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Clinical Genetics|January 7, 2026
Discovery of a Pathogenic NME5 Variant Underlying Acephalic Spermatozoa Syndrome: Unraveling a Novel Genotype-Phenotype Association in Male InfertilityYunchuan Tian, Yingteng Zhang, Xinyao Tang, et al.Clinical Genetics|August 1, 2025
Loss of Different Domains of TDRD12 Leads to Distinct Male Infertility-Related PhenotypesXinyao Tang, Jinhui Li, Yunchuan Tian, et al.Elife|November 6, 2024
DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and miceXiang Wang, Gan Shen, Yihong Yang, et al.Human Genetics|August 14, 2025
Biallelic loss-of-function variants of DNAH7 cause male infertility associated with asthenozoospermia in humansGuicheng Zhao, Jun Ma, Yingteng Zhang, et al.Proceedings of the National Academy of Sciences of the United States of America|March 31, 2026
ASB9 promotes ubiquitin-mediated degradation of TNP2 to facilitate histone-to-protamine transition in humans and miceShikun Zhao, Gan Shen, Tiechao Ruan, et al.Nucleic Acids Research|January 23, 2026
A novel dual histone mark reader ZCWPW2 regulates meiotic recombination through lactylation and transcriptional regulation in humans and miceTiechao Ruan, Jun Ma, Gan Shen, et al.Pageof 2