Associated Papers
Novel Loss-of-function Variants of ZP3 Associated with Premature Ovarian Insufficiency.
Zhou L et al.
Reproductive Sciences (thousand Oaks, Calif.), 2024
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
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
Zona Pellucida Genes and Proteins: Essential Players in Mammalian Oogenesis and Fertility.
Wassarman PM et al.
Genes, 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
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
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
Select a paper to view details