Similar articles for PMID: 7911697

Year	Number of Results
1973	2
1982	1
1985	1
1987	1
1988	1
1989	5
1990	5
1991	4
1992	4
1993	11
1994	37
1995	49
1996	41
1997	46
1998	45
1999	29
2000	28
2001	39
2002	21
2003	14
2004	7
2005	2
2006	3
2007	1
2008	1
2009	2
2011	1
2012	2
2013	1
2014	1
2018	1
2020	1
2021	1
2022	2
2024	0

1

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.

Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Scheumann GF, Jackson CE, Tunnacliffe A, et al. Eng C, et al. Hum Mol Genet. 1994 Feb;3(2):237-41. doi: 10.1093/hmg/3.2.237. Hum Mol Genet. 1994. PMID: 7911697

2

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. Komminoth P. Verh Dtsch Ges Pathol. 1995;79:L-LV. Verh Dtsch Ges Pathol. 1995. PMID: 8600671

3

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, et al. Hofstra RM, et al. Nature. 1994 Jan 27;367(6461):375-6. doi: 10.1038/367375a0. Nature. 1994. PMID: 7906866

4

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. Bugalho MJ, et al. Eur J Endocrinol. 1997 Apr;136(4):423-6. doi: 10.1530/eje.0.1360423. Eur J Endocrinol. 1997. PMID: 9150704

5

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. Eng C, et al. Oncogene. 1995 Feb 2;10(3):509-13. Oncogene. 1995. PMID: 7845675

6

Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease.

Eng C, Mulligan LM. Eng C, et al. Hum Mutat. 1997;9(2):97-109. doi: 10.1002/(SICI)1098-1004(1997)9:2<97::AID-HUMU1>3.0.CO;2-M. Hum Mutat. 1997. PMID: 9067749 Review.

7

Mutations of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas.

Zedenius J, Larsson C, Bergholm U, Bovée J, Svensson A, Hallengren B, Grimelius L, Bäckdahl M, Weber G, Wallin G. Zedenius J, et al. J Clin Endocrinol Metab. 1995 Oct;80(10):3088-90. doi: 10.1210/jcem.80.10.7559902. J Clin Endocrinol Metab. 1995. PMID: 7559902

8

[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. Sansó G, et al. Medicina (B Aires). 1998;58(2):179-84. Medicina (B Aires). 1998. PMID: 9706252 Spanish.

9

Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. "Study Group Multiple Endocrine Neoplasia Austria (SMENA)".

Fink M, Weinhüsel A, Niederle B, Haas OA. Fink M, et al. Int J Cancer. 1996 Aug 22;69(4):312-6. doi: 10.1002/(SICI)1097-0215(19960822)69:4<312::AID-IJC13>3.0.CO;2-7. Int J Cancer. 1996. PMID: 8797874 Free article.

10

Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A (Sipple's syndrome).

Oishi S, Sato T, Takiguchi-Shirahama S, Nakamura Y. Oishi S, et al. Endocr J. 1995 Aug;42(4):527-36. doi: 10.1507/endocrj.42.527. Endocr J. 1995. PMID: 8556060 Free article.

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