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Glycosphingolipid
- The ST3GAL5 gene provides instructions for making an enzyme called GM3 synthase. This enzyme carries out a chemical reaction that is the first step in the ...
- Fabry disease is an inherited disorder that results from the buildup of a type of fat, called globotriaosylceramide, in the body's cells. Beginning in childhood, ...
- GM2 activator deficiency (sometimes called GM2 gangliosidosis, AB variant) is a rare inherited disorder that causes progressive brain injury. Most individuals ...
- The HEXA gene provides instructions for making one part (subunit) of an enzyme called beta-hexosaminidase A. Specifically, the protein produced from the HEXA ...
- The GLA gene provides instructions for making an enzyme called alpha-galactosidase A. This enzyme is active in lysosomes, which are structures that act as ...
- ... the Platelet Glycoprotein Ib-IX Complex to the Glycosphingolipid-enriched Membrane Domain. J Biol Chem. 2015 Sep ...
- ... on PubMed Essentials of Glycobiology (first edition, 1999): Glycosphingolipid Degradation Gieselmann V, Krageloh-Mann I. Metachromatic leukodystrophy-- ...
- ... the Platelet Glycoprotein Ib-IX Complex to the Glycosphingolipid-enriched Membrane Domain. J Biol Chem. 2015 Sep ...
- ... on PubMed Essentials of Glycobiology (first edition, 1999): Glycosphingolipid Degradation Grossi S, Regis S, Rosano C, Corsolini ...
- ... storage disease" where abnormal amounts of lipids called "glycosphingolipids" are stored in special cells called reticuloendothelial cells. ...