Caburet S - Search Results

1

The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles.

Benayoun BA, Caburet S, Dipietromaria A, Bailly-Bechet M, Batista F, Fellous M, Vaiman D, Veitia RA. Benayoun BA, et al. Among authors: caburet s. Hum Mol Genet. 2008 Oct 15;17(20):3118-27. doi: 10.1093/hmg/ddn209. Epub 2008 Jul 16. Hum Mol Genet. 2008. PMID: 18635577

2

A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation.

Caburet S, Demarez A, Moumné L, Fellous M, De Baere E, Veitia RA. Caburet S, et al. J Med Genet. 2004 Dec;41(12):932-6. doi: 10.1136/jmg.2004.024356. J Med Genet. 2004. PMID: 15591279 Free PMC article.

3

The post-translational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modification pathways.

Benayoun BA, Auer J, Caburet S, Veitia RA. Benayoun BA, et al. Among authors: caburet s. Proteomics. 2008 Aug;8(15):3118-23. doi: 10.1002/pmic.200800084. Proteomics. 2008. PMID: 18604817

4

Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).

Benayoun BA, Caburet S, Dipietromaria A, Georges A, D'Haene B, Pandaranayaka PJ, L'Hôte D, Todeschini AL, Krishnaswamy S, Fellous M, De Baere E, Veitia RA. Benayoun BA, et al. Among authors: caburet s. PLoS One. 2010 Jan 20;5(1):e8789. doi: 10.1371/journal.pone.0008789. PLoS One. 2010. PMID: 20098707 Free PMC article.

5

Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase.

Benayoun BA, Georges AB, L'Hôte D, Andersson N, Dipietromaria A, Todeschini AL, Caburet S, Bazin C, Anttonen M, Veitia RA. Benayoun BA, et al. Among authors: caburet s. Hum Mol Genet. 2011 May 1;20(9):1673-86. doi: 10.1093/hmg/ddr042. Epub 2011 Feb 2. Hum Mol Genet. 2011. PMID: 21289058

6

Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency.

Bouhali K, Dipietromaria A, Fontaine A, Caburet S, Barbieri O, Bellessort B, Fellous M, Veitia RA, Levi G. Bouhali K, et al. Among authors: caburet s. Hum Mol Genet. 2011 Jul 1;20(13):2642-50. doi: 10.1093/hmg/ddr166. Epub 2011 Apr 19. Hum Mol Genet. 2011. PMID: 21505076

7

Forkhead transcription factors: key players in health and disease.

Benayoun BA, Caburet S, Veitia RA. Benayoun BA, et al. Among authors: caburet s. Trends Genet. 2011 Jun;27(6):224-32. doi: 10.1016/j.tig.2011.03.003. Epub 2011 Apr 18. Trends Genet. 2011. PMID: 21507500 Review.

8

The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology.

Caburet S, Georges A, L'Hôte D, Todeschini AL, Benayoun BA, Veitia RA. Caburet S, et al. Mol Cell Endocrinol. 2012 Jun 5;356(1-2):55-64. doi: 10.1016/j.mce.2011.06.019. Epub 2011 Jul 8. Mol Cell Endocrinol. 2012. PMID: 21763750 Review.

9

The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2.

Elzaiat M, Todeschini AL, Caburet S, Veitia RA. Elzaiat M, et al. Among authors: caburet s. Clin Genet. 2017 Feb;91(2):173-182. doi: 10.1111/cge.12862. Epub 2016 Sep 29. Clin Genet. 2017. PMID: 27604691 Review.

10

Compositional biases and polyalanine runs in humans.

Cocquet J, De Baere E, Caburet S, Veitia RA. Cocquet J, et al. Among authors: caburet s. Genetics. 2003 Nov;165(3):1613-7. doi: 10.1093/genetics/165.3.1613. Genetics. 2003. PMID: 14668408 Free PMC article.

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