A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.
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Environmental Influences on Genomic ImprintingAltered gene expression in human placentas after IVF/ICSIIn utero exposures to environmental organic pollutants disrupt epigenetic marks linked to fetoplacental developmentHigh-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.Epigenetics in the placenta.Maternal bias and escape from X chromosome imprinting in the midgestation mouse placenta.Developmental origins of child mental health disorders.Quantitative allele-specific expression and DNA methylation analysis of H19, IGF2 and IGF2R in the human placenta across gestation reveals H19 imprinting plasticity.Methylation allelic polymorphism (MAP) in chorionic gonadotropin beta5 (CGB5) and its association with pregnancy success.DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation.The human placental methylomePlacenta-imprinted gene expression association of infant neurobehavior.MethPat: a tool for the analysis and visualisation of complex methylation patterns obtained by massively parallel sequencing.Imprinted gene expression in fetal growth and developmentUsing RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta.DNA methylation in the human placenta and fetal growth (review).Pyrosequencing for accurate imprinted allele expression analysisThe prevalence of loss of imprinting of H19 and IGF2 at birth.Inactive X chromosome-specific reduction in placental DNA methylation.Placental pseudo-malignancy from a DNA methylation perspective: unanswered questions and future directions.Demonstration of all-or-none loss of imprinting in mRNA expression in single cells.Pyrosequencing for the rapid and efficient quantification of allele-specific expressionEpigenetics and the placenta.DNA methylation profiling highlights the unique nature of the human placental epigenome.Neurodevelopmental consequences in offspring of mothers with preeclampsia during pregnancy: underlying biological mechanism via imprinting genes.Allelic Imbalance in TOR1A mRNA Expression in Manifesting and Non-Manifesting Carriers of the GAG-Deletion.Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.Genomic imprinting and conflict-induced decanalization.The dysfunctional placenta epigenome: causes and consequences.Prenatal Depression and Infant Temperament: The Moderating Role of Placental Gene Expression
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P2860
A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 07 September 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A sensitive functional assay r ...... imprinting in human placenta.
@en
A sensitive functional assay r ...... imprinting in human placenta.
@nl
type
label
A sensitive functional assay r ...... imprinting in human placenta.
@en
A sensitive functional assay r ...... imprinting in human placenta.
@nl
prefLabel
A sensitive functional assay r ...... imprinting in human placenta.
@en
A sensitive functional assay r ...... imprinting in human placenta.
@nl
P2093
P2860
P356
P1433
P1476
A sensitive functional assay r ...... imprinting in human placenta.
@en
P2093
Andreas I Diplas
James Wetmur
Luca Lambertini
Men-Jean Lee
Rhoda Sperling
P2860
P304
P356
10.4161/EPI.3.5.6755
P577
2008-09-07T00:00:00Z