From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Myosin-15 also known as myosin, heavy chain 15 is a
protein that in humans is encoded by the MYH15
gene.
[5]
Function
MYH15 is a
slow-twitch
myosin.
[5]
References
Further reading
- Luke MM, O'Meara ES, Rowland CM, et al. (2009).
"Gene variants associated with ischemic stroke: the cardiovascular health study". Stroke. 40 (2): 363–8.
doi:
10.1161/STROKEAHA.108.521328.
PMC
2881155.
PMID
19023099.
- Rossi AC, Mammucari C, Argentini C, et al. (2010).
"Two novel/ancient myosins in mammalian skeletal muscles: MYH14/7b and MYH15 are expressed in extraocular muscles and muscle spindles". J. Physiol. 588 (Pt 2): 353–64.
doi:
10.1113/jphysiol.2009.181008.
PMC
2821527.
PMID
19948655.
- Olsen JV, Blagoev B, Gnad F, et al. (2006).
"Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48.
doi:
10.1016/j.cell.2006.09.026.
PMID
17081983.
S2CID
7827573.
- Stedman HH, Kozyak BW, Nelson A, et al. (2004). "Myosin gene mutation correlates with anatomical changes in the human lineage". Nature. 428 (6981): 415–8.
Bibcode:
2004Natur.428..415S.
doi:
10.1038/nature02358.
PMID
15042088.
S2CID
4304466.
- Nagase T, Ishikawa K, Suyama M, et al. (1999).
"Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 6 (1): 63–70.
doi:
10.1093/dnares/6.1.63.
PMID
10231032.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004).
"Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5.
doi:
10.1038/ng1285.
PMID
14702039.
- McGuigan K, Phillips PC, Postlethwait JH (2004).
"Evolution of sarcomeric myosin heavy chain genes: evidence from fish". Mol. Biol. Evol. 21 (6): 1042–56.
doi:
10.1093/molbev/msh103.
PMID
15014174.
- Shiffman D, O'Meara ES, Bare LA, et al. (2008).
"Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study". Arterioscler. Thromb. Vasc. Biol. 28 (1): 173–9.
doi:
10.1161/ATVBAHA.107.153981.
PMC
2636623.
PMID
17975119.
- Bare LA, Morrison AC, Rowland CM, et al. (2007).
"Five common gene variants identify elevated genetic risk for coronary heart disease". Genet. Med. 9 (10): 682–9.
doi:
10.1097/GIM.0b013e318156fb62.
PMID
18073581.
