Works matching AU Zha, Xiaomin

Results: 12

A homozygous loss‐of‐function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans.

Published in:

Andrology, 2025, v. 13, n. 5, p. 1285, doi. 10.1111/andr.13827

By:

Xiang, Mingfei;
Wang, Yu;
Jiao, Yuying;
Guo, Rui;
Zheng, Na;
Yu, Kexin;
Zhu, Xiaoya;
Hu, Pengcheng;
Zhang, Jingjing;
Zha, Xiaomin;
Duan, Zongliu;
Wang, Fengsong;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription.

Published in:

Andrology, 2025, v. 13, n. 5, p. 1261, doi. 10.1111/andr.13743

By:

Wang, Yu;
Xiang, Mingfei;
Zhou, Yiru;
Zheng, Na;
Zhang, Jingjing;
Zha, Xiaomin;
Duan, Zongliu;
Wang, Fengsong;
Zhang, Ying;
Wang, Zhongxin;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

Unraveling the Impact of the PROCA1 Mutation in Male Infertility: Incorporating Whole Exome Sequencing in Teratozoospermia Patients and Analyzing Proca1 Knockout Mice.

Published in:

Reproductive Sciences, 2025, v. 32, n. 4, p. 1080, doi. 10.1007/s43032-024-01624-6

By:

Zheng, Na;
Shen, Yiru;
Wang, Yu;
Xiang, Mingfei;
Yu, Kexin;
Zhang, Jingjing;
Zha, Xiaomin;
Duan, Zongliu;
Wang, Fengsong;
Zhu, Fuxi;
Cao, Yunxia

Publication type:

Article

Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa Syndrome.

Published in:

Reproductive Sciences, 2022, v. 29, n. 2, p. 646, doi. 10.1007/s43032-021-00665-5

By:

Xiang, Mingfei;
Wang, Yu;
Wang, Ke;
Kong, Shuai;
Lu, Mengmeng;
Zhang, Jingjing;
Duan, Zongliu;
Zha, Xiaomin;
Shi, Xuanming;
Wang, Fengsong;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

Published in:

SCIENCE CHINA Life Sciences, 2024, v. 67, n. 8, p. 1697, doi. 10.1007/s11427-023-2539-1

By:

Wu, Huan;
Zhang, Yanman;
Li, Yuqian;
Sun, Shuya;
Zhang, Jintao;
Xie, Qingsong;
Dong, Yue;
Zhou, Shushu;
Sha, Xuan;
Li, Kuokuo;
Chen, Jinyi;
Zhang, Xin;
Gao, Yang;
Shen, Qunshan;
Wang, Guanxiong;
Zha, Xiaomin;
Duan, Zongliu;
Tang, Dongdong;
Xu, Chuan;
Geng, Hao

Publication type:

Article

Association of lifestyle and occupational exposure factors with human semen quality: a cross-sectional study of 1060 participants.

Published in:

Systems Biology in Reproductive Medicine, 2024, v. 70, n. 1, p. 150, doi. 10.1080/19396368.2024.2357348

By:

Yang, Wen;
Duan, Zongliu;
Li, Guanjian;
Geng, Hao;
Gao, Yang;
Shen, Qunshan;
Liu, Liting;
Wang, Guanxiong;
Zha, Xiaomin;
Xu, Chuan;
Zhou, Ping;
Song, Bing;
Tang, Dongdong;
Wu, Huan;
Wei, Zhaolian;
Tang, Feng;
He, Xiaojin

Publication type:

Article

A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 1, p. 261, doi. 10.1007/s10815-021-02363-2

By:

Xiang, Mingfei;
Wang, Yu;
Xu, Weilong;
Zheng, Na;
Deng, Hongshi;
Zhang, Jingjing;
Duan, Zongliu;
Zha, Xiaomin;
Zhang, Wenjun;
Song, Gaojie;
Shi, Xuanming;
Wang, Fengsong;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 10, p. 2791, doi. 10.1007/s10815-021-02295-x

By:

Xiang, Mingfei;
Wang, Yu;
Xu, Weilong;
Zheng, Na;
Zhang, Jingjing;
Duan, Zongliu;
Zha, Xiaomin;
Shi, Xuanming;
Wang, Fengsong;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 4, p. 949, doi. 10.1007/s10815-021-02075-7

By:

Lu, Mengmeng;
Kong, Shuai;
Xiang, Mingfei;
Wang, Yu;
Zhang, Jingjing;
Duan, Zongliu;
Zha, Xiaomin;
Wang, Fengsong;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 4, p. 821, doi. 10.1007/s10815-020-01719-4

By:

Wang, Fengsong;
Zhang, Jingjing;
Kong, Shuai;
Li, Chanjuan;
Zhang, Zhiguo;
He, Xiaojin;
Wu, Huan;
Tang, Dongdong;
Zha, Xiaomin;
Tan, Qing;
Duan, Zongliu;
Cao, Yunxia;
Zhu, Fuxi

Publication type:

Article

Rational construction of genome-minimized Streptomyces host for the expression of secondary metabolite gene clusters.

Published in:

Synthetic & Systems Biotechnology, 2024, v. 9, n. 3, p. 600, doi. 10.1016/j.synbio.2024.04.017

By:

Hui Li;
Sheng Gao;
Sanyuan Shi;
Xiaomin Zha;
Haoyu Ye;
Yunzi Luo

Publication type:

Article

Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.

Published in:

Human Mutation, 2022, v. 43, n. 12, p. 2079, doi. 10.1002/humu.24475

By:

Wang, Guanxiong;
Zhu, Xiaoyu;
Gao, Yang;
Lv, Mingrong;
Li, Kuokuo;
Tang, Dongdong;
Wu, Huan;
Xu, Chuan;
Geng, Hao;
Shen, Qunshan;
Zha, Xiaomin;
Duan, Zongliu;
Zhang, Jingjing;
Hua, Rong;
Tao, Fangbiao;
Zhou, Ping;
Wei, Zhaolian;
Cao, Yunxia;
Guo, Rui;
He, Xiaojin

Publication type:

Article