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收藏分享 收藏 Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertilityMEI4中的双等位基因错义变异导致植入前胚胎停滞和女性不育
Pan, Zhiqi; Wang, Weijie; Wu, Ling; Yao, Zhongyuan; Wang, Wenjing; Chen, Yao; Gu, Hao; Dong, Jie; Mu, Jian; Zhang, Zhihua; Fu, Jing; Li, Qiaoli; Wang, Lei; Sun, Xiaoxi; Kuang, Yanping; Sang, Qing; Chen, Biaobang 分享 收藏 PATL2 regulates mRNA homeostasis in oocytes by interacting with EIF4E and CPEB1Zhang, Zhihua; Liu, Ruyi; Zhou, Hongbin; Li, Qun; Qu, Ronggui; Wang, Weijie; Zhou, Zhou; Yu, Ran; Zeng, Yang; Mu, Jian; Chen, Biaobang; Guo, Xuejiang; Sang, Qing; Wang, Lei 分享 收藏 分享 收藏 Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects从头突变的大规模分析确定了以卵母细胞和早期胚胎缺陷为特征的女性不育的危险基因Li, Qun; Zhao, Lin; Zeng, Yang; Kuang, Yanping; Guan, Yichun; Chen, Biaobang; Xu, Shiru; Tang, Bin; Wu, Ling; Mao, Xiaoyan; Sun, Xiaoxi; Shi, Juanzi; Xu, Peng; Diao, Feiyang; Xue, Songguo; Bao, Shihua; Meng, Qingxia; Yuan, Ping; Wang, Wenjun; Ma, Ning; Song, Di; Xu, Bei; Dong, Jie; Mu, Jian; Zhang, Zhihua; Fan, Huizhen; Gu, Hao; Li, Qiaoli; He, Lin; Jin, Li; Wang, Lei; Sang, Qing 分享 收藏 ADGB variants cause asthenozoospermia and male infertilityADGB变体导致弱精子症和男性不育Qu, Ronggui; Zhang, Zhihua; Wu, Ling; Li, Qun; Mu, Jian; Zhao, Lin; Yan, Zheng; Wang, Wenjing; Zeng, Yang; Liu, Ruyi; Dong, Jie; Li, Qiaoli; Sun, Xiaoxi; Wang, Lei; Sang, Qing; Chen, Biaobang; Kuang, Yanping 分享 收藏 Karyopherin α deficiency contributes to human preimplantation embryo arrest核蛋白 α 缺乏导致人类植入前胚胎停滞Wang, Wenjing; Miyamoto, Yoichi; Chen, Biaobang; Shi, Juanzi; Diao, Feiyang; Zheng, Wei; Li, Qun; Yu, Lan; Li, Lin; Xu, Yao; Wu, Ling; Mao, Xiaoyan; Fu, Jing; Li, Bin; Yan, Zheng; Shi, Rong; Xue, Xia; Mu, Jian; Zhang, Zhihua; Wu, Tianyu; Zhao, Lin; Wang, Weijie; Zhou, Zhou; Dong, Jie; Li, Qiaoli; Jin, Li; He, Lin; Sun, Xiaoxi; Lin, Ge; Kuang, Yanping; Wang, Lei; Sang, Qing 分享 收藏 Electric Power Audit Text Classification With Multi-Grained Pre-Trained Language Model基于多粒度预训练语言模型的电力审计文本分类Meng, Qinglin; Song, Yan; Mu, Jian; Lv, Yuanxu; Yang, Jiachen; Xu, Liang; Zhao, Jin; Ma, Junwei; Yao, Wei; Wang, Rui; Xiao, Maoxiang; Meng, Qingyu 分享 收藏 IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3Zhang, Zhihua; Zhou, Hongbin; Deng, Xujing; Zhang, Ruixiu; Qu, Ronggui; Mu, Jian; Liu, Ruyi; Zeng, Yang; Chen, Biaobang; Wang, Lei; Sang, Qing; Bao, Shihua 分享 收藏 分享 收藏 分享 收藏 Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertilityLiu, Ruyi; Yan, Zheng; Fan, Yong; Qu, Ronggui; Chen, Biaobang; Li, Bin; Wu, Ling; Wu, Haibo; Mu, Jian; Zhao, Lin; Wang, Wenjing; Dong, Jie; Zeng, Yang; Li, Qiaoli; Wang, Lei; Sang, Qing; Zhang, Zhihua; Kuang, Yanping 分享 收藏 FBXO43 variants in patients with female infertility characterized by early embryonic arrest以早期胚胎停滞为特征的女性不孕症患者的FBXO43变体Wang, Weijie; Wang, Wenjing; Xu, Yao; Shi, Juanzi; Fu, Jing; Chen, Biaobang; Mu, Jian; Zhang, Zhihua; Zhao, Lin; Lin, Jing; Du, Jing; Li, Qiaoli; He, Lin; Jin, Li; Sun, Xiaoxi; Wang, Lei; Sang, Qing 分享 收藏 Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failureDong, Jie; Zhang, Hong; Mao, Xiaoyan; Zhu, Junhua; Li, Da; Fu, Jing; Hu, Jijun; Wu, Ling; Chen, Biaobang; Sun, Yiming; Mu, Jian; Zhang, Zhihua; Sun, Xiaoxi; Zhao, Lin; Wang, Wenjing; Wang, Weijie; Zhou, Zhou; Zeng, Yang; Du, Jing; Li, Qiaoli; He, Lin; Jin, Li; Kuang, Yanping; Wang, Lei; Sang, Qing 分享 收藏 分享 收藏 A novel splicing variant in DNAH8 causes asthenozoospermiaDNAH8中一种新的剪接变体导致弱精子症Zhou, Zhou; Mao, Xiaoyan; Chen, Biaobang; Mu, Jian; Wang, Wenjing; Li, Bin; Yan, Zheng; Dong, Jie; Li, Qiaoli; Kuang, Yanping; Wang, Lei; Wu, Ling; Sang, Qing 分享 收藏 Homozygous variants in PANX1 cause human oocyte death and female infertilityWang, 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 分享 收藏 Novel mutations inLHCGR(luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndromeZhang, Zhihua; Wu, Ling; Diao, Feiyang; Chen, Biaobang; Fu, Jing; Mao, Xiaoyan; Yan, Zheng; Li, Bin; Mu, Jian; Zhou, Zhou; Wang, Wenjing; Zhao, Lin; Dong, Jie; Zeng, Yang; Du, Jing; Kuang, Yanping; Sun, Xiaoxi; He, Lin; Sang, Qing; Wang, Lei 分享 收藏 
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