Associated Papers
Association of Zona Pellucida Gene Variants With Female Infertility: A Retrospective Genetic Analysis.
Sa SW et al.
Bjog : an International Journal of Obstetrics and Gynaecology, 2025
ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans.
Cao G et al.
Frontiers in Genetics, 2024
Clinical and Genetic Characteristics of a Cohort with Distal Vaginal Atresia.
Kang J et al.
International Journal of Molecular Sciences, 2022
Zona Pellucida Genes and Proteins: Essential Players in Mammalian Oogenesis and Fertility.
Wassarman PM et al.
Genes, 2021
A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.
Wang J et al.
Journal of Assisted Reproduction and Genetics, 2021
Novel mutations in ZP1: Expanding the mutational spectrum associated with empty follicle syndrome in infertile women.
Wu L et al.
Clinical Genetics, 2021
[The human zona pellucida: New genetic findings].
Trocka D et al.
Medecine Sciences : M/s, 0
Genetic variations in zona pellucida glycoproteins: Implications for fertility and ART outcomes.
Rajput N et al.
Mutation Research. Reviews in Mutation Research, 0
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