Fellous M - Search Results

1

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. Among authors: fellous m. J Med Genet. 2004 Dec;41(12):932-6. doi: 10.1136/jmg.2004.024356. J Med Genet. 2004. PMID: 15591279 Free PMC article.

2

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

Moumné L, Fellous M, Veitia RA. Moumné L, et al. Among authors: fellous m. Hum Mol Genet. 2005 Dec 1;14(23):3557-64. doi: 10.1093/hmg/ddi383. Epub 2005 Oct 11. Hum Mol Genet. 2005. PMID: 16219626

3

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. Moumné L, et al. Among authors: fellous m. Hum Mol Genet. 2008 Apr 1;17(7):1010-9. doi: 10.1093/hmg/ddm373. Epub 2007 Dec 24. Hum Mol Genet. 2008. PMID: 18158309

4

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: fellous m. 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

5

Structure, evolution and expression of the FOXL2 transcription unit.

Cocquet J, De Baere E, Gareil M, Pannetier M, Xia X, Fellous M, Veitia RA. Cocquet J, et al. Among authors: fellous m. Cytogenet Genome Res. 2003;101(3-4):206-11. doi: 10.1159/000074338. Cytogenet Genome Res. 2003. PMID: 14684984 Review.

6

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. Moumné L, et al. Among authors: fellous m. Mol Cell Endocrinol. 2008 Jan 30;282(1-2):2-11. doi: 10.1016/j.mce.2007.11.006. Epub 2007 Nov 19. Mol Cell Endocrinol. 2008. PMID: 18155828 Review.

7

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. Laissue P, et al. Among authors: fellous m. J Med Genet. 2009 Jul;46(7):455-7. doi: 10.1136/jmg.2008.065086. Epub 2009 May 7. J Med Genet. 2009. PMID: 19429596 Free article.

8

The transcription factor FOXL2 in ovarian function and dysfunction.

De Baere E, Fellous M, Veitia RA. De Baere E, et al. Among authors: fellous m. Folia Histochem Cytobiol. 2009;47(5):S43-9. doi: 10.2478/v10042-009-0062-7. Folia Histochem Cytobiol. 2009. PMID: 20067892 Review.

9

Sense and antisense Foxl2 transcripts in mouse.

Cocquet J, Pannetier M, Fellous M, Veitia RA. Cocquet J, et al. Among authors: fellous m. Genomics. 2005 May;85(5):531-41. doi: 10.1016/j.ygeno.2005.01.007. Genomics. 2005. PMID: 15820304

10

FOXL2 mutation screening in a large panel of POF patients and XX males.

De Baere E, Lemercier B, Christin-Maitre S, Durval D, Messiaen L, Fellous M, Veitia R. De Baere E, et al. Among authors: fellous m. J Med Genet. 2002 Aug;39(8):e43. doi: 10.1136/jmg.39.8.e43. J Med Genet. 2002. PMID: 12161610 Free PMC article. No abstract available.

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