Хайлтын үр дүнгүүд - Seung‐Yun Yoo

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  1. 1
    Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin–proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation

    Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin–proteasome system impairment and inversely correlates with the degree of nuclear inclusion... -н Aaron B. Bowman, Seung-Yun Yoo, Nico P. Dantuma, Huda Y. Zoghbi

    Хэвлэсэн 2005
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    Artigo
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  2. 2
    Genetic Interactions between Doublecortin and Doublecortin-like Kinase in Neuronal Migration and Axon Outgrowth

    Genetic Interactions between Doublecortin and Doublecortin-like Kinase in Neuronal Migration and Axon Outgrowth -н Thomas A.S Deuel, Judy S. Liu, Joseph C. Corbo, Seung-Yun Yoo, Lucy B. Rorke‐Adams, Christopher A. Walsh

    Хэвлэсэн 2006
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    Artigo
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  3. 3
    SCA7 Knockin Mice Model Human SCA7 and Reveal Gradual Accumulation of Mutant Ataxin-7 in Neurons and Abnormalities in Short-Term Plasticity

    SCA7 Knockin Mice Model Human SCA7 and Reveal Gradual Accumulation of Mutant Ataxin-7 in Neurons and Abnormalities in Short-Term Plasticity -н Seung-Yun Yoo, Mark E. Pennesi, Edwin J. Weeber, Bisong Xu, Richard Atkinson, Shiming Chen, Dawna L. Armstrong, Samuel M. Wu, J. David Sweatt, Huda Y. Zoghbi

    Хэвлэсэн 2003
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    Artigo
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  4. 4
    Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry

    Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry -н Eric M. Morrow, Seung-Yun Yoo, Steven W. Flavell, Tae-Kyung Kim, Yingxi Lin, Robert Hill, Nahit Motavallı Mukaddes, Soher Balkhy, Generoso G. Gascon, Asif Hashmi, Samira Al-Saad, Janice Ware, Robert M. Joseph, Rachel Greenblatt, Danielle Gleason, Julia A. Ertelt, Kira Apse, Adria Bodell, Jennifer N. Partlow, Brenda J. Barry, Hui Yao, Kyriacos Markianos, Russell J. Ferland, Michael E. Greenberg, Christopher A. Walsh

    Хэвлэсэн 2008
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    Artigo
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  5. 5
    Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

    Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features -н Qing Ouyang, Tojo Nakayama, Ozan Baytaş, Shawn M. Davidson, Chendong Yang, M Schmidt, Sofia B. Lizarraga, Sasmita Mishra, Malak EI-Quessny, Saima Niaz, Mirrat Gul Butt, Syed Imran Murtaza, Afzal Javed, Haroon Rashid Chaudhry, Dylan J. Vaughan, Robert Hill, Jennifer N. Partlow, Seung-Yun Yoo, Anh-Thu N. Lam, Ramzi Nasir, Muna Al‐Saffar, A. James Barkovich, Matthew Schwede, Shailender Nagpal, Anna Rajab, Ralph J. DeBerardinis, David E. Housman, Ganeshwaran H. Mochida, Eric M. Morrow

    Хэвлэсэн 2016
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    Artigo
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  6. 6
    Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders

    Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders -н Michael S. Ching, Yiping Shen, Wen‐Hann Tan, Shafali Jeste, Eric M. Morrow, Xiaoli Chen, Nahit Motavallı Mukaddes, Seung‐Yun Yoo, Ellen Hanson, Rachel J. Hundley, Christina L. Austin, Ronald E. Becker, Gerard T. Berry, Katherine Driscoll, Elizabeth C. Engle, Sandra Friedman, James F. Gusella, Fuki M. Hisama, Mira Irons, Tina Lafiosca, Elaine LeClair, David T. Miller, Michael Neessen, Jonathan Picker, Leonard Rappaport, Cynthia M. Rooney, Dean Sarco, Joan M. Stoler, Christopher A. Walsh, Robert R. Wolff, Ting Zhang, Ramzi H. Nasir, Bai‐Lin Wu

    Хэвлэсэн 2010
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    Artigo
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