Associated Papers
A novel candidate missense variant in the catalytic domain of USP26 associated with asthenoteratozoospermia.
Mousavi SZ et al.
Gene, 2026
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
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.
Arafat M et al.
Molecular Genetics & Genomic Medicine, 2020
A novel frameshift mutation in ubiquitin-specific protease 26 gene in a patient with severe oligozoospermia.
Li L et al.
Bioscience Reports, 2020
The impacts of nineteen mutations on the enzymatic activity of USP26.
Liu YL et al.
Gene, 2018
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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