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

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice

DNAH3 双等位基因变异导致人类和小鼠出现弱精子症和男性不育症

Gui-Quan Meng, Yaling Wang, Chen Luo, Yu-Mei Tan, Yong Li, Chen Tan, Chaofeng Tu, Qian-Jun Zhang, Liang Hu, Huan Zhang, Lan-Lan Meng, Chun-Yu Liu, Leiyu Deng, Guang-Xiu Lu, Ge Lin, Juan Du, Yue-Qiu Tan, Yanwei Sha, Lingbo Wang, Wen-Bin He

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants

来自 DNAH12 的进一步证据表明,携带动力蛋白轴丝重链基因家族变异的不育男性具有良好的生育能力。

Hao Geng ,Kai Wang ,Dan Liang ,Xiaoqing Ni ,Hui Yu ,Dongdong Tang ,Mingrong Lv ,Huan Wu ,Kuokuo Li ,Qunshan Shen ,Yang Gao ,Chuan Xu ,Ping Zhou ,Zhaolian Wei ,Yunxia Cao ,Yanwei Sha ,Xiaoyu Yang ,Xiaojin He

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

新型 DNAH11 变异与弱畸精子症的关联导致男性不育

Senzhao Guo #, Dongdong Tang #, Yuge Chen #, Hui Yu #, Meng Gu #, Hao Geng, Jiajun Fang, Baoyan Wu, Lewen Ruan, Kuokuo Li, Chuan Xu, Yang Gao, Qing Tan, Zongliu Duan, Huan Wu, Rong Hua, Rui Guo, Zhaolian Wei, Ping Zhou, Yuping Xu, Yunxia Cao, Xiaojin He, Yanwei Sha, Mingrong Lv

Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis

AK9 缺乏会破坏精子核苷酸稳态,导致弱精子症和男性不育

Yanwei Sha, Wensheng Liu, Shu Li, Ludmila V Osadchuk, Yongjie Chen, Hua Nie, Shuai Gao, Linna Xie, Weibing Qin, Huiliang Zhou, Lin Li

Eif4enif1 haploinsufficiency disrupts oocyte mitochondrial dynamics and leads to subfertility

Eif4enif1 单倍体不足会破坏卵母细胞线粒体动力学并导致生育力低下

Yuxi Ding, Zequn He, Yanwei Sha, Kehkooi Kee, Lin Li

Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced in vitro fertilization

TAF7L中的有害变体导致人类少弱畸形精子症及其损害组蛋白与鱼精蛋白的交换,从而诱导体外受精减少

Haowei Bai, Yanwei Sha, Yueqiu Tan, Peng Li, Yuxiang Zhang, Junwei Xu, Shuai Xu, Zhiyong Ji, Xiaobo Wang, Wei Chen, Jianxiong Zhang, Chencheng Yao, Zheng Li, Erlei Zhi

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice

DNHD1基因的双等位基因变异会导致人类和小鼠出现鞭毛轴丝缺陷和弱精子症。

Chen Tan ,Lanlan Meng ,Mingrong Lv ,Xiaojin He ,Yanwei Sha ,Dongdong Tang ,Yaqi Tan ,Tongyao Hu ,Wenbin He ,Chaofeng Tu ,Hongchuan Nie ,Huan Zhang ,Juan Du ,Guangxiu Lu ,Li-Qing Fan ,Yunxia Cao ,Ge Lin ,Yue-Qiu Tan

TBC1D21 is an essential factor for sperm mitochondrial sheath assembly and male fertility‡

TBC1D21 是精子线粒体鞘组装和男性生育力的必要因素‡

Yongjie Chen, Xiu Chen, Haihang Zhang, Yanwei Sha, Ranran Meng, Tianyu Shao, Xiaoyan Yang, Pengpeng Jin, Yinghua Zhuang, Wanping Min, Dan Xu, Zhaodi Jiang, Yuhua Li, Lin Li, Wentao Yue, Chenghong Yin

Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome

ACTRT1 致病变异导致无头精子综合征

Yanwei Sha, Wensheng Liu, Lin Li, Mario Serafimovski, Vladimir Isachenko, Youzhu Li, Jing Chen, Bangrong Zhao, Yifeng Wang, Xiaoli Wei

Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella

DNAH2 中的新型双等位基因变异导致严重的弱畸形精子症,伴有多种鞭毛形态异常

Yang Gao, Shixiong Tian, Yanwei Sha, Xiaomin Zha, Huiru Cheng, Anyong Wang, Chunyu Liu, Mingrong Lv, Xiaoqing Ni, Qiang Li, Huan Wu, Qing Tan, Dongdong Tang, Bing Song, Ding Ding, Jiangshan Cong, Yuping Xu, Ping Zhou, Zhaolian Wei, Yunxia Cao, Yuanhong Xu, Feng Zhang, Xiaojin He