Associated Papers
Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectives.
Wang X et al.
Reproductive Biology and Endocrinology : Rb&e, 2025
Whole-Genome Sequencing Reveals a Novel GATA2 Mutation in Lower-Grade Glioma: Bioinformatics Analysis of Functional and Therapeutic Implications.
Handoko et al.
Cancers, 2025
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
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Analysis of 29 Targeted Genes for Non-Obstructive Azoospermia: The Relationship between Genetic Testing and Testicular Histology.
Cannarella R et al.
The World Journal of Men's Health, 2023
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.
Xie C et al.
Human Reproduction Update, 2022
Alterations in synaptonemal complex coding genes and human infertility.
Zhang F et al.
International Journal of Biological Sciences, 2022
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
Autosomal single-gene disorders involved in human infertility.
Jedidi I et al.
Saudi Journal of Biological Sciences, 2018
The landscape of somatic mutation in sporadic Chinese colorectal cancer.
Liu Z et al.
Oncotarget, 2018
Human male infertility and its genetic causes.
Miyamoto T et al.
Reproductive Medicine and Biology, 2017
Mutations in Genes Coding for Synaptonemal Complex Proteins and Their Impact on Human Fertility.
Geisinger A et al.
Cytogenetic and Genome Research, 2016
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies.
Roos A et al.
Archives of Gynecology and Obstetrics, 2013
Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population.
Gurkan H et al.
Andrologia, 2013
SYCP3 mutation may not be associated with recurrent miscarriage caused by aneuploidy.
Mizutani E et al.
Human Reproduction (oxford, England), 2011
Mutations of the SYCP3 gene in women with recurrent pregnancy loss.
Bolor H et al.
American Journal of Human Genetics, 2009
Mutations of SYCP3 are rare in infertile Spanish men with meiotic arrest.
Martínez J et al.
Fertility and Sterility, 2007
[Idiopathic male infertility and partial copy deletion of DAZ gene family].
Yang Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
Azoospermia in patients heterozygous for a mutation in SYCP3.
Miyamoto T et al.
Lancet (london, England), 2003
The formation and repair of DNA double-strand breaks in mammalian meiosis.
Qu W et al.
Asian Journal of Andrology, 0