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31 results for Viville,+Stéphane

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Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility
Author / Creator:Stallmeyer, Birgit ; Bühlmann, Clara ; Stakaitis, Rytis ; Dicke, Ann-Kristin ; Ghieh, Farah ; Meier, Luisa ; Zoch, Ansgar ; MacKenzie MacLeod, David ; Steingröver, Johanna ; Okutman, Özlem ; Fietz, Daniela ; Pilatz, Adrian ; Riera-Escamilla, Antoni ; Xavier, Miguel J. ; Ruckert, Christian ; Di Persio, Sara ; Neuhaus, Nina ; Gurbuz, Ali Sami ; Şalvarci, Ahmet ; Le May, Nicolas ; McEleny, Kevin ; Friedrich, Corinna ; van der Heijden, Godfried ; Wyrwoll, Margot J. ; Kliesch, Sabine ; Veltman, Joris A. ; Krausz, Csilla ; Viville, Stéphane ; Conrad, Donald F. ; O’Carroll, Dónal ; Tüttelmann, Frank
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2024-08, Vol.15 (1), p.6637-18, Article 6637
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Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways
Author / Creator:Sabou, Marcela ; Doderer-Lang, Cécile ; Leyer, Caroline ; Konjic, Ana ; Kubina, Sophie ; Lennon, Sarah ; Rohr, Olivier ; Viville, Stéphane ; Cianférani, Sarah ; Candolfi, Ermanno ; Pfaff, Alexander W. ; Brunet, Julie
Publisher:Cham: Springer International Publishing
Journal title:Cellular and molecular life sciences : CMLS, 2020-06, Vol.77 (11), p.2141-2156
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Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility
Author / Creator:Okutman, Ozlem ; Tarabeux, Julien ; Muller, Jean ; Viville, Stéphane
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2021-03, Vol.12 (3), p.410
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Genetic evaluation of patients with non-syndromic male infertility
Author / Creator:Okutman, Ozlem ; Rhouma, Maroua Ben ; Benkhalifa, Moncef ; Muller, Jean ; Viville, Stéphane
Publisher:New York: Springer US
Journal title:Journal of assisted reproduction and genetics, 2018-11, Vol.35 (11), p.1939-1951
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Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia
Author / Creator:Hick, Aurore ; Wattenhofer-Donzé, Marie ; Chintawar, Satyan ; Tropel, Philippe ; Simard, Jodie P. ; Vaucamps, Nadège ; Gall, David ; Lambot, Laurie ; André, Cécile ; Reutenauer, Laurence ; Rai, Myriam ; Teletin, Marius ; Messaddeq, Nadia ; Schiffmann, Serge N. ; Viville, Stéphane ; Pearson, Christopher E. ; Pandolfo, Massimo ; Puccio, Hélène
Publisher:England: The Company of Biologists Ltd
Journal title:Disease models & mechanisms, 2013-05, Vol.6 (3), p.608-621
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A new mutation identified in SPATA16 in two globozoospermic patients
Author / Creator:ElInati, Elias ; Fossard, Camille ; Okutman, Ozlem ; Ghédir, Houda ; Ibala-Romdhane, Samira ; Ray, Pierre F. ; Saad, Ali ; Hennebicq, Sylvianne ; Viville, Stéphane
Publisher:New York: Springer US
Journal title:Journal of assisted reproduction and genetics, 2016-06, Vol.33 (6), p.815-820
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Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect
Author / Creator:Okutman, Özlem ; Demirel, Cem ; Tülek, Firat ; Pfister, Veronique ; Büyük, Umut ; Muller, Jean ; Charlet-Berguerand, Nicolas ; Viville, Stéphane
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2020-04, Vol.11 (4), p.382
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Highly Dynamic and Sex-Specific Expression of microRNAs During Early ES Cell Differentiation
Author / Creator:Ciaudo, Constance ; Servant, Nicolas ; Cognat, Valérie ; Sarazin, Alexis ; Kieffer, Emmanuelle ; Viville, Stéphane ; Colot, Vincent ; Barillot, Emmanuel ; Heard, Edith ; Voinnet, Olivier
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2009-08, Vol.5 (8), p.e1000620
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A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Author / Creator:Okutman, Ozlem ; Muller, Jean ; Skory, Valerie ; Garnier, Jean Marie ; Gaucherot, Angeline ; Baert, Yoni ; Lamour, Valérie ; Serdarogullari, Munevver ; Gultomruk, Meral ; Röpke, Albrecht ; Kliesch, Sabine ; Herbepin, Viviana ; Aknin, Isabelle ; Benkhalifa, Moncef ; Teletin, Marius ; Bakircioglu, Emre ; Goossens, Ellen ; Charlet-Berguerand, Nicolas ; Bahceci, Mustafa ; Tüttelmann, Frank ; Viville, STéphane
