Searching journal content for articles similar to Edwards et al. 20 (7): 972.

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  1. ...of chromatin looping (Davidson et al. 2019; Gabriele et al. 2022). An integrated analysis of stripes with genomic and epigenomic features at a -wide scale also shows vast potential in understanding the cooperation between regulatory elements in 3D space (Barrington et al. 2019; Kraft et al. 2019; Zhang et al...
  2. ...contribution to neurodevelopment. We begin by defining several features of chromatin architecture, including the interplay between histone modifications, DNA methylation, and 3D organization. In the context of neurodevelopment, the dramatic alterations throughout normal neurodevelopment highlight...
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  3. ...Francisco, San Francisco, California 94158, USA; 3Chan-Zuckerberg Biohub, San Francisco, California 94158, USA Corresponding author: kpollard@gladstone.ucsf.eduAbstractChromatin interactions and linkage disequilibrium (LD) are both pairwise measurements between genomic loci that show block patterns along...
  4. ...-throughput genomic technologies to study DNA methylation profiles in cancer cells has demonstrated that DNA hypomethylation preferentially affects large chromatin blocks exhibiting gene expression variability and definite chromatin features ( Hansen et al. 2011 ; Berman et al. 2012 ; Hon et al. 2012 ; Timp et al...
  5. ...associated with seedling tissue. (B) Seedling-specific and callus-specific DH sites within promoters showed higher levels of methylation than the average of all seedling DH sites within promoters. Randomly selected 3061 DH sites within promoters were used as a control. Open chromatin maps of rice Genome...
  6. ...more broadly distributed, with most occurring within CpG islands or CpG island ‘‘shores,’’ but many without (Supplemental Fig. 6), consistent with these loci having significant average preexisting methylation. Analysis of chromatin immunoprecipitation and massively parallel sequencing (ChIP-seq) data...
  7. ...chromatin organization and methylation, such relationships can be explored systematically. As well-defined surrogates for heterochromatin, we tested the relationship between DNA replication timing and DNase hypersensitivity with cytosine methylation in two human cell types, unexpectedly finding the later...
  8. ...gene across multiple TADs (Schertzer et al. 2019). However, this deposition is not uniform along the domain, suggesting that genomic features contribute to the mechanism by which these lncRNAs silence their target genes. The observation that Airn expression is accompanied by changes in 3D chromatin...
  9. ..., Fu Y, Su T, Hibshoosh H, et al. 2010. Chromatin and sequence features that define the fine and gross structure of genomic methylation patterns. Genome Res 20: 972–980. Elsik CG, Tellam RL, Worley KC, Gibbs RA, Muzny DM, Weinstock GM, Adelson DL, Eichler EE, Elnitski L, Guigo R, et al. 2009...
  10. ...barriers across the . However, recent in vivo measurements present a puzzle: reported CTCF residence times on chromatin are in the range of a few minutes, whereas cohesin lifetimes are much longer. Can the observed features of folding result from relatively transient barriers? To address this question, we...
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