CDC73 Gene

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1		Vicky Zhou	+ 750 word(s)	750	2020-12-15 07:47:06

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Zhou, V. CDC73 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5082 (accessed on 16 September 2026).

Zhou V. CDC73 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5082. Accessed September 16, 2026.

Zhou, Vicky. "CDC73 Gene" Encyclopedia, https://encyclopedia.pub/entry/5082 (accessed September 16, 2026).

Zhou, V. (2020, December 24). CDC73 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5082

Zhou, Vicky. "CDC73 Gene." Encyclopedia. Web. 24 December, 2020.

CDC73 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/cdc73

cell division cycle 73

genes

References

Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, Besser GM,Conceição Pereira M, Davie MW, Dudley N, Leite V, Sadler GP, Seller A, ThakkerRV. Parafibromin mutations in hereditary hyperparathyroidism syndromes andparathyroid tumours. Clin Endocrinol (Oxf). 2006 Mar;64(3):299-306.
Cetani F, Pardi E, Marcocci C. Update on parathyroid carcinoma. J EndocrinolInvest. 2016 Jun;39(6):595-606. doi: 10.1007/s40618-016-0447-3.Review.
Fernandez-Ranvier GG, Khanafshar E, Tacha D, Wong M, Kebebew E, Duh QY, Clark OH. Defining a molecular phenotype for benign and malignant parathyroid tumors.Cancer. 2009 Jan 15;115(2):334-44. doi: 10.1002/cncr.24037.
Masi G, Barzon L, Iacobone M, Viel G, Porzionato A, Macchi V, De Caro R, FaviaG, Palù G. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr Relat Cancer. 2008 Dec;15(4):1115-26. doi:10.1677/ERC-08-0066.
Newey PJ, Bowl MR, Cranston T, Thakker RV. Cell division cycle protein 73homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Hum Mutat. 2010 Mar;31(3):295-307. doi:10.1002/humu.21188.
Newey PJ, Bowl MR, Thakker RV. Parafibromin--functional insights. J InternMed. 2009 Jul;266(1):84-98. doi: 10.1111/j.1365-2796.2009.02107.x. Review.
Serrano-Gonzalez M, Shay S, Austin J, Maceri DR, Pitukcheewanont P. A germlinemutation of HRPT2/CDC73 (70 G>T) in an adolescent female with parathyroidcarcinoma: first case report and a review of the literature. J Pediatr EndocrinolMetab. 2016 Sep 1;29(9):1005-12. doi: 10.1515/jpem-2016-0109. Review.
Villablanca A, Calender A, Forsberg L, Höög A, Cheng JD, Petillo D, Bauters C,Kahnoski K, Ebeling T, Salmela P, Richardson AL, Delbridge L, Meyrier A, Proye C,Carpten JD, Teh BT, Robinson BG, Larsson C. Germline and de novo mutations in theHRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). JMed Genet. 2004 Mar;41(3):e32.
Wang PF, Tan MH, Zhang C, Morreau H, Teh BT. HRPT2, a tumor suppressor genefor hyperparathyroidism-jaw tumor syndrome. Horm Metab Res. 2005 Jun;37(6):380-3.Review.
Westin G. Molecular genetics and epigenetics of nonfamilial (sporadic)parathyroid tumours. J Intern Med. 2016 Dec;280(6):551-558. doi:10.1111/joim.12458.

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Subjects: Genetics & Heredity

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Update Date: 24 Dec 2020

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