RYR3
RYR3 (Ryanodine receptor 3) هوَ بروتين يُشَفر بواسطة جين RYR3 في الإنسان.[1][2]
المراجع
- "Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization"، Genomics، 18 (1): 163–5، فبراير 1994، doi:10.1006/geno.1993.1446، PMID 8276408.
- "Expression levels of RyR1 and RyR3 control resting free Ca2+ in skeletal muscle"، Am. J. Physiol., Cell Physiol.، 288 (3): C640–9، مارس 2005، doi:10.1152/ajpcell.00407.2004، PMID 15548569.
قراءة متعمقة
- Bertocchini F؛ Ovitt CE؛ Conti A؛ وآخرون (1997)، "Requirement for the ryanodine receptor type 3 for efficient contraction in neonatal skeletal muscles"، EMBO J.، 16 (23): 6956–63، doi:10.1093/emboj/16.23.6956، PMC 1170299، PMID 9384575.
- Bultynck G؛ De Smet P؛ Rossi D؛ وآخرون (2001)، "Characterization and mapping of the 12 kDa FK506-binding protein (FKBP12)-binding site on different isoforms of the ryanodine receptor and of the inositol 1,4,5-trisphosphate receptor"، Biochem. J.، 354 (Pt 2): 413–22، doi:10.1042/bj3540413، PMC 1221670، PMID 11171121.
- Schwarzmann N؛ Kunerth S؛ Weber K؛ وآخرون (2002)، "Knock-down of the type 3 ryanodine receptor impairs sustained Ca2+ signaling via the T cell receptor/CD3 complex"، J. Biol. Chem.، 277 (52): 50636–42، doi:10.1074/jbc.M209061200، PMID 12354756.
- Nakashima Y؛ Nishimura S؛ Maeda A؛ وآخرون (1997)، "Molecular cloning and characterization of a human brain ryanodine receptor"، FEBS Lett.، 417 (1): 157–62، doi:10.1016/S0014-5793(97)01275-1، PMID 9395096.
- Xiao B؛ Masumiya H؛ Jiang D؛ وآخرون (2002)، "Isoform-dependent formation of heteromeric Ca2+ release channels (ryanodine receptors)"، J. Biol. Chem.، 277 (44): 41778–85، doi:10.1074/jbc.M208210200، PMID 12213830.
- Davis MR؛ Haan E؛ Jungbluth H؛ وآخرون (2003)، "Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene"، Neuromuscul. Disord.، 13 (2): 151–7، doi:10.1016/S0960-8966(02)00218-3، PMID 12565913.
- Kitahara K؛ Kawa S؛ Katsuyama Y؛ وآخرون (2008)، "Microsatellite scan identifies new candidate genes for susceptibility to alcoholic chronic pancreatitis in Japanese patients"، Dis. Markers، 25 (3): 175–80، doi:10.1155/2008/426764، PMID 19096130.
- Tochigi M؛ Kato C؛ Ohashi J؛ وآخرون (2008)، "No association between the ryanodine receptor 3 gene and autism in a Japanese population"، Psychiatry Clin. Neurosci.، 62 (3): 341–4، doi:10.1111/j.1440-1819.2008.01802.x، PMID 18588595.
- Masumiya H؛ Yamamoto H؛ Hemberger M؛ وآخرون (2003)، "The mouse sino-atrial node expresses both the type 2 and type 3 Ca(2+) release channels/ryanodine receptors"، FEBS Lett.، 553 (1–2): 141–4، doi:10.1016/S0014-5793(03)00999-2، PMID 14550562.
- "Smooth muscle tissues express a major dominant negative splice variant of the type 3 Ca2+ release channel (ryanodine receptor)"، J. Biol. Chem.، 278 (7): 4763–9، 2003، doi:10.1074/jbc.M210410200، PMID 12471029.
- Mohaupt MG؛ Karas RH؛ Babiychuk EB؛ وآخرون (2009)، "Association between statin-associated myopathy and skeletal muscle damage"، Canadian Medical Association Journal، 181 (1–2): E11–8، doi:10.1503/cmaj.081785، PMC 2704421، PMID 19581603.
- Balschun D؛ Wolfer DP؛ Bertocchini F؛ وآخرون (1999)، "Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning"، EMBO J.، 18 (19): 5264–73، doi:10.1093/emboj/18.19.5264، PMC 1171597، PMID 10508160.
- "Partial cloning and differential expression of ryanodine receptor/calcium-release channel genes in human tissues including the hippocampus and cerebellum"، Neuroscience، 85 (1): 205–16، 1998، doi:10.1016/S0306-4522(97)00612-X، PMID 9607712.
- Ota T؛ Suzuki Y؛ Nishikawa T؛ وآخرون (2004)، "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، doi:10.1038/ng1285، PMID 14702039.
- Van Acker K؛ Bultynck G؛ Rossi D؛ وآخرون (2004)، "The 12 kDa FK506-binding protein, FKBP12, modulates the Ca(2+)-flux properties of the type-3 ryanodine receptor"، J. Cell Sci.، 117 (Pt 7): 1129–37، doi:10.1242/jcs.00948، PMID 14970260.
- Bultynck G؛ Rossi D؛ Callewaert G؛ وآخرون (2001)، "The conserved sites for the FK506-binding proteins in ryanodine receptors and inositol 1,4,5-trisphosphate receptors are structurally and functionally different"، J. Biol. Chem.، 276 (50): 47715–24، doi:10.1074/jbc.M106573200، PMID 11598113.
- "cDNA cloning and sequencing of the human ryanodine receptor type 3 (RYR3) reveals a novel alternative splice site in the RYR3 gene"، FEBS Lett.، 423 (3): 367–70، 1998، doi:10.1016/S0014-5793(98)00124-0، PMID 9515741.
- Lynn S؛ Morgan JM؛ Lamb HK؛ وآخرون (1995)، "Isolation and partial cloning of ryanodine-sensitive Ca2+ release channel protein isoforms from human myometrial smooth muscle"، FEBS Lett.، 372 (1): 6–12، doi:10.1016/0014-5793(95)00924-X، PMID 7556644.
- بوابة طب
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة الكيمياء الحيوية
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