Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
Jia W et al.
Journal of Assisted Reproduction and Genetics, 2022
Gene Spectrum and Clinical Traits of Nine Patients With Oocyte Maturation Arrest.
Huo M et al.
Frontiers in Genetics, 2022
A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.
Zhang D et al.
Journal of Assisted Reproduction and Genetics, 2021
Human Zona Pellucida Glycoproteins: Binding Characteristics With Human Spermatozoa and Induction of Acrosome Reaction.
Gupta SK
Frontiers in Cell and Developmental Biology, 2021
Cryo-EM structure of native human uromodulin, a zona pellucida module polymer.
Stsiapanava A et al.
The Embo Journal, 2020
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
[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
Select a paper to view details