Associated Papers
ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans.
Cao G et al.
Frontiers in Genetics, 2024
Can successful pregnancy be achieved and predicted from patients with identified ZP mutations? A literature review.
Zhou J et al.
Reproductive Biology and Endocrinology : Rb&e, 2022
A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females.
Loeuillet C et al.
Clinical Genetics, 2022
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
Jia W et al.
Journal of Assisted Reproduction and Genetics, 2022
A novel gene mutation in ZP3 loop region identified in patients with empty follicle syndrome.
Zhang Z et al.
Human Mutation, 2022
A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.
Wang J et al.
Journal of Assisted Reproduction and Genetics, 2021
Novel mutations in ZP1: Expanding the mutational spectrum associated with empty follicle syndrome in infertile women.
Wu L et al.
Clinical Genetics, 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
Zona pellucida genes and proteins and human fertility.
Litscher ES et al.
Trends in Developmental Biology, 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
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