For: | Deng TQ, Xie YL, Pu JB, Xuan J, Li XM. Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report. World J Clin Cases 2022; 10(34): 12761-12767 [PMID: 36579083 DOI: 10.12998/wjcc.v10.i34.12761] |
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URL: | https://www.wjgnet.com/2307-8960/full/v10/i34/12761.htm |
Number | Citing Articles |
1 |
Mingfei Xiang, Yu Wang, Yuying Jiao, Rui Guo, Na Zheng, Kexin Yu, Xiaoya Zhu, Pengcheng Hu, Jingjing Zhang, Xiaomin Zha, Zongliu Duan, Fengsong Wang, Yunxia Cao, Fuxi Zhu. A homozygous loss‐of‐function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans. Andrology 2024; doi: 10.1111/andr.13827
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2 |
Thomas Greither, Mario Dejung, Hermann M. Behre, Falk Butter, Holger Herlyn. The human sperm proteome—Toward a panel for male fertility testing. Andrology 2023; 11(7): 1418 doi: 10.1111/andr.13431
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3 |
Manvi Arora, Poonam Mehta, Shruti Sethi, George Anifandis, Mary Samara, Rajender Singh. Genetic etiological spectrum of sperm morphological abnormalities. Journal of Assisted Reproduction and Genetics 2024; 41(11): 2877 doi: 10.1007/s10815-024-03274-8
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4 |
Weilong Xu, Zhoujuan Yao, Yunzhi Li, Ke Wang, Shuai Kong, Yu Wang, Mingfei Xiang, Fuxi Zhu, Fengsong Wang, Hui Zhang. Loss of PMFBP1 Disturbs Mouse Spermatogenesis by Downregulating HDAC3 Expression. Journal of Assisted Reproduction and Genetics 2023; 40(8): 1865 doi: 10.1007/s10815-023-02874-0
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5 |
Bingbing Wu, Chenghong Long, Yuzhuo Yang, Zhe Zhang, Shuang Ma, Yanjie Ma, Huafang Wei, Jinghe Li, Hui Jiang, Wei Li, Chao Liu. CCDC113 stabilizes sperm axoneme and head-tail coupling apparatus to ensure male fertility. eLife 2024; 13 doi: 10.7554/eLife.98016.3
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