TBX3

An Error has occured retrieving Wikidata item for infobox TBX3‏ (T-box 3) هوَ بروتين يُشَفر بواسطة جين TBX3 في الإنسان.

الوظيفة

هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.

الأهمية السريرية

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قراءة متعمقة

• "Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome". Nature Genetics. 16 (3): 311–5. Jul 1997. doi:10.1038/ng0797-311. PMID 9207801.
• "The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome". American Journal of Human Genetics. 64 (6): 1550–62. Jun 1999. doi:10.1086/302417. PMC 1377898. PMID 10330342.
• "Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome". Proceedings of the National Academy of Sciences of the United States of America. 96 (18): 10212–7. Aug 1999. doi:10.1073/pnas.96.18.10212. PMC 17868. PMID 10468588.
• "A dominant repression domain in Tbx3 mediates transcriptional repression and cell immortalization: relevance to mutations in Tbx3 that cause ulnar-mammary syndrome". Human Molecular Genetics. 10 (21): 2403–13. Oct 2001. doi:10.1093/hmg/10.21.2403. PMID 11689487.
• "TBX-3, the gene mutated in Ulnar-Mammary Syndrome, is a negative regulator of p19ARF and inhibits senescence". The Journal of Biological Chemistry. 277 (8): 6567–72. Feb 2002. doi:10.1074/jbc.M110492200. PMID 11748239.
• "The T-box repressors TBX2 and TBX3 specifically regulate the tumor suppressor gene p14ARF via a variant T-site in the initiator". The Journal of Biological Chemistry. 277 (29): 26120–7. Jul 2002. doi:10.1074/jbc.M200403200. PMID 12000749.
• "Structure of the DNA-bound T-box domain of human TBX3, a transcription factor responsible for ulnar-mammary syndrome". Structure. 10 (3): 343–56. Mar 2002. doi:10.1016/S0969-2126(02)00722-0. PMID 12005433.
• "Tbx3 impinges on the p53 pathway to suppress apoptosis, facilitate cell transformation and block myogenic differentiation". Oncogene. 21 (24): 3827–35. May 2002. doi:10.1038/sj.onc.1205476. PMID 12032820.
• "Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development". American Journal of Medical Genetics. 110 (4): 365–9. Jul 2002. doi:10.1002/ajmg.10447. PMID 12116211.
• "Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family". Annales De Génétique. 45 (4): 213–7. 2003. doi:10.1016/S0003-3995(02)01144-9. PMID 12668170.
• "TBX3 and its isoform TBX3+2a are functionally distinctive in inhibition of senescence and are overexpressed in a subset of breast cancer cell lines". Cancer Research. 64 (15): 5132–9. Aug 2004. doi:10.1158/0008-5472.CAN-04-0615. PMID 15289316.
• "Increased expression of cSHMT, Tbx3 and utrophin in plasma of ovarian and breast cancer patients". International Journal of Cancer. 118 (2): 412–21. Jan 2006. doi:10.1002/ijc.21332. PMID 16049973.
• "Isl1Cre reveals a common Bmp pathway in heart and limb development". Development. 133 (8): 1575–85. Apr 2006. doi:10.1242/dev.02322. PMID 16556916.
• "Tbx3, a transcriptional factor, involves in proliferation and osteogenic differentiation of human adipose stromal cells". Molecular and Cellular Biochemistry. 296 (1–2): 129–36. Feb 2007. doi:10.1007/s11010-006-9306-4. PMID 16955224.
• "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. Nov 2006. doi:10.1016/j.cell.2006.09.026. PMID 17081983.
• "Molecular pathway for the localized formation of the sinoatrial node". Circulation Research. 100 (3): 354–62. Feb 2007. doi:10.1161/01.RES.0000258019.74591.b3. PMID 17234970.

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