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Page 1
Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.
McKay JD, Lesueur F, Jonard L, Pastore A, Williamson J, Hoffman L, Burgess J, Duffield A, Papotti M, Stark M, Sobol H, Maes B, Murat A, Kääriäinen H, Bertholon-Grégoire M, Zini M, Rossing MA, Toubert ME, Bonichon F, Cavarec M, Bernard AM, Boneu A, Leprat F, Haas O, Lasset C, Schlumberger M, Canzian F, Goldgar DE, Romeo G. McKay JD, et al. Among authors: murat a. Am J Hum Genet. 2001 Aug;69(2):440-6. doi: 10.1086/321979. Epub 2001 Jul 2. Am J Hum Genet. 2001. PMID: 11438887 Free PMC article.
RET rearrangements in familial papillary thyroid carcinomas.
Corvi R, Lesueur F, Martinez-Alfaro M, Zini M, Decaussin M, Murat A, Romeo G. Corvi R, et al. Among authors: murat a. Cancer Lett. 2001 Sep 20;170(2):191-8. doi: 10.1016/s0304-3835(01)00596-1. Cancer Lett. 2001. PMID: 11463498
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.
Giraud S, Zhang CX, Serova-Sinilnikova O, Wautot V, Salandre J, Buisson N, Waterlot C, Bauters C, Porchet N, Aubert JP, Emy P, Cadiot G, Delemer B, Chabre O, Niccoli P, Leprat F, Duron F, Emperauger B, Cougard P, Goudet P, Sarfati E, Riou JP, Guichard S, Rodier M, Meyrier A, Caron P, Vantyghem MC, Assayag M, Peix JL, Pugeat M, Rohmer V, Vallotton M, Lenoir G, Gaudray P, Proye C, Conte-Devolx B, Chanson P, Shugart YY, Goldgar D, Murat A, Calender A. Giraud S, et al. Among authors: murat a. Am J Hum Genet. 1998 Aug;63(2):455-67. doi: 10.1086/301953. Am J Hum Genet. 1998. PMID: 9683585 Free PMC article.
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
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
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
190 results