Associated Papers
Tex11 Mutant Mouse Models of Human Azoospermia.
Atkins GR et al.
Biorxiv : the Preprint Server for Biology, 2026
Molecular characterization of recessively inherited ataxic and neuropathic disorders in consanguineous Pakistani families.
Aslam F et al.
Scientific Reports, 2026
41606223 (PubMed )
Supplement: 41598_2026_37808_MOESM5_ESM.xlsx › Sheet1
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
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Novel mutations of TEX11 are associated with non-obstructive azoospermia.
Song J et al.
Frontiers in Endocrinology, 2023
Clinical Evaluation of a Custom Gene Panel as a Tool for Precision Male Infertility Diagnosis by Next-Generation Sequencing.
Cannarella R et al.
Life (basel, Switzerland), 2020
A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.
Sha Y et al.
Bmc Medical Genetics, 2018
TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.
Yang F et al.
Embo Molecular Medicine, 2015
Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure.
Cannarella R et al.
Asian Journal of Andrology, 0
A new TEX11 mutation causes azoospermia and testicular meiotic arrest.
Yu XC et al.
Asian Journal of Andrology, 0
The formation and repair of DNA double-strand breaks in mammalian meiosis.
Qu W et al.
Asian Journal of Andrology, 0
Select a paper to view details