REEP1: Difference between revisions
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'''Receptor expression-enhancing protein 1''' is a [[protein]] that in humans is encoded by the ''REEP1'' [[gene]].<ref name="pmid16271481">{{cite journal | vauthors = Clark AJ, Metherell LA, Cheetham ME, Huebner A | title = Inherited ACTH insensitivity illuminates the mechanisms of ACTH action | journal = Trends Endocrinol Metab | volume = 16 | issue = 10 | pages = 451–7 |date=Nov 2005 | pmid = 16271481 | pmc = | doi = 10.1016/j.tem.2005.10.006 }}</ref><ref name="pmid15550249">{{cite journal | vauthors = Saito H, Kubota M, Roberts RW, Chi Q, Matsunami H | title = RTP family members induce functional expression of mammalian odorant receptors | journal = Cell | volume = 119 | issue = 5 | pages = 679–91 |date=Nov 2004 | pmid = 15550249 | pmc = | doi = 10.1016/j.cell.2004.11.021 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: REEP1 receptor accessory protein 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=65055| accessdate = }}</ref> | '''Receptor expression-enhancing protein 1''' is a [[protein]] that in humans is encoded by the ''REEP1'' [[gene]].<ref name="pmid16271481">{{cite journal | vauthors = Clark AJ, Metherell LA, Cheetham ME, Huebner A | title = Inherited ACTH insensitivity illuminates the mechanisms of ACTH action | journal = Trends Endocrinol Metab | volume = 16 | issue = 10 | pages = 451–7 |date=Nov 2005 | pmid = 16271481 | pmc = | doi = 10.1016/j.tem.2005.10.006 }}</ref><ref name="pmid15550249">{{cite journal | vauthors = Saito H, Kubota M, Roberts RW, Chi Q, Matsunami H | title = RTP family members induce functional expression of mammalian odorant receptors | journal = Cell | volume = 119 | issue = 5 | pages = 679–91 |date=Nov 2004 | pmid = 15550249 | pmc = | doi = 10.1016/j.cell.2004.11.021 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: REEP1 receptor accessory protein 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=65055| accessdate = }}</ref> | ||
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==References== | ==References== | ||
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Latest revision as of 02:21, 18 January 2019
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Receptor expression-enhancing protein 1 is a protein that in humans is encoded by the REEP1 gene.[1][2][3]
References
- ↑ Clark AJ, Metherell LA, Cheetham ME, Huebner A (Nov 2005). "Inherited ACTH insensitivity illuminates the mechanisms of ACTH action". Trends Endocrinol Metab. 16 (10): 451–7. doi:10.1016/j.tem.2005.10.006. PMID 16271481.
- ↑ Saito H, Kubota M, Roberts RW, Chi Q, Matsunami H (Nov 2004). "RTP family members induce functional expression of mammalian odorant receptors". Cell. 119 (5): 679–91. doi:10.1016/j.cell.2004.11.021. PMID 15550249.
- ↑ "Entrez Gene: REEP1 receptor accessory protein 1".
Further reading
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- 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.
- Ballif BA, Villén J, Beausoleil SA, et al. (2005). "Phosphoproteomic analysis of the developing mouse brain". Mol. Cell. Proteomics. 3 (11): 1093–101. doi:10.1074/mcp.M400085-MCP200. PMID 15345747.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Hillier LW, Graves TA, Fulton RS, et al. (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4". Nature. 434 (7034): 724–31. doi:10.1038/nature03466. PMID 15815621.
- Behrens M, Bartelt J, Reichling C, et al. (2006). "Members of RTP and REEP gene families influence functional bitter taste receptor expression". J. Biol. Chem. 281 (29): 20650–9. doi:10.1074/jbc.M513637200. PMID 16720576.
- Züchner S, Wang G, Tran-Viet KN, et al. (2006). "Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31". Am. J. Hum. Genet. 79 (2): 365–9. doi:10.1086/505361. PMC 1559498. PMID 16826527.
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