about
Permissive transcriptional activity at the centromere through pockets of DNA hypomethylation.DNA methylation biomarkers: cancer and beyondSmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivationAnalysis of mammalian proteins involved in chromatin modification reveals new metaphase centromeric proteins and distinct chromosomal distribution patternsWheel running and environmental enrichment differentially modify exon-specific BDNF expression in the hippocampus of wild-type and pre-motor symptomatic male and female Huntington's disease mice.Quantitative microscopy after fluorescence in situ hybridization - a comparison between repeat-depleted and non-depleted DNA probes.Postnatal stability, tissue, and time specific effects of AHRR methylation change in response to maternal smoking in pregnancyEpigenetic deregulation in pediatric acute lymphoblastic leukemia.DNA methylation-mediated down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta.Stability of gene expression and epigenetic profiles highlights the utility of patient-derived paediatric acute lymphoblastic leukaemia xenografts for investigating molecular mechanisms of drug resistance.Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndromeMeiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis.Expression discordance of monozygotic twins at birth: effect of intrauterine environment and a possible mechanism for fetal programming.Transcription within a functional human centromere.Maternal vitamin D predominates over genetic factors in determining neonatal circulating vitamin D concentrations.Evaluation of microRNA expression in patient bone marrow aspirate slides.Human active X-specific DNA methylation events showing stability across time and tissuesValidation of DNA methylation biomarkers for diagnosis of acute lymphoblastic leukemia.International network of twin registries (INTR): building a platform for international collaboration.Prospects for epigenetic epidemiology.The establishment of DOHaD working groups in Australia and New Zealand.Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence.Kiss and break up--a safe passage to anaphase in mitosis and meiosis.DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adultsGenome-scale case-control analysis of CD4+ T-cell DNA methylation in juvenile idiopathic arthritis reveals potential targets involved in disease.Going back to the future with Guthrie-powered epigenome-wide association studies.The chromosomal distribution of CpG islands in the mouse: evidence for genome scrambling in the rodent lineage.Removal of repetitive sequences from FISH probes using PCR-assisted affinity chromatography.Placenta-specific methylation of the vitamin D 24-hydroxylase gene: implications for feedback autoregulation of active vitamin D levels at the fetomaternal interface.Wide-ranging DNA methylation differences of primary trophoblast cell populations and derived cell lines: implications and opportunities for understanding trophoblast function.Copy number variation and mosaicism.Analysis of epigenetic changes in survivors of preterm birth reveals the effect of gestational age and evidence for a long term legacy.Intersections of epigenetics, twinning and developmental asymmetries: insights into monogenic and complex diseases and a role for 3D facial analysis.DNA methylation and miRNA expression profiling in childhood B-cell acute lymphoblastic leukemia.Effects of early-life environment and epigenetics on cardiovascular disease risk in children: highlighting the role of twin studies.The utility of dried blood spots for proteomic studies: looking forward to looking back.Nutritional influences on epigenetic programming: asthma, allergy, and obesity.A 330 kb CENP-A binding domain and altered replication timing at a human neocentromere.A rapid method of genomic array analysis of scaffold/matrix attachment regions (S/MARs) identifies a 2.5-Mb region of enhanced scaffold/matrix attachment at a human neocentromere.A distinct DNA methylation signature defines pediatric pre-B cell acute lymphoblastic leukemia.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Craig JM
@ast
Craig JM
@es
Craig JM
@sl
Jeffrey M. Craig
@en
type
label
Craig JM
@ast
Craig JM
@es
Craig JM
@sl
Jeffrey M. Craig
@en
altLabel
Craig J
@en
Craig JM
@en
prefLabel
Craig JM
@ast
Craig JM
@es
Craig JM
@sl
Jeffrey M. Craig
@en
P108
P1053
B-3484-2012
P106
P108
P21
P31
P3829
P496
0000-0003-3979-7849