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Page 1
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: bouchard p. Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819. Hum Mutat. 2008. PMID: 18642388
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
D'haene B, Attanasio C, Beysen D, Dostie J, Lemire E, Bouchard P, Field M, Jones K, Lorenz B, Menten B, Buysse K, Pattyn F, Friedli M, Ucla C, Rossier C, Wyss C, Speleman F, De Paepe A, Dekker J, Antonarakis SE, De Baere E. D'haene B, et al. Among authors: bouchard p. PLoS Genet. 2009 Jun;5(6):e1000522. doi: 10.1371/journal.pgen.1000522. Epub 2009 Jun 19. PLoS Genet. 2009. PMID: 19543368 Free PMC article.
FOXO3a variants in patients with premature ovarian failure.
Vinci G, Christin-Maitre S, Pasquier M, Bouchard P, Fellous M, Veitia RA. Vinci G, et al. Among authors: bouchard p. Clin Endocrinol (Oxf). 2008 Mar;68(3):495-7. doi: 10.1111/j.1365-2265.2007.03052.x. Epub 2007 Sep 19. Clin Endocrinol (Oxf). 2008. PMID: 17888023 No abstract available.
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: bouchard p. Eur J Endocrinol. 2006 May;154(5):739-44. doi: 10.1530/eje.1.02135. Eur J Endocrinol. 2006. PMID: 16645022
[Genes and ovarian insufficiency].
Christin-Maitre S, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Ann Endocrinol (Paris). 1999 Jul;60(2):118-22. Ann Endocrinol (Paris). 1999. PMID: 10456183 Review. French.
[Physiopathologic anomalies in ovarian response].
Christin-Maitre S, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Contracept Fertil Sex. 1996 Feb;24(2):105-10. Contracept Fertil Sex. 1996. PMID: 8611930 Review. French. No abstract available.
Genes and premature ovarian failure.
Christin-Maitre S, Vasseur C, Portnoï MF, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Mol Cell Endocrinol. 1998 Oct 25;145(1-2):75-80. doi: 10.1016/s0303-7207(98)00172-5. Mol Cell Endocrinol. 1998. PMID: 9922102 Review.
Bioassays of gonadotropins based on cloned receptors.
Christin-Maitre S, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Mol Cell Endocrinol. 1996 Dec 20;125(1-2):151-9. doi: 10.1016/s0303-7207(96)03946-9. Mol Cell Endocrinol. 1996. PMID: 9027353 Review.
605 results