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176 related items for PubMed ID: 9398735
1. A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma. Hofstra RM, Fattoruso O, Quadro L, Wu Y, Libroia A, Verga U, Colantuoni V, Buys CH. J Clin Endocrinol Metab; 1997 Dec; 82(12):4176-8. PubMed ID: 9398735 [Abstract] [Full Text] [Related]
2. A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC. Eng C, Smith DP, Mulligan LM, Healey CS, Zvelebil MJ, Stonehouse TJ, Ponder MA, Jackson CE, Waterfield MD, Ponder BA. Oncogene; 1995 Feb 02; 10(3):509-13. PubMed ID: 7845675 [Abstract] [Full Text] [Related]
3. Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A. Landsvater RM, Jansen RP, Hofstra RM, Buys CH, Lips CJ, Ploos van Amstel HK. Hum Genet; 1996 Jan 02; 97(1):11-4. PubMed ID: 8557249 [Abstract] [Full Text] [Related]
4. A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A. Berndt I, Reuter M, Saller B, Frank-Raue K, Groth P, Grussendorf M, Raue F, Ritter MM, Höppner W. J Clin Endocrinol Metab; 1998 Mar 02; 83(3):770-4. PubMed ID: 9506724 [Abstract] [Full Text] [Related]
5. Rudolf-Virchow-Preis 1995. The role of RET proto-oncogene mutation analysis in the diagnosis of multiple endocrine neoplasia type 2 (MEN 2) gene carriers and in the discrimination of sporadic and familial medullary thyroid carcinomas and pheochromocytomas. Komminoth P. Verh Dtsch Ges Pathol; 1995 Mar 02; 79():L-LV. PubMed ID: 8600671 [Abstract] [Full Text] [Related]
6. Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas. Komminoth P, Kunz EK, Matias-Guiu X, Hiort O, Christiansen G, Colomer A, Roth J, Heitz PU. Cancer; 1995 Aug 01; 76(3):479-89. PubMed ID: 8625130 [Abstract] [Full Text] [Related]
7. Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group. Frank-Raue K, Höppner W, Frilling A, Kotzerke J, Dralle H, Haase R, Mann K, Seif F, Kirchner R, Rendl J, Deckart HF, Ritter MM, Hampel R, Klempa J, Scholz GH, Raue F. J Clin Endocrinol Metab; 1996 May 01; 81(5):1780-3. PubMed ID: 8626834 [Abstract] [Full Text] [Related]
8. Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma. Shirahama S, Ogura K, Takami H, Ito K, Tohsen T, Miyauchi A, Nakamura Y. J Hum Genet; 1998 May 01; 43(2):101-6. PubMed ID: 9621513 [Abstract] [Full Text] [Related]
9. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Hofstra RM, Landsvater RM, Ceccherini I, Stulp RP, Stelwagen T, Luo Y, Pasini B, Höppener JW, van Amstel HK, Romeo G. Nature; 1994 Jan 27; 367(6461):375-6. PubMed ID: 7906866 [Abstract] [Full Text] [Related]
10. Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma. Oriola J, Páramo C, Halperin I, García-Mayor RV, Rivera-Fillat F. Am J Med Genet; 1998 Jul 07; 78(3):271-3. PubMed ID: 9677065 [Abstract] [Full Text] [Related]
11. [Early diagnosis of multiple endocrine neoplasia type 2 (MEN 2) by detection of mutated RET proto-oncogene carriers]. Sansó G, Domené HM, Iorcansky S, Barontini M. Medicina (B Aires); 1998 Jul 07; 58(2):179-84. PubMed ID: 9706252 [Abstract] [Full Text] [Related]
15. Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence. Romei C, Elisei R, Pinchera A, Ceccherini I, Molinaro E, Mancusi F, Martino E, Romeo G, Pacini F. J Clin Endocrinol Metab; 1996 Apr 07; 81(4):1619-22. PubMed ID: 8636377 [Abstract] [Full Text] [Related]
17. Molecular analysis of the RET proto-oncogene in patients with sporadic medullary thyroid carcinoma: a novel point mutation in the extracellular cysteine-rich domain. Bugalho MJ, Frade JP, Santos JR, Limbert E, Sobrinho L. Eur J Endocrinol; 1997 Apr 07; 136(4):423-6. PubMed ID: 9150704 [Abstract] [Full Text] [Related]