RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/23690138http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23690138http://www.w3.org/2000/01/rdf-schema#comment"Neural tube defects (NTDs) are serious congenital malformation of fusion failure of the neural tube during early embryogenesis. DNA methylation disorders have been found in NTD-affected fetuses, and are correlated to the risk of NTDs. The insulin-like growth factor 2 (IGF2) gene, maternally imprinted, has a key role in fetal development. IGF2 transcription is partly controlled by differentially methylated regions (DMRs) 0 and 2. To assess whether disturbed methylation pattern increases the incidence of NTDs, we employed matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) to quantify CpG methylation levels of DMR2 and 0 in fetuses with or without NTDs. We found that the methylation level of IGF2 DMR0 increased significantly in the brain tissues of NTD-affected fetuses. And hypermethylation of DMR0 was associated with an increased risk of NTDs, with an odds ratio of 5.375 (95 % CI: 1.447-19.965; p = 0.007). IGF2 mRNA expression was negatively correlated with the methylation level of DMR0 (R (2) = 0.893; p = 0.000) in HCT15 cells. These results highlights that IGF2 DMR0 hypermethylation is a potential risk factor of NTD, and IGF2 gene is a promising candidate gene to study for a greater understanding of the cause of NTDs."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.org/dc/terms/identifier"doi:10.1007/s11010-013-1655-1"xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Chang S."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Guo J."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Lu X."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Guo J.'"xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Zhang Q."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Wang J."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Zhao H."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Wang Z."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Zhang T."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Wang F."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Wang L."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Wu L."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Niu B."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/author"Shangguan S."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/name"Mol Cell Biochem"xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/pages"33-42"xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/title"Altered methylation of IGF2 DMR0 is associated with neural tube defects."xsd:string
http://purl.uniprot.org/citations/23690138http://purl.uniprot.org/core/volume"380"xsd:string
http://purl.uniprot.org/citations/23690138http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23690138
http://purl.uniprot.org/citations/23690138http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23690138
http://purl.uniprot.org/uniprot/#_B2MUX6-mappedCitation-23690138http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23690138