Fellous M - Search Results

1

Recent advances in the study of genes involved in non-syndromic premature ovarian failure.

Laissue P, Vinci G, Veitia RA, Fellous M. Laissue P, et al. Among authors: fellous m. Mol Cell Endocrinol. 2008 Jan 30;282(1-2):101-11. doi: 10.1016/j.mce.2007.11.005. Epub 2007 Nov 19. Mol Cell Endocrinol. 2008. PMID: 18164539 Review.

2

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.

Laissue P, Christin-Maitre S, Touraine P, Kuttenn F, Ritvos O, Aittomaki K, Bourcigaux N, Jacquesson L, Bouchard P, Frydman R, Dewailly D, Reyss AC, Jeffery L, Bachelot A, Massin N, Fellous M, Veitia RA. Laissue P, et al. Among authors: fellous m. Eur J Endocrinol. 2006 May;154(5):739-44. doi: 10.1530/eje.1.02135. Eur J Endocrinol. 2006. PMID: 16645022

3

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. Caburet S, et al. Among authors: fellous m. PLoS One. 2012;7(3):e33412. doi: 10.1371/journal.pone.0033412. Epub 2012 Mar 13. PLoS One. 2012. PMID: 22428046 Free PMC article.

4

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. Caburet S, et al. Among authors: fellous m. N Engl J Med. 2014 Mar 6;370(10):943-949. doi: 10.1056/NEJMoa1309635. N Engl J Med. 2014. PMID: 24597867 Free PMC article.

5

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.

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. 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.

7

[Genetic analysis of premature ovarian failure: role of forkhead and TGF-beta genes].

Lakhal B, Laissue P, Elghèzal H, Fellous M. Lakhal B, et al. Among authors: fellous m. Gynecol Obstet Fertil. 2008 Sep;36(9):862-71. doi: 10.1016/j.gyobfe.2008.07.002. Epub 2008 Aug 8. Gynecol Obstet Fertil. 2008. PMID: 18692424 Review. French.

8

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. De Baere E, et al. Among authors: fellous m. Pediatr Endocrinol Rev. 2005 Jun;2(4):653-60. Pediatr Endocrinol Rev. 2005. PMID: 16208278 Review.

9

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

10

Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita.

Laissue P, Copelli S, Bergada I, Bergada C, Barrio G, Karaboga S, Wurtz JM, Fellous M, Lalli E, Veitia RA. Laissue P, et al. Among authors: fellous m. Clin Endocrinol (Oxf). 2006 Nov;65(5):681-6. doi: 10.1111/j.1365-2265.2006.02649.x. Clin Endocrinol (Oxf). 2006. PMID: 17054473

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