Zoekresultaten - Katherina Walz

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  1. 1
    Unconventional Transcriptional Response to Environmental Enrichment in a Mouse Model of Rett Syndrome

    Unconventional Transcriptional Response to Environmental Enrichment in a Mouse Model of Rett Syndrome door Bredford Kerr, Pamela A. Silva, Katherina Walz, Juan I. Young

    Gepubliceerd in 2010
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  2. 2
    Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)

    Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2) door Katherina Walz, Richard Paylor, Jiong Yan, Weimin Bi, James R. Lupski

    Gepubliceerd in 2006
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  3. 3
    Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes

    Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes door Bredford Kerr, Jessica Soto C, Mauricio A. Sáez, Alexander J. Abrams, Katherina Walz, Juan I. Young

    Gepubliceerd in 2011
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  4. 4
    Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome

    Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome door Jéssica Molina, Paulina Carmona-Mora, Jacqueline Chrast, Paola Krall, César P. Canales, James R. Lupski, Alexandre Reymond, Katherina Walz

    Gepubliceerd in 2008
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  5. 5
    Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development

    Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development door Matías Alvarez-Saavedra, Loreto Carrasco, Sylvia Sura‐Trueba, Vera Demarchi Aiello, Katherina Walz, José Xavier Neto, Juan I. Young

    Gepubliceerd in 2010
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  6. 6
    COP9 Signalosome Subunit 3 Is Essential for Maintenance of Cell Proliferation in the Mouse Embryonic Epiblast

    COP9 Signalosome Subunit 3 Is Essential for Maintenance of Cell Proliferation in the Mouse Embryonic Epiblast door Jiong Yan, Katherina Walz, Hisashi Nakamura, Sandra Carattini-Rivera, Qi Zhao, Hannes Vogel, Ning Wei, Monica J. Justice, Allan Bradley, James R. Lupski

    Gepubliceerd in 2003
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  7. 7
    Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models

    Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models door Guénola Ricard, Jéssica Molina, Jacqueline Chrast, Wenli Gu, Nele Gheldof, Sylvain Pradervand, Frédéric Schütz, Juan I. Young, James R. Lupski, Alexandre Reymond, Katherina Walz

    Gepubliceerd in 2010
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  8. 8
    Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) Contiguous Gene Syndromes by Chromosome Engineering in Mice: Phenotypic Consequences of Gene Dosage Imbalance

    Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) Contiguous Gene Syndromes by Chromosome Engineering in Mice: Phenotypic Consequences of Gene Dosage Imbalance door Katherina Walz, Sandra Caratini-Rivera, Weimin Bi, Patricia Fonseca, Dena L. Mansouri, Jennifer Lynch, Hannes Vogel, Jeffrey L. Noebels, Allan Bradley, James R. Lupski

    Gepubliceerd in 2003
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  9. 9
    Podocyte-Specific Overexpression of Wild Type or Mutant Trpc6 in Mice Is Sufficient to Cause Glomerular Disease

    Podocyte-Specific Overexpression of Wild Type or Mutant Trpc6 in Mice Is Sufficient to Cause Glomerular Disease door Paola Krall, César P. Canales, Pamela Kairath, Paulina Carmona-Mora, Jéssica Molina, J. Daniel Carpio, Phillip Ruiz, Sergio Mezzano, Jing Li, Changli Wei, Jochen Reiser, Juan I. Young, Katherina Walz

    Gepubliceerd in 2010
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  10. 10
    Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse

    Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse door Weimin Bi, Jiong Yan, Paweł Stankiewicz, Sung Sup Park, Katherina Walz, Cornelius F. Boerkoel, Lorraine Potocki, Lisa G. Shaffer, Koenraad Devriendt, Małgorzata J.M. Nowaczyk, Ken Inoue, James R. Lupski

    Gepubliceerd in 2002
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  11. 11
    Ankrd11 Is a Chromatin Regulator Involved in Autism that Is Essential for Neural Development

    Ankrd11 Is a Chromatin Regulator Involved in Autism that Is Essential for Neural Development door Denis Gallagher, Anastassia Voronova, Mark Zander, Gonzalo I. Cancino, Alexa N. Bramall, Matthew P. Krause, Clemer Abad, Mustafa Tekin, Paul M. Neilsen, David F. Callen, Stephen W. Scherer, Gordon Keller, David R. Kaplan, Katherina Walz, Freda D. Miller

    Gepubliceerd in 2014
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  12. 12
    Transient Receptor Potential Channel 6 (TRPC6) Protects Podocytes during Complement-mediated Glomerular Disease

    Transient Receptor Potential Channel 6 (TRPC6) Protects Podocytes during Complement-mediated Glomerular Disease door Andreas D. Kistler, Geetika Singh, Mehmet M. Altintas, Hao Yu, Isabel Cuesta Fernández, Changkyu Gu, Cory Wilson, Sandeep Srivastava, Alexander Dietrich, Katherina Walz, Dontscho Kerjaschki, Phillip Ruiz, Stuart E. Dryer, Sanja Sever, Amit Kumar Dinda, Christian Faul, Jochen Reiser

    Gepubliceerd in 2013
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  13. 13
    Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith–Magenis syndrome

    Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith–Magenis syndrome door Gustavo Henrique Apolinário Vieira, Jayson Rodriguez, Paulina Carmona-Mora, Lei Cao, Bruno Faulin Gamba, Daniel R. Carvalho, Andréa de Rezende Duarte, Suely Rodrigues dos Santos, Deise Helena de Souza, Barbara R. DuPont, Katherina Walz, Danilo Moretti‐Ferreira, Anand K. Srivastava

    Gepubliceerd in 2011
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  14. 14
    FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing

    FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing door Oscar Diaz‐Horta, Asli Subasioglu-Uzak, M’hamed Grati, Alexandra A. DeSmidt, Joseph Foster, Lei Cao, Güney Bademci, Suna Tokgöz-Yılmaz, Duygu Duman, Filiz Başak Cengiz, Clemer Abad, Rahul Mittal, Susan H. Blanton, Xue Z. Liu, Amjad Farooq, Katherina Walz, Zhongmin Lu, Mustafa Tekin

    Gepubliceerd in 2014
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  15. 15
    Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome

    Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome door Katherina Walz, Devon Cohen, Paul M. Neilsen, Joseph Foster, Francesco Brancati, Korcan Demir, Richard Fisher, Michelle Moffat, Nienke E. Verbeek, Kathrine Bjørgo, Adriana Lo Castro, Paolo Curatolo, Giuseppe Novelli, Clemer Abad, Lei Cao, Lily Zhang, Oscar Diaz‐Horta, Juan I. Young, David F. Callen, Mustafa Tekin

    Gepubliceerd in 2014
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  16. 16
    ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

    ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice door Oscar Diaz‐Horta, Clemer Abad, Levent Sennaroğlu, Joseph Foster, Alexandra A. DeSmidt, Güney Bademci, Suna Tokgöz-Yılmaz, Duygu Duman, Filiz Başak Cengiz, M’hamed Grati, Suat Fítöz, Xue Z. Liu, Amjad Farooq, Faiqa Imtiaz, Benjamin Currall, Cynthia C. Morton, Michiru Nishita, Yasuhiro Minami, Zhongmin Lu, Katherina Walz, Mustafa Tekin

    Gepubliceerd in 2016
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