Resultados de procura - Bernard Grisart

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  1. 1
    Cinematographic analysis of bovine embryo development in serum-free oviduct-conditioned medium

    Cinematographic analysis of bovine embryo development in serum-free oviduct-conditioned medium por Bernard Grisart, A. Massip, F. Dessy

    Publicado 1994
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  2. 2
    Glucose metabolism during bovine preimplantation development: Analysis of gene expression in single oocytes and embryos

    Glucose metabolism during bovine preimplantation development: Analysis of gene expression in single oocytes and embryos por Anne‐Sophie Lequarré, Bernard Grisart, Benoît Moreau, N. Schuurbiers, A. Massip, F. Dessy

    Publicado 1997
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  3. 3
    Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome

    Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome por Damien Lederer, Bernard Grisart, M. Cristina Digilio, Valérie Benoît, Marianne Crespin, S. Ghariani, Isabelle Maystadt, Bruno Dallapiccola, Christine Verellen‐Dumoulin

    Publicado 2011
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  4. 4
    Genetic and functional confirmation of the causality of the <i>DGAT1 K232A</i> quantitative trait nucleotide in affecting milk yield and composition

    Genetic and functional confirmation of the causality of the <i>DGAT1 K232A</i> quantitative trait nucleotide in affecting milk yield and composition por Bernard Grisart, Frédéric Farnir, Latifa Karim, Nadine Cambisano, Jong-Joo Kim, Alex Kvasz, Myriam Mni, Patricia Simon, Jean‐Marie Frère, Wouter Coppieters, Michel Georges

    Publicado 2004
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  5. 5
    Simultaneous Mining of Linkage and Linkage Disequilibrium to Fine Map Quantitative Trait Loci in Outbred Half-Sib Pedigrees: Revisiting the Location of a Quantitative Trait Locus With Major Effect on Milk Production on Bovine Chromosome 14

    Simultaneous Mining of Linkage and Linkage Disequilibrium to Fine Map Quantitative Trait Loci in Outbred Half-Sib Pedigrees: Revisiting the Location of a Quantitative Trait Locus W... por Frédéric Farnir, Bernard Grisart, Wouter Coppieters, Juliette Riquet, Paulette Berzi, Nadine Cambisano, Latifa Karim, Myriam Mni, Sirja Moisio, Patricia Simon, Danny Wagenaar, Johanna Vilkki, Michel Georges

    Publicado 2002
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  6. 6
    Positional Candidate Cloning of a QTL in Dairy Cattle: Identification of a Missense Mutation in the Bovine <i>DGAT1</i> Gene with Major Effect on Milk Yield and Composition

    Positional Candidate Cloning of a QTL in Dairy Cattle: Identification of a Missense Mutation in the Bovine <i>DGAT1</i> Gene with Major Effect on Milk Yield and Composition por Bernard Grisart, Wouter Coppieters, Frédéric Farnir, Latifa Karim, Christine A. Ford, Paulette Berzi, Nadine Cambisano, Myriam Mni, Suzanne J. Reid, Patricia Simon, Richard Spelman, Michel Georges, Russell G. Snell

    Publicado 2002
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  7. 7
    Extensive Genome-wide Linkage Disequilibrium in Cattle

    Extensive Genome-wide Linkage Disequilibrium in Cattle por Frédéric Farnir, Wouter Coppieters, Juan-José Arranz, Paulette Berzi, Nadine Cambisano, Bernard Grisart, Latifa Karim, Fabienne Marcq, Laurence Moreau, Myriam Mni, Carine Nezer, Patricia Simon, Pascal Vanmanshoven, Danny Wagenaar, Michel Georges

    Publicado 2000
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  8. 8
    Fine-mapping of quantitative trait loci by identity by descent in outbred populations: Application to milk production in dairy cattle

    Fine-mapping of quantitative trait loci by identity by descent in outbred populations: Application to milk production in dairy cattle por Juliette Riquet, Wouter Coppieters, Nadine Cambisano, Juan-José Arranz, Paulette Berzi, Scott K. Davis, Bernard Grisart, Frédérick Farnir, Latifa Karim, Myriam Mni, Patricia Simon, Jeremy F. Taylor, Pascal Vanmanshoven, Danny Wagenaar, James E. Womack, Michel Georges

    Publicado 1999
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  9. 9
    Molecular Dissection of a Quantitative Trait Locus: A Phenylalanine-to-Tyrosine Substitution in the Transmembrane Domain of the Bovine Growth Hormone Receptor Is Associated With a Major Effect on Milk Yield and Composition

