Lenoir GM - Search Results

1

Development of medullary thyroid carcinoma in transgenic mice expressing the RET protooncogene altered by a multiple endocrine neoplasia type 2A mutation.

Michiels FM, Chappuis S, Caillou B, Pasini A, Talbot M, Monier R, Lenoir GM, Feunteun J, Billaud M. Michiels FM, et al. Among authors: lenoir gm. Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3330-5. doi: 10.1073/pnas.94.7.3330. Proc Natl Acad Sci U S A. 1997. PMID: 9096393 Free PMC article.

2

Distinct biological properties of two RET isoforms activated by MEN 2A and MEN 2B mutations.

Rossel M, Pasini A, Chappuis S, Geneste O, Fournier L, Schuffenecker I, Takahashi M, van Grunsven LA, Urdiales JL, Rudkin BB, Lenoir GM, Billaud M. Rossel M, et al. Among authors: lenoir gm. Oncogene. 1997 Jan 23;14(3):265-75. doi: 10.1038/sj.onc.1200831. Oncogene. 1997. PMID: 9018112

3

[Neural crest and multiple endocrinopathies].

Pasini A, Michiels FM, Chappuis-Flament S, Geneste O, Rossel M, Fournier L, Feunteun J, Lenoir G, Schuffenecker I, Billaud M. Pasini A, et al. C R Seances Soc Biol Fil. 1996;190(5-6):557-67. C R Seances Soc Biol Fil. 1996. PMID: 9074721 Review. French.

4

RET proto-oncogene mutations in French MEN 2A and FMTC families.

Schuffenecker I, Billaud M, Calender A, Chambe B, Ginet N, Calmettes C, Modigliani E, Lenoir GM. Schuffenecker I, et al. Among authors: lenoir gm. Hum Mol Genet. 1994 Nov;3(11):1939-43. doi: 10.1093/hmg/3.11.1939. Hum Mol Genet. 1994. PMID: 7874109

5

Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain.

Pasini A, Geneste O, Legrand P, Schlumberger M, Rossel M, Fournier L, Rudkin BB, Schuffenecker I, Lenoir GM, Billaud M. Pasini A, et al. Among authors: lenoir gm. Oncogene. 1997 Jul 24;15(4):393-402. doi: 10.1038/sj.onc.1201199. Oncogene. 1997. PMID: 9242375

6

Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines.

Chappuis-Flament S, Pasini A, De Vita G, Ségouffin-Cariou C, Fusco A, Attié T, Lenoir GM, Santoro M, Billaud M. Chappuis-Flament S, et al. Among authors: lenoir gm. Oncogene. 1998 Dec 3;17(22):2851-61. doi: 10.1038/sj.onc.1202202. Oncogene. 1998. PMID: 9879991

7

Various mechanisms cause RET-mediated signaling defects in Hirschsprung's disease.

Pelet A, Geneste O, Edery P, Pasini A, Chappuis S, Atti T, Munnich A, Lenoir G, Lyonnet S, Billaud M. Pelet A, et al. J Clin Invest. 1998 Mar 15;101(6):1415-23. doi: 10.1172/JCI375. J Clin Invest. 1998. PMID: 9502784 Free PMC article.

8

BRCA1, a gene involved in inherited predisposition to breast and ovarian cancer.

Feunteun J, Lenoir GM. Feunteun J, et al. Among authors: lenoir gm. Biochim Biophys Acta. 1996 Mar 18;1242(3):177-80. doi: 10.1016/0304-419x(95)00016-9. Biochim Biophys Acta. 1996. PMID: 8603070 Review. No abstract available.

9

Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.

Geneste O, Bidaud C, De Vita G, Hofstra RM, Tartare-Deckert S, Buys CH, Lenoir GM, Santoro M, Billaud M. Geneste O, et al. Among authors: lenoir gm. Hum Mol Genet. 1999 Oct;8(11):1989-99. doi: 10.1093/hmg/8.11.1989. Hum Mol Genet. 1999. PMID: 10484767

10

Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function?

Takahashi M, Iwashita T, Santoro M, Lyonnet S, Lenoir GM, Billaud M. Takahashi M, et al. Among authors: lenoir gm. Hum Mutat. 1999;13(4):331-6. doi: 10.1002/(SICI)1098-1004(1999)13:4<331::AID-HUMU11>3.0.CO;2-#. Hum Mutat. 1999. PMID: 10220148

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