...
机译:奈梅亨断裂综合征动物模型中与小脑减员相关的星形胶质细胞功能障碍。
Department of Neurobiology, George S. Wise, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel;
Leibniz Institute for Age Research–Fritz Lipmann Institute e.V., Jena, Germany;
Department of Neurobiology, George S. Wise, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel;
Leibniz Institute for Age Research–Fritz Lipmann Institute e.V., Jena, Germany;
Department of Neurobiology, George S. Wise, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel;
Department of Neurobiology, George S. Wise, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel;
Leibniz Institute for Age Research–Fritz Lipmann Institute e.V., Jena, Germany;
The David and Inez Myers Laboratory for Genetic Research, Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv, 69978, Israel;
Department;
Nijmegen breakage syndrome; Asrocyte; Microglia; Glia; Cerebellum; Purkinje cells; BDNF; NT3;
机译:奈梅亨人破损综合征动物模型中与小脑减退相关的星形胶质细胞功能障碍。
机译:奈梅亨断裂综合征小鼠模型的白质损伤的MRI证据。
机译:奈梅亨断裂综合症的可诱导的无效突变小鼠模型证明了NBS1在染色体稳定性和细胞活力中的基本功能。
机译:内皮功能障碍,血小板多动和氧化应激与急性冠状动脉综合征中的结果和左心室收缩功能障碍
机译:共济失调毛细血管扩张突变和奈梅亨断裂综合症蛋白-1在UVC诱导的DNA复制依赖性双链断裂积累中的作用。
机译:端粒磨损和功能障碍:奈梅亨断裂综合征中早衰表型的潜在触发因素
机译:Nijmegen破裂综合征成纤维细胞和IPSCS:用于揭露疾病相关的信号通路的细胞模型,并建立抗氧化剂的筛选平台