Associated Papers
The RAD51 paralogue HvXRCC2 affects meiosis and recombination in barley.
Colas I et al.
Journal of Experimental Botany, 2025
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
The role of RAD51 regulators and variants in primary ovarian insufficiency, endometriosis, and polycystic ovary syndrome.
Witham M et al.
Nar Molecular Medicine, 2024
RAD51 and Infertility: A Review and Case-Control Study.
Sahota JS et al.
Biochemical Genetics, 2024
Positive and negative regulators of RAD51/DMC1 in homologous recombination and DNA replication.
Ito M et al.
Dna Repair, 2024
Pathogenic variants in human DNA damage repair genes mostly arose after the latest human out-of-Africa migration.
He J et al.
Frontiers in Genetics, 2024
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Landscape of pathogenic mutations in premature ovarian insufficiency.
Ke H et al.
Nature Medicine, 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
Distinct landscapes of deleterious variants in DNA damage repair system in ethnic human populations.
Qin Z et al.
Life Science Alliance, 2022
Fanconi Anemia Gene Variants in Patients with Gonadal Dysfunction.
Daum H et al.
Reproductive Sciences (thousand Oaks, Calif.), 2022
Genetics of Azoospermia.
Cioppi F et al.
International Journal of Molecular Sciences, 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C et al.
Frontiers in Cell and Developmental Biology, 2021
Germline Profiling and Molecular Characterization of Early Onset Metastatic Colorectal Cancer.
Xu T et al.
Frontiers in Oncology, 2020
XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans.
Zhang YX et al.
Clinical Genetics, 2019
XRCC2 mutation causes meiotic arrest, azoospermia and infertility.
Yang Y et al.
Journal of Medical Genetics, 2018