Hasil Pencarian - Scott M Wilson

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  1. 1
    Genetic background alters the severity and onset of neuromuscular disease caused by the loss of ubiquitin-specific protease 14 (usp14).

    Genetic background alters the severity and onset of neuromuscular disease caused by the loss of ubiquitin-specific protease 14 (usp14). oleh Andrea G Marshall, Jennifer A Watson, Jada J Hallengren, Brandon J Walters, Lynn E Dobrunz, Ludwig Francillon, Julie A Wilson, Scott E Phillips, Scott M Wilson

    Diterbitkan 2013-01-01
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  2. 2
    The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice.

    The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice. oleh Corinna Lappe-Siefke, Sven Loebrich, Wulf Hevers, Oliver B Waidmann, Michaela Schweizer, Susanne Fehr, Jean-Marc Fritschy, Ivan Dikic, Jens Eilers, Scott M Wilson, Matthias Kneussel

    Diterbitkan 2009-09-01
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  3. 3
    Usp14 deficiency increases tau phosphorylation without altering tau degradation or causing tau-dependent deficits.

    Usp14 deficiency increases tau phosphorylation without altering tau degradation or causing tau-dependent deficits. oleh Youngnam N Jin, Ping-Chung Chen, Jennifer A Watson, Brandon J Walters, Scott E Phillips, Karen Green, Robert Schmidt, Julie A Wilson, Gail V Johnson, Erik D Roberson, Lynn E Dobrunz, Scott M Wilson

    Diterbitkan 2012-01-01
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  4. 4
    Motor and Sensory Deficits in the teetering Mice Result from Mutation of the ESCRT Component HGS.

    Motor and Sensory Deficits in the teetering Mice Result from Mutation of the ESCRT Component HGS. oleh Jennifer A Watson, Bula J Bhattacharyya, Jada H Vaden, Julie A Wilson, Mert Icyuz, Alan D Howard, Edward Phillips, Tara M DeSilva, Gene P Siegal, Andrew J Bean, Gwendalyn D King, Scott E Phillips, Richard J Miller, Scott M Wilson

    Diterbitkan 2015-06-01
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