Searching journal content for articles similar to Hon et al. 22 (2): 246.

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  1. ...than 30 years in the MPN clinical area, effects on DNA methylation have not been comprehensively studied -wide in relevant cell types, and currently there is a limited understanding about the global mechanistic effects of this agent. To gain insight into the effects of HC, gene expression analysis...
  2. ...tumors, thus paving the way for better targeted therapies for PB.Cis-regulatory elements (CREs) including promoters, enhancers, and repressors are noncoding DNA sequences harboring binding sites for transcription factors (TFs) required to activate or repress target gene expression (Ong and Corces 2011...
  3. ...expression regulation. We illustrate how DO gene expression can be27 aligned with inbred epigenetic states to identify putative cis-regulatory regions. Finally, we provide28 a data resource that documents strain-specific variation in chromatin state and DNA methylation29 in hepatocytes across nine widely...
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  4. ...relationship between cytosine modifications and the chromatin architecture of enhancers remains elusive. To gain insights into their function, 5mC and 5hmC levels were perturbed by inhibiting DNA methyltransferases and TETs during differentiation of mouse embryonal carcinoma cells into neural progenitors...
  5. ...Diagenode. A detailed protocol is described in the Supplemental Methods. Genome-wide methylation and gene expression analyses Genome-wide DNA methylation is measured by Infinium HumanMethylation450 (HM450) BeadChip array (Illumina) according to the manufacturer’s instructions. Global gene expression profiles were...
  6. ...inhibitor used for the induction of global DNA demethylation in both mammals and plants (Zhou et al. 2002). Zebularine treatment reduced overall DNA methylation levels by ∼30%, and this led to a global reduction in R-loop intensities of ∼22% (Fig. 3D; Supplemental Fig. S6C).To investigate which types of TEs...
  7. ...for this article.] A hallmark of many cancers is the decrease in 5-methylcytosine in genomic DNA relative to non-neoplastic cells or tissue, termed global hypomethylation (Feinberg and Vogelstein 1983; GamaSosa et al. 1983; Wild and Flanagan 2010). Although the degree of global hypomethylation can be severe...
  8. ...; Widschwendter et al. 2007) and is postulated to be part of a global “epigenetic switch” from Polycomb repression to DNA methylation (Gal-Yam et al. 2008; Jin et al. 2009). Indeed, the histone marks and expression levels of NP genes in DKO1 cells strongly resembled those of normal colonic mucosa (Supplemental...
  9. ...) and noncancer samples (GM12878 and H1-HESC). The chromatin ChIP-seq tracks demonstrate that the hypomethylated region is marked by cancer-specific repressive H3K27me3 and EZH2 binding (cancer = K562, HeLa, HepG2; noncancer = HMEC, GM12878, NH-A). Dynamic DNA methylation across human tissues Genome Research 559...
  10. ...-translational histone modifications, and nucleosome occupancy (Coolen et al. 2010; Taberlay and Jones 2011; Bert et al. 2013), can lead to global changes of the cancer epi coupled with associated deregulation of cancer gene expression signatures. DNA methylation currently remains the most characterized epigenetic...
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