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
Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans.
Liu C et al.
The Embo Journal, 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
New insights into the genetics of spermatogenic failure: a review of the literature.
Cannarella R et al.
Human Genetics, 2019
Single nucleotide polymorphisms of USP26 in azoospermic men.
Luddi A et al.
Systems Biology in Reproductive Medicine, 2016
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
Novel mutations in ubiquitin-specific protease 26 gene might cause spermatogenesis impairment and male infertility.
Zhang J et al.
Asian Journal of Andrology, 2007
Alterations of the USP26 gene in Caucasian men.
Stouffs K et al.
International Journal of Andrology, 2006
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