RYR3: Difference between revisions
Jump to navigation
Jump to search
m (→Further reading: task using AWB) |
m (Add: pmc. You can use this bot yourself. Report bugs here. | User-activated.) |
||
| Line 17: | Line 17: | ||
*{{cite journal |author=Xiao B |title=Isoform-dependent formation of heteromeric Ca2+ release channels (ryanodine receptors) |journal=J. Biol. Chem. |volume=277 |issue= 44 |pages= 41778–85 |year= 2002 |pmid= 12213830 |doi= 10.1074/jbc.M208210200 |name-list-format=vanc|author2=Masumiya H |author3=Jiang D |display-authors=3 |author4=<Please add first missing authors to populate metadata.> }} | *{{cite journal |author=Xiao B |title=Isoform-dependent formation of heteromeric Ca2+ release channels (ryanodine receptors) |journal=J. Biol. Chem. |volume=277 |issue= 44 |pages= 41778–85 |year= 2002 |pmid= 12213830 |doi= 10.1074/jbc.M208210200 |name-list-format=vanc|author2=Masumiya H |author3=Jiang D |display-authors=3 |author4=<Please add first missing authors to populate metadata.> }} | ||
*{{cite journal |author=Davis MR |title=Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene |journal=Neuromuscul. Disord. |volume=13 |issue= 2 |pages= 151–7 |year= 2003 |pmid= 12565913 |doi=10.1016/S0960-8966(02)00218-3 |name-list-format=vanc|author2=Haan E |author3=Jungbluth H |display-authors=3 |last4=Sewry |first4=C |last5=North |first5=K |last6=Muntoni |first6=F |last7=Kuntzer |first7=T |last8=Lamont |first8=P |last9=Bankier |first9=A }} | *{{cite journal |author=Davis MR |title=Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene |journal=Neuromuscul. Disord. |volume=13 |issue= 2 |pages= 151–7 |year= 2003 |pmid= 12565913 |doi=10.1016/S0960-8966(02)00218-3 |name-list-format=vanc|author2=Haan E |author3=Jungbluth H |display-authors=3 |last4=Sewry |first4=C |last5=North |first5=K |last6=Muntoni |first6=F |last7=Kuntzer |first7=T |last8=Lamont |first8=P |last9=Bankier |first9=A }} | ||
*{{cite journal |author=Kitahara K |title=Microsatellite scan identifies new candidate genes for susceptibility to alcoholic chronic pancreatitis in Japanese patients |journal=Dis. Markers |volume=25 |issue= 3 |pages= 175–80 |year= 2008 |pmid= 19096130 |doi= 10.1155/2008/426764|name-list-format=vanc|author2=Kawa S |author3=Katsuyama Y |display-authors=3 |author4=<Please add first missing authors to populate metadata.> }} | *{{cite journal |author=Kitahara K |title=Microsatellite scan identifies new candidate genes for susceptibility to alcoholic chronic pancreatitis in Japanese patients |journal=Dis. Markers |volume=25 |issue= 3 |pages= 175–80 |year= 2008 |pmid= 19096130 |pmc=3827802 |doi= 10.1155/2008/426764|name-list-format=vanc|author2=Kawa S |author3=Katsuyama Y |display-authors=3 |author4=<Please add first missing authors to populate metadata.> }} | ||
*{{cite journal |author=Tochigi M |title=No association between the ryanodine receptor 3 gene and autism in a Japanese population |journal=Psychiatry Clin. Neurosci. |volume=62 |issue= 3 |pages= 341–4 |year= 2008 |pmid= 18588595 |doi= 10.1111/j.1440-1819.2008.01802.x |name-list-format=vanc|author2=Kato C |author3=Ohashi J |display-authors=3 |last4=Koishi |first4=Shinko |last5=Kawakubo |first5=Yuki |last6=Yamamoto |first6=Kenji |last7=Matsumoto |first7=Hideo |last8=Hashimoto |first8=Ohiko |last9=Kim |first9=Soo-Yung }} | *{{cite journal |author=Tochigi M |title=No association between the ryanodine receptor 3 gene and autism in a Japanese population |journal=Psychiatry Clin. Neurosci. |volume=62 |issue= 3 |pages= 341–4 |year= 2008 |pmid= 18588595 |doi= 10.1111/j.1440-1819.2008.01802.x |name-list-format=vanc|author2=Kato C |author3=Ohashi J |display-authors=3 |last4=Koishi |first4=Shinko |last5=Kawakubo |first5=Yuki |last6=Yamamoto |first6=Kenji |last7=Matsumoto |first7=Hideo |last8=Hashimoto |first8=Ohiko |last9=Kim |first9=Soo-Yung }} | ||
