CDC42EP3

An Error has occured retrieving Wikidata item for infobox CDC42EP3‏ (CDC42 effector protein 3) هوَ بروتين يُشَفر بواسطة جين CDC42EP3 في الإنسان.^[1]^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

^ ^أ ^ب "Entrez Gene: CDC42EP3 CDC42 effector protein (Rho GTPase binding) 3". مؤرشف من الأصل في 2010-12-05.
^ Hirsch DS، Pirone DM، Burbelo PD (مارس 2001). "A new family of Cdc42 effector proteins, CEPs, function in fibroblast and epithelial cell shape changes". J Biol Chem. ج. 276 ع. 2: 875–83. DOI:10.1074/jbc.M007039200. PMID:11035016.
^ Alberts AS، Bouquin N، Johnston LH، Treisman R (مايو 1998). "Analysis of RhoA-binding proteins reveals an interaction domain conserved in heterotrimeric G protein beta subunits and the yeast response regulator protein Skn7". J Biol Chem. ج. 273 ع. 15: 8616–22. DOI:10.1074/jbc.273.15.8616. PMID:9535835.

قراءة متعمقة

Joberty G، Perlungher RR، Macara IG (2000). "The Borgs, a new family of Cdc42 and TC10 GTPase-interacting proteins". Mol. Cell. Biol. ج. 19 ع. 10: 6585–97. PMC:84628. PMID:10490598.
Hartley JL، Temple GF، Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. ج. 10 ع. 11: 1788–95. DOI:10.1101/gr.143000. PMC:310948. PMID:11076863.
Wiemann S، Weil B، Wellenreuther R، وآخرون (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. ج. 11 ع. 3: 422–35. DOI:10.1101/gr.GR1547R. PMC:311072. PMID:11230166.
Simpson JC، Wellenreuther R، Poustka A، وآخرون (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. ج. 1 ع. 3: 287–92. DOI:10.1093/embo-reports/kvd058. PMC:1083732. PMID:11256614.
Joberty G، Perlungher RR، Sheffield PJ، وآخرون (2001). "Borg proteins control septin organization and are negatively regulated by Cdc42". Nat. Cell Biol. ج. 3 ع. 10: 861–6. DOI:10.1038/ncb1001-861. PMID:11584266.
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. Bibcode:2002PNAS...9916899M. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
Ballif BA، Villén J، Beausoleil SA، وآخرون (2005). "Phosphoproteomic analysis of the developing mouse brain". Mol. Cell. Proteomics. ج. 3 ع. 11: 1093–101. DOI:10.1074/mcp.M400085-MCP200. PMID:15345747.
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.
Wiemann S، Arlt D، Huber W، وآخرون (2004). "From ORFeome to biology: a functional genomics pipeline". Genome Res. ج. 14 ع. 10B: 2136–44. DOI:10.1101/gr.2576704. PMC:528930. PMID:15489336.
Hillier LW، Graves TA، Fulton RS، وآخرون (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4". Nature. ج. 434 ع. 7034: 724–31. Bibcode:2005Natur.434..724H. DOI:10.1038/nature03466. PMID:15815621.
Stelzl U، Worm U، Lalowski M، وآخرون (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. ج. 122 ع. 6: 957–68. DOI:10.1016/j.cell.2005.08.029. PMID:16169070.
Rual JF، Venkatesan K، Hao T، وآخرون (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. ج. 437 ع. 7062: 1173–8. Bibcode:2005Natur.437.1173R. DOI:10.1038/nature04209. PMID:16189514.
Mehrle A، Rosenfelder H، Schupp I، وآخرون (2006). "The LIFEdb database in 2006". Nucleic Acids Res. ج. 34 ع. Database issue: D415–8. DOI:10.1093/nar/gkj139. PMC:1347501. PMID:16381901.
Olsen JV، Blagoev B، Gnad F، وآخرون (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. ج. 127 ع. 3: 635–48. DOI:10.1016/j.cell.2006.09.026. PMID:17081983.

هذه بذرة مقالة عن جين على كروموسوم 2 بحاجة للتوسيع. فضلًا شارك في تحريرها.

[entrez-1] أ ^ب "Entrez Gene: CDC42EP3 CDC42 effector protein (Rho GTPase binding) 3". مؤرشف من الأصل في 2010-12-05.

[pmid11035016-2] Hirsch DS، Pirone DM، Burbelo PD (مارس 2001). "A new family of Cdc42 effector proteins, CEPs, function in fibroblast and epithelial cell shape changes". J Biol Chem. ج. 276 ع. 2: 875–83. DOI:10.1074/jbc.M007039200. PMID:11035016.

[pmid9535835-3] Alberts AS، Bouquin N، Johnston LH، Treisman R (مايو 1998). "Analysis of RhoA-binding proteins reveals an interaction domain conserved in heterotrimeric G protein beta subunits and the yeast response regulator protein Skn7". J Biol Chem. ج. 273 ع. 15: 8616–22. DOI:10.1074/jbc.273.15.8616. PMID:9535835.

[1]

[2]

[3]