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

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

Development and assessment of a knowledge, attitude, and practice (KAP) questionnaire for genetic counselees with preimplantation genetic testing (PGT) indications

针对有植入前遗传学检测 (PGT) 指征的遗传咨询者,开发和评估知识、态度和实践 (KAP) 问卷

Luo, Zhen; Tu, Chaofeng; Li, Li; Peng, Lingli

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

Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.

新型 SPEF2 变异体导致男性不育,并可能引起原发性纤毛运动障碍

Lu Wenqing, Li Yong, Meng Lanlan, Tan Chen, Nie Hongchuan, Zhang Qianjun, Song Yuying, Zhang Huan, Tan Yue-Qiu, Tu Chaofeng, Guo Haichun, Wu Longxiang, Du Juan

Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression

人类C12orf40基因的功能缺失变异会阻断减数分裂进程,从而导致男性不育。

Tu, Chaofeng; Wen, Junfei; Wang, Weili; Zhu, Qifan; Chen, Ying; Cheng, Jianglu; Li, Zeye; Meng, Lanlan; Li, Yong; He, Wenbin; Tan, Chen; Xie, Chunbo; Fu, Shao-Mei; Du, Juan; Lu, Guangxiu; Lin, Ge; Gou, Lan-Tao; Tan, Yue-Qiu

Estimation for volunteer web survey samples using a model-averaging approach

使用模型平均法估计志愿者网络调查样本

Liu, Zhan; Zheng, Junbo; Tu, Chaofeng; Pan, Yingli

GPC6 Promotes Cell Proliferation, Migration, and Invasion in Nasopharyngeal Carcinoma

GPC6促进鼻咽癌细胞的增殖、迁移和侵袭

Fan, Chunmei; Tu, Chaofeng; Qi, Peng; Guo, Can; Xiang, Bo; Zhou, Ming; Li, Xiayu; Wu, Xu; Li, Xiaoling; Li, Guiyuan; Xiong, Wei; Zeng, Zhaoyang