Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
Single-cell RNA sequencing of human oocytes reveals a differential transcriptomic profile associated with agar-like zona pellucida.
Zhang X et al.
Journal of Ovarian Research, 2024
A heterozygous ZP2 mutation causes zona pellucida defects and female infertility in mouse and human.
Liu SL et al.
Iscience, 2023
Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.
Hou M et al.
Reproductive Sciences (thousand Oaks, Calif.), 2022
Gene mutations impede oocyte maturation, fertilization, and early embryonic development.
Fei CF et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology, 2022
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
Jia W et al.
Journal of Assisted Reproduction and Genetics, 2022
Human Zona Pellucida Glycoproteins: Binding Characteristics With Human Spermatozoa and Induction of Acrosome Reaction.
Gupta SK
Frontiers in Cell and Developmental Biology, 2021
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
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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