Molecular Forms of GM2-Activator Protein. A Study on its Biosynthesis in Human Skin Fibroblasts
Author:
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry
Link
https://www.degruyter.com/document/doi/10.1515/bchm3.1985.366.2.887/pdf
Reference14 articles.
1. AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2.
2. Eine Cerebrosidsulfatase aus Schweineniere
3. An activator stimulating the enzymic hydrolysis of sphingoglycolipids.
4. Enzyme-linked Immunosorbent Assay for the Ganglioside GM2-Activator Protein. Screening of Normal Human Tissues and Body Fluids, of Tissues of GM2Gangliosidosis, and for Its Subcellular Localization
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1. GM2 activator deficiency/GM2 gangliosidosis – deficiency of the activator protein;Atlas of Inherited Metabolic Diseases 3E;2011-12-30
2. Activator Proteins for Lysosomal Glycolipid Hydrolysis;Methods of Biochemical Analysis;2006-10-31
3. 8. The GM2-gangliosidoses and the elucidation of the β-hexosaminidase system;Tay-Sachs Disease;2001
4. The GM2 activator protein, its roles as a co-factor in GM2 hydrolysis and as a general glycolipid transport protein;Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism;1998-07
5. Biochemical Characterization of the Cys138Arg Substitution Associated with the AB Variant Form of GM2 Gangliosidosis: Evidence That Cys138 Is Required for the Recognition of the GM2 Activator/GM2 Ganglioside Complex by β-Hexosaminidase A;Biochemistry;1998-01-01
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