Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology
Reference34 articles.
1. Significance of egg's zona pellucida glycoproteins in sperm-egg interaction and fertilization;Abou-Haila;Minerva Ginecol,2014
2. Exome sequencing shines in empty follicle syndrome: zona pellucida gene mutations manifest genuine empty follicle syndrome;Altaf;Fertil Steril,2021
3. Oocyte morphology does not affect fertilization rate, embryo quality and implantation rate after intracytoplasmic sperm injection;Balaban;Hum. Reprod.,1998
4. Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human;Cao;J. Cell. Mol. Med.,2020
5. A recurrent missense mutation in ZP3 causes empty follicle syndrome and female infertility;Chen;Am. J. Hum. Genet.,2017
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1. Exome sequencing in genuine empty follicle syndrome: Novel candidate genes;European Journal of Obstetrics & Gynecology and Reproductive Biology;2024-06
2. Comparative Analysis of the Ovary Transcriptome among Wanyue Black and Yorkshire Gilts Using RNA-Seq;Veterinary Sciences;2024-03-04
3. The correlation between sperm percentage with a small acrosome and unexplained in vitro fertilization failure;BMC Pregnancy and Childbirth;2024-01-11
4. Intracellular fraction of zona pellucida protein 3 is required for the oocyte-to-embryo transition in mice;Molecular Human Reproduction;2023-10-31
5. Case report: A novel homozygous variant in ZP3 is associated with human empty follicle syndrome;Frontiers in Genetics;2023-10-16
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