about
Folate and DNA methylation: a review of molecular mechanisms and the evidence for folate's roleImprinted and X-linked non-coding RNAs as potential regulators of human placental functionChromatin regulators of genomic imprintingCNVs: harbingers of a rare variant revolution in psychiatric geneticsEpigenetic genome-wide association methylation in aging and longevityImprinted gene expression in hybrids: perturbed mechanisms and evolutionary implications.Oncogenic potential of yin yang 1 mediated through control of imprinted genesHigh-Throughput Analysis of Global DNA Methylation Using Methyl-Sensitive DigestionDegree of methylation of ZAC1 (PLAGL1) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort.A genome-wide survey of imprinted genes in rice seeds reveals imprinting primarily occurs in the endospermQuantitative allele-specific expression and DNA methylation analysis of H19, IGF2 and IGF2R in the human placenta across gestation reveals H19 imprinting plasticity.Resolving the variable genome and epigenome in human disease.Adolescent idiopathic scoliosis (AIS), environment, exposome and epigenetics: a molecular perspective of postnatal normal spinal growth and the etiopathogenesis of AIS with consideration of a network approach and possible implications for medical thAllele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expressionNatural variability of minimotifs in 1092 people indicates that minimotifs are targets of evolution.Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib.Importance of the matriline for genomic imprinting, brain development and behaviour.Characterization of the imprinting signature of mouse embryo fibroblasts by RNA deep sequencing.Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruptionSexual selection modulates genetic conflicts and patterns of genomic imprinting.Deregulation of small non-coding RNAs at the DLK1-DIO3 imprinted locus predicts lung cancer patient outcome.Epigenetics and the environment: emerging patterns and implications.Functions of DNA methyltransferase 3-like in germ cells and beyond.Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications.Genomic imprinting--the struggle of the genders at the molecular level.Epigenetic regulation of stemness maintenance in the neurogenic niches.BDNF/TRKB/P75NTR polymorphisms and their consequences on antidepressant efficacy in depressed patients.Non-Invasive Approaches to Epigenetic-Based Sperm Selection.The interplay between DNA methylation, folate and neurocognitive development.Genomic Imprinting and the Regulation of Postnatal Neurogenesis.
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on September 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genomic imprinting and human disease.
@en
Genomic imprinting and human disease.
@nl
type
label
Genomic imprinting and human disease.
@en
Genomic imprinting and human disease.
@nl
prefLabel
Genomic imprinting and human disease.
@en
Genomic imprinting and human disease.
@nl
P2860
P356
P1476
Genomic imprinting and human disease.
@en
P2093
Ryutaro Hirasawa
P2860
P304
P356
10.1042/BSE0480187
P50
P577
2010-09-01T00:00:00Z