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Items: 35

1.

Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome-wide analysis.

Penrad-Mobayed M, Perrin C, Herman L, Todeschini AL, Nigon F, Cosson B, Caburet S, Veitia RA.

FASEB J. 2020 Jan;34(1):571-587. doi: 10.1096/fj.201901573R. Epub 2019 Nov 25.

PMID:
31914586
2.

A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.

Caburet S, Todeschini AL, Petrillo C, Martini E, Farran ND, Legois B, Livera G, Younis JS, Shalev S, Veitia RA.

EBioMedicine. 2019 Apr;42:524-531. doi: 10.1016/j.ebiom.2019.03.075. Epub 2019 Apr 15.

3.

Natural and molecular history of prolactinoma: insights from a Prlr-/- mouse model.

Bernard V, Villa C, Auguste A, Lamothe S, Guillou A, Martin A, Caburet S, Young J, Veitia RA, Binart N.

Oncotarget. 2017 Dec 27;9(5):6144-6155. doi: 10.18632/oncotarget.23713. eCollection 2018 Jan 19.

4.

A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.

Fouquet B, Pawlikowska P, Caburet S, Guigon C, Mäkinen M, Tanner L, Hietala M, Urbanska K, Bellutti L, Legois B, Bessieres B, Gougeon A, Benachi A, Livera G, Rosselli F, Veitia RA, Misrahi M.

Elife. 2017 Dec 12;6. pii: e30490. doi: 10.7554/eLife.30490.

5.

Mechanisms of Mendelian dominance.

Veitia RA, Caburet S, Birchler JA.

Clin Genet. 2018 Mar;93(3):419-428. doi: 10.1111/cge.13107. Epub 2017 Oct 26. Review.

PMID:
28755412
6.

A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.

Paris F, Flatters D, Caburet S, Legois B, Servant N, Lefebvre H, Sultan C, Veitia RA.

Clin Endocrinol (Oxf). 2017 Nov;87(5):539-544. doi: 10.1111/cen.13420. Epub 2017 Aug 13.

PMID:
28708305
7.

A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome.

Caburet S, Fruchter RB, Legois B, Fellous M, Shalev S, Veitia RA.

Eur J Endocrinol. 2017 May;176(5):K9-K14. doi: 10.1530/EJE-16-0968.

PMID:
28348023
8.

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

Elzaiat M, Todeschini AL, Caburet S, Veitia RA.

Clin Genet. 2017 Feb;91(2):173-182. doi: 10.1111/cge.12862. Epub 2016 Sep 29. Review.

PMID:
27604691
9.

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency.

Fauchereau F, Shalev S, Chervinsky E, Beck-Fruchter R, Legois B, Fellous M, Caburet S, Veitia RA.

Clin Genet. 2016 May;89(5):603-7. doi: 10.1111/cge.12736. Epub 2016 Feb 10.

PMID:
26771056
10.

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Auguste A, Bessière L, Todeschini AL, Caburet S, Sarnacki S, Prat J, D'angelo E, De La Grange P, Ariste O, Lemoine F, Legois B, Sultan C, Zider A, Galmiche L, Kalfa N, Veitia RA.

Hum Mol Genet. 2015 Dec 1;24(23):6687-98. doi: 10.1093/hmg/ddv373. Epub 2015 Sep 11.

PMID:
26362254
11.

Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes.

Caburet S, Anttonen M, Todeschini AL, Unkila-Kallio L, Mestivier D, Butzow R, Veitia RA.

BMC Cancer. 2015 Apr 10;15:251. doi: 10.1186/s12885-015-1283-0.

12.

[STAG3 in premature ovarian failure].

Caburet S, Vilain É.

Med Sci (Paris). 2015 Feb;31(2):129-31. doi: 10.1051/medsci/20153102005. Epub 2015 Mar 4. French. No abstract available.

13.

STAG3 is a strong candidate gene for male infertility.

Llano E, Gomez-H L, García-Tuñón I, Sánchez-Martín M, Caburet S, Barbero JL, Schimenti JC, Veitia RA, Pendas AM.

Hum Mol Genet. 2014 Jul 1;23(13):3421-31. doi: 10.1093/hmg/ddu051. Epub 2014 Mar 7.

14.

Mutant cohesin in premature ovarian failure.

Caburet S, Arboleda VA, Llano E, Overbeek PA, Barbero JL, Oka K, Harrison W, Vaiman D, Ben-Neriah Z, García-Tuñón I, Fellous M, Pendás AM, Veitia RA, Vilain E.

N Engl J Med. 2014 Mar 6;370(10):943-949. doi: 10.1056/NEJMoa1309635.

15.

Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.