Publisher:New York: Springer US
Journal title:Journal of assisted reproduction and genetics, 2017-05, Vol.34 (5), p.683-694
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Extended passaging increases the efficiency of neural differentiation from induced pluripotent stem cells
Author / Creator:Koehler, Karl R ; Tropel, Philippe ; Theile, Jonathan W ; Kondo, Takako ; Cummins, Theodore R ; Viville, Stéphane ; Hashino, Eri
Publisher:England: BioMed Central Ltd
Journal title:BMC neuroscience, 2011-08, Vol.12 (1), p.82-82, Article 82
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Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development
Author / Creator:Houston, Brendan J ; Oud, Manon S ; Aguirre, Daniel M ; Merriner, D Jo ; Anne E O’Connor ; Okutman, Ozlem ; Viville, Stéphane ; Burke, Richard ; Veltman, Joris A ; Moira K O’Bryan
Publisher:Oxford: Oxford University Press
Journal title:G3 : genes - genomes - genetics, 2020-12, Vol.10 (12), p.4449-4457
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Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy
Author / Creator:Harper, Joyce C ; Geraedts, Joep ; Borry, Pascal ; Cornel, Martina C ; Dondorp, Wybo ; Gianaroli, Luca ; Harton, Gary ; Milachich, Tanya ; Kääriäinen, Helena ; Liebaers, Inge ; Morris, Michael ; Sequeiros, Jorge ; Sermon, Karen ; Shenfield, Françoise ; Skirton, Heather ; Soini, Sirpa ; Spits, Claudia ; Veiga, Anna ; Vermeesch, Joris Robert ; Viville, Stéphane ; de Wert, Guido ; Macek, Milan
Publisher:Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-11, Vol.21 (S2), p.S1-S21
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Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes
Author / Creator:Bianchetti, Laurent ; Tarabay, Yara ; Lecompte, Odile ; Stote, Roland ; Poch, Olivier ; Dejaegere, Annick ; Viville, Stéphane
Publisher:England: BioMed Central Ltd
Journal title:BMC evolutionary biology, 2015-10, Vol.15 (1), p.222-222, Article 222
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Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres
Author / Creator:Van Rij, Maartje C ; De Rademaeker, Marjan ; Moutou, Céline ; Dreesen, Jos CFM ; De Rycke, Martine ; Liebaers, Inge ; Geraedts, Joep PM ; De Die-Smulders, Christine EM ; Viville, Stéphane
Publisher:Basingstoke: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2012-04, Vol.20 (4), p.368-375
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Autism, imprinting and epigenetic disorders: a metabolic syndrome linked to anomalies in homocysteine recycling starting in early life??
Author / Creator:Ménézo, Yves ; Mares, Pierre ; Cohen, Marc ; Brack, Michel ; Viville, Stephane ; Elder, Kay
Publisher:Boston: Springer US
Journal title:Journal of assisted reproduction and genetics, 2011-12, Vol.28 (12), p.1143-1145
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CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders
Author / Creator:Thauvin-Robinet, Christel ; Munck, Anne ; Huet, Frédéric ; de Becdelièvre, Alix ; Jimenez, Clément ; Lalau, Guy ; Gautier, Elodie ; Rollet, Jacques ; Flori, Jean ; Nové-Josserand, Raphaëlle ; Soufir, Jean-Claude ; Haloun, Alain ; Hubert, Dominique ; Houssin, Elise ; Bellis, Gil ; Rault, Gilles ; David, Albert ; Janny, Laurent ; Chiron, Raphaël ; Rives, Nathalie ; Hairion, Dominique ; Collignon, Patrick ; Valeri, Antoine ; Karsenty, Gilles ; Rossi, Annick ; Audrézet, Marie-Pierre ; Férec, Claude ; Leclerc, Julie ; Georges, Marie des ; Claustres, Mireille ; Bienvenu, Thierry ; Gérard, Bénédicte ; Boisseau, Pierre ; Cabet-Bey, Faïza ; Cheillan, David ; Feldmann, Delphine ; Clavel, Christine ; Bieth, Eric ; Iron, Albert ; Simon-Bouy, Brigitte ; Izard, Vincent ; Steffann, Julie ; Viville, Stéphane ; Costa, Catherine ; Drouineaud, Véronique ; Fauque, Patricia ; Binquet, Christine ; Bonithon-Kopp, Claire ; Morris, Mike A ; Faivre, Laurence ; Goossens, Michel ; Roussey, Michel ; Girodon, Emmanuelle
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2013-04, Vol.50 (4), p.220-227
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High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis
