Associated Papers
ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans.
Cao G et al.
Frontiers in Genetics, 2024
A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females.
Loeuillet C et al.
Clinical Genetics, 2022
Zona Pellucida Genes and Proteins: Essential Players in Mammalian Oogenesis and Fertility.
Wassarman PM et al.
Genes, 2021
Human Zona Pellucida Glycoproteins: Binding Characteristics With Human Spermatozoa and Induction of Acrosome Reaction.
Gupta SK
Frontiers in Cell and Developmental Biology, 2021
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
Molecular basis of egg coat cross-linking sheds light on ZP1-associated female infertility.
Nishimura K et al.
Nature Communications, 2019
Novel zona pellucida gene variants identified in patients with oocyte anomalies.
Yang P et al.
Fertility and Sterility, 2017
[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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