Utrophin
"Utrophin" 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 autosomally-encoded 376-kDa cytoskeletal protein that is similar in structure and function to DYSTROPHIN. It is a ubiquitously-expressed protein that plays a role in anchoring the CYTOSKELETON to the PLASMA MEMBRANE.
Descriptor ID |
D049411
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MeSH Number(s) |
D12.776.220.987 D12.776.543.985
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Concept/Terms |
Utrophin- Utrophin
- UTRN Protein
- Dystrophin-Related Protein
- Dystrophin Related Protein
- Dystrophin-Related Protein 1
- Dystrophin Related Protein 1
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Below are MeSH descriptors whose meaning is more general than "Utrophin".
Below are MeSH descriptors whose meaning is more specific than "Utrophin".
This graph shows the total number of publications written about "Utrophin" by people in this website by year, and whether "Utrophin" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2009 | 0 | 1 | 1 | 2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Utrophin" by people in Profiles.
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Gutpell KM, Hrinivich WT, Hoffman LM. Skeletal muscle fibrosis in the mdx/utrn+/- mouse validates its suitability as a murine model of Duchenne muscular dystrophy. PLoS One. 2015; 10(1):e0117306.
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Ahmad N, Bygrave M, Chhem R, Hoffman L, Welch I, Grange R, Fenster A, Hill D, Lee TY. High-frequency ultrasound to grade disease progression in murine models of Duchenne muscular dystrophy. J Ultrasound Med. 2009 Jun; 28(6):707-16.
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Porter JD, Merriam AP, Hack AA, Andrade FH, McNally EM. Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice. Neuromuscul Disord. 2001 Mar; 11(2):197-207.
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