Glycogen Phosphorylase, Muscle Form
"Glycogen Phosphorylase, Muscle Form" 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 isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in muscle. Mutation of the gene coding this enzyme is the cause of McArdle disease (GLYCOGEN STORAGE DISEASE TYPE V).
MeSH Number(s)
D08.811.913.400.450.460.400.186.312
Below are MeSH descriptors whose meaning is more general than "Glycogen Phosphorylase, Muscle Form".
Below are MeSH descriptors whose meaning is more specific than "Glycogen Phosphorylase, Muscle Form".
This graph shows the total number of publications written about "Glycogen Phosphorylase, Muscle Form" by people in Harvard Catalyst Profiles by year, and whether "Glycogen Phosphorylase, Muscle Form" was a major or minor topic of these publication.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
Below are the most recent publications written about "Glycogen Phosphorylase, Muscle Form" by people in Profiles.
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Glucopyranosylidene-spiro-iminothiazolidinone, a new bicyclic ring system: synthesis, derivatization, and evaluation for inhibition of glycogen phosphorylase by enzyme kinetic and crystallographic methods. Bioorg Med Chem. 2014 Aug 01; 22(15):4028-41.
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Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families. Neuromuscul Disord. 2002 Nov; 12(9):824-7.