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机译:通过X染色体失活分离MECP2空Rett综合征患者hiPS细胞和同基因对照
Program in Developmental and Stem Cell Biology and|Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S1A8,;
Department of Biochemistry and Molecular Biology, Pennsylvania State College of Medicine, Hershey, PA 17033, USA and;
Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada M5G1L7,;
Program in Developmental and Stem Cell Biology and;
Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada M5G1L7,;
Program in Developmental and Stem Cell Biology and|Ontario Human Induced Pluripotent Stem Cell Facility, Toronto, Ontario, Canada M5G1L7;
Department of Biochemistry and Molecular Biology, Pennsylvania State College of Medicine, Hershey, PA 17033, USA and;
机译:通过X染色体失活分离MECP2空Rett综合征患者hiPS细胞和同基因对照。
机译:具有p.R168X或p.T158M MECP2突变的Rett综合征患者的临床严重程度与X染色体失活的方向和偏斜之间的相关性。
机译:使用Talen介导的SCN1A基因编辑的Dravet综合征患者IPSC的D1-1鹰帽的IPSCs的产生
机译:使用限制Boltzmann Machine的RETT综合征患者呼吸紊乱分类
机译:用患者特异性诱导多能干细胞模拟Rett综合征。
机译:通过X染色体失活分离MECP2空Rett综合征患者hiPS细胞和同基因对照
机译:通过X染色体失活分离MECP2空Rett综合征患者hiPS细胞和同基因对照