15q11.2 BP1-BP2 microdeletion presenting as progressive spastic paraplegia and brain images of small vessel disease

por Sha, Qianqian, Xia, Yu, Shen, Xiya, Du, Ailian
Publicado 2022

Two patients with congenital myasthenic syndrome caused by COLQ gene mutations and the consequent ColQ protein defect

por Zhang, Qiting, Sha, Qianqian, Qiao, Kai, Liu, Xiaoli, Gong, Xiaohui, Du, Ailian
Publicado 2023

IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency

por Wan, Yanling, Muhammad, Tahir, Huang, Tao, Lv, Yue, Sha, Qianqian, Yang, Shuang, Lu, Gang, Chan, Wai-yee, Ma, Jinlong, Liu, Hongbin
Publicado 2022

IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice

por Muhammad, Tahir, Wan, Yanling, Sha, Qianqian, Wang, Jianfeng, Huang, Tao, Cao, Yongzhi, Li, Mengjing, Yu, Xiaochen, Yin, Yingying, Chan, Wai Yee, Chen, Zi-Jiang, You, Li, Lu, Gang, Liu, Hongbin
Publicado 2020