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

A testis-specific E3 ubiquitin ligase complex governs spermiogenesis and male fertility

睾丸特异性E3泛素连接酶复合物调控精子发生和男性生育能力

Wu, Tiantian; Tu, Chaofeng; Feng, Yuxuan; Qu, Wenying; Chen, Jinyi; Wu, Huan; Gao, Wenxin; Xu, Bingya; Yu, Xiangling; Bao, Mingyuan; Xu, Jinfu; Zhou, Nianchao; Hu, Haoyue; Jiang, Bing; Xie, Qingsong; Meng, Lanlan; Tan, Chen; Lin, Ge; Shen, Cong; Chen, Xia; Guo, Yueshuai; Zhou, Tao; Liang, Yuting; Hua, Rong; Cao, Yunxia; Liu, Mingxi; Yu, Jun; Huang, Xiaoyan; Tan, Yue-Qiu; Zheng, Bo

Novel INSL3 variants cause male infertility with cryptorchidism

新型INSL3变异导致男性隐睾症和不育

Wei, Chunjia; Lu, Wenqing; Li, Yong; Liang, Yaoqiong; Meng, Lanlan; Tan, Chen; Lin, Ge; Tan, Yue-Qiu; Zhang, Qianjun; Tu, Chaofeng; Du, Juan

A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics

非梗阻性无精子症的常见病因:MEI1双等位基因变异及其对不孕症诊断的意义

Tan, Chen; Wang, Tiantian; Tu, Chaofeng; Xie, Chunbo; Chen, Zixu; Yuan, Shimin; Hu, Tongyao; He, Wenbin; Li, Yong; Wang, Yurong; Luo, Chen; Zhang, Qianjun; Nie, Hongchuan; Zhang, Huan; Lu, Guangxiu; Lin, Ge; Tan, Yue-Qiu; Meng, Lanlan; Du, Juan

METTL5 deficiency induces oligoasthenoteratozoospermia via impaired 18S rRNA m(6)A methylation in humans and mice.

METTL5 缺陷通过损害人类和小鼠的 18S rRNA m(6)A 甲基化而诱发少弱畸精子症。

Zhang Mengya, Zhang Xueguang, Tan Chen, Jiang Ting, Cao Zheng, Chen Yufei, Qiao Feng, Huang Gelin, Ma Chaoye, Li Huixia, Ye Mei, Wang Lei, Zuo Liandong, Yu Jun, Li Xiaofeng, Zhang Yunfang, Tan Yue-Qiu, Lin Shuibin, Xu Wenming, Chen Hao

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha

遗传罕见病防控:长沙市基于家庭的筛查和生殖干预

Lin, Ge; He, Jun; Wang, Yuankun; Liu, Xiangyan; Du, Juan; Zhang, Qianjun; Zhou, Shihao; Hu, Lanping; He, Jing; Li, Xiurong; Hu, Hao; Hu, Liang; Zhong, Changgao; He, Wen-Bin; Peng, Chan; Xu, Zhen; Zhang, Jingjing; Shu, Yan; Song, Xuan; Zhang, Wenqian; Lu, Guangxiu; Ou, Zhiming; Tan, Yue-Qiu; Liu, Jiyang

Hemizygous IL2RG Variants Impair IL-2-Induced STAT5 Phosphorylation and Transcriptional Activity Causing X-Linked Severe Combined Immunodeficiency

半合子IL2RG变异体损害IL-2诱导的STAT5磷酸化和转录活性,导致X连锁重症联合免疫缺陷

Zhang, Ning; Sang, Yi-Lin; Zhu, Wu; Wang, Yu-Rong; Yu, Yan-Yan; Chen, Ya-Hui; Du, Juan; He, Wen-Bin; Tan, Yue-Qiu; Wang, Fu-Yan

Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermia.

ZMYND15 中的新突变与少精子症/无精子症引起的男性不育有关

Wei Chunjia, Lu Yingchi, Yi Sibing, Liang Yaoqiong, Meng Lanlan, Tan Chen, Du Juan, Lin Ge, Tan Yue-Qiu, Gan Xianyou, Tu Chaofeng, Qin Zailong

CFAP47 is Implicated in X-Linked Polycystic Kidney Disease

CFAP47与X连锁多囊肾病有关

Mori, Takayasu; Fujimaru, Takuya; Liu, Chunyu; Patterson, Karynne; Yamamoto, Kouhei; Suzuki, Takefumi; Chiga, Motoko; Sekine, Akinari; Ubara, Yoshifumi; Miller, Danny E; Zalusky, Miranda P G; Mandai, Shintaro; Ando, Fumiaki; Mori, Yutaro; Kikuchi, Hiroaki; Susa, Koichiro; Chong, Jessica X; Bamshad, Michael J; Tan, Yue-Qiu; Zhang, Feng; Uchida, Shinichi; Sohara, Eisei

Extended application of PGT-M strategies for small pathogenic CNVs

PGT-M策略在小型致病性CNV中的扩展应用

Hu, Xiao; Wang, Weili; Luo, Keli; Dai, Jing; Zhang, Yi; Wan, Zhenxing; He, Wenbin; Zhang, Shuoping; Yang, Lanlin; Tan, Qin; Li, Wen; Zhang, Qianjun; Gong, Fei; Lu, Guangxiu; Tan, Yue-Qiu; Lin, Ge; Du, Juan

Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella.

鉴定出与精子鞭毛多种形态异常相关的、导致弱精子畸形的新型纯合ARMC2突变

Zhao Siyi, Liu Qiong, Su Lilan, Meng Lanlan, Tan Chen, Wei Chunjia, Zhang Huan, Luo Tao, Zhang Qianjun, Tan Yue-Qiu, Tu Chaofeng, Chen Houyang, Gao Xingcheng