AAV-mediated gene therapy produces fertile offspring in the Lhcgr-deficient mouse model of Leydig cell failure
AAV 介导的基因疗法在 Lhcgr 缺陷的 Leydig 细胞衰竭小鼠模型中产生了可生育的后代
期刊:Cell Reports Medicine
影响因子:11.7
doi:10.1016/j.xcrm.2022.100792
Kai Xia, Fulin Wang, Xingqiang Lai, Lin Dong, Peng Luo, Suyuan Zhang, Cuifeng Yang, Hong Chen, Yuanchen Ma, Weijun Huang, Wangsheng Ou, Yuyan Li, Xin Feng, Bin Yang, Congyuan Liu, Zhenmin Lei, Xiang'an Tu, Qiong Ke, Frank Fuxiang Mao, Chunhua Deng, Andy Peng Xiang
细胞生物学
其它细胞
FCM
IF
IHC-P
WB
Mouse
STP2