Low frequency of imprinting defects in ICSI children born small for gestational age.
about
The human retinoblastoma gene is imprinted.DNA methylation errors at imprinted loci after assisted conception originate in the parental spermNo evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age.Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study.A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeA systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously.Dynamic expression patterns of imprinted genes in human embryonic stem cells following prolonged passaging and differentiation.Assisted reproduction treatment and epigenetic inheritance.Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques.The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders.DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome.DNA methylation signatures in cord blood of ICSI children.Epigenetic status in the offspring of spontaneous and assisted conception.Altered methylations of H19, Snrpn, Mest and Peg3 are reversible by developmental reprogramming in kidney tissue of ICSI-derived mice.Genomic imprinting, small babies and assisted reproduction.Abnormal methylation of KCNQ1OT1 and differential methylation of H19 imprinting control regions in human ICSI embryos.Imprinting alterations in sperm may not significantly influence ART outcomes and imprinting patterns in the cord blood of offspring.Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer.
P2860
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P2860
Low frequency of imprinting defects in ICSI children born small for gestational age.
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Low frequency of imprinting defects in ICSI children born small for gestational age.
@ast
Low frequency of imprinting defects in ICSI children born small for gestational age.
@en
Low frequency of imprinting defects in ICSI children born small for gestational age.
@nl
type
label
Low frequency of imprinting defects in ICSI children born small for gestational age.
@ast
Low frequency of imprinting defects in ICSI children born small for gestational age.
@en
Low frequency of imprinting defects in ICSI children born small for gestational age.
@nl
prefLabel
Low frequency of imprinting defects in ICSI children born small for gestational age.
@ast
Low frequency of imprinting defects in ICSI children born small for gestational age.
@en
Low frequency of imprinting defects in ICSI children born small for gestational age.
@nl
P2093
P2860
P356
P1476
Low frequency of imprinting defects in ICSI children born small for gestational age.
@en
P2093
Bernhard Horsthemke
Deniz Kanber
Michael Ludwig
Michael Zeschnigk
P2860
P2888
P356
10.1038/EJHG.2008.177
P577
2008-10-22T00:00:00Z