Interaction of GM2 Activator Protein with Glycosphingolipids
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference37 articles.
1. Lysosomes in Biology and Pathology;Li,1984
2. Hydrolysis of Tay-Sachs Ganglioside by β-Hexosaminidase A of Human Liver and Urine
3. Characterization of an activating factor required for hydrolysis of Gm2 ganglioside catalyzed by hexosaminidase A
4. Purification and Characterization of an Activator Protein for the Degradation of Glycolipids GM2and GA2by Hexosaminidase A
5. AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2.
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2. Identification and characterization of the Onchocerca volvulus Excretory Secretory Product Ov28CRP, a putative GM2 activator protein;PLOS Neglected Tropical Diseases;2019-07-22
3. Membrane lipids and their degradation compounds control GM2 catabolism at intralysosomal luminal vesicles;Journal of Lipid Research;2019-06
4. GM2 activator protein deficiency, mimic of Tay-Sachs disease;International Journal of Epilepsy;2017-12
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