檢索結果 - Kim Cryns

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  1. 1
    A genotype-phenotype correlation for GJB2 (connexin 26) deafness

    A genotype-phenotype correlation for GJB2 (connexin 26) deafness 由 Kim Cryns

    出版 2004
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    Artigo
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  2. 2
    Transgenic Mice Overexpressing Glycogen Synthase Kinase 3β: A Putative Model of Hyperactivity and Mania

    Transgenic Mice Overexpressing Glycogen Synthase Kinase 3β: A Putative Model of Hyperactivity and Mania 由 Jos Prickaerts, Dieder Moechars, Kim Cryns, Ilse Lenaerts, Hansfried Van Craenendonck, Ilse Goris, Guy Daneels, J. Adriaan Bouwknecht, Thomas Steckler

    出版 2006
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  3. 3
    IMPA1 is Essential for Embryonic Development and Lithium-Like Pilocarpine Sensitivity

    IMPA1 is Essential for Embryonic Development and Lithium-Like Pilocarpine Sensitivity 由 Kim Cryns, Alon Shamir, Nathalie Van Acker, Itzhak Levi, Guy Daneels, Ilse Goris, J Adriaan Bouwknecht, Luc Andries, Stefan U. Kass, Galila Agam, H. Belmaker, Yuly Bersudsky, Thomas Steckler, Dieder Moechars

    出版 2007
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    Artigo
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  4. 4
    Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease

    Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease 由 Kim Cryns, Theru A. Sivakumaran, Jody M.W. van den Ouweland, Ronald J. E. Pennings, Cor W. R. J. Cremers, Kris Flothmann, Terry‐Lynn Young, Richard J. Smith, Marci M. Lesperance, Guy Van Camp

    出版 2003
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    Revisão
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  5. 5
    Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice

    Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice 由 Diana Dominguez, Jos Tournoy, Dieter Hartmann, Tobias Huth, Kim Cryns, Siska Deforce, Lutgarde Serneels, Ira Espuny-Camacho, Els Marjaux, Katleen Craessaerts, Anton Roebroek, Michael Schwake, Rudi D’Hooge, Patricia Bach, Ulrich Kalinke, Dieder Moechars, Christian Alzheimer, Karina Reiß, Paul Säftig, Bart De Strooper

    出版 2005
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  6. 6
    Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

    Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss 由 Irina N. Bespalova, Guy Van Camp, Steven J. H. Bom, David J. Brown, Kim Cryns, Andrew T. DeWan, Ayse Elif Erson‐Bensan, Kris Flothmann, Henricus P. M. Kunst, Purnima Kurnool, Theru A. Sivakumaran, Cor W. R. J. Cremers, Suzanne M. Leal, Margit Burmeister, Marci M. Lesperance

    出版 2001
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  7. 7
    GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

    GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study 由 Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, J Waligora, Małgorzata Mueller‐Malesińska, Agnieszka Pollak, Rafał Płoski, Alessandra Murgia, Eva Orzan, Pierangela Castorina, Umberto Ambrosetti, Ewa Nowakowska-Szyrwińska, Jerzy Bal, Wojciech Wiszniewski, Andreas Janecke, Doris Nekahm-Heis, Pavel Seeman, O. Bendová, Margaret A. Kenna, Anna Frangulov, Heidi L. Rehm, Mustafa Tekin, Armağan İncesulu, Hans‐Henrik M. Dahl, Desirée du Sart, Lucy Jenkins, Deirdre Lucas, Maria Bitner‐Glindzicz, Karen B. Avraham, Zippora Brownstein, Ignacio del Castillo, Felipe Moreno, Nikolaus Blin, Markus Pfister, István Sziklai, Tímea Tóth, Philip M. Kelley, Edward Cohn, Lionel Van Maldergem, Pascale Hilbert, Anne‐Françoise Roux, M. Mondain, Lies H. Hoefsloot, Cor W. R. J. Cremers, Tuija Löppönen, Heikki Löppönen, Agnete Parving, Karen Grønskov, Iris Schrijver, Joseph Roberson, Francesca Gualandi, Alessandro Martini, Geneviève Lina‐Granade, Nathalie Pallares‐Ruiz, Céu Correia, Graça Fialho, Kim Cryns, Nele Hilgert, Paul Van de Heyning, Carla Nishimura, Richard J. Smith, Guy Van Camp

    出版 2005
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