檢索結果 - Divya Jayaraman

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  1. 1
    Genetic Changes Shaping the Human Brain

    Genetic Changes Shaping the Human Brain 由 Byoung-Il Bae, Divya Jayaraman, Christopher A. Walsh

    出版 2015
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    Revisão
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  2. 2
    Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate

    Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate 由 Divya Jayaraman, Andrew Kodani, Dilenny M. Gonzalez, Joseph D. Mancias, Ganeshwaran H. Mochida, Cristiana Vagnoni, Jeffrey R. Johnson, Nevan J. Krogan, J. Wade Harper, Jeremy F. Reiter, Timothy W. Yu, Byoung-Il Bae, Christopher A. Walsh

    出版 2016
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    Artigo
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  3. 3
    Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication

    Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication 由 Andrew Kodani, Timothy W. Yu, Jeffrey R. Johnson, Divya Jayaraman, Tasha L. Johnson, Lihadh Al‐Gazali, László Sztriha, Jennifer N. Partlow, Hanjun Kim, Alexis Leigh Krup, Alexander Dammermann, Nevan J. Krogan, Christopher A. Walsh, Jeremy F. Reiter

    出版 2015
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    Artigo
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  4. 4
    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 由 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

    出版 2017
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    Artigo
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  5. 5
    Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy

    Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy 由 Hyun Yong Koh, Lacey Smith, Kimberly Wiltrout, Archana Podury, Nitish Chourasia, Alissa M. D’Gama, Meredith Park, Devon Knight, Emma Sexton, Julia Koh, Brandon T. Oby, Rebecca Pinsky, Diane D. Shao, Courtney E. French, Wanqing Shao, Shira Rockowitz, Piotr Sliz, Bo Zhang, Sonal Mahida, Christelle Moufawad El Achkar, Christopher J. Yuskaitis, Heather E. Olson, Beth Rosen Sheidley, Annapurna Poduri, Elizabeth Barkoudah, Ann M. Bergin, Miya E. Bernson‐Leung, Elizabeth Binney, Jeffrey Bolton, Stephanie Donatelli, Darius Ebrahimi‐Fakhari, Mark Gorman, Chellamani Harini, Divya Jayaraman, Agnieszka Kielian, Lauren LaFortune, Kerri L. LaRovere, Mark H. Libenson, David N. Lieberman, Tobias Loddenkemper, Candice Marti, Anna Minster, Kate Mysak, Ann Paris, Archana A. Patel, Phillip L. Pearl, Jurriaan M. Peters, A Gomes Pinto, Peter Raffalli, Alexander Rotenberg, Catherine L. Salussolia, Rebecca Sarvendram, Hannah Shapiro, Janet S. Soul, Sarah Spence, Karen Spencer, Robert C. Stowe, Coral M. Stredny, Masanori Takeoka, Molly Tracy, Sara Trowbridge, Melissa Tsuboyama, David K. Urion

    出版 2023
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    Artigo
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