Inactive X chromosome-specific reduction in placental DNA methylation.
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Recent progress towards understanding the role of DNA methylation in human placental developmentPrenatal exposure to mixtures of xenoestrogens and repetitive element DNA methylation changes in human placentaRegulation of TIMP-1 in Human Placenta and Fetal Membranes by lipopolysaccharide and demethylating agent 5-aza-2'-deoxycytidinePlacental methylome analysis from a prospective autism studyEndogenous Retroviruses: With Us and against UsImproved reporting of DNA methylation data derived from studies of the human placenta.DNA methylation-mediated down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta.DNA methylation is globally disrupted and associated with expression changes in chronic obstructive pulmonary disease small airwaysParental ages and levels of DNA methylation in the newborn are correlated.Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expressionExtensive epigenetic reprogramming in human somatic tissues between fetus and adultChromosome-wide DNA methylation analysis predicts human tissue-specific X inactivationGenome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies.Differentially methylated CpG island within human XIST mediates alternative P2 transcription and YY1 binding.A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N)The human placental methylomeEarly Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas.DNA methylation signatures in development and aging of the human prefrontal cortex.Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation.Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.Different measures of "genome-wide" DNA methylation exhibit unique properties in placental and somatic tissues.Targeting of >1.5 Mb of human DNA into the mouse X chromosome reveals presence of cis-acting regulators of epigenetic silencing.The human placenta methylomePlacental Hypomethylation Is More Pronounced in Genomic Loci Devoid of Retroelements.DNA methylation profiling highlights the unique nature of the human placental epigenome.Genome-wide oxidative bisulfite sequencing identifies sex-specific methylation differences in the human placenta.Truncation of MIMT1 gene in the PEG3 domain leads to major changes in placental gene expression and stillbirth in cattle.The Genes of Life and Death: A Potential Role for Placental-Specific Genes in Cancer: Active retrotransposons in the placenta encode unique functional genes that may also be used by cancer cells to promote malignancy.Genome-wide analysis of DNA methylation in human amnion.
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Inactive X chromosome-specific reduction in placental DNA methylation.
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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 July 2009
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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
Inactive X chromosome-specific reduction in placental DNA methylation.
@en
Inactive X chromosome-specific reduction in placental DNA methylation.
@nl
type
label
Inactive X chromosome-specific reduction in placental DNA methylation.
@en
Inactive X chromosome-specific reduction in placental DNA methylation.
@nl
prefLabel
Inactive X chromosome-specific reduction in placental DNA methylation.
@en
Inactive X chromosome-specific reduction in placental DNA methylation.
@nl
P2093
P2860
P356
P1476
Inactive X chromosome-specific reduction in placental DNA methylation.
@en
P2093
Joslynn G Affleck
Luana Avila
Maria S Penaherrera
Wendy P Robinson
P2860
P304
P356
10.1093/HMG/DDP299
P577
2009-07-07T00:00:00Z