CDK5RAP1
CDK5RAP1 (CDK5 regulatory subunit associated protein 1) هوَ بروتين يُشَفر بواسطة جين CDK5RAP1 في الإنسان.[1][2][3][4]
الوظيفة
المراجع
- "Entrez Gene: CDK5RAP1 CDK5 regulatory subunit associated protein 1". مؤرشف من الأصل في 2010-12-05.
- Zou X، Ji C، Jin F، Liu J، Wu M، Zheng H، Wang Y، Li X، Xu J، Gu S، Xie Y، Mao Y (أغسطس 2004). "Cloning, characterization and expression of CDK5RAP1_v3 and CDK5RAP1_v4, two novel splice variants of human CDK5RAP1". Genes Genet Syst. ج. 79 ع. 3: 177–82. DOI:10.1266/ggs.79.177. PMID:15329498.
- Ching YP، Pang AS، Lam WH، Qi RZ، Wang JH (أبريل 2002). "Identification of a neuronal Cdk5 activator-binding protein as Cdk5 inhibitor". J Biol Chem. ج. 277 ع. 18: 15237–40. DOI:10.1074/jbc.C200032200. PMID:11882646.
- Ching YP، Qi Z، Wang JH (أبريل 2000). "Cloning of three novel neuronal Cdk5 activator binding proteins". Gene. ج. 242 ع. 1–2: 285–94. DOI:10.1016/S0378-1119(99)00499-0. PMID:10721722.
قراءة متعمقة
- Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
- Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
- Lai CH، Chou CY، Ch'ang LY، وآخرون (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". Genome Res. ج. 10 ع. 5: 703–13. DOI:10.1101/gr.10.5.703. PMC:310876. PMID:10810093.
- Wang X، Ching YP، Lam WH، وآخرون (2000). "Identification of a common protein association region in the neuronal Cdk5 activator". J. Biol. Chem. ج. 275 ع. 41: 31763–9. DOI:10.1074/jbc.M004358200. PMID:10915792.
- Zhang QH، Ye M، Wu XY، وآخرون (2001). "Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells". Genome Res. ج. 10 ع. 10: 1546–60. DOI:10.1101/gr.140200. PMC:310934. PMID:11042152.
- Deloukas P، Matthews LH، Ashurst J، وآخرون (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. ج. 414 ع. 6866: 865–71. DOI:10.1038/414865a. PMID:11780052.
- 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. 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.
- Lehner B، Sanderson CM (2004). "A protein interaction framework for human mRNA degradation". Genome Res. ج. 14 ع. 7: 1315–23. DOI:10.1101/gr.2122004. PMC:442147. PMID:15231747.
- 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.
- 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. DOI:10.1038/nature04209. PMID:16189514.
- بوابة الكيمياء الحيوية
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة طب
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