"Hexosaminidase B" 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.
A mammalian beta-hexosaminidase isoform that is comprized of hexosaminidase beta subunits. Deficiency of hexosaminidase B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.
| Descriptor ID |
D054819
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| MeSH Number(s) |
D08.811.277.450.483.180.875
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hexosaminidase B".
Below are MeSH descriptors whose meaning is more specific than "Hexosaminidase B".
This graph shows the total number of publications written about "Hexosaminidase B" by people in this website by year, and whether "Hexosaminidase B" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hexosaminidase B" by people in Profiles.
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Preferential beta-hexosaminidase (Hex) A (alpha beta) formation in the absence of beta-Hex B (beta beta) due to heterozygous point mutations present in beta-Hex beta-chain alleles of a motor neuron disease patient. J Biol Chem. 1994 Feb 18; 269(7):4819-26.