Хайлтын үр дүнгүүд - Casper Shyr

  • 9-н 1 - 9 үр дүнгүүдийг харуулж байна
Үр дүнг сайжруулах
  1. 1
    FLAGS, frequently mutated genes in public exomes

    FLAGS, frequently mutated genes in public exomes -н Casper Shyr, Maja Tarailo‐Graovac, Michael Gottlieb, Jessica J. Y. Lee, Clara van Karnebeek, Wyeth W. Wasserman

    Хэвлэсэн 2014
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    Artigo
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  2. 2
    Global mapping of binding sites for Nrf2 identifies novel targets in cell survival response through ChIP-Seq profiling and network analysis

    Global mapping of binding sites for Nrf2 identifies novel targets in cell survival response through ChIP-Seq profiling and network analysis -н Deepti Malhotra, Élodie Portales-Casamar, Anju Singh, Siddhartha Srivastava, David J. Arenillas, Christine Happel, Casper Shyr, Nobunao Wakabayashi, Thomas W. Kensler, Wyeth W. Wasserman, Shyam Biswal

    Хэвлэсэн 2010
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    Artigo
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  3. 3
    A novel recurrent mutation in ATP1A3 causes CAPOS syndrome

    A novel recurrent mutation in ATP1A3 causes CAPOS syndrome -н Michelle Demos, Clara DM van Karnebeek, Colin J.D. Ross, Shelin Adam, Yaoqing Shen, Shing H. Zhan, Casper Shyr, Gabriella Horváth, Mohnish Suri, Alan Fryer, Steven J.M. Jones, Jan M. Friedman

    Хэвлэсэн 2014
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    Artigo
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  4. 4
    JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles

    JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles -н Anthony Mathelier, Oriol Fornés, David J. Arenillas, Chih‐Yu Chen, Grégoire Denay, Jessica Lee, Wenqiang Shi, Casper Shyr, Ge Tan, Rebecca Worsley-Hunt, Allen W. Zhang, François Parcy, Boris Lenhard, Albin Sandelin, Wyeth W. Wasserman

    Хэвлэсэн 2015
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    Artigo
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  5. 5
    JASPAR 2014: an extensively expanded and updated open-access database of transcription factor binding profiles

    JASPAR 2014: an extensively expanded and updated open-access database of transcription factor binding profiles -н Anthony Mathelier, Xiaobei Zhao, Allen W. Zhang, François Parcy, Rebecca Worsley-Hunt, David J. Arenillas, Sorana Buchman, Chih‐Yu Chen, Alice Chou, Hans Ienasescu, Jonathan Lim, Casper Shyr, Ge Tan, Michelle Zhou, Boris Lenhard, Albin Sandelin, Wyeth W. Wasserman

    Хэвлэсэн 2013
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    Artigo
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  6. 6
    The genotypic and phenotypic spectrum of PIGA deficiency

    The genotypic and phenotypic spectrum of PIGA deficiency -н Maja Tarailo‐Graovac, Graham Sinclair, Sylvia Stöckler‐Ipsiroglu, Margot Van Allen, Jacob Rozmus, Casper Shyr, Roberta Biancheri, Tracey Oh, Bryan Sayson, Mirafe Lafek, Colin J.D. Ross, Wendy P. Robinson, Wyeth W. Wasserman, Andrea Rossi, Clara DM van Karnebeek

    Хэвлэсэн 2015
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    Artigo
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  7. 7
    Atypical cerebral palsy: genomics analysis enables precision medicine

    Atypical cerebral palsy: genomics analysis enables precision medicine -н Allison Matthews, Ingrid Blydt-Hansen, Basma Al-Jabri, John Andersen, Maja Tarailo‐Graovac, Magda Price, Katherine Selby, Michelle Demos, Mary Connolly, Britt I. Drögemöller, Casper Shyr, Jill Mwenifumbo, Alison M. Elliott, Jessica Lee, Aisha Ghani, Sylvia Stöckler, Ramona Salvarinova, Hilary Vallance, Graham Sinclair, Colin J.D. Ross, Wyeth W. Wasserman, Margaret L. McKinnon, Gabriella Horváth, Helly Goez, Clara D.M. van Karnebeek

    Хэвлэсэн 2018
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    Artigo
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  8. 8
    Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood

    Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood -н Clara D.M. van Karnebeek, William S. Sly, Colin J.D. Ross, Ramona Salvarinova, Joy Yaplito‐Lee, Saikat Santra, Casper Shyr, Gabriella Horváth, Patrice Eydoux, Anna Lehman, Virginie Bernard, Theresa Newlove, Henry Ukpeh, Anupam Chakrapani, Mary Anne Preece, Sarah Ball, James Pitt, Hilary Vallance, Marion B. Coulter-Mackie, Hien Anh Thi Nguyen, Linhua Zhang, Amit P. Bhavsar, Graham Sinclair, Abdul Waheed, Wyeth W. Wasserman, Sylvia Stöckler‐Ipsiroglu

    Хэвлэсэн 2014
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    Artigo
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  9. 9
    Exome Sequencing and the Management of Neurometabolic Disorders

    Exome Sequencing and the Management of Neurometabolic Disorders -н Maja Tarailo‐Graovac, Casper Shyr, Colin J.D. Ross, Gabriella Horváth, Ramona Salvarinova, Xin C. Ye, Lin-Hua Zhang, Amit P. Bhavsar, Jessica J. Y. Lee, Britt I. Drögemöller, Mena Abdelsayed, Majid Alfadhel, Linlea Armstrong, Matthias R. Baumgartner, Patricie Burda, Mary Connolly, Jessie M. Cameron, Michelle Demos, Tammie Dewan, Janis M. Dionne, A. Mark Evans, Jan M. Friedman, Ian Garber, M. E. Suzanne Lewis, Jiqiang Ling, Rupasri Mandal, André Mattman, Margaret L. McKinnon, Aspasia Michoulas, Daniel L. Metzger, Oluseye A. Ogunbayo, Bojana Rakić, Jacob Rozmus, Peter C. Ruben, Bryan Sayson, Saikat Santra, Kirk R. Schultz, Kathryn Selby, Paul Shekel, Sandra Sirrs, Cristina Skrypnyk, Andrea Superti‐Furga, Stuart E. Turvey, Margot I. Van Allen, David S. Wishart, Jiang Wu, John K. Wu, Dimitrios Zafeiriou, Leo A. J. Kluijtmans, Ron A. Wevers, Patrice Eydoux, Anna Lehman, Hilary Vallance, Sylvia Stöckler‐Ipsiroglu, Graham Sinclair, Wyeth W. Wasserman, Clara D.M. van Karnebeek

    Хэвлэсэн 2016
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    Artigo
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