Author / Creator:Tropel, Philippe ; Tournois, Johana ; Côme, Julien ; Varela, Christine ; Moutou, Céline ; Fragner, Pascal ; Cailleret, Michel ; Laâbi, Yacine ; Peschanski, Marc ; Viville, Stéphane
Publisher:New York: New York : Springer-Verlag
Journal title:In vitro cellular & developmental biology. Animal, 2010-04, Vol.46 (3-4), p.376-385
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Genetic diagnosis of embryos: Clear explanation, not rhetoric, is needed
Author / Creator:Bouffard, C. ; Viville, S. ; Knoppers, B. M.
Publisher:Canada: CMA Impact Inc
Journal title:Canadian Medical Association journal (CMAJ), 2009-09, Vol.181 (6-7), p.387-391
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New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications
Author / Creator:Moutou, Céline ; Gardes, Nathalie ; Viville, Stéphane
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2004-12, Vol.12 (12), p.1007-1014
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Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policyEuropean Society of Human Genetics and European Society of Human R...
Author / Creator:Harper, Joyce C ; Geraedts, Joep ; Borry, Pascal ; Cornel, Martina C ; Dondorp, Wybo ; Gianaroli, Luca ; Harton, Gary ; Milachich, Tanya ; Kääriäinen, Helena ; Liebaers, Inge ; Morris, Michael ; Sequeiros, Jorge ; Sermon, Karen ; Shenfield, Françoise ; Skirton, Heather ; Soini, Sirpa ; Spits, Claudia ; Veiga, Anna ; Vermeesch, Joris Robert ; Viville, Stéphane ; De Wert, Guido ; Macek, Milan
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-11, Vol.21 (S2), p.S1-S21
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Showing 1 to 20 of 31 results

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Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility

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Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways

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Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility

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Genetic evaluation of patients with non-syndromic male infertility

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Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia

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A new mutation identified in SPATA16 in two globozoospermic patients

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Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect

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Highly Dynamic and Sex-Specific Expression of microRNAs During Early ES Cell Differentiation

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A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family

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Extended passaging increases the efficiency of neural differentiation from induced pluripotent stem cells

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Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development

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Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy

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Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes

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Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

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Autism, imprinting and epigenetic disorders: a metabolic syndrome linked to anomalies in homocysteine recycling starting in early life??

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CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders

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High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis

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Genetic diagnosis of embryos: Clear explanation, not rhetoric, is needed

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New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications

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Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policyEuropean Society of Human Genetics and European Society of Human R...

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