Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency
Huhtaniemi, Ilpo, Hovatta, Outi, La Marca, Antonio, Livera, Gabriel, Monniaux, Danielle, Persani, Luca, Heddar, Abdelkader, Jarzabek, Katarzyna, Laisk-Podar, Triin, Salumets, Andres, Tapanainen, Juha S., Veitia, Reiner A., Visser, Jenny A., Wieacker, Peter, Wolczynski, Slawomir, Misrahi, Micheline
Published in Trends in endocrinology and metabolism (01.06.2018)
Published in Trends in endocrinology and metabolism (01.06.2018)
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A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency
Fauchereau, F., Shalev, S., Chervinsky, E., Beck-Fruchter, R., Legois, B., Fellous, M., Caburet, S., Veitia, R.A.
Published in Clinical genetics (01.05.2016)
Published in Clinical genetics (01.05.2016)
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The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2
Elzaiat, M., Todeschini, A.‐L., Caburet, S., Veitia, R.A.
Published in Clinical genetics (01.02.2017)
Published in Clinical genetics (01.02.2017)
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Dosage balance in gene regulation: biological implications
Birchler, James A., Riddle, Nicole C., Auger, Donald L., Veitia, Reiner A.
Published in Trends in genetics (01.04.2005)
Published in Trends in genetics (01.04.2005)
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FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)
Hersmus, R, Kalfa, N, de Leeuw, B, Stoop, H, Oosterhuis, JW, de Krijger, R, Wolffenbuttel, KP, Drop, SLS, Veitia, RA, Fellous, M, Jaubert, F, Looijenga, LHJ
Published in The Journal of pathology (01.05.2008)
Published in The Journal of pathology (01.05.2008)
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Evolution and expression of FOXL2
Cocquet, J, Pailhoux, E, Jaubert, F, Servel, N, Xia, X, Pannetier, M, De Baere, E, Messiaen, L, Cotinot, C, Fellous, M, Veitia, R A
Published in Journal of medical genetics (01.12.2002)
Published in Journal of medical genetics (01.12.2002)
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An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation
Baron, Daniel, Cocquet, Julie, Xia, Xuhua, Fellous, Marc, Guiguen, Yann, Veitia, Reiner A
Published in Journal of molecular endocrinology (01.12.2004)
Published in Journal of molecular endocrinology (01.12.2004)
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Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients
Lakhal, B, Braham, R, Berguigua, R, Bouali, N, Zaouali, M, Chaieb, M, Veitia, RA, Saad, A, Elghezal, H
Published in Clinical genetics (01.08.2010)
Published in Clinical genetics (01.08.2010)
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A sigmoidal transcriptional response: cooperativity, synergy and dosage effects
VEITIA, REINER A.
Published in Biological reviews of the Cambridge Philosophical Society (01.02.2003)
Published in Biological reviews of the Cambridge Philosophical Society (01.02.2003)
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Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome
Beysen, D., Raes, J., Leroy, B.P., Lucassen, A., Yates, J.R.W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J.P., Kim, J.R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L.M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R.A., De Paepe, A., De Baere, E.
Published in American journal of human genetics (01.08.2005)
Published in American journal of human genetics (01.08.2005)
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Structure, evolution and expression of the FOXL2 transcription unit
Cocquet, J., De Baere, E., Gareil, M., Pannetier, M., Xia, X., Fellous, M., Veitia, R.A.
Published in Cytogenetic and genome research (01.01.2003)
Published in Cytogenetic and genome research (01.01.2003)
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