Associated Papers
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 control of meiosis surveillance mechanisms in mammals.
Huang Y et al.
Frontiers in Cell and Developmental Biology, 2023
36910159 (PubMed )
Supplement: DataSheet2.PDF
Novel mutations of TEX11 are associated with non-obstructive azoospermia.
Song J et al.
Frontiers in Endocrinology, 2023
Genetic defects in human azoospermia.
Ghieh F et al.
Basic and Clinical Andrology, 2019
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
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
Yatsenko AN et al.
The New England Journal of Medicine, 2015
A new TEX11 mutation causes azoospermia and testicular meiotic arrest.
Yu XC et al.
Asian Journal of Andrology, 0
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