Glycosphingolipid β-Galactosidases
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference41 articles.
1. Metabolic Basis of Inherited Disease;Stanbury,1972
2. Globoid Cell Leucodystrophy (Krabbe's Disease): Deficiency of Galactocerebroside -Galactosidase
3. Lactosyl Ceramidosis: Catabolic Enzyme Defect of Glycosphingolipid Metabolism
4. Fabry's Disease: Alpha-Galactosidase Deficiency
5. Generalized Gangliosidosis: Beta-Galactosidase Deficiency
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3. Molecular basis of GM1 gangliosidosis and Morquio disease, type B. Structure–function studies of lysosomal β-galactosidase and the non-lysosomal β-galactosidase-like protein;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1999-10
4. Hydrolysis of lactosylceramide by human galactosylceramidase and GM1-beta-galactosidase in a detergent-free system and its stimulation by sphingolipid activator proteins, sap-B and sap-C Activator proteins stimulate lactosylceramide hydrolysis;European Journal of Biochemistry;1994-05
5. Chloride binding proteins: mechanistic implications for the oxygen-evolving complex of Photosystem II;Photosynthesis Research;1990-01
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