Gangliosides

O-GlcNAcase ; Homo sapiens







13 Article(s)
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Title
Pub. Year
#Total Relationships
1 31097363 Ganglioside GM2 catabolism is inhibited by storage compounds of mucopolysaccharidoses and by cationic amphiphilic drugs. 2019 Sep - Oct 1
2 20821051 Substrate reduction therapy with miglustat in chronic GM2 gangliosidosis type Sandhoff: results of a 3-year follow-up. 2010 Dec 1
3 19898953 Miglustat therapy in juvenile Sandhoff disease. 2009 Dec 1
4 18588514 Identification and characterization of mature beta-hexosaminidases associated with human placenta lysosomal membrane. 2008 Aug 1
5 17994285 Increased lung surfactant phosphatidylcholine in patients affected by lysosomal storage diseases. 2007 Nov 1
6 12662933 Crystal structure of human beta-hexosaminidase B: understanding the molecular basis of Sandhoff and Tay-Sachs disease. 2003 Apr 11 1
7 12760286 Thermodynamic determination of plasma and leukocyte beta-hexosaminidase isoenzymes in homozygote and heterozygote carriers for the GM2 gangliosidosis B1 variant. 2003 May 2
8 11278374 Degradation of membrane-bound ganglioside GM2 by beta -hexosaminidase A. Stimulation by GM2 activator protein and lysosomal lipids. 2001 Apr 20 1
9 9572057 Biology and potential strategies for the treatment of GM2 gangliosidoses. 1998 Apr 1
10 7766021 Purification of a chitooligosaccharidolytic beta-N-acetylglucosaminidase from Bombyx mori larvae during metamorphosis and the nucleotide sequence of its cDNA. 1995 Feb 1
11 3935131 Molecular forms of GM2-activator protein. A study on its biosynthesis in human skin fibroblasts. 1985 Sep 1
12 6225718 Activating proteins for ganglioside GM2 degradation by beta-hexosaminidase isoenzymes in tissue extracts from different species. 1983 Jul 1
13 7451432 Isolation and characterization of a novel monosialosylpentahexosyl ceramide from Tay-Sachs brain. 1981 Jan 10 1