미오신-15 는 미오신이라고도 알려져 있으며, 헤비 체인 15 는 인간에게 MYH15 유전자 에 의해 암호화된 단백질 이다.[5]
함수 MYH15는 느린 트위치 마이오신 이다.[5]
참조 추가 읽기 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. 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 .
