Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans

Ensuring meiotic DNA break formation in the mouse pseudoautosomal region

(2020) Laurent Acquaviva et al.   NATURE

USP26 deubiquitinates androgen receptor (AR) in the maintenance of sperm maturation and spermatogenesis through the androgen receptor signaling pathway

(2020) Jing Wang et al.   Advances in Clinical and Experimental Medicine

Ubiquitin-specific protease 26 (USP26) is not essential for mouse gametogenesis and fertility

(2019) Natalia Felipe-Medina et al.   CHROMOSOMA

Usp26 mutation in mice leads to defective spermatogenesis depending on genetic background

(2019) Kohei Sakai et al.   Scientific Reports

Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome

(2018) Fuxi Zhu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

(2018) Yanwei Sha et al.   BMC Medical Genetics

SHOC1 is a ERCC4-(HhH)2-like protein, integral to the formation of crossover recombination intermediates during mammalian meiosis

(2018) Michel F. Guiraldelli et al.   PLoS Genetics

Disruption of Usp26 gene causes male subfertility associated with spermatogenesis defects in mice§

(2018) Hong Tian et al.   BIOLOGY OF REPRODUCTION

Sperm recovery and ICSI outcomes in Klinefelter syndrome: a systematic review and meta-analysis

(2017) Giovanni Corona et al.   HUMAN REPRODUCTION UPDATE

USP26 functions as a negative regulator of cellular reprogramming by stabilising PRC1 complex components

(2017) Bo Ning et al.   Nature Communications

A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia

(2016) Qian Ma et al.   Reproductive Sciences

Single nucleotide polymorphisms of USP26 in azoospermic men

(2016) Alice Luddi et al.   Systems Biology in Reproductive Medicine

Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism

(2016) M. Bonomi et al.   JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

Double-strand break repair on sex chromosomes: challenges during male meiotic prophase

(2015) Lin-Yu Lu et al.   CELL CYCLE

CRISPR-Cas9-Mediated Genetic Screening in Mice with Haploid Embryonic Stem Cells Carrying a Guide RNA Library

(2015) Cuiqing Zhong et al.   Cell Stem Cell

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse

(2015) F. Yang et al.   EMBO Molecular Medicine

X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

(2015) Alexander N. Yatsenko et al.   NEW ENGLAND JOURNAL OF MEDICINE

Evidence from enzymatic and meta-analyses does not support a direct association betweenUSP26gene variants and male infertility

(2015) W. Zhang et al.   Andrology

Association of 370-371insACA, 494T>C, and 1423C>T haplotype in ubiquitin-specific protease 26 gene and male infertility: a meta-analysis

(2014) Yu-Tian Dai et al.   ASIAN JOURNAL OF ANDROLOGY

Regulation of the DNA damage response on male meiotic sex chromosomes

(2013) Lin-Yu Lu et al.   Nature Communications

Klinefelter Syndrome—A Clinical Update

(2012) Kristian A. Groth et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mouse model for men with klinefelter syndrome: a multifaceted fit for a complex disorder

(2011) Ronald S Swerdloff et al.   ACTA PAEDIATRICA

Spindle assembly checkpoint and its regulators in meiosis

(2011) Shao-Chen Sun et al.   HUMAN REPRODUCTION UPDATE

Distinct Properties of the XY Pseudoautosomal Region Crucial for Male Meiosis

(2011) L. Kauppi et al.   SCIENCE

The Pseudoautosomal Region and Sex Chromosome Aneuploidies in Domestic Species

(2011) T. Raudsepp et al.   Sexual Development

Meiotic recombination errors, the origin of sperm aneuploidy and clinical recommendations

(2011) Helen G. Tempest   Systems Biology in Reproductive Medicine

The Deubiquitinating Enzyme USP26 Is a Regulator of Androgen Receptor Signaling

(2010) A. M. G. Dirac et al.   MOLECULAR CANCER RESEARCH

Novel genetic aspects of Klinefelter's syndrome

(2010) F. Tuttelmann et al.   MOLECULAR HUMAN REPRODUCTION

Meiotic failure in male mice lacking an X-linked factor

(2008) F. Yang et al.   GENES & DEVELOPMENT

ATM Promotes the Obligate XY Crossover and both Crossover Control and Chromosome Axis Integrity on Autosomes

(2008) Marco Barchi et al.   PLoS Genetics

ZIP4H (TEX11) Deficiency in the Mouse Impairs Meiotic Double Strand Break Repair and the Regulation of Crossing Over

(2008) Carrie A. Adelman et al.   PLoS Genetics