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

CEP112 coordinates translational regulation of essential fertility genes during spermiogenesis through phase separation in humans and mice

CEP112 通过人类和小鼠的相分离来协调精子发生过程中必需生育基因的翻译调控

Xueguang Zhang #, Gelin Huang #, Ting Jiang #, Lanlan Meng #, Tongtong Li #, Guohui Zhang, Nan Wu, Xinyi Chen, Bingwang Zhao, Nana Li, Sixian Wu, Junceng Guo, Rui Zheng, Zhiliang Ji, Zhigang Xu, Zhenbo Wang, Dong Deng, Yueqiu Tan, Wenming Xu

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models

灵长类特异性 SSX1 缺乏导致男性不育症、食蟹猴和树鼩模型中出现弱畸形精子症

Chunyu Liu, Wei Si, Chaofeng Tu, Shixiong Tian, Xiaojin He, Shengnan Wang, Xiaoyu Yang, Chencheng Yao, Cong Li, Zine-Eddine Kherraf, Maosen Ye, Zixue Zhou, Yuhua Ma, Yang Gao, Yu Li, Qiwei Liu, Shuyan Tang, Jiaxiong Wang, Hexige Saiyin, Liangyu Zhao, Liqun Yang, Lanlan Meng, Bingbing Chen, Dongdong

Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella

TTC12 中的新型纯合变异会导致男性不育,并伴有弱畸精子症,这是由于鞭毛中的运动蛋白臂复合体和线粒体鞘缺陷造成的

Lanlan Meng, Qiang Liu, Chen Tan, Xilin Xu, Wenbin He, Tongyao Hu, Chaofeng Tu, Yong Li, Juan Du, Qianjun Zhang, Guangxiu Lu, Li-Qing Fan, Ge Lin, Hongchuan Nie, Huan Zhang, Yue-Qiu Tan

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA

CFAP54 的双等位基因突变可导致男性不育,并伴有严重的 MMAF 和 NOA

Shixiong Tian, Chaofeng Tu, Xiaojin He, Lanlan Meng, Jiaxiong Wang, Shuyan Tang, Yang Gao, Chunyu Liu, Huan Wu, Yiling Zhou, Mingrong Lv, Ge Lin, Li Jin, Yunxia Cao, Dongdong Tang, Feng Zhang, Yue-Qiu Tan

Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility

在中国男性原发性纤毛运动障碍和不育症患者中鉴定新的双等位基因 LRRC6 变异

Yunhao Li #, Yong Li #, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu

Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype

CCIN 的新型纯合变异体因精子头部异常且具有核沉降表型而导致男性不育

Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan

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

Identification of Hub Genes in Colorectal Adenocarcinoma by Integrated Bioinformatics

利用整合生物信息学方法鉴定结直肠腺癌中的关键基因

Liu, Yang; Chen, Lanlan; Meng, Xiangbo; Ye, Shujun; Ma, Lianjun

TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation

TDRD7 通过介导自噬体成熟参与晶状体发育和精子发生

Chaofeng Tu, Haiyu Li, Xuyang Liu, Ying Wang, Wei Li, Lanlan Meng, Weili Wang, Yong Li, Dongyan Li, Juan Du, Guangxiu Lu, Ge Lin, Yue-Qiu Tan

Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly

人类WDR63基因的双等位基因变异通过异常的内动力蛋白臂组装导致男性不育

Shuai Lu,Yayun Gu,Yifei Wu,Shenmin Yang,Chenmeijie Li,Lanlan Meng,Wenwen Yuan,Tao Jiang,Xin Zhang,Yang Li,Cheng Wang,Mingxi Liu,Lan Ye,Xuejiang Guo,Hongbing Shen,Xiaoyu Yang,Yueqiu Tan,Zhibin Hu