Billaud M - Search Results

1

The RET proto-oncogene induces apoptosis: a novel mechanism for Hirschsprung disease.

Bordeaux MC, Forcet C, Granger L, Corset V, Bidaud C, Billaud M, Bredesen DE, Edery P, Mehlen P. Bordeaux MC, et al. Among authors: billaud m. EMBO J. 2000 Aug 1;19(15):4056-63. doi: 10.1093/emboj/19.15.4056. EMBO J. 2000. PMID: 10921886 Free PMC article.

2

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: billaud m. Hum Mol Genet. 1999 Oct;8(11):1989-99. doi: 10.1093/hmg/8.11.1989. Hum Mol Genet. 1999. PMID: 10484767

3

Dialogue between LKB1 and AMPK: a hot topic at the cellular pole.

Forcet C, Billaud M. Forcet C, et al. Among authors: billaud m. Sci STKE. 2007 Sep 18;2007(404):pe51. doi: 10.1126/stke.4042007pe51. Sci STKE. 2007. PMID: 17878409 Review.

4

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. Among authors: billaud m. J Clin Invest. 1998 Mar 15;101(6):1415-23. doi: 10.1172/JCI375. J Clin Invest. 1998. PMID: 9502784 Free PMC article.

5

The RET receptor: function in development and dysfunction in congenital malformation.

Manié S, Santoro M, Fusco A, Billaud M. Manié S, et al. Among authors: billaud m. Trends Genet. 2001 Oct;17(10):580-9. doi: 10.1016/s0168-9525(01)02420-9. Trends Genet. 2001. PMID: 11585664

6

Functional analysis of Peutz-Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity.

Forcet C, Etienne-Manneville S, Gaude H, Fournier L, Debilly S, Salmi M, Baas A, Olschwang S, Clevers H, Billaud M. Forcet C, et al. Among authors: billaud m. Hum Mol Genet. 2005 May 15;14(10):1283-92. doi: 10.1093/hmg/ddi139. Epub 2005 Mar 30. Hum Mol Genet. 2005. PMID: 15800014

7

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: billaud m. Hum Mol Genet. 1994 Nov;3(11):1939-43. doi: 10.1093/hmg/3.11.1939. Hum Mol Genet. 1994. PMID: 7874109

8

[The RET gene in thyroid pathology].

Michiels FM, Billaud M. Michiels FM, et al. Among authors: billaud m. Arch Anat Cytol Pathol. 1998;46(1-2):19-30. Arch Anat Cytol Pathol. 1998. PMID: 9754357 Review. French.

9

Molecular chaperone complexes with antagonizing activities regulate stability and activity of the tumor suppressor LKB1.

Gaude H, Aznar N, Delay A, Bres A, Buchet-Poyau K, Caillat C, Vigouroux A, Rogon C, Woods A, Vanacker JM, Höhfeld J, Perret C, Meyer P, Billaud M, Forcet C. Gaude H, et al. Among authors: billaud m. Oncogene. 2012 Mar 22;31(12):1582-91. doi: 10.1038/onc.2011.342. Epub 2011 Aug 22. Oncogene. 2012. PMID: 21860411

10

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: billaud m. Oncogene. 1998 Dec 3;17(22):2851-61. doi: 10.1038/sj.onc.1202202. Oncogene. 1998. PMID: 9879991

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