CDC73
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هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.
هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.
CDC73 (Cell division cycle 73) هوَ بروتين يُشَفر بواسطة جين CDC73 في الإنسان.[1][2][3]
الوظيفة[عدل]

الأهمية السريرية[عدل]

المراجع[عدل]
- ^ Sood R, Bonner TI, Makalowska I, Stephan DA, Robbins CM, Connors TD, Morgenbesser SD, Su K, Faruque MU, Pinkett H, Graham C, Baxevanis AD, Klinger KW, Landes GM, Trent JM, Carpten JD (April 2001). "Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus". Genomics. 73 (2): 211–22. doi:10.1006/geno.2001.6500. PMID 11318611. الوسيط
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تم تجاهله (مساعدة) - ^ "Entrez Gene: CDC73 Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae)". مؤرشف من الأصل في 05 ديسمبر 2010. الوسيط
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تم تجاهله (مساعدة) - ^ Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, Petillo D, Leotlela PD, Harding B, Cameron D, Pannett AA, Höög A, Heath H, James-Newton LA, Robinson B, Zarbo RJ, Cavaco BM, Wassif W, Perrier ND, Rosen IB, Kristoffersson U, Turnpenny PD, Farnebo LO, Besser GM, Jackson CE, Morreau H, Trent JM, Thakker RV, Marx SJ, Teh BT, Larsson C, Hobbs MR (December 2002). "HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome". Nat. Genet. 32 (4): 676–80. doi:10.1038/ng1048. PMID 12434154. الوسيط
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تم تجاهله (مساعدة)
قراءة متعمقة[عدل]
- Szabó J, Heath B, Hill VM, et al. (1995). "Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31". Am. J. Hum. Genet. 56 (4): 944–50. PMC 1801214. PMID 7717405. الوسيط
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تم تجاهله (مساعدة) - Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298. الوسيط
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تم تجاهله (مساعدة) - Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149. الوسيط
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تم تجاهله (مساعدة) - Sood R, Bonner TI, Makalowska I, et al. (2001). "Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus". Genomics. 73 (2): 211–22. doi:10.1006/geno.2001.6500. PMID 11318611. الوسيط
|CitationClass=
تم تجاهله (مساعدة) - Hobbs MR, Rosen IB, Jackson CE (2002). "Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2". Am. J. Hum. Genet. 70 (5): 1376–7. doi:10.1086/340093. PMC 447614. PMID 11951180. الوسيط
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تم تجاهله (مساعدة) - Carpten JD, Robbins CM, Villablanca A, et al. (2003). "HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome". Nat. Genet. 32 (4): 676–80. doi:10.1038/ng1048. PMID 12434154. الوسيط
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تم تجاهله (مساعدة) - Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. الوسيط
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تم تجاهله (مساعدة) - Howell VM, Haven CJ, Kahnoski K, et al. (2003). "HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours". J. Med. Genet. 40 (9): 657–63. doi:10.1136/jmg.40.9.657. PMC 1735580. PMID 12960210. الوسيط
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تم تجاهله (مساعدة) - Shattuck TM, Välimäki S, Obara T, et al. (2003). "Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma". N. Engl. J. Med. 349 (18): 1722–9. doi:10.1056/NEJMoa031237. PMID 14585940. الوسيط
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تم تجاهله (مساعدة) - Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039. الوسيط
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تم تجاهله (مساعدة) - Simonds WF, Robbins CM, Agarwal SK, et al. (2004). "Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome". J. Clin. Endocrinol. Metab. 89 (1): 96–102. doi:10.1210/jc.2003-030675. PMID 14715834. الوسيط
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تم تجاهله (مساعدة) - Warner J, Epstein M, Sweet A, et al. (2004). "Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications". J. Med. Genet. 41 (3): 155–60. doi:10.1136/jmg.2003.016725. PMC 1735699. PMID 14985373. الوسيط
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تم تجاهله (مساعدة) - Villablanca A, Calender A, Forsberg L, et al. (2004). "Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)". J. Med. Genet. 41 (3): e32. doi:10.1136/jmg.2003.012369. PMC 1735713. PMID 14985403. الوسيط
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تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 221. doi:10.1007/s00439-003-1060-z. PMID 15046050. الوسيط
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تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 222. doi:10.1007/s00439-003-1060-z. PMID 15046094. الوسيط
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تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 222. doi:10.1007/s00439-003-1060-z. PMID 15046098. الوسيط
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تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 223. doi:10.1007/s00439-003-1060-z. PMID 15046102. الوسيط
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تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 223. doi:10.1007/s00439-003-1060-z. PMID 15046105. الوسيط
|CitationClass=
تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 223. doi:10.1007/s00439-003-1060-z. PMID 15046107. الوسيط
|CitationClass=
تم تجاهله (مساعدة) - Teh BT, Howell VM, Haven CJ, et al. (2004). "Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome". Hum. Genet. 114 (2): 224. doi:10.1007/s00439-003-1060-z. PMID 15046109. الوسيط
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