Rare variants in GPR3 in POI patients: a case series with review of literature

por Ren, Shuting, Zhang, Feng, Shang, Lingyue, Yang, Xi, Pan, Yuncheng, Zhang, Xiaojin, Wu, Yanhua
Publicado 2023

Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging

por Zhou, Zixue, Yang, Xi, Pan, Yuncheng, Shang, Lingyue, Chen, Siyuan, Yang, Jialin, Jin, Li, Zhang, Feng, Wu, Yanhua
Publicado 2021

Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient

por Wang, Yingchen, Chen, Qing, Zhang, Feng, Yang, Xi, Shang, Lingyue, Ren, Shuting, Pan, Yuncheng, Zhou, Zixue, Li, Guoqing, Fang, Yunzheng, Jin, Li, Wu, Yanhua, Zhang, Xiaojin
Publicado 2021

Rare variants in FANCA induce premature ovarian insufficiency

por Yang, Xi, Zhang, Xiaojin, Jiao, Jiao, Zhang, Feng, Pan, Yuncheng, Wang, Qiqi, Chen, Qing, Cai, Baozhu, Tang, Shuyan, Zhou, Zixue, Chen, Siyuan, Yin, Hao, Fu, Wei, Luo, Yang, Li, Da, Li, Guoqing, Shang, Lingyue, Yang, Jialing, Jin, Li, Shi, Qinghua, Wu, Yanhua
Publicado 2019