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Items: 1 to 20 of 220

1.

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.

3.

The human FOXL2 mutation database.

Beysen D, Vandesompele J, Messiaen L, De Paepe A, De Baere E.

Hum Mutat. 2004 Sep;24(3):189-93.

PMID:
15300845
4.

Foxl2 function in ovarian development.

Uhlenhaut NH, Treier M.

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

PMID:
16647286
5.

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.

6.

Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure.

Bodega B, Porta C, Crosignani PG, Ginelli E, Marozzi A.

Mol Hum Reprod. 2004 Aug;10(8):555-7. Epub 2004 Jun 4.

7.

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
8.

A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis-ptosis-epicanthus inversus.

Qian X, Shu A, Qin W, Xing Q, Gao J, Yang J, Feng G, He L.

Mutat Res. 2004 Oct 4;554(1-2):19-22.

PMID:
15450400
9.

A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome.

Corrêa FJ, Tavares AB, Pereira RW, Abrão MS.

Fertil Steril. 2010 Feb;93(3):1006.e3-6. doi: 10.1016/j.fertnstert.2009.08.034. Epub 2009 Dec 6.

PMID:
19969293
10.

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.

PMID:
19429596
11.
13.

Comparative analysis of the FOXL2 gene and characterization of mutations in BPES patients.

Udar N, Yellore V, Chalukya M, Yelchits S, Silva-Garcia R, Small K; BPES Consortium.

Hum Mutat. 2003 Sep;22(3):222-8.

PMID:
12938087
14.

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.

15.

Transcriptional factor FOXL2 interacts with DP103 and induces apoptosis.

Lee K, Pisarska MD, Ko JJ, Kang Y, Yoon S, Ryou SM, Cha KY, Bae J.

Biochem Biophys Res Commun. 2005 Oct 28;336(3):876-81.

PMID:
16153597
16.

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development.

Uda M, Ottolenghi C, Crisponi L, Garcia JE, Deiana M, Kimber W, Forabosco A, Cao A, Schlessinger D, Pilia G.

Hum Mol Genet. 2004 Jun 1;13(11):1171-81. Epub 2004 Mar 31.

17.

Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.

Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, Messiaen LM, Oley C, Splitt M, Thomson J, Van de Peer Y, Veitia RA, De Paepe A, De Baere E.

Am J Hum Genet. 2005 Aug;77(2):205-18. Epub 2005 Jun 16.

18.

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.

19.

Interplay between paracrine signaling and gap junctional communication in ovarian follicles.

Gittens JE, Barr KJ, Vanderhyden BC, Kidder GM.

J Cell Sci. 2005 Jan 1;118(Pt 1):113-22. Epub 2004 Dec 7.

20.

Suppression of ovarian follicle activation in mice by the transcription factor Foxo3a.

Castrillon DH, Miao L, Kollipara R, Horner JW, DePinho RA.

Science. 2003 Jul 11;301(5630):215-8.

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