TBCE

An Error has occured retrieving Wikidata item for infobox TBCE‏ (Tubulin folding cofactor E) هوَ بروتين يُشَفر بواسطة جين TBCE في الإنسان.

قراءة متعمقة

• Lewis SA، Tian G، Vainberg IE، Cowan NJ (1996). "Chaperonin-mediated folding of actin and tubulin". J. Cell Biol. ج. 132 ع. 1–2: 1–4. DOI:10.1083/jcb.132.1.1. PMC:2120700. PMID:8567715.
• Parvari R، Diaz GA، Hershkovitz E (2007). "Parathyroid development and the role of tubulin chaperone E". Horm. Res. ج. 67 ع. 1: 12–21. DOI:10.1159/000095944. PMID:17008776.
• Tian G، Lewis SA، Feierbach B، وآخرون (1997). "Tubulin subunits exist in an activated conformational state generated and maintained by protein cofactors". J. Cell Biol. ج. 138 ع. 4: 821–32. DOI:10.1083/jcb.138.4.821. PMC:2138046. PMID:9265649.
• Parvari R، Hershkovitz E، Kanis A، وآخرون (1998). "Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43". Am. J. Hum. Genet. ج. 63 ع. 1: 163–9. DOI:10.1086/301915. PMC:1377236. PMID:9634513.
• Diaz GA، Khan KT، Gelb BD (1999). "The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43". Genomics. ج. 54 ع. 1: 13–8. DOI:10.1006/geno.1998.5530. PMID:9806825.
• Roobol A، Sahyoun ZP، Carden MJ (1999). "Selected subunits of the cytosolic chaperonin associate with microtubules assembled in vitro". J. Biol. Chem. ج. 274 ع. 4: 2408–15. DOI:10.1074/jbc.274.4.2408. PMID:9891010.
• Parvari R، Hershkovitz E، Grossman N، وآخرون (2002). "Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome". Nat. Genet. ج. 32 ع. 3: 448–52. DOI:10.1038/ng1012. PMID:12389028.
• Martin N، Jaubert J، Gounon P، وآخرون (2002). "A missense mutation in Tbce causes progressive motor neuronopathy in mice". Nat. Genet. ج. 32 ع. 3: 443–7. DOI:10.1038/ng1016. PMID:12389029.
• Bommel H، Xie G، Rossoll W، وآخرون (2003). "Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease". J. Cell Biol. ج. 159 ع. 4: 563–9. DOI:10.1083/jcb.200208001. PMC:2173089. PMID:12446740.
• 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.
• Gevaert K، Goethals M، Martens L، وآخرون (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. ج. 21 ع. 5: 566–9. DOI:10.1038/nbt810. PMID:12665801.
• 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.
• 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.
• Kimura K، Wakamatsu A، Suzuki Y، وآخرون (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. ج. 16 ع. 1: 55–65. DOI:10.1101/gr.4039406. PMC:1356129. PMID:16344560.
• Gregory SG، Barlow KF، McLay KE، وآخرون (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. ج. 441 ع. 7091: 315–21. DOI:10.1038/nature04727. PMID:16710414.
• Kortazar D، Fanarraga ML، Carranza G، وآخرون (2007). "Role of cofactors B (TBCB) and E (TBCE) in tubulin heterodimer dissociation". Exp. Cell Res. ج. 313 ع. 3: 425–36. DOI:10.1016/j.yexcr.2006.09.002. PMID:17184771.