TBCE

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

الوظيفة

هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.

الأهمية السريرية

هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.

قراءة متعمقة

• "Chaperonin-mediated folding of actin and tubulin". J. Cell Biol. 132 (1–2): 1–4. 1996. doi:10.1083/jcb.132.1.1. PMC 2120700. PMID 8567715.
• "Parathyroid development and the role of tubulin chaperone E". Horm. Res. 67 (1): 12–21. 2007. doi:10.1159/000095944. PMID 17008776.
• "Tubulin subunits exist in an activated conformational state generated and maintained by protein cofactors". J. Cell Biol. 138 (4): 821–32. 1997. doi:10.1083/jcb.138.4.821. PMC 2138046. PMID 9265649.
• "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. 63 (1): 163–9. 1998. doi:10.1086/301915. PMC 1377236. PMID 9634513.
• "The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43". Genomics. 54 (1): 13–8. 1999. doi:10.1006/geno.1998.5530. PMID 9806825.
• "Selected subunits of the cytosolic chaperonin associate with microtubules assembled in vitro". J. Biol. Chem. 274 (4): 2408–15. 1999. doi:10.1074/jbc.274.4.2408. PMID 9891010.
• "Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome". Nat. Genet. 32 (3): 448–52. 2002. doi:10.1038/ng1012. PMID 12389028.
• "A missense mutation in Tbce causes progressive motor neuronopathy in mice". Nat. Genet. 32 (3): 443–7. 2002. doi:10.1038/ng1016. PMID 12389029.
• "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. 159 (4): 563–9. 2003. doi:10.1083/jcb.200208001. PMC 2173089. PMID 12446740.
• "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. 2003. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. 2004. doi:10.1038/nbt810. PMID 12665801.
• "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. 2004. doi:10.1038/ng1285. PMID 14702039.
• "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. 2005. doi:10.1038/nature04209. PMID 16189514.
• "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. 2006. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315–21. 2006. doi:10.1038/nature04727. PMID 16710414.
• "Role of cofactors B (TBCB) and E (TBCE) in tubulin heterodimer dissociation". Exp. Cell Res. 313 (3): 425–36. 2007. doi:10.1016/j.yexcr.2006.09.002. PMID 17184771.

هذه بذرة مقالة عن جين على كروموسوم 1 بحاجة للتوسيع. شارك في تحريرها.