日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Novel missense variants in COX15 cause oocyte degeneration and female infertility

COX15基因中发现的新型错义变异会导致卵母细胞退化和女性不孕。

Yu, Ran; Zhang, Xuelin; Dou, Qian; Li, Chunyi; Ye, Zhiqi; Xu, Fangzhou; Xiong, Chi; Chen, Biaobang; Wang, Weijie; Li, Qiaoli; Wang, Lei; Sang, Qing; Zhang, Zhihua

Novel variants in PABPC1L cause female infertility due to oocyte maturation defects.

PABPC1L 的新变异会导致卵母细胞成熟缺陷,从而导致女性不孕。

Pan Zhiqi, Ye Zhiqi, Ye Hongjuan, Chen Biaobang, Mu Jian, Zhang Zhihua, Li Qiaoli, Kuang Yanping, Wang Lei, Sang Qing, Guan Yichun, Wang Weijie

Genetic landscape of human oocyte/embryo defects

人类卵母细胞/胚胎缺陷的遗传图谱

Chen, Biaobang; Wang, Weijie; Shi, Juanzi; Sun, Xiaoxi; Guan, Yichun; Hao, Guimin; Zhao, Junli; Mu, Jian; Zhang, Zhihua; Xu, Fangzhou; Gao, Dengying; Pan, Zhiqi; Yu, Ran; Gu, Hao; Fan, Huizhen; Luo, Yuxi; Xie, Siyuan; Du, Xingzhu; Jing, Huixia; Ye, Zhiqi; Zhang, Xuelin; Hai, Ruiqi; Zhu, Hongying; Wu, Tianyu; Li, Qiaoli; Fu, Jing; Wu, Ling; Wang, Wenjing; Li, Chunyi; Diao, Feiyang; Shi, Qiuwen; Li, Lin; Xu, Shiru; Li, Da; Dong, Xi; Xu, Peng; Wang, Jiucun; He, Lin; Kuang, Yanping; Sang, Qing; Wang, Lei

The E3 ubiquitin ligase adaptor KLHL8 targets ZAR1 to regulate maternal mRNA degradation in oocytes.

E3泛素连接酶接头蛋白KLHL8靶向ZAR1,调节卵母细胞中母源mRNA的降解

Fan Huizhen, Liu Ruyi, Yu Ran, Chen Biaobang, Li Qiaoli, Mu Jian, Wang Weijie, Wu Tianyu, He Lin, Wang Lei, Sang Qing, Zhang Zhihua

Novel homozygous variants in ASTL and WEE2 responsible for female infertility characterized by abnormal fertilization

ASTL 和 WEE2 中的新型纯合变异导致女性不孕,其特征是受精异常

Xie, Siyuan; Zhang, Meiling; Wu, Fengyan; Yu, Ran; Fu, Jing; Shi, Rong; Li, Qiaoli; Chen, Biaobang; Shi, Juanzi; Wu, Tianyu; Sun, Xiaoxi; Sang, Qing; Wang, Lei; Wang, Weijie; Mu, Jian

COX15 deficiency causes oocyte ferroptosis.

COX15 缺乏会导致卵母细胞铁死亡

Zhang Zhihua, Yu Ran, Shi Qiuwen, Wu Zhi-Jing, Li Qingchun, Mu Jian, Chen Biaobang, Shi Juanzi, Ni Renmin, Wu Ling, Li Qiaoli, Fu Jing, Li Rong, Sun Xiaoxi, Wang Jiucun, He Lin, Kuang Yanping, Sang Qing, Wang Lei

Identification novel mutations and phenotypic spectrum expanding in PATL2 in infertile women with IVF/ICSI failure

在体外受精/卵胞浆内单精子注射(IVF/ICSI)失败的不孕女性中,PATL2基因存在新的突变,并伴有表型谱的扩展。

Ye, Zhiqi; Li, Da; Niu, Xiangli; Yang, Aimin; Pan, Zhiqi; Yu, Ran; Gu, Hao; Shi, Rong; Wu, Ling; Xiang, Yanfang; Hao, Guimin; Kuang, Yanping; Chen, Biaobang; Wang, Lei; Sang, Qing; Li, Lin; Shi, Juanzi; Li, Qiaoli

YBX2-dependent stabilization of oocyte mRNA through a reversible sponge-like cortical partition

YBX2依赖性卵母细胞mRNA通过可逆的海绵状皮质隔膜稳定化

Zhang, Zhihua; Liu, Ruyi; Zhou, Hongbin; Luo, Yuxi; Mu, Jian; Fu, Jing; Wu, Tianyu; Chen, Biaobang; Sang, Qing; Wang, Lei

Homozygous variants in PANX1 cause human oocyte death and female infertility

PANX1基因的纯合变异会导致人类卵母细胞死亡和女性不孕。

Wang, Weijie; Qu, Ronggui; Dou, Qian; Wu, Fengyan; Wang, Wenjing; Chen, Biaobang; Mu, Jian; Zhang, Zhihua; Zhao, Lin; Zhou, Zhou; Dong, Jie; Zeng, Yang; Liu, Ruyi; Du, Jing; Zhu, Shujia; Li, Qiaoli; He, Lin; Jin, Li; Wang, Lei; Sang, Qing

Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development

CDC20基因的双等位基因突变会导致女性不孕,其特征是卵母细胞成熟和早期胚胎发育异常。

Zhao, Lin; Xue, Songguo; Yao, Zhongyuan; Shi, Juanzi; Chen, Biaobang; Wu, Ling; Sun, Lihua; Xu, Yao; Yan, Zheng; Li, Bin; Mao, Xiaoyan; Fu, Jing; Zhang, Zhihua; Mu, Jian; Wang, Wenjing; Du, Jing; Liu, Shuai; Dong, Jie; Wang, Weijie; Li, Qiaoli; He, Lin; Jin, Li; Liang, Xiaozhen; Kuang, Yanping; Sun, Xiaoxi; Wang, Lei; Sang, Qing