Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
about
Non-invasive prenatal diagnosis of fetal trisomy 21 using cell-free fetal DNA in maternal bloodLoss of the maternal H19 gene induces changes in Igf2 methylation in both cis and transChild health, developmental plasticity, and epigenetic programmingA conserved structural element in horse and mouse IGF2 genes binds a methylation sensitive factorMosaic uniparental disomy in Beckwith-Wiedemann syndrome.Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndromeBeckwith-Wiedemann syndrome in a child with chromosome 18q deletionPromoter-specific expression and imprint status of marsupial IGF2Epigenetic approaches for the detection of fetal DNA in maternal plasma.Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor.The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome.Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.Epigenetics and developmental programming of adult onset diseases.Molecular biology of Beckwith-Wiedemann syndrome.Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patients.New insights reveal complex mechanisms involved in genomic imprinting.Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques.Effect of budesonide on the methylation and mRNA expression of the insulin-like growth factor 2 and c-myc genes in mouse lung tumors.Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.Specific hypomethylated CpGs at the IGF2 locus act as an epigenetic biomarker for familial adenomatous polyposis colorectal cancer.Epigenetic modulation of DNA methylation by nutrition and its mechanisms in animals.
P2860
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P2860
Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
description
1993 nî lūn-bûn
@nan
1993 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@ast
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@en
type
label
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@ast
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@en
prefLabel
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@ast
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@en
P2093
P2860
P356
P1476
Parental allele specific methy ...... nd Beckwith-Wiedemann syndrome
@en
P2093
P2860
P304
P356
10.1136/JMG.30.5.353
P407
P577
1993-05-01T00:00:00Z