*{{cite journal |author=Masumiya H |title=The mouse sino-atrial node expresses both the type 2 and type 3 Ca(2+) release channels/ryanodine receptors |journal=FEBS Lett. |volume=553 |issue= 1–2 |pages= 141–4 |year= 2003 |pmid= 14550562 |doi=10.1016/S0014-5793(03)00999-2 |name-list-format=vanc|author2=Yamamoto H |author3=Hemberger M |display-authors=3 |last4=Tanaka |first4=H |last5=Shigenobu |first5=K |last6=Chen |first6=SR |last7=Furukawa |first7=T }} | *{{cite journal |author=Masumiya H |title=The mouse sino-atrial node expresses both the type 2 and type 3 Ca(2+) release channels/ryanodine receptors |journal=FEBS Lett. |volume=553 |issue= 1–2 |pages= 141–4 |year= 2003 |pmid= 14550562 |doi=10.1016/S0014-5793(03)00999-2 |name-list-format=vanc|author2=Yamamoto H |author3=Hemberger M |display-authors=3 |last4=Tanaka |first4=H |last5=Shigenobu |first5=K |last6=Chen |first6=SR |last7=Furukawa |first7=T }} | ||
Revision as of 13:50, 7 November 2018
| VALUE_ERROR (nil) | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Aliases | |||||||
| External IDs | GeneCards: [1] | ||||||
| Orthologs | |||||||
| Species | Human | Mouse | |||||
| Entrez |
|
| |||||
| Ensembl |
|
| |||||
| UniProt |
|
| |||||
| RefSeq (mRNA) |
|
| |||||
| RefSeq (protein) |
|
| |||||
| Location (UCSC) | n/a | n/a | |||||
| PubMed search | n/a | n/a | |||||
| Wikidata | |||||||
| |||||||
Ryanodine receptor 3 is a protein that in humans is encoded by the RYR3 gene.[1] The protein encoded by this gene is both a calcium channel and a receptor for the plant alkaloid ryanodine. RYR3 and RYR1 control the resting calcium ion concentration in skeletal muscle.[2]
See also
References
- ↑ Sorrentino V, Giannini G, Malzac P, Mattei MG (Feb 1994). "Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization". Genomics. 18 (1): 163–5. doi:10.1006/geno.1993.1446. PMID 8276408.
- ↑ Perez CF, López JR, Allen PD (March 2005). "Expression levels of RyR1 and RyR3 control resting free Ca2+ in skeletal muscle". Am. J. Physiol., Cell Physiol. 288 (3): C640–9. doi:10.1152/ajpcell.00407.2004. PMID 15548569.
Further reading
- Bertocchini F, Ovitt CE, Conti A, et al. (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, et al. (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, et al. (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, et al. (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, et al. (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, et al. (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, et al. (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. PMC 3827802. PMID 19096130.
- Tochigi M, Kato C, Ohashi J, et al. (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, et al. (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.
- Jiang D, Xiao B, Li X, Chen SR (2003). "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. doi:10.1074/jbc.M210410200. PMID 12471029.
- Mohaupt MG, Karas RH, Babiychuk EB, et al. (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, et al. (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.
- Martin C, Chapman KE, Seckl JR, Ashley RH (1998). "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. doi:10.1016/S0306-4522(97)00612-X. PMID 9607712.
- 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.
- Van Acker K, Bultynck G, Rossi D, et al. (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, et al. (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.
- Leeb T, Brenig B (1998). "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. doi:10.1016/S0014-5793(98)00124-0. PMID 9515741.
- Lynn S, Morgan JM, Lamb HK, et al. (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.
External links
- RYR3+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
 | This article on a gene on human chromosome 15 is a stub. You can help Wikipedia by expanding it. |