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
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Correlation of Novel Single Nucleotide Polymorphisms ofUSP26, TEX15, and TNP2 Genes with Male Infertility in North West of Iran.
Ghadirkhomi E et al.
International Journal of Fertility & Sterility, 2022
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
A novel frameshift mutation in ubiquitin-specific protease 26 gene in a patient with severe oligozoospermia.
Li L et al.
Bioscience Reports, 2020
Ubiquitin-specific protease 26 (USP26) is not essential for mouse gametogenesis and fertility.
Felipe-Medina N et al.
Chromosoma, 2019
New insights into the genetics of spermatogenic failure: a review of the literature.
Cannarella R et al.
Human Genetics, 2019
Basic and clinical genetic studies on male infertility in Iran during 2000-2016: A review.
Moghbelinejad S et al.
International Journal of Reproductive Biomedicine, 2018
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
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia.
Ma Q et al.
Reproductive Sciences (thousand Oaks, Calif.), 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
Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men.
Shi YC et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2011
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
Sequence analysis of the X-linked USP26 gene in severe male factor infertility patients and fertile controls.
Christensen GL et al.
Fertility and Sterility, 2008
Alterations of the USP26 gene in Caucasian men.
Stouffs K et al.
International Journal of Andrology, 2006
Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26.
Ravel C et al.
Molecular Human Reproduction, 2006
Novel mutations in testis-specific ubiquitin protease 26 gene may cause male infertility and hypogonadism.
Paduch DA et al.
Reproductive Biomedicine Online, 2005
Possible role of USP26 in patients with severely impaired spermatogenesis.
Stouffs K et al.
European Journal of Human Genetics : Ejhg, 2005
The association between mutations in ubiquitin-specific protease 26 (USP26) and male infertility: a systematic review and meta-analysis.
Li QY et al.
Asian Journal of Andrology, 0