Caburet S, Zavadakova P, Ben-Neriah Z, Bouhali K, Dipietromaria A, Charon C, Besse C, Laissue P, Chalifa-Caspi V, Christin-Maitre S, Vaiman D, Levi G, Veitia RA, Fellous M.

PLoS One. 2012;7(3):e33412. doi: 10.1371/journal.pone.0033412. Epub 2012 Mar 13.

16.

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.

Mol Cell Endocrinol. 2012 Jun 5;356(1-2):55-64. doi: 10.1016/j.mce.2011.06.019. Epub 2011 Jul 8. Review.

PMID:
21763750
17.

Forkhead transcription factors: key players in health and disease.

Benayoun BA, Caburet S, Veitia RA.

Trends Genet. 2011 Jun;27(6):224-32. doi: 10.1016/j.tig.2011.03.003. Epub 2011 Apr 18. Review.

PMID:
21507500
18.

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.

Hum Mol Genet. 2011 Jul 1;20(13):2642-50. doi: 10.1093/hmg/ddr166. Epub 2011 Apr 19.

PMID:
21505076
19.

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.

Hum Mol Genet. 2011 May 1;20(9):1673-86. doi: 10.1093/hmg/ddr042. Epub 2011 Feb 2.

PMID:
21289058
20.

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.

PLoS One. 2010 Jan 20;5(1):e8789. doi: 10.1371/journal.pone.0008789.

21.

Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?

Georges AB, Benayoun BA, Caburet S, Veitia RA.

FASEB J. 2010 Feb;24(2):346-56. doi: 10.1096/fj.09-142117. Epub 2009 Sep 17. Review.

PMID:
19762556
22.
23.

Molecular combing.

Conti C, Caburet S, Schurra C, Bensimon A.

Curr Protoc Cytom. 2001 May;Chapter 8:Unit 8.10. doi: 10.1002/0471142956.cy0810s16.

PMID:
18770738
24.

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.

Hum Mol Genet. 2008 Oct 15;17(20):3118-27. doi: 10.1093/hmg/ddn209. Epub 2008 Jul 16.

PMID:
18635577
25.

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.

Proteomics. 2008 Aug;8(15):3118-23. doi: 10.1002/pmic.200800084.

PMID:
18604817
26.

Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.

De Baere E, Copelli S, Caburet S, Laissue P, Beysen D, Christin-Maitre S, Bouchard P, Veitia R, Fellous M.

Pediatr Endocrinol Rev. 2005 Jun;2(4):653-60. Review.

PMID:
16208278
27.

Human ribosomal RNA gene arrays display a broad range of palindromic structures.

Caburet S, Conti C, Schurra C, Lebofsky R, Edelstein SJ, Bensimon A.

Genome Res. 2005 Aug;15(8):1079-85. Epub 2005 Jul 15.

28.

Coding repeats and evolutionary "agility".

Caburet S, Cocquet J, Vaiman D, Veitia RA.

Bioessays. 2005 Jun;27(6):581-7. Review.

PMID:
15892112
29.

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.

J Med Genet. 2004 Dec;41(12):932-6.

30.
31.

Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments.

Koszul R, Caburet S, Dujon B, Fischer G.

EMBO J. 2004 Jan 14;23(1):234-43. Epub 2003 Dec 18.

32.

GermOnline, a cross-species community knowledgebase on germ cell differentiation.

Wiederkehr C, Basavaraj R, Sarrauste de Menthière C, Hermida L, Koch R, Schlecht U, Amon A, Brachat S, Breitenbach M, Briza P, Caburet S, Cherry M, Davis R, Deutschbauer A, Dickinson HG, Dumitrescu T, Fellous M, Goldman A, Grootegoed JA, Hawley R, Ishii R, Jégou B, Kaufman RJ, Klein F, Lamb N, Maro B, Nasmyth K, Nicolas A, Orr-Weaver T, Philippsen P, Pineau C, Rabitsch KP, Reinke V, Roest H, Saunders W, Schröder M, Schedl T, Siep M, Villeneuve A, Wolgemuth DJ, Yamamoto M, Zickler D, Esposito RE, Primig M.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D560-7.

33.

Compositional biases and polyalanine runs in humans.

Cocquet J, De Baere E, Caburet S, Veitia RA.

Genetics. 2003 Nov;165(3):1613-7.

34.

Combing the genome for genomic instability.

Caburet S, Conti C, Bensimon A.

Trends Biotechnol. 2002 Aug;20(8):344-50. Review.

PMID:
12127282
35.

Targeting the molecular mechanism of DNA replication.

Conti C, Caburet S, Bensimon A.

Drug Discov Today. 2001 Aug 1;6(15):786-792.

PMID:
11470587

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