Identification of a Novel GJA8 (Cx50) Point Mutation Causes Human Dominant Congenital Cataracts

por Ge, Xiang-Lian, Zhang, Yilan, Wu, Yaming, LV, Jineng, Zhang, Wei, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Publicado 2014

AAV-Mediated Lysophosphatidylcholine Acyltransferase 1 (Lpcat1) Gene Replacement Therapy Rescues Retinal Degeneration in rd11 Mice

por Dai, Xufeng, Han, Juanjuan, Qi, Yan, Zhang, Hua, Xiang, Lue, Lv, Jineng, Li, Jie, Deng, Wen-Tao, Chang, Bo, Hauswirth, William W., Pang, Ji-jing
Publicado 2014

Engineered FnCas12a with enhanced activity through directional evolution in human cells

por Liu, Xiexie, Liu, Xiaoyu, Zhou, Chenchen, Lv, Jineng, He, Xiubin, Liu, Yuanyuan, Xie, Haihua, Wang, Bang, Lv, Xiujuan, Tang, Lianchao, Li, Mingchun, Liu, Changbao, Zhao, Junzhao, Liu, Yong, Song, Zongming, Gu, Feng
Publicado en J Biol Chem (2021)