Associated Papers
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.
Guzmán-Jiménez A et al.
Human Reproduction Open, 2024
39678461 (PubMed )
Supplement: hoae069_supplementary_data.zip › supplementary_tables.xlsx › _S13
An RNF12-USP26 amplification loop drives germ cell specification and is disrupted by disease-associated mutations.
Segarra-Fas A et al.
Science Signaling, 2022
35857630 (PubMed )
Supplement: EMS155062-supplement-Supplementary_Material.pdf
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.
Arafat M et al.
Molecular Genetics & Genomic Medicine, 2020
Ubiquitin-specific protease (USP26) gene alterations associated with male infertility and recurrent pregnancy loss (RPL) in Iranian infertile patients.
Asadpor U et al.
Journal of Assisted Reproduction and Genetics, 2013
[Polymorphism of Usp26 correlates with idiopathic male infertility].
Zhang J et al.
Zhonghua Nan Ke Xue = National Journal of Andrology, 2012
USP26 gene variations in fertile and infertile men.
Ribarski I et al.
Human Reproduction (oxford, England), 2009
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