Výsledky vyhledávání - Steven C. Ryu

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  1. 1
    Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids

    Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids Autor Priya Srikanth, Valentina N. Lagomarsino, Christina Muratore, Steven C. Ryu, Amy He, Walter M. Taylor, Constance Zhou, Marlise Arellano, Tracy L. Young‐Pearse

    Vydáno 2018
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  2. 2
    Aging and neurodegeneration are associated with increased mutations in single human neurons

    Aging and neurodegeneration are associated with increased mutations in single human neurons Autor Michael A. Lodato, Rachel E. Rodin, Craig L. Bohrson, Michael E. Coulter, Alison R. Barton, Min‐Seok Kwon, Maxwell A. Sherman, Carl Vitzthum, Lovelace J. Luquette, Chandri Yandava, Pengwei Yang, Thomas W. Chittenden, Nicole E. Hatem, Steven C. Ryu, Mollie B. Woodworth, Peter J. Park, Christopher A. Walsh

    Vydáno 2017
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  3. 3
    Somatic genomic changes in single Alzheimer’s disease neurons

    Somatic genomic changes in single Alzheimer’s disease neurons Autor Michael B. Miller, August Yue Huang, Jun‐Ho Kim, Zinan Zhou, Samantha L. Kirkham, Eduardo A. Maury, Jennifer S. Ziegenfuss, Hannah C. Reed, Jennifer E. Neil, Lariza M. Rento, Steven C. Ryu, C. Chanthia, Lovelace J. Luquette, Heather M. Ames, Derek H. Oakley, Matthew P. Frosch, Bradley T. Hyman, Michael A. Lodato, Eunjung Alice Lee, Christopher A. Walsh

    Vydáno 2022
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  4. 4
    Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size

    Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size Autor Matthew B. Johnson, Xingshen Sun, Andrew Kodani, Rebeca Borges-Monroy, Kelly M. Girskis, Steven C. Ryu, Peter P. Wang, Komal Patel, Dilenny M. Gonzalez, Yu Mi Woo, Ziying Yan, Bo Liang, Richard S. Smith, Manavi Chatterjee, Daniel Coman, Xenophon Papademetris, Lawrence H. Staib, Fahmeed Hyder, Joseph B. Mandeville, P. Ellen Grant, Kiho Im, Hojoong Kwak, John F. Engelhardt, Christopher A. Walsh, Byoung-Il Bae

    Vydáno 2018
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  5. 5
    Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor <i>DONSON</i> as the cause of microcephaly-micromelia syndrome

    Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor <i>DONSON</i> as the cause of microcephaly-micromelia syndrome Autor Gilad D. Evrony, Dwight R. Cordero, Jun Shen, Jennifer N. Partlow, Timothy W. Yu, Rachel E. Rodin, Robert Hill, Michael E. Coulter, Anh-Thu N. Lam, Divya Jayaraman, Dianne Gerrelli, Diana Gold Diaz, Chloe Santos, Victoria Morrison, Antonella Galli, Ulrich Tschulena, Stefan Wiemann, Marie-Jocelyne Martel, Betty Anne Spooner, Steven C. Ryu, Princess C. Elhosary, Jillian M. Richardson, Danielle Tierney, Christopher A. Robinson, Rajni Chibbar, Dana Diudea, Rebecca D. Folkerth, Sheldon Wiebe, A. James Barkovich, Ganeshwaran H. Mochida, James Irvine, Edmond G. Lemire, Patricia M. Blakley, Christopher A. Walsh

    Vydáno 2017
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