Associated Papers
ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans.
Cao G et al.
Frontiers in Genetics, 2024
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
Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida.
Luo G et al.
Journal of Assisted Reproduction and Genetics, 2020
Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome.
Liu M et al.
Journal of Assisted Reproduction and Genetics, 2020
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 mutation in the ZP1 gene and clinical implications.
Yuan P et al.
Journal of Assisted Reproduction and 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