Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
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Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometryThe role and interaction of imprinted genes in human fetal growthFrequent loss of imprinting of IGF2 and MEST in lung adenocarcinomaAn imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoaChromosomal DNA demethylation specified by protein bindingInduction and maintenance of nonsymmetrical DNA methylation in Neurospora.Human imprinted chromosomal regions are historical hot-spots of recombination.Widespread epigenetic abnormalities suggest a broad DNA methylation erasure defect in abnormal human sperm.Insulin gene expression is regulated by DNA methylationCancer epigenetics: a brief review.Loss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells.Analysis of DNA methylation acquisition at the imprinted Dlk1 locus reveals asymmetry at CpG dyadsMetakaryotic stem cell nuclei use pangenomic dsRNA/DNA intermediates in genome replication and segregation.Early demethylation of non-CpG, CpC-rich, elements in the myogenin 5'-flanking region: a priming effect on the spreading of active demethylation.Impact of DNA methylation on trophoblast function.Covalent genomic DNA modification patterns revealed by denaturing gradient gel blotsTransgenerational glucose intolerance with Igf2/H19 epigenetic alterations in mouse islet induced by intrauterine hyperglycemia.Placental 5-methylcytosine and 5-hydroxymethylcytosine patterns associate with size at birth.Single-base resolution of mouse offspring brain methylome reveals epigenome modifications caused by gestational folic acid.Protein binding protects sites on stable episomes and in the chromosome from de novo methylation.Down-regulation of achaete-scute complex homolog 1 (ASCL1) in neuroblastoma cells induces up-regulation of insulin-like growth factor 2 (IGF2).A methylated oligonucleotide inhibits IGF2 expression and enhances survival in a model of hepatocellular carcinomaTissue-specific DNA methylation profiles in newborns.Impairment of IGF2 gene expression in prostate cancer is triggered by epigenetic dysregulation of IGF2-DMR0 and its interaction with KLF4.Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.DNA methylation of imprinted loci of autosomal chromosomes and IGF2 is not affected in Parkinson's disease patients' peripheral blood mononuclear cells.Specific hypomethylated CpGs at the IGF2 locus act as an epigenetic biomarker for familial adenomatous polyposis colorectal cancer.Epigenetic Mechanisms in Cancer Formation and ProgressionA Loss of Insulin-like Growth Factor-2 Imprinting Is Modulated by CCCTC-binding Factor Down-regulation at Senescence in Human Epithelial CellsAssociations between the maternal circulating lipid profile in pregnancy and fetal imprinted gene alleles: a cohort study
P2860
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P2860
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
@en
type
label
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
@en
prefLabel
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
@en
P2093
P356
P1433
P1476
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
@en
P2093
Hoffman AR
P304
P356
10.1006/GENO.1999.6094
P577
2000-03-01T00:00:00Z