"Cardiac Myosins" 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.
Myosin type II isoforms found in cardiac muscle.
| Descriptor ID |
D024722
|
| MeSH Number(s) |
D05.750.078.730.475.475.124 D08.811.277.040.025.193.750.750.124 D12.776.210.500.600.470.249 D12.776.220.525.475.475.124
|
| Concept/Terms |
Cardiac Myosins- Cardiac Myosins
- Cardiac Myosin
- Myosin, Cardiac
- Myosins, Cardiac
- Cardiac Muscle Myosins
- Muscle Myosins, Cardiac
- Myosins, Cardiac Muscle
|
Below are MeSH descriptors whose meaning is more general than "Cardiac Myosins".
Below are MeSH descriptors whose meaning is more specific than "Cardiac Myosins".
This graph shows the total number of publications written about "Cardiac Myosins" by people in this website by year, and whether "Cardiac Myosins" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
| 2007 | 1 | 1 | 2 |
| 2008 | 1 | 1 | 2 |
| 2009 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 0 | 2 | 2 |
| 2016 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cardiac Myosins" by people in Profiles.
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Genetic Variation in Enhancers Modifies Cardiomyopathy Gene Expression and Progression. Circulation. 2021 03 30; 143(13):1302-1316.
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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel. Genet Med. 2018 03; 20(3):351-359.
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Oxidized LDL signals through Rho-GTPase to induce endothelial cell stiffening and promote capillary formation. J Lipid Res. 2016 05; 57(5):791-808.
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Two strikes and you're out: gene-gene mutation interactions in HCM. Circ Res. 2014 Jul 07; 115(2):208-10.
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Genetic mutations and mechanisms in dilated cardiomyopathy. J Clin Invest. 2013 Jan; 123(1):19-26.
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Population-based variation in cardiomyopathy genes. Circ Cardiovasc Genet. 2012 Aug 01; 5(4):391-9.
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Pathogenic properties of the N-terminal region of cardiac myosin binding protein-C in vitro. J Muscle Res Cell Motil. 2012 May; 33(1):17-30.
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Anticardiac myosin immunity and chronic allograft vasculopathy in heart transplant recipients. J Immunol. 2011 Jul 15; 187(2):1023-30.
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HDAC3-dependent reversible lysine acetylation of cardiac myosin heavy chain isoforms modulates their enzymatic and motor activity. J Biol Chem. 2011 Feb 18; 286(7):5567-77.
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Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation. Circ Cardiovasc Genet. 2009 Oct; 2(5):442-9.