Activated mTOR signaling pathway in myofibers with inherited metabolic defect might be an evidence for mTOR inhibition therapies

por Lyu, Jing-Wei, Xu, Xue-Bi, Ji, Kun-Qian, Zhang, Na, Sun, Yuan, Zhao, Dan-Dan, Zhao, Yu-Ying, Yan, Chuan-Zhu
Publicado 2019

Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations

por Yu, Xiao-Lin, Yan, Chuan-Zhu, Ji, Kun-Qian, Lin, Peng-Fei, Xu, Xue-Bi, Dai, Ting-Jun, Li, Wei, Zhao, Yu-Ying
Publicado 2018

Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation

por Xu, Xue-Bi, Ji, Kun-Qian, Lyu, Jing-Wei, Zhang, Shu, Lyu, Xiao-Qing, Liu, Chang, Li, Wei, Yan, Chuan-Zhu, Zhao, Yu-Ying
Publicado 2019