Searching journal content for articles similar to Platt et al. 27 (4): 591.

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  1. ...factors bind directly to the DNA to activate or repress transcription (Marr et al. 2021; Minnoye et al. 2021). Recent advances in sequencing technology have enabled the characterization of chromatin remodelers, nucleosome positioning, and chromatin accessibility using high-throughput assays like Ch...
  2. ...in promoters but also in distal regulatory regions. Additional analyses reveal their colocalization with the chromatin remodelers CHD6, CHD8, and EP400. In summary, SEM provides an effective platform for exploration of nonstandard nucleosome subtypes.The nucleosome is the basic packaging unit of chromatin...
  3. ...expectations for when differential gene expression should matter. Here, we collated existing data into a gene-regulatory network (GRN) and performed developmental transcriptomics across different environmental conditions, genetic backgrounds, and mutants to assess the regulatory logic of mouth-form plasticity...
  4. ...was calculated as the log2FE (Log2[average mark signal/H3 (input) signal]) and then plotted at the TSS of genes categorized by their expression level. Arrowheads indicate the position of nucleosomes at which a difference in H3K27me3 enrichment is observed between the GSC-like and CySC-like chromatin profiles...
  5. ...enriched with BRG1 (Fig. 2I). The regions that gained nucleosomes in both M-CLL and U-CLL versus NBCs had a more than threefold enrichment of BRG1 in comparison with neighboring regions (Fig. 2J). (2) The loci bound by another chromatin remodeler, CHD1, in lymphoblastoid B cells (The ENCODE Project...
  6. ...this enhancer. These results demonstrate the power of caQTLs to characterize regulatory mechanisms at GWAS loci.Chromatin accessibility quantitative trait loci (caQTLs) have successfully identified functional variants and regulatory elements at a subset of gene expression QTLs (eQTLs) and -wide association...
  7. ...lying within the IES might be more easily accessible than one outside.Besides nucleosome positioning, precise IES boundary targeting might also depend on the DNA topology, which influences protein binding and can be exploited in regulation (Baranello et al. 2012). Some ISWI family chromatin remodelers...
  8. ...chromatin loops between convergent CTCF sites (van Ruiten and Rowland 2021). The genomic positions of boundaries and dots anchor all display enrichment for cohesin by ChIP-seq. Acute depletion of CTCF leads to -wide loss of TADs and dots in Hi-C contact maps as well as a loss of cohesin ChIP-seq enrichment...
  9. ...by the TP53 (MA0106.3) or TP63 (MA0525.2) motif occurring within each ChIP-seq peak. Locations with multiple motifs were excluded from the analysis. Appropriate MNase-seq data were not available for TP73. To capture nucleosome positioning before TP53 or TP63 binding and any resultant chromatin remodeling...
  10. ..., modeling 3D chromatin organization, and predicting gene expression (Thibodeau et al. 2021; Karbalayghareh et al. 2022; Tan et al. 2023; Zhang et al. 2023; Grover et al. 2024). Although experimental assays such as FAIRE-seq (Giresi et al. 2007), DNase-seq (Song and Crawford 2010), and ATAC-seq (Buenrostro...
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