"Caveolin 3" 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 caveolin that is expressed exclusively in MUSCLE CELLS and is sufficient to form CAVEOLAE in SARCOLEMMA. Mutations in caveolin 3 are associated with multiple muscle diseases including DISTAL MYOPATHY and LIMB-GIRDLE MUSCULAR DYSTROPHY.
| Descriptor ID |
D051244
|
| MeSH Number(s) |
D12.776.210.500.235 D12.776.543.990.100.875
|
| Concept/Terms |
Caveolin 3- Caveolin 3
- M-Caveolin
- Muscle Caveolin
- Caveolin, Muscle
- Caveolin-3
|
Below are MeSH descriptors whose meaning is more general than "Caveolin 3".
Below are MeSH descriptors whose meaning is more specific than "Caveolin 3".
This graph shows the total number of publications written about "Caveolin 3" by people in this website by year, and whether "Caveolin 3" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 0 | 1 | 1 |
| 2002 | 0 | 2 | 2 |
| 2003 | 0 | 3 | 3 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Caveolin 3" by people in Profiles.
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Dysregulation of nuclear receptor COUP-TFII impairs skeletal muscle development. Sci Rep. 2017 06 09; 7(1):3136.
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CAV3 mutation in a patient with transient hyperCKemia and myalgia. Neurol Neurochir Pol. 2016 Nov - Dec; 50(6):468-473.
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Ultrasound-mediated stimulation of microbubbles after acute myocardial infarction and reperfusion ameliorates left-ventricular remodelling in mice via improvement of borderzone vascularization. PLoS One. 2013; 8(2):e56841.
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Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome. Circulation. 2006 Nov 14; 114(20):2104-12.
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MR imaging of caveolin gene-specific alterations in right ventricular wall thickness. Magn Reson Imaging. 2005 Jan; 23(1):61-8.
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Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases. Neurology. 2004 Feb 24; 62(4):538-43.
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Phosphofructokinase muscle-specific isoform requires caveolin-3 expression for plasma membrane recruitment and caveolar targeting: implications for the pathogenesis of caveolin-related muscle diseases. Am J Pathol. 2003 Dec; 163(6):2619-34.
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Phenotypic behavior of caveolin-3 R26Q, a mutant associated with hyperCKemia, distal myopathy, and rippling muscle disease. Am J Physiol Cell Physiol. 2003 Nov; 285(5):C1150-60.
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Mechanical unloading increases caveolin expression in the failing human heart. Cardiovasc Res. 2003 Jul 01; 59(1):57-66.
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Caveolin-3 knock-out mice develop a progressive cardiomyopathy and show hyperactivation of the p42/44 MAPK cascade. J Biol Chem. 2002 Oct 11; 277(41):38988-97.