Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
A novel mutation in ZP3 causes human ovulatory dysfunction and oocyte maturation arrest.
Liu Y et al.
Journal of Ovarian Research, 2025
Novel Loss-of-function Variants of ZP3 Associated with Premature Ovarian Insufficiency.
Zhou L et al.
Reproductive Sciences (thousand Oaks, Calif.), 2024
Novel mutations in TUBB8 and ZP3 cause human oocyte maturation arrest and female infertility.
Li W et al.
European Journal of Obstetrics, Gynecology, and Reproductive 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
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.
Shen Y et al.
Human Reproduction (oxford, England), 2022
A novel gene mutation in ZP3 loop region identified in patients with empty follicle syndrome.
Zhang Z et al.
Human Mutation, 2022
Gene Spectrum and Clinical Traits of Nine Patients With Oocyte Maturation Arrest.
Huo M et al.
Frontiers in Genetics, 2022
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
Cryo-EM structure of native human uromodulin, a zona pellucida module polymer.
Stsiapanava A et al.
The Embo Journal, 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
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 mutation in the ZP1 gene and clinical implications.
Yuan P et al.
Journal of Assisted Reproduction and Genetics, 2019
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation.
Zhou Z et al.
Human Genetics, 2019
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.
Chen T et al.
American Journal of Human Genetics, 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