storage Diseases
Information about Lysosomal Storage 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 Lysosomal Storage Diseases
Most recent studies have shown that Lysosomal Storage Diseases shares some biological mechanisms with aspartylglucosaminuria, fabry-disease, gangliosidoses, gaucher-disease, glycogen-storage-disease-type-ii, inborn-errors-of-metabolism, leukodystrophy, leukodystrophy-metachromatic, metabolic-diseases, mucolipidoses, mucopolysaccharidoses, mucopolysaccharidosis-i, mucopolysaccharidosis-vii, nerve-degeneration, nervousness, neurodegenerative-disorders, neuronal-ceroid-lipofuscinoses, niemann-pick-diseases, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Lysosomal Storage Diseases, and have been seen in publications frequently: Aging, Autophagy, Cell Death, Endocytosis, Excretion, Exocytosis, Fatty Acid Oxidation, Glycosylation, Immune Response, Intracellular Transport, Lipid Storage, Localization, Myelination, Pathogenesis, Proteolysis, Receptor-mediated Endocytosis, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Lysosomal Storage Diseases, such as AGA, ARSA, ARSB, ASAH1, CTSA, ELF3, GAA, GBA, GLA, GLB1, GUSB, MCOLN1, PPT1, PSAP, SGSH, SMPD1, TPP1. 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.