Associated Papers
Genetic control of meiosis surveillance mechanisms in mammals.
Huang Y et al.
Frontiers in Cell and Developmental Biology, 2023
36910159 (PubMed )
Supplement: DataSheet2.PDF
The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review.
Allouch A et al.
Frontiers in Endocrinology, 2023
Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency.
Sirchia F et al.
Journal of Assisted Reproduction and Genetics, 2022
Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.
Mei L et al.
Molecular Medicine Reports, 2022
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Primary ovarian insufficiency, meiosis and DNA repair.
Veitia RA
Biomedical Journal, 2020
GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families.
Schubert S et al.
Genes & Cancer, 2017
No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency.
Norling A et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2014
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.
Zangen D et al.
American Journal of Human Genetics, 2011
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