"Connectin" 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 giant elastic protein of molecular mass ranging from 2,993 kDa (cardiac), 3,300 kDa (psoas), to 3,700 kDa (soleus) having a kinase domain. The amino- terminal is involved in a Z line binding, and the carboxy-terminal region is bound to the myosin filament with an overlap between the counter-connectin filaments at the M line.
| Descriptor ID |
D064211
|
| MeSH Number(s) |
D08.811.913.696.620.682.324 D12.776.210.500.246
|
| Concept/Terms |
Myomesin- Myomesin
- M-Line 185 kDa Protein
- M Line 185 kDa Protein
- M-Protein (muscle)
- Muscle M-Line Protein
- M-Line Protein, Muscle
- Muscle M Line Protein
- Protein, Muscle M-Line
- Skelemins
- M-Band Proteins
- M Band Proteins
- Proteins, M-Band
|
Below are MeSH descriptors whose meaning is more general than "Connectin".
Below are MeSH descriptors whose meaning is more specific than "Connectin".
This graph shows the total number of publications written about "Connectin" by people in this website by year, and whether "Connectin" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 0 | 2 | 2 |
| 2018 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Connectin" by people in Profiles.
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Ghahremani S, Kanwal A, Pettinato A, Ladha F, Legere N, Thakar K, Zhu Y, Tjong H, Wilderman A, Stump WT, Greenberg L, Greenberg MJ, Cotney J, Wei CL, Hinson JT. CRISPR Activation Reverses Haploinsufficiency and Functional Deficits Caused by TTN Truncation Variants. Circulation. 2024 Apr 16; 149(16):1285-1297.
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Fu Y, Eisen HJ. Genetics of Dilated Cardiomyopathy. Curr Cardiol Rep. 2018 09 27; 20(11):121.
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Waterfall JJ, Arons E, Walker RL, Pineda M, Roth L, Killian JK, Abaan OD, Davis SR, Kreitman RJ, Meltzer PS. High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias. Nat Genet. 2014 Jan; 46(1):8-10.
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Toro C, Oliv? M, Dalakas MC, Sivakumar K, Bilbao JM, Tyndel F, Vidal N, Farrero E, Sambuughin N, Goldfarb LG. Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins. BMC Neurol. 2013 Mar 20; 13:29.