    Molecular Dissection of a Quantitative Trait Locus: A Phenylalanine-to-Tyrosine Substitution in the Transmembrane Domain of the Bovine Growth Hormone Receptor Is Associated With a... por Sarah Blott, Jong-Joo Kim, Sirja Moisio, Anne Schmidt‐Küntzel, Anne Cornet, Paulette Berzi, Nadine Cambisano, Christine A. Ford, Bernard Grisart, Dave Johnson, Latifa Karim, Patricia Simon, Russell G. Snell, Richard Spelman, Jerry Wong, Johanna Vilkki, Michel Georges, Frédéric Farnir, Wouter Coppieters

    Publicado 2003
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  10. 10
    Spectrum of Mutations in Gitelman Syndrome

    Spectrum of Mutations in Gitelman Syndrome por Rosa Vargas‐Poussou, Karin Dahan, Diana Kahila, Annabelle Vénisse, Eva Riveira‐Muñoz, Huguette Debaix, Bernard Grisart, Frank Bridoux, Robert J. Unwin, Bruno Moulin, Jean‐Philippe Haymann, Marie‐Christine Vantyghem, Claire Rigothier, Bertrand Dussol, M. Godin, Hubert Nivet, Laurence Dubourg, Ivan Tack, Anne‐Paule Gimenez‐Roqueplo, Pascal Houillier, Anne Blanchard, Olivier Devuyst, Xavier Jeunemaı̂tre

    Publicado 2011
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  11. 11
    Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

    Outcome of publicly funded nationwide first-tier noninvasive prenatal screening por Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gâtinois, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Vincent Bours, Anne De Leener, Marjan De Rademaeker, Julie Désir, Annelies Dheedene, Armelle Duquenne, Nathalie Fieremans, Annelies Fieuw, Jean‐Stéphane Gatot, Bernard Grisart, Katrien Janssens, Sandra Janssens, Damien Lederer, Axel Marichal, Björn Menten, Colombine Meunier, Léonor Palmeira, Bruno Pichon, Eva Sammels, Guillaume Smits, Yves Sznajer, Elise Vantroys, Koenraad Devriendt, Joris Vermeesch

    Publicado 2021
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  12. 12
    Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

    Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan por Tony Roscioli, Erik‐Jan Kamsteeg, Karen Buysse, Isabelle Maystadt, Jeroen van Reeuwijk, Christa van den Elzen, Ellen van Beusekom, Moniek Riemersma, Rolph Pfundt, Lisenka E.L.M. Vissers, Margit Schraders, Umut Altunoğlu, Michael F. Buckley, Han G. Brunner, Bernard Grisart, Huiqing Zhou, Joris A. Veltman, Christian Gilissen, Grazia M.S. Mancini, P. Delrée, Michèl A.A.P. Willemsen, Danijela Petković Ramadža, David Chitayat, Christopher Bennett, Eamonn Sheridan, E Peeters, Gita Tan-Sindhunata, C E de Die-Smulders, Koenraad Devriendt, Hülya Kayserili, Osama Abd El-Fattah El-Hashash, Derek L. Stemple, Dirk J. Lefeber, Yung‐Yao Lin, Hans van Bokhoven

    Publicado 2012
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  13. 13
    Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

    Clinical and molecular delineation of the 17q21.31 microdeletion syndrome por David A. Koolen, Andrew J. Sharp, Jane A. Hurst, Helen V. Firth, Samantha J.L. Knight, Alice Goldenberg, Pascale Saugier‐Veber, Rolph Pfundt, Lisenka E.L.M. Vissers, Anne Destrèe, Bernard Grisart, Liesbeth Rooms, Nathalie Van der Aa, Michael Field, Anna Hackett, Katrina M. Bell, M.J.M. Nowaczyk, Grazia M.S. Mancini, Pino J. Poddighe, Charles E. Schwartz, Elena Rossi, Manuela De Gregori, Lucinda Antonacci-Fulton, Michael D. McLellan, J M Garrett, Maddy Wiechert, Tracie L. Miner, Seth D. Crosby, Roberto Ciccone, Lionel Willatt, Anita Rauch, Martin Zenker, Swaroop Aradhya, Melanie A. Manning, Tim M. Strom, Janine Wagenstaller, Ana Cristina Victorino Krepischi, Angela Maria Vianna‐Morgante, Carla Rosenberg, Sue Price, Helen Stewart, Charles Shaw‐Smith, Han G. Brunner, Andrew O.M. Wilkie, Joris A. Veltman, Orsetta Zuffardi, Evan E. Eichler, Bert B.A. de Vries

    Publicado 2008
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