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31 results for Viville,+Stéphane

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Select record 21
ArticlesPeer ReviewedFull Text
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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Select record 27
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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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Select record 28
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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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Select record 30
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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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Select record 31
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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 C F M ; De Rycke, Martine ; Liebaers, Inge ; Geraedts, Joep P M ; De Die-smulders, Christine E M ; Viville, Stéphane
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2012-09, Vol.20 (9), p.1010-1010
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Select record 32
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Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis
Author / Creator:Moutou, Céline ; Gardes, Nathalie ; Viville, Stéphane
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2002-04, Vol.10 (4), p.231-238
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Select record 33
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Diversity of Endogenous Epitopes Bound to MHC Class II Molecules Limited by Invariant Chain
Author / Creator:Bodmer, Helen ; Viville, Stéphane ; Benoist, Christophe ; Mathis, Diane
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1994-03, Vol.263 (5151), p.1284-1286
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Select record 34
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RNA Polymerase II Transcription in Murine Cells Lacking the TATA Binding Protein
Author / Creator:Martianov, Igor ; Viville, Stephane ; Davidson, Irwin
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2002-11, Vol.298 (5595), p.1036-1039
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A quantitative and morphological analysis of oocytes collected during 438 IVF cycles
Author / Creator:Wittemer, C ; Ohl, J ; Bettahar-Lebugle, K ; Viville, S ; Nisand, I
Publisher:Netherlands: Springer Nature B.V
Journal title:Journal of assisted reproduction and genetics, 2000-01, Vol.17 (1), p.44-50
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Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy: European Society of Human Genetics and European Society of Human...
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:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-11, Vol.21 (S2), p.S1-S21
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Select record 37
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Chromosome abnormalities in sperm from infertile men with normal somatic karyotypes: teratozoospermia
Author / Creator:Machev, N. ; Gosset, P. ; Viville, S.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Cytogenetic and genome research, 2005-01, Vol.111 (3-4), p.352-357
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Select record 38
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Erratum: 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 C F M ; De Rycke, Martine ; Liebaers, Inge ; Geraedts, Joep P M ; De Die-Smulders, Christine E M ; Viville, Stéphane
Journal title:European journal of human genetics : EJHG, 2012-08, Vol.20 (9), p.1010-1010
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Select record 39
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Highly Dynamic and Sex-Specific Expression of microRNAs During Early ES Cell Differentiation: e1000620
Author / Creator:Ciaudo, Constance ; Servant, Nicolas ; Cognat, Valérie ; Sarazin, Alexis ; Kieffer, Emmanuelle ; Viville, Stéphane ; Colot, Vincent ; Barillot, Emmanuel ; Heard, Edith ; Voinnet, Olivier
Publisher:San Francisco: Public Library of Science
Journal title:PLoS genetics, 2009-08, Vol.5 (8)
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Select record 40
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A Silencer Element Identified in Drosophila Is Required for Imprinting of H19 Reporter Transgenes in Mice
Author / Creator:Brenton, J. D. ; Drewell, R. A. ; Viville, S. ; Hilton, K. J. ; Barton, S. C. ; J. F-X. Ainscough ; Surani, M. A.
Publisher:United States: National Academy of Sciences of the United States of America
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (16), p.9242-9247
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Showing 21 to 40 of 31 results

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

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Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis

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Diversity of Endogenous Epitopes Bound to MHC Class II Molecules Limited by Invariant Chain

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RNA Polymerase II Transcription in Murine Cells Lacking the TATA Binding Protein

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A quantitative and morphological analysis of oocytes collected during 438 IVF cycles

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

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Chromosome abnormalities in sperm from infertile men with normal somatic karyotypes: teratozoospermia

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

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Highly Dynamic and Sex-Specific Expression of microRNAs During Early ES Cell Differentiation: e1000620

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A Silencer Element Identified in Drosophila Is Required for Imprinting of H19 Reporter Transgenes in Mice

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