CCDC50

CCDC50

Coiled-coil domain containing 50, also known as CCDC50, is a human gene.cite web | title = Entrez Gene: CCDC50 coiled-coil domain containing 50| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=152137| accessdate = ]

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References

Further reading

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*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, "et al." |title=A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29. |journal=Hum. Genet. |volume=112 |issue= 1 |pages= 24–8 |year= 2003 |pmid= 12483295 |doi= 10.1007/s00439-002-0836-x
*cite journal | author=Vazza G, Picelli S, Bozzato A, Mostacciuolo ML |title=Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28. |journal=Gene |volume=314 |issue= |pages= 113–20 |year= 2003 |pmid= 14527723 |doi=
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Blagoev B, Ong SE, Kratchmarova I, Mann M |title=Temporal analysis of phosphotyrosine-dependent signaling networks by quantitative proteomics. |journal=Nat. Biotechnol. |volume=22 |issue= 9 |pages= 1139–45 |year= 2005 |pmid= 15314609 |doi= 10.1038/nbt1005
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Zhang Y, Wolf-Yadlin A, Ross PL, "et al." |title=Time-resolved mass spectrometry of tyrosine phosphorylation sites in the epidermal growth factor receptor signaling network reveals dynamic modules. |journal=Mol. Cell Proteomics |volume=4 |issue= 9 |pages= 1240–50 |year= 2005 |pmid= 15951569 |doi= 10.1074/mcp.M500089-MCP200
*cite journal | author=Tashiro K, Konishi H, Sano E, "et al." |title=Suppression of the ligand-mediated down-regulation of epidermal growth factor receptor by Ymer, a novel tyrosine-phosphorylated and ubiquitinated protein. |journal=J. Biol. Chem. |volume=281 |issue= 34 |pages= 24612–22 |year= 2006 |pmid= 16803894 |doi= 10.1074/jbc.M604184200
*cite journal | author=Olsen JV, Blagoev B, Gnad F, "et al." |title=Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. |journal=Cell |volume=127 |issue= 3 |pages= 635–48 |year= 2006 |pmid= 17081983 |doi= 10.1016/j.cell.2006.09.026
*cite journal | author=Modamio-Hoybjor S, Mencia A, Goodyear R, "et al." |title=A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss. |journal=Am. J. Hum. Genet. |volume=80 |issue= 6 |pages= 1076–89 |year= 2007 |pmid= 17503326 |doi= 10.1086/518311

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  • Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… …   Wikipedia

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