"Sarcomeres" 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 repeating contractile units of the MYOFIBRIL, delimited by Z bands along its length.
| Descriptor ID |
D012518
|
| MeSH Number(s) |
A10.690.552.875.700 A11.284.430.214.190.875.820 A11.620.249.850.700 A11.620.500.500.700
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Sarcomeres".
Below are MeSH descriptors whose meaning is more specific than "Sarcomeres".
This graph shows the total number of publications written about "Sarcomeres" by people in this website by year, and whether "Sarcomeres" 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 |
|---|
| 1993 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 2 | 3 |
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sarcomeres" by people in Profiles.
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Mechanical stimulation enhances development of scaffold-free, 3D-printed, engineered heart tissue grafts. J Tissue Eng Regen Med. 2021 05; 15(5):503-512.
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Baseline Characteristics of the VANISH Cohort. Circ Heart Fail. 2019 12; 12(12):e006231.
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Altered C10 domain in cardiac myosin binding protein-C results in hypertrophic cardiomyopathy. Cardiovasc Res. 2019 12 01; 115(14):1986-1997.
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Myofilaments: Movers and Rulers of the Sarcomere. Compr Physiol. 2017 03 16; 7(2):675-692.
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Alterations in Multi-Scale Cardiac Architecture in Association With Phosphorylation of Myosin Binding Protein-C. J Am Heart Assoc. 2016 Mar 15; 5(3):e002836.
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Histone Deacetylase 3 (HDAC3)-dependent Reversible Lysine Acetylation of Cardiac Myosin Heavy Chain Isoforms Modulates Their Enzymatic and Motor Activity. J Biol Chem. 2015 Jun 19; 290(25):15559-15569.
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Contractile dysfunction in a mouse model expressing a heterozygous MYBPC3 mutation associated with hypertrophic cardiomyopathy. Am J Physiol Heart Circ Physiol. 2014 Mar; 306(6):H807-15.
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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.