"alpha-L-Fucosidase" 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 an alpha L-fucoside to yield an alcohol and L-fucose. Deficiency of this enzyme can cause FUCOSIDOSIS. EC 3.2.1.51.
Descriptor ID |
D005644
|
MeSH Number(s) |
D08.811.277.450.050
|
Concept/Terms |
alpha-L-Fucosidase- alpha-L-Fucosidase
- alpha L Fucosidase
- Fucosidase
- alpha-Fucosidase
- alpha Fucosidase
|
Below are MeSH descriptors whose meaning is more general than "alpha-L-Fucosidase".
Below are MeSH descriptors whose meaning is more specific than "alpha-L-Fucosidase".
This graph shows the total number of publications written about "alpha-L-Fucosidase" by people in this website by year, and whether "alpha-L-Fucosidase" was a major or minor topic of these publications.
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Below are the most recent publications written about "alpha-L-Fucosidase" by people in Profiles.
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The genes encoding the peripheral cannabinoid receptor and alpha-L-fucosidase are located near a newly identified common virus integration site, Evi11. J Virol. 1997 Sep; 71(9):6796-804.
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Prenatal diagnosis of mucolipidosis type II on first-trimester amniotic fluid. Prenat Diagn. 1990 Apr; 10(4):231-5.
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[Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1985 Dec; 7(6):475-7.