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MYH2
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An Error has occured retrieving Wikidata item for infobox MYH2 (Myosin heavy chain 2) هوَ بروتين يُشَفر بواسطة جين MYH2 في الإنسان.[1][2]
الوظيفة
![[أيقونة]](/%D9%85%D9%84%D9%81:Crystal_xedit.svg){kind=small} | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
| هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
- ^ Smerdu V، Karsch-Mizrachi I، Campione M، Leinwand L، Schiaffino S (يناير 1995). "Type IIx myosin heavy chain transcripts are expressed in type IIb fibers of human skeletal muscle". Am J Physiol. ج. 267 ع. 6 Pt 1: C1723–8. PMID:7545970.
- ^ "Entrez Gene: MYH2 myosin, heavy chain 2, skeletal muscle, adult". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
- Schwartz CE، McNally E، Leinwand L، Skolnick MH (1987). "A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13". Cytogenet. Cell Genet. ج. 43 ع. 1–2: 117–20. DOI:10.1159/000132307. PMID:2877813.
- Ennion S، Sant'ana Pereira J، Sargeant AJ، وآخرون (1995). "Characterization of human skeletal muscle fibres according to the myosin heavy chains they express". J. Muscle Res. Cell. Motil. ج. 16 ع. 1: 35–43. DOI:10.1007/BF00125308. PMID:7751403.
- Hisatome I، Morisaki T، Kamma H، وآخرون (1998). "Control of AMP deaminase 1 binding to myosin heavy chain". Am. J. Physiol. ج. 275 ع. 3 Pt 1: C870–81. PMID:9730972.
- Weiss A، McDonough D، Wertman B، وآخرون (1999). "Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved". Proc. Natl. Acad. Sci. U.S.A. ج. 96 ع. 6: 2958–63. DOI:10.1073/pnas.96.6.2958. PMC:15877. PMID:10077619.
- Weiss A، Schiaffino S، Leinwand LA (1999). "Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity". J. Mol. Biol. ج. 290 ع. 1: 61–75. DOI:10.1006/jmbi.1999.2865. PMID:10388558.
- Onuoha GN، Alpar EK، Laprade M، وآخرون (1999). "Effects of bone fracture and surgery on plasma myosin heavy chain fragments of skeletal muscle". Clinical and investigative medicine. Médecine clinique et experimentale. ج. 22 ع. 5: 180–4. PMID:10579056.
- Martinsson T، Oldfors A، Darin N، وآخرون (2001). "Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene". Proc. Natl. Acad. Sci. U.S.A. ج. 97 ع. 26: 14614–9. DOI:10.1073/pnas.250289597. PMC:18967. PMID:11114175.
- Tajsharghi H، Thornell LE، Darin N، وآخرون (2002). "Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age". Neurology. ج. 58 ع. 5: 780–6. DOI:10.1212/wnl.58.5.780. PMID:11889243.
- England K، Ashford D، Kidd D، Rumsby M (2002). "PKC epsilon is associated with myosin IIA and actin in fibroblasts". Cell. Signal. ج. 14 ع. 6: 529–36. DOI:10.1016/S0898-6568(01)00277-7. PMID:11897493.
- Allen DL، Leinwand LA (2003). "Intracellular calcium and myosin isoform transitions. Calcineurin and calcium-calmodulin kinase pathways regulate preferential activation of the IIa myosin heavy chain promoter". J. Biol. Chem. ج. 277 ع. 47: 45323–30. DOI:10.1074/jbc.M208302200. PMID:12235157.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Kim EJ، Helfman DM (2003). "Characterization of the metastasis-associated protein, S100A4. Roles of calcium binding and dimerization in cellular localization and interaction with myosin". J. Biol. Chem. ج. 278 ع. 32: 30063–73. DOI:10.1074/jbc.M304909200. PMID:12756252.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
- Chung MC، Kawamoto S (2005). "IRF-2 is involved in up-regulation of nonmuscle myosin heavy chain II-A gene expression during phorbol ester-induced promyelocytic HL-60 differentiation". J. Biol. Chem. ج. 279 ع. 53: 56042–52. DOI:10.1074/jbc.M404791200. PMID:15496418.
- Tajsharghi H، Darin N، Rekabdar E، وآخرون (2005). "Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2)". Eur. J. Hum. Genet. ج. 13 ع. 5: 617–22. DOI:10.1038/sj.ejhg.5201375. PMID:15741996.
- Kimura K، Wakamatsu A، Suzuki Y، وآخرون (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. ج. 16 ع. 1: 55–65. DOI:10.1101/gr.4039406. PMC:1356129. PMID:16344560.
- Li M، Lionikas A، Yu F، وآخرون (2006). "Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys)". Neuromuscul. Disord. ج. 16 ع. 11: 782–91. DOI:10.1016/j.nmd.2006.07.023. PMC:1693964. PMID:17005402.
- Ewing RM، Chu P، Elisma F، وآخرون (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. ج. 3 ع. 1: 89. DOI:10.1038/msb4100134. PMC:1847948. PMID:17353931.
