Related references
Note: Only part of the references are listed.Mutations in ZP4 are associated with abnormal zona pellucida and female infertility
Xiaoli Wei et al.
JOURNAL OF CLINICAL PATHOLOGY (2022)
Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report
Karim Arafah et al.
HUMAN REPRODUCTION (2021)
A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation
Dazhi Zhang et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2021)
Novel ZP1 pathogenic variants identified in an infertile patient and a successful live birth following ICSI treatment
Kun Chu et al.
CLINICAL GENETICS (2020)
Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect
Ozlem Okutman et al.
GENES (2020)
Diversity of RNA-Binding Proteins Modulating Post-Transcriptional Regulation of Protein Expression in the Maturing Mammalian Oocyte
Marie Christou-Kent et al.
CELLS (2020)
A novel homozygous nonsense ZP1 variant causes human female infertility associated with empty follicle syndrome (EFS)
Qianhua Xu et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2020)
Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome
Mohan Liu 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
Qiqi Cao et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2020)
Novel mutations inZP1andZP2cause primary infertility due to empty follicle syndrome and abnormal zona pellucida
Geng Luo et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2020)
Novel mutation in the ZP1 gene and clinical implications
Ping Yuan et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2019)
Genetics of human female infertility
Svetlana A. Yatsenko et al.
BIOLOGY OF REPRODUCTION (2019)
Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters
Ling Sun et al.
HUMAN MUTATION (2019)
Mutation analysis of ZP1, ZP2, ZP3 and ZP4 genes in 152 Han Chinese samples with ovarian endometriosis
Yang Zou et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2019)
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility
Qing Sang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
fastp: an ultra-fast all-in-one FASTQ preprocessor
Shifu Chen et al.
BIOINFORMATICS (2018)
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Marie Christou-Kent et al.
EMBO MOLECULAR MEDICINE (2018)
Novel mutations in PATL2 cause female infertility with oocyte germinal vesicle arrest
Lingli Huang et al.
HUMAN REPRODUCTION (2018)
Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development
C. Chen et al.
HUMAN REPRODUCTION (2018)
Strelka2: fast and accurate calling of germline and somatic variants
Sangtae Kim et al.
NATURE METHODS (2018)
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility
Zine-Eddine Kherraf et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Novel zona pellucida gene variants identified in patients with oocyte anomalies
Ping Yang et al.
FERTILITY AND STERILITY (2017)
Empty follicle syndrome revisited: definition, incidence, aetiology, early diagnosis and treatment
Alberto Revelli et al.
REPRODUCTIVE BIOMEDICINE ONLINE (2017)
Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest
Biaobang Chen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility
Tailai Chen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
The Galectin-9/Tim-3 pathway is involved in the regulation of NK cell function at the maternal-fetal interface in early pregnancy
Yan-Hong Li et al.
CELLULAR & MOLECULAR IMMUNOLOGY (2016)
Mutations in TUBB8 and Human Oocyte Meiotic Arrest
Ruizhi Feng et al.
NEW ENGLAND JOURNAL OF MEDICINE (2016)
The Ensembl Variant Effect Predictor
William McLaren et al.
GENOME BIOLOGY (2016)
Oocyte maturation: gamete-somatic cells interactions, meiotic resumption, cytoskeletal dynamics and cytoplasmic reorganization
Giovanni Coticchio et al.
HUMAN REPRODUCTION UPDATE (2015)
SAMBLASTER: fast duplicate marking and structural variant read extraction
Gregory G. Faust et al.
BIOINFORMATICS (2014)
Mutant ZP1 in Familial Infertility
Hua-Lin Huang et al.
NEW ENGLAND JOURNAL OF MEDICINE (2014)
Fine Characterisation of a Recombination Hotspot at the DPY19L2 Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population
Charles Coutton et al.
PLOS GENETICS (2013)
Influence of the zona pellucida of the mouse egg on folliculogenesis and fertility
Paul M. Wassarman et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2012)
Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome
Kemal O. Yariz et al.
FERTILITY AND STERILITY (2011)
Insights into Egg Coat Assembly and Egg-Sperm Interaction from the X-Ray Structure of Full-Length ZP3
Ling Han et al.
CELL (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Zona pellucida glycoproteins
Paul M. Wassarman
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility
Klaus Dieterich et al.
NATURE GENETICS (2007)
Association between sequence variations in genes encoding human zona pellucida glycoproteins and fertilization failure in IVF
M Männikkö et al.
HUMAN REPRODUCTION (2005)
Comparative recombination rates in the rat, mouse, and human genomes
MI Jensen-Seaman et al.
GENOME RESEARCH (2004)