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机译:Tk2缺乏症的发作和器官特异性取决于Tk1下调和转录补偿
Department of Neurology, Columbia University Medical Center, 630 West 168th Street, P&S 4-423, New York, NY 10032, USA;
Department of Neurology, Columbia University Medical Center, 630 West 168th Street, P&S 4-423, New York, NY 10032, USA;
Department of Neurology, Columbia University Medical Center, 630 West 168th Street, P&S 4-423, New York, NY 10032, USA;
机译:Tk2缺乏症的发作和器官特异性取决于Tk1下调和转录补偿。
机译:核苷生物利用度和TK1稳态水平调节对TK2缺乏引起的线粒体DNA消耗综合征的DC Plus DT治疗的反应
机译:核苷生物利用度和TK1稳态水平调节对TK2缺乏引起的线粒体DNA消耗综合征的DC Plus DT治疗的反应
机译:拟南芥中两个边界特异性MYB转录因子LATERAL ORGAN FUSION1和LATERAL ORGAN FUSION2的表征
机译:Tk2缺乏症的发作和器官特异性取决于Tk1下调和转录补偿
机译:Tk2缺乏症的发作和器官特异性取决于Tk1下调和转录补偿