Associated Papers
Tex11 Mutant Mouse Models of Human Azoospermia.
Atkins GR et al.
Biorxiv : the Preprint Server for Biology, 2026
The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility.
Gao Y et al.
Human Reproduction Update, 2026
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
Ibrahim R et al.
Reproductive Biology, 2025
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes.
Rotte N et al.
Embo Molecular Medicine, 2025
40374915 (PubMed )
Supplement: 44321_2025_244_MOESM2_ESM.pdf
Analysis of genes implicated in non-obstructive azoospermia.
Wang J et al.
Steroids, 2025
Genetic determinants of testicular sperm extraction outcomes: insights from a large multicentre study of men with non-obstructive azoospermia.
Riera-Escamilla A et al.
Human Reproduction Open, 2025
40896145 (PubMed )
Supplement: hoaf049_supplementary_data.zip › HRO-25-0045-R2-SuppTablesS2-S4_and_S6-S9.xlsx › ST6
The landscape of RNA binding proteins in mammalian spermatogenesis.
Li Y et al.
Science (new York, N.y.), 2024
39208083 (PubMed )
Supplement: science.adj8172_tables_s1_to_s16.zip › science.adj8172_table_s14.xlsx › Candidate_Hom_DNS_LOF
A partial deletion within the meiosis-specific sporulation domain SPO22 of Tex11 is not associated with infertility in mice.
Ghieh F et al.
Plos One, 2024
Novel mutations of TEX11 are associated with non-obstructive azoospermia.
Song J et al.
Frontiers in Endocrinology, 2023
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