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  1. ...Dynamic barriers modulate cohesin positioning and folding at fixed occupancy Hadi Rahmaninejad, Yao Xiao, Maxime M.C. Tortora and Geoffrey Fudenberg Department of Quantitative and Computational Biology, University of Southern California, Los Angeles, California 90089, USA Corresponding authors...
  2. ...://hgdownload.soe.ucsc.edu/goldenPath/hg19/database/ cpgIslandExt.txt.gz). Heatmap representations of ChIP-seq, MeDIP-seq, and GRO-seq tag densities were generated by summing the total number of tags in 20-bp bins for 3 kb to either side of the TSS or from the midpoint of the CGI domain and visualized with Java Treeview v.1.1.6. To compare...
  3. ...are available for predicting the presence of CpG islands in DNA sequences. Examples include the CpGplot tool from the European Molecular Biology Open Software Suite (EMBOSS) (Rice et al. 2000), the CpG Island Searcher (Takai and Jones 2003), CpGProD (Ponger and Mouchiroud 2002), and CpGPAP (Chuang et al. 2012...
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  4. ...in MCF-7. (E) A model demonstrating the relationship of ZFX to other components of CpG island promoter structure. ZFX binds at +240 bp in the nucleosome-depleted region of CpG island promoters, between the general transcription preinitiation complex (PIC) and the first nucleosome in the transcribed...
  5. ..., SOX10, TCF4, ETS1, SREBF1, CEBPB, KLF2, and ETV5) were higher in either skeletal muscle or heart nonmyelinating Schwann cells. Analysis of the transcription regulatory programs by the SCENIC software predicted that FOXO1 (and YY1) could regulate XIST in heart and skeletal muscle Schwann cells...
  6. ...of RNAPII complexes. Notably, ZC3H4, a component of the restrictor complex involved in transcription termination of early nonproductive elongation (Estell et al. 2023; Rouvière et al. 2023), showed a negative correlation between its enrichment along the gene body occupancy and RNAPII elongation rates (Fig...
  7. ...Gs in the are methylated, DNA methylation is absent or reduced in regions bound by transcription factors such as in CpG islands, gene promoters, and distal regulatory elements (Stadler et al. 2011; Hon et al. 2013; Ziller et al. 2013). This observation led to the proposal that DNA methylation may limit transcription...
  8. ...of DNA to transcription factors. It is catalyzed by ATP-dependent chromatin remodeling complexes such as the SWI/SNF and NuRD remodelers, both of which bind to numerous common target gene promoters as revealed by the chromatin occupancy profiles of their ATPase subunits (BRG1–SWI/SNF and CHD4–Nu...
  9. ...the activation domain of the transcriptional activator Gal4 that binds in their shared promoter (Lohr et al. 1995; Platt and Reece 1998). Accordingly, when we deleted GAL80, we observed a significant gain of TF occupancy at the GAL1-10 promoter and a decrease in nucleosome occupancy in both gene bodies...
  10. ..., North Carolina 27708, USA Corresponding author: amink@cs.duke.eduAbstractOver a thousand different transcription factors (TFs) bind with varying occupancy across the human . Chromatin immunoprecipitation (ChIP) can assay occupancy -wide, but only one TF at a time, limiting our ability to comprehensively...
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