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Germline-sequence variants S836S and L769L in the RE arranged during Transfection (RET) proto-oncogene are not associated with predisposition to sporadic medullary carcinoma in the French population.
Berard I, Kraimps JL, Savagner F, Murat A, Renaudin K, Nicolli-Sire P, Bertrand G, Moisan JP, Bezieau S. Berard I, et al. Among authors: murat a. Clin Genet. 2004 Feb;65(2):150-2. doi: 10.1111/j.0009-9163.2004.00172.x. Clin Genet. 2004. PMID: 14984475 No abstract available.
Familial medullary thyroid carcinoma with noncysteine ret mutations: phenotype-genotype relationship in a large series of patients.
Niccoli-Sire P, Murat A, Rohmer V, Franc S, Chabrier G, Baldet L, Maes B, Savagner F, Giraud S, Bezieau S, Kottler ML, Morange S, Conte-Devolx B; French Calcitonin Tumors Group (GETC). Niccoli-Sire P, et al. Among authors: murat a. J Clin Endocrinol Metab. 2001 Aug;86(8):3746-53. doi: 10.1210/jcem.86.8.7767. J Clin Endocrinol Metab. 2001. PMID: 11502806
The clinical spectrum of RET proto-oncogene mutations in codon 790.
Bihan H, Murat A, Fysekidis M, Al-Salameh A, Schwartz C, Baudin E, Thieblot P, Borson-Chazot F, Guillausseau PJ, Cardot-Bauters C, Raingeard I, Requeda E, Sadoul JL, Reznik Y; Régis Cohen for the French Group of Endocrine Tumours. Bihan H, et al. Among authors: murat a. Eur J Endocrinol. 2013 Jul 29;169(3):271-6. doi: 10.1530/EJE-13-0050. Print 2013 Sep. Eur J Endocrinol. 2013. PMID: 23756355
When should thyroidectomy be performed in familial medullary thyroid carcinoma gene carriers with non-cysteine RET mutations?
Niccoli-Sire P, Murat A, Rohmer V, Gibelin H, Chabrier G, Conte-Devolx B, Visset J, Ronceray J, Jaeck D, Henry JF, Proye C, Carnaille B, Kraimps JL; Groupe D'étude Des Tumeurs Endocrines. Niccoli-Sire P, et al. Among authors: murat a. Surgery. 2003 Dec;134(6):1029-36; discussion 1036-7. doi: 10.1016/j.surg.2003.07.019. Surgery. 2003. PMID: 14668737
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
Burnichon N, Rohmer V, Amar L, Herman P, Leboulleux S, Darrouzet V, Niccoli P, Gaillard D, Chabrier G, Chabolle F, Coupier I, Thieblot P, Lecomte P, Bertherat J, Wion-Barbot N, Murat A, Venisse A, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP; PGL.NET network. Burnichon N, et al. Among authors: murat a. J Clin Endocrinol Metab. 2009 Aug;94(8):2817-27. doi: 10.1210/jc.2008-2504. Epub 2009 May 19. J Clin Endocrinol Metab. 2009. PMID: 19454582
RET mutations in exons 13 and 14 of FMTC patients.
Bolino A, Schuffenecker I, Luo Y, Seri M, Silengo M, Tocco T, Chabrier G, Houdent C, Murat A, Schlumberger M, et al. Bolino A, et al. Among authors: murat a. Oncogene. 1995 Jun 15;10(12):2415-9. Oncogene. 1995. PMID: 7784092
190 results