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Items: 1 to 20 of 151


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.


Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development.

Moumné L, Dipietromaria A, Batista F, Kocer A, Fellous M, Pailhoux E, Veitia RA.

Hum Mol Genet. 2008 Apr 1;17(7):1010-9. Epub 2007 Dec 24.


Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutations.

Benayoun BA, Batista F, Auer J, Dipietromaria A, L'Hôte D, De Baere E, Veitia RA.

Hum Mol Genet. 2009 Feb 15;18(4):632-44. doi: 10.1093/hmg/ddn389. Epub 2008 Nov 14.


Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.

Beysen D, Moumné L, Veitia R, Peters H, Leroy BP, De Paepe A, De Baere E.

Hum Mol Genet. 2008 Jul 1;17(13):2030-8. doi: 10.1093/hmg/ddn100. Epub 2008 Mar 27.


The mutations and potential targets of the forkhead transcription factor FOXL2.

Moumné L, Batista F, Benayoun BA, Nallathambi J, Fellous M, Sundaresan P, Veitia RA.

Mol Cell Endocrinol. 2008 Jan 30;282(1-2):2-11. Epub 2007 Nov 19. Review.


A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction.

Nallathambi J, Moumné L, De Baere E, Beysen D, Usha K, Sundaresan P, Veitia RA.

Hum Genet. 2007 Mar;121(1):107-12. Epub 2006 Nov 7.


Foxl2 function in ovarian development.

Uhlenhaut NH, Treier M.

Mol Genet Metab. 2006 Jul;88(3):225-34. Epub 2006 May 2. Review.


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.


Molecular cloning and gene expression of Foxl2 in the frog Rana rugosa.

Oshima Y, Uno Y, Matsuda Y, Kobayashi T, Nakamura M.

Gen Comp Endocrinol. 2008 Nov-Dec;159(2-3):170-7. doi: 10.1016/j.ygcen.2008.08.013. Epub 2008 Sep 6.


Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.

Laissue P, Lakhal B, Benayoun BA, Dipietromaria A, Braham R, Elghezal H, Philibert P, Saâd A, Sultan C, Fellous M, Veitia RA.

J Med Genet. 2009 Jul;46(7):455-7. doi: 10.1136/jmg.2008.065086. Epub 2009 May 7.


Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation.

Moumné L, Fellous M, Veitia RA.

Hum Mol Genet. 2005 Dec 1;14(23):3557-64. Epub 2005 Oct 11.


FOXL2 activates P450 aromatase gene transcription: towards a better characterization of the early steps of mammalian ovarian development.

Pannetier M, Fabre S, Batista F, Kocer A, Renault L, Jolivet G, Mandon-Pépin B, Cotinot C, Veitia R, Pailhoux E.

J Mol Endocrinol. 2006 Jun;36(3):399-413.


The combination of polyalanine expansion mutation and a novel missense substitution in transcription factor FOXL2 leads to different ovarian phenotypes in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) patients.

Fan J, Zhou Y, Huang X, Zhang L, Yao Y, Song X, Chen J, Hu J, Ge S, Song H, Fan X.

Hum Reprod. 2012 Nov;27(11):3347-57. doi: 10.1093/humrep/des306. Epub 2012 Aug 27.


Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems.

Dipietromaria A, Benayoun BA, Todeschini AL, Rivals I, Bazin C, Veitia RA.

Hum Mol Genet. 2009 Sep 1;18(17):3324-33. doi: 10.1093/hmg/ddp273. Epub 2009 Jun 10.


FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report.

Méduri G, Bachelot A, Duflos C, Bständig B, Poirot C, Genestie C, Veitia R, De Baere E, Touraine P.

Hum Reprod. 2010 Jan;25(1):235-43. doi: 10.1093/humrep/dep355. Epub 2009 Oct 9.


An investigation into FOXE1 polyalanine tract length in premature ovarian failure.

Watkins WJ, Harris SE, Craven MJ, Vincent AL, Winship IM, Gersak K, Shelling AN.

Mol Hum Reprod. 2006 Mar;12(3):145-9. Epub 2006 Feb 15.


Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation.

De Baere E, Dixon MJ, Small KW, Jabs EW, Leroy BP, Devriendt K, Gillerot Y, Mortier G, Meire F, Van Maldergem L, Courtens W, Hjalgrim H, Huang S, Liebaers I, Van Regemorter N, Touraine P, Praphanphoj V, Verloes A, Udar N, Yellore V, Chalukya M, Yelchits S, De Paepe A, Kuttenn F, Fellous M, Veitia R, Messiaen L.

Hum Mol Genet. 2001 Jul 15;10(15):1591-600.


Molecular cloning and analysis of gonadal expression of Foxl2 in the medaka, Oryzias latipes.

Nakamoto M, Matsuda M, Wang DS, Nagahama Y, Shibata N.

Biochem Biophys Res Commun. 2006 May 26;344(1):353-61.


The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance.

Schmidt D, Ovitt CE, Anlag K, Fehsenfeld S, Gredsted L, Treier AC, Treier M.

Development. 2004 Feb;131(4):933-42. Epub 2004 Jan 21.


Synergistic activation of the Mc2r promoter by FOXL2 and NR5A1 in mice.

Yang WH, Gutierrez NM, Wang L, Ellsworth BS, Wang CM.

Biol Reprod. 2010 Nov;83(5):842-51. doi: 10.1095/biolreprod.110.085621. Epub 2010 Jul 21.

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