Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Abnormal zona pellucida and follicular development in ZP1-mutant macaques.
Meng W et al.
Zoological Research, 2025
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
Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human.
Cao Q et al.
Journal of Cellular and Molecular Medicine, 2020
A novel homozygous nonsense ZP1 variant causes human female infertility associated with empty follicle syndrome (EFS).
Xu Q et al.
Molecular Genetics & Genomic Medicine, 2020
Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect.
Okutman Ö et al.
Genes, 2020
Zona pellucida genes and proteins and human fertility.
Litscher ES et al.
Trends in Developmental Biology, 2020
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation.
Zhou Z et al.
Human Genetics, 2019
[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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