"Muscle Proteins" 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.
The protein constituents of muscle, the major ones being ACTINS and MYOSINS. More than a dozen accessory proteins exist including TROPONIN; TROPOMYOSIN; and DYSTROPHIN.
| Descriptor ID |
D009124
|
| MeSH Number(s) |
D12.776.210.500
|
| Concept/Terms |
Muscle Proteins- Muscle Proteins
- Proteins, Muscle
- Muscle Protein
- Protein, Muscle
|
Below are MeSH descriptors whose meaning is more general than "Muscle Proteins".
Below are MeSH descriptors whose meaning is more specific than "Muscle Proteins".
This graph shows the total number of publications written about "Muscle Proteins" by people in this website by year, and whether "Muscle Proteins" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2016 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Muscle Proteins" by people in Profiles.
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Mining the Secretome of C2C12 Muscle Cells: Data Dependent Experimental Approach To Analyze Protein Secretion Using Label-Free Quantification and Peptide Based Analysis. J Proteome Res. 2018 02 02; 17(2):879-890.
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DNA methylation array analysis identifies breast cancer associated RPTOR, MGRN1 and RAPSN hypomethylation in peripheral blood DNA. Oncotarget. 2016 Sep 27; 7(39):64191-64202.
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Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing. PLoS One. 2016; 11(1):e0146040.
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Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. Am J Hum Genet. 2011 May 13; 88(5):621-7.
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Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3. Biol Chem. 2005 Jan; 386(1):61-7.
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Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease. Ann Neurol. 2003 Apr; 53(4):512-20.
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Control of facial muscle development by MyoR and capsulin. Science. 2002 Dec 20; 298(5602):2378-81.
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Measurement of fluorescence changes of NAD(P)H and of fluorescent flavoproteins in saponin-skinned human skeletal muscle fibers. Anal Biochem. 1994 Feb 01; 216(2):322-7.
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Induction of endogenous myosin light chain 1 and cardiac alpha-actin expression in L6E9 cells by MyoD1. J Biol Chem. 1992 Sep 15; 267(26):18728-34.
MeSH information
