Rong Hua

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 12

Top Topics

Polycystic Ovary Syndrome

Escherichia Coli

Top Venues

Cell death & disease

Cellular and molecular life sciences : CMLS

Human reproduction (Oxford, England)

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Chang Wang, Qingsong Xie, Xun Xia, Chuanying Zhang, Shan Jiang, Sihan Wang, Xi Zhang, Rong Hua, Jiangyang Xue, Haoyu Zheng
ZMYND12 serves as an IDAd subunit that is essential for sperm motility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Yang Gao, Rufeng Xue, Rui Guo, Fan Yang, Xuan Sha, Yuqian Li, Rong Hua, Guotong Li, Qunshan Shen, Kuokuo Li, Wenwen Liu, Yuping Xu, Ping Zhou, ZhaoLian Wei, Zhiguo Zhang, Yun-Xia Cao, Xiao-Jin He, Huan Wu
CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches. Human reproduction (Oxford, England) (2024)
Chang Wang, Qingsong Xie, Xun Xia, Chuanying Zhang, Shan Jiang, Sihan Wang, Xi Zhang, Rong Hua, Jiangyang Xue, Haoyu Zheng
ZMYND12 serves as an IDAd subunit that is essential for sperm motility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Chang Wang, Qingsong Xie, Xun Xia, Chuanying Zhang, Shan Jiang, Sihan Wang, Xi Zhang, Rong Hua, Jiangyang Xue, Haoyu Zheng
ZMYND12 serves as an IDAd subunit that is essential for sperm motility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Rong Hua, Rufeng Xue, Yiyuan Liu, Yuqian Li, Xuan Sha, Kuokuo Li, Yang Gao, Qunshan Shen, Mingrong Lv, Yuping Xu, Zhiguo Zhang, Xiao-Jin He, Yun-Xia Cao, Huan Wu
ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida. Human reproduction (Oxford, England) (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Wen Yang, Rong Hua, Yunxia Cao, Xiaojin He
A metabolomic perspective on the mechanisms by which environmental pollutants and lifestyle lead to male infertility. Andrology (2023)
Yiyuan Liu, Yuqian Li, Lanlan Meng, Kuokuo Li, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Xiaojin He, Yunxia Cao, Huan Wu, Yue-Qiu Tan, Rong Hua
Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia due to acrosomal hypoplasia and reduced progressive motility. Human molecular genetics (2023)
Shushu Zhou, Huan Wu, Jintao Zhang, Xiaojin He, Siyu Liu, Ping Zhou, Rong Hua, Yunxia Cao, Mingxi Liu
Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility. European journal of human genetics : EJHG 30 (6) (2022)