Laissue P - Search Results

1

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: laissue p. Pediatr Endocrinol Rev. 2005 Jun;2(4):653-60. Pediatr Endocrinol Rev. 2005. PMID: 16208278 Review.

2

Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.

Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, Decock C, Delbeke P, Ensenauer R, Ebinger F, Gillessen-Kaesbach G, Hendriks Y, Kimonis V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: laissue p. Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819. Hum Mutat. 2008. PMID: 18642388

3

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. 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.

4

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. Eur J Endocrinol. 2006 May;154(5):739-44. doi: 10.1530/eje.1.02135. Eur J Endocrinol. 2006. PMID: 16645022

5

Mutations in the NOG gene are not a common cause of nonsyndromic premature ovarian failure.

Laissue P, Christin-Maitre S, Bouchard P, Fellous M, Veitia RA. Laissue P, et al. Clin Endocrinol (Oxf). 2007 Jun;66(6):900. doi: 10.1111/j.1365-2265.2007.02797.x. Epub 2007 Mar 23. Clin Endocrinol (Oxf). 2007. PMID: 17381491 No abstract available.

6

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. 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.

7

Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients.

Nallathambi J, Laissue P, Batista F, Benayoun BA, Lesaffre C, Moumné L, Pandaranayaka PE, Usha K, Krishnaswamy S, Sundaresan P, Veitia RA. Nallathambi J, et al. Among authors: laissue p. Hum Mutat. 2008 Aug;29(8):E123-31. doi: 10.1002/humu.20809. Hum Mutat. 2008. PMID: 18484667

8

BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?

Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA. Lakhal B, et al. Among authors: laissue p. Clin Endocrinol (Oxf). 2010 Mar;72(3):425-6. doi: 10.1111/j.1365-2265.2009.03651.x. Epub 2009 Jun 8. Clin Endocrinol (Oxf). 2010. PMID: 19508678 No abstract available.

9

[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: laissue p. 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.

10

A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure.

Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA. Lakhal B, et al. Among authors: laissue p. Clin Endocrinol (Oxf). 2009 Nov;71(5):752-3. doi: 10.1111/j.1365-2265.2009.03571.x. Epub 2009 May 8. Clin Endocrinol (Oxf). 2009. PMID: 19486016 No abstract available.

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