| CST | Cerebroside sulfotransferase |
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| CBS | cerebroside sulfate |
| cerebroside | <biochemistry> Glycolipid found in brain (11% of dry matter). Sphingosine core with fatty amide or hydroxy fatty amide and a single monosaccharide on the alcohol group (either glucose or galactose). (18 Nov 1997) |
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| cerebroside lipidosis | <disease> A chronic congenital disease of lipid metabolism caused by a deficiency of the beta-glucocerebrosidase enzyme. The defect is most common in Ashkenazi Jews. Clinical features are hepatosplenomegaly (enlargement of liver and spleen) and in severe early onset forms of the disease, with neurological dysfunction. Inheritance: autosomal recessive. (27 Sep 1997) |
| cerebroside-sulfatase | <enzyme> An enzyme that catalyses the hydrolysis of cerebroside 3-sulfate (sulfatide) to yield a cerebroside and inorganic sulfate. A marked deficiency of arylsulfatase a, which is considered the heat-labile component of cerebroside sulfatase, has been demonstrated in all forms of metachromatic leukodystrophy (leukodystrophy, metachromatic). Chemical name: Cerebroside-3-sulfate 3-sulfohydrolase Registry number: EC 3.1.6.8 (12 Dec 1998) |
Synonyms : Cerebroside Sulfatase, Sulfatase, Sulfatidate
Synonyms :
| cerebroside sulfatase |
[EC 3.1.6.8] an enzyme of the hydrolase class that catalyzes the cleavage of sulfate residues from sulfatides to form cerebrosides. Deficiency of the enzyme, an autosomal recessive trait, is one of the causes of metachromatic leukodystrophy. Called also arylsulfatase A.
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| cerebroside |
leiten sich von den Ceramiden ab: Verbindung von Zucker u. Ceramiden
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