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Items: 1 to 20 of 26

1.

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.

PMID:
18372316
2.

FOXL2 mutations and genomic rearrangements in BPES.

Beysen D, De Paepe A, De Baere E.

Hum Mutat. 2009 Feb;30(2):158-69. doi: 10.1002/humu.20807. Review.

PMID:
18726931
3.

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.

PMID:
18155828
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.

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
6.

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
7.

FOXL2 impairment in human disease.

Verdin H, De Baere E.

Horm Res Paediatr. 2012;77(1):2-11. doi: 10.1159/000335236. Epub 2012 Jan 12. Review.

8.

The transcription factor FOXL2 in ovarian function and dysfunction.

De Baere E, Fellous M, Veitia RA.

Folia Histochem Cytobiol. 2009;47(5):S43-9. doi: 10.2478/v10042-009-0062-7. Review.

PMID:
20067892
9.

Structure, evolution and expression of the FOXL2 transcription unit.

Cocquet J, De Baere E, Gareil M, Pannetier M, Xia X, Fellous M, Veitia RA.

Cytogenet Genome Res. 2003;101(3-4):206-11. Review.

PMID:
14684984
10.

FOXL2: at the crossroads of female sex determination and ovarian function.

Benayoun BA, Dipietromaria A, Bazin C, Veitia RA.

Adv Exp Med Biol. 2009;665:207-26. Review.

PMID:
20429427
11.

Laboratory diagnosis and molecular classification of von Willebrand disease.

Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ.

Acta Haematol. 2009;121(2-3):71-84. doi: 10.1159/000214846. Epub 2009 Jun 8. Review.

PMID:
19506352
13.

FOXL2: a central transcription factor of the ovary.

Georges A, Auguste A, Bessière L, Vanet A, Todeschini AL, Veitia RA.

J Mol Endocrinol. 2013 Dec 19;52(1):R17-33. doi: 10.1530/JME-13-0159. Print 2014 Feb. Review.

PMID:
24049064
14.

Missense mutations of human homeoboxes: A review.

D'Elia AV, Tell G, Paron I, Pellizzari L, Lonigro R, Damante G.

Hum Mutat. 2001 Nov;18(5):361-74. Review. Erratum in: Hum Mutat 2002 Apr;19(4):457.

PMID:
11668629
15.

Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review.

Dellinger MT, Thome K, Bernas MJ, Erickson RP, Witte MH.

Lymphology. 2008 Sep;41(3):98-102. Review.

PMID:
19013876
16.

Impact of FOXL2 mutations on signaling in ovarian granulosa cell tumors.

Leung DT, Fuller PJ, Chu S.

Int J Biochem Cell Biol. 2016 Mar;72:51-4. doi: 10.1016/j.biocel.2016.01.003. Epub 2016 Jan 11. Review.

PMID:
26791928
17.

LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.

Nobile C, Michelucci R, Andreazza S, Pasini E, Tosatto SC, Striano P.

Hum Mutat. 2009 Apr;30(4):530-6. doi: 10.1002/humu.20925. Review.

PMID:
19191227
18.

In control of biology: of mice, men and Foxes.

Wijchers PJ, Burbach JP, Smidt MP.

Biochem J. 2006 Jul 15;397(2):233-46. Review.

19.

Minireview: roles of the forkhead transcription factor FOXL2 in granulosa cell biology and pathology.

Pisarska MD, Barlow G, Kuo FT.

Endocrinology. 2011 Apr;152(4):1199-208. doi: 10.1210/en.2010-1041. Epub 2011 Jan 19. Review.

20.

Foxl-2 in gonad development and pathology.

Jaubert F, Galmiche L, Lortat-Jacob S, Fournet JC, Fellous M.

Arkh Patol. 2011 Jul-Aug;73(4):10-3. Review.

PMID:
22164424

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