Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida.
Sun L et al.
Reproductive Biomedicine Online, 2023
Identification of zona pellucida defects revealed a novel loss-of-function mutation in ZP2 in humans and rats.
Zeng J et al.
Frontiers in Endocrinology, 2023
Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.
Hou M et al.
Reproductive Sciences (thousand Oaks, Calif.), 2022
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
Jia W et al.
Journal of Assisted Reproduction and Genetics, 2022
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.
Shen Y et al.
Human Reproduction (oxford, England), 2022
Zona Pellucida Genes and Proteins: Essential Players in Mammalian Oogenesis and Fertility.
Wassarman PM et al.
Genes, 2021
A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility.
Sun Y et al.
Journal of Assisted Reproduction and Genetics, 2021
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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