Hasil Pencarian - Koen Devriendt

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  1. 1
    Haploinsufficiency of the autism candidate gene Neurobeachin induces autism-like behaviors and affects cellular and molecular processes of synaptic plasticity in mice

    Haploinsufficiency of the autism candidate gene Neurobeachin induces autism-like behaviors and affects cellular and molecular processes of synaptic plasticity in mice oleh Kim Nuytens, Ilse Gantois, Pieter Stijnen, Emilia Iscru, Annelies Laeremans, Lutgarde Serneels, Lien Van Eylen, Stephen A. Liebhaber, Koen Devriendt, Detlef Balschun, Lutgarde Arckens, John W.M. Creemers, Rudi D'Hooge

    Diterbitkan 2013-03-01
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  2. 2
    Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction.

    Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction. oleh Benedetta Izzi, Inge Francois, Veerle Labarque, Chantal Thys, Christine Wittevrongel, Koen Devriendt, Eric Legius, Annick Van den Bruel, Marc D'Hooghe, Diether Lambrechts, Francis de Zegher, Chris Van Geet, Kathleen Freson

    Diterbitkan 2012-01-01
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  3. 3
    Pseudoautosomal region 1 length polymorphism in the human population.

    Pseudoautosomal region 1 length polymorphism in the human population. oleh Martin A Mensah, Matthew S Hestand, Maarten H D Larmuseau, Mala Isrie, Nancy Vanderheyden, Matthias Declercq, Erika L Souche, Jeroen Van Houdt, Radka Stoeva, Hilde Van Esch, Koen Devriendt, Thierry Voet, Ronny Decorte, Peter N Robinson, Joris R Vermeesch

    Diterbitkan 2014-11-01
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  4. 4
    Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

    Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders oleh Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koen Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad, Moises A. Serrano, D. James Stavropoulos, Hope Twede, Joris R. Vermeesch, Jacob A. S. Vorstman, Stephen W. Scherer

    Diterbitkan 2019-02-01
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  5. 5
    Enhanced MCP-1 Release in Early Autosomal Dominant Polycystic Kidney Disease

    Enhanced MCP-1 Release in Early Autosomal Dominant Polycystic Kidney Disease oleh Peter Janssens, Jean-Paul Decuypere, Stéphanie De Rechter, Luc Breysem, Dorien Van Giel, Jaak Billen, An Hindryckx, Luc De Catte, Marcella Baldewijns, Kathleen B.M. Claes, Karl M. Wissing, Koen Devriendt, Bert Bammens, Isabelle Meyts, Vicente E. Torres, Rudi Vennekens, Djalila Mekahli

    Diterbitkan 2021-06-01
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  6. 6
    Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the Congo

    Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the Congo oleh Daan Van Brusselen, MD, Tony Kayembe-Kitenge, MD, Sébastien Mbuyi-Musanzayi, PhD, Toni Lubala Kasole, PhD, Leon Kabamba Ngombe, PhD, Paul Musa Obadia, MD, Daniel Kyanika wa Mukoma, MSc, Koen Van Herck, ProfPhD, Dirk Avonts, ProfPhD, Koen Devriendt, ProfPhD, Erik Smolders, ProfPhD, Célestin Banza Lubaba Nkulu, ProfPhD, Benoit Nemery, ProfPhD

    Diterbitkan 2020-04-01
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