MYH9
From Wikipedia, the free encyclopedia
Myosin, heavy chain 9, non-muscle, also known as MYH9, is a human gene.
[edit] See also
[edit] Further reading
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- Lee CL, Atassi MZ (1978). "Enzymic and immunochemical properties of lysozyme. Accurate definition of the antigenic site around the disulphide bridge 30-115 (site 3) by 'surface-simulation' synthesis.". Biochem. J. 167 (3): 571–81. PMID 603622.
- Tweed WA, Phua WT, Chong KY, et al. (1992). "Large tidal volume ventilation improves pulmonary gas exchange during lower abdominal surgery in Trendelenburg's position.". Canadian journal of anaesthesia = Journal canadien d'anesthésie 38 (8): 989–95. PMID 1752022.
- Simons M, Wang M, McBride OW, et al. (1991). "Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes.". Circ. Res. 69 (2): 530–9. PMID 1860190.
- Toothaker LE, Gonzalez DA, Tung N, et al. (1991). "Cellular myosin heavy chain in human leukocytes: isolation of 5' cDNA clones, characterization of the protein, chromosomal localization, and upregulation during myeloid differentiation.". Blood 78 (7): 1826–33. PMID 1912569.
- Saez CG, Myers JC, Shows TB, Leinwand LA (1990). "Human nonmuscle myosin heavy chain mRNA: generation of diversity through alternative polyadenylylation.". Proc. Natl. Acad. Sci. U.S.A. 87 (3): 1164–8. PMID 1967836.
- Moos C, Feng IN (1980). "Effect of C-protein on actomyosin ATPase.". Biochim. Biophys. Acta 632 (2): 141–9. PMID 6448079.
- Obermann WM, Plessmann U, Weber K, Fürst DO (1995). "Purification and biochemical characterization of myomesin, a myosin-binding and titin-binding protein, from bovine skeletal muscle.". Eur. J. Biochem. 233 (1): 110–5. PMID 7588733.
- Maupin P, Phillips CL, Adelstein RS, Pollard TD (1995). "Differential localization of myosin-II isozymes in human cultured cells and blood cells.". J. Cell. Sci. 107 ( Pt 11): 3077–90. PMID 7699007.
- Bement WM, Hasson T, Wirth JA, et al. (1994). "Identification and overlapping expression of multiple unconventional myosin genes in vertebrate cell types.". Proc. Natl. Acad. Sci. U.S.A. 91 (14): 6549–53. PMID 8022818.
- Eilertsen KJ, Kazmierski ST, Keller TC (1994). "Cellular titin localization in stress fibers and interaction with myosin II filaments in vitro.". J. Cell Biol. 126 (5): 1201–10. PMID 8063857.
- Shoeman RL, Sachse C, Höner B, et al. (1993). "Cleavage of human and mouse cytoskeletal and sarcomeric proteins by human immunodeficiency virus type 1 protease. Actin, desmin, myosin, and tropomyosin.". Am. J. Pathol. 142 (1): 221–30. PMID 8424456.
- Lalwani AK, Linthicum FH, Wilcox ER, et al. (1998). "A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration.". Audiol. Neurootol. 2 (3): 139–54. PMID 9390828.
- Ford HL, Silver DL, Kachar B, et al. (1998). "Effect of Mts1 on the structure and activity of nonmuscle myosin II.". Biochemistry 36 (51): 16321–7. doi: . PMID 9405067.
- Obermann WM, van der Ven PF, Steiner F, et al. (1998). "Mapping of a myosin-binding domain and a regulatory phosphorylation site in M-protein, a structural protein of the sarcomeric M band.". Mol. Biol. Cell 9 (4): 829–40. PMID 9529381.
- Dunham I, Shimizu N, Roe BA, et al. (1999). "The DNA sequence of human chromosome 22.". Nature 402 (6761): 489–95. doi: . PMID 10591208.
- Miyamoto CA, Fischman DA, Reinach FC (2000). "The interface between MyBP-C and myosin: site-directed mutagenesis of the CX myosin-binding domain of MyBP-C.". J. Muscle Res. Cell. Motil. 20 (7): 703–15. PMID 10672519.
- Sajid M, Hu Z, Lele M, Stouffer GA (2000). "Protein complexes involving alpha v beta 3 integrins, nonmuscle myosin heavy chain-A, and focal adhesion kinase from in thrombospondin-treated smooth muscle cells.". J. Investig. Med. 48 (3): 190–7. PMID 10822899.
- Husi H, Ward MA, Choudhary JS, et al. (2000). "Proteomic analysis of NMDA receptor-adhesion protein signaling complexes.". Nat. Neurosci. 3 (7): 661–9. doi: . PMID 10862698.
- Kelley MJ, Jawien W, Lin A, et al. (2000). "Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13.". Hum. Genet. 106 (5): 557–64. PMID 10914687.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.