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机译:小鼠神经病性戈谢病:可行的联合选择性鞘脂蛋白C缺乏症和突变型葡糖脑苷脂酶(V394L)小鼠合并糖基鞘氨醇和葡萄糖基神经酰胺蓄积和进行性神经功能缺损
The Division of Human Genetics,|Department of Pediatrics,;
The Division of Human Genetics,|Department of Pediatrics,;
The Division of Human Genetics,|Department of Pediatrics,;
Division of Neurology,|Department of Pediatrics,;
Division of Neurology,|Department of Pediatrics,;
Division of Neurology,|Department of Pediatrics,;
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA;
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA;
Division of Pediatric Pathology, Cincinnati Children's Hospital Medical Center,|Department of Pathology, University of Cincinnati College of Medicine, Cincinnati, OH 45229-3039, USA and;
The Division of Human Genetics,|Department of Pediatrics,;
机译:小鼠神经性戈谢病:可行的联合选择性鞘脂蛋白C缺乏症和突变型葡糖脑苷脂酶(V394L)小鼠与葡糖鞘氨醇和葡糖神经酰胺积聚和进行性神经功能缺损。
机译:小鼠中saposin C和D的联合缺乏会导致神经病性表型,葡萄糖基神经酰胺和α-羟基神经酰胺蓄积,并改变prosaposin的运输。
机译:小鼠中鞘脂蛋白C和D的联合缺乏导致神经病性表型,葡萄糖基神经酰胺和α-羟基神经酰胺的积累,并改变了鞘脂蛋白的运输
机译:小鼠神经病性戈谢病:可行的联合选择性鞘脂蛋白C缺乏症和突变型葡糖脑苷脂酶(V394L)小鼠合并糖基鞘氨醇和葡萄糖基神经酰胺蓄积和进行性神经功能缺损
机译:小鼠神经病性戈谢病:可行的联合选择性鞘脂蛋白C缺乏症和突变型葡糖脑苷脂酶(V394L)小鼠合并糖基鞘氨醇和葡萄糖基神经酰胺蓄积和进行性神经功能缺损