Cerebroside-Sulfatase
"Cerebroside-Sulfatase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An enzyme that catalyzes 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). EC 3.1.6.8.
Descriptor ID |
D002553
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MeSH Number(s) |
D08.811.277.352.827.070.250
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Concept/Terms |
Cerebroside-Sulfatase- Cerebroside-Sulfatase
- Cerebroside Sulfatase
- Sulfatidate Sulfatase
- Sulfatase, Sulfatidate
- Arylsulfatase A
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Below are MeSH descriptors whose meaning is more general than "Cerebroside-Sulfatase".
Below are MeSH descriptors whose meaning is more specific than "Cerebroside-Sulfatase".
This graph shows the total number of publications written about "Cerebroside-Sulfatase" by people in this website by year, and whether "Cerebroside-Sulfatase" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2005 | 0 | 1 | 1 |
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Below are the most recent publications written about "Cerebroside-Sulfatase" by people in Profiles.
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Cho YS, Iguchi N, Yang J, Handel MA, Hecht NB. Meiotic messenger RNA and noncoding RNA targets of the RNA-binding protein Translin (TSN) in mouse testis. Biol Reprod. 2005 Oct; 73(4):840-7.
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Penzien JM, Kappler J, Herschkowitz N, Schuknecht B, Leinekugel P, Propping P, T?nnesen T, Lou H, Moser H, Zierz S, et al. Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease. Am J Hum Genet. 1993 Mar; 52(3):557-64.
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Kappler J, Leinekugel P, Conzelmann E, Kleijer WJ, Kohlsch?tter A, T?nnesen T, Rochel M, Freycon F, Propping P. Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency. Hum Genet. 1991 Mar; 86(5):463-70.
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