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
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.
Arafat M et al.
Molecular Genetics & Genomic Medicine, 2020
The impacts of nineteen mutations on the enzymatic activity of USP26.
Liu YL et al.
Gene, 2018
Single nucleotide polymorphisms of USP26 in azoospermic men.
Luddi A et al.
Systems Biology in Reproductive Medicine, 2016
Evidence from enzymatic and meta-analyses does not support a direct association between USP26 gene variants and male infertility.
Zhang W et al.
Andrology, 2015
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
Association of USP26 haplotypes in men in Taiwan, China with severe spermatogenic defect.
Lee IW et al.
Asian Journal of Andrology, 2008
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