Associated Papers
A novel candidate missense variant in the catalytic domain of USP26 associated with asthenoteratozoospermia.
Mousavi SZ et al.
Gene, 2026
Genetic determinants of testicular sperm extraction outcomes: insights from a large multicentre study of men with non-obstructive azoospermia.
Riera-Escamilla A et al.
Human Reproduction Open, 2025
40896145 (PubMed )
Supplement: hoaf049_supplementary_data.zip › HRO-25-0045-R2-SuppTablesS2-S4_and_S6-S9.xlsx › ST6
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans.
Liu C et al.
The Embo Journal, 2021
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.
Arafat M et al.
Molecular Genetics & Genomic Medicine, 2020
Molecular Characterization of Astrocytoma Progression Towards Secondary Glioblastomas Utilizing Patient-Matched Tumor Pairs.
Seifert M et al.
Cancers, 2020
32604718 (PubMed )
Supplement: cancers-12-01696-s001.zip › Supporting_Tables_and_Figures › Table_S8_ExomeSeq_Predictions.xlsx › MuTect_SNV_Predictions
A novel frameshift mutation in ubiquitin-specific protease 26 gene in a patient with severe oligozoospermia.
Li L et al.
Bioscience Reports, 2020
New insights into the genetics of spermatogenic failure: a review of the literature.
Cannarella R et al.
Human Genetics, 2019
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia.
Ma Q et al.
Reproductive Sciences (thousand Oaks, Calif.), 2016
Select a paper to view details