在R1-pS262陶氏诱导的内源性陶氏聚合,突触损伤和认知障碍中,对R1-pS262陶氏的构造模式发生了变化

Gang Wu1,2, Yong Luo1,2, Qian Guo1

  • 1School of Basic Medicine, Key Laboratory of Education Ministry/Hubei province of China for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

PubMed
概括

在Ser262的陶酸化驱动蛋白质聚合和神经退行在阿尔茨海默氏症 (AD). 这一发现为陶病和潜在的治疗点提供了新的见解.