Searching journal content for articles similar to Moyers et al. 33 (11): 1879.

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  1. ...of the PVT1 promoter was significant in HuH-7 cells but not in Hep G2 cells. HBV-Enh I was the core sequence for transcriptional activation of the MYC promoter (Fig. 7D–F). Analysis of the inserted HBV sequences in the gene regions revealed that the integration of HBV-Enh I could occur near the regions...
  2. ...knockdown (Fig. 6C; Supplemental Table S8), consistent with the findings of previous reports in HepG2 cells (Middleton et al. 2017). The majority (1741/1879, ∼93%) of genes with significant changes in IR showed only regulated LIRs or regulated CIRs (Fig. 6D). Although most of the genes generally possessed...
  3. ...not work alone; they cooperate and interact with each other and thus create complex transcription patterns of the (Lemon and Tjian 2000; Perez-Pinera et al. 2013; Li et al. 2014; Ang et al. 2016).Studying the collaborative patterns of TFs is a much more complicated problem than characterizing...
  4. ...through RNA polymerase III transcription factor C (TFIIIC) recruitment with subsequent altered chromatin looping and histone acetylation resulting in gene expression changes in cis (Ferrari et al. 2020). Alu RNA may also play a role in reducing transcription of RNA polymerase II (Pol II) transcripts...
  5. ...the promoter of the known HSF1 target gene, HSP90AA1 (Hickey et al. 1989), is displayed in Figure 2D. ChIP-seq reveals -wide patterns of TF binding and colocalization of PPARGC1A and its network partners Our initial ChIP-seq studies suggested that PPARGC1A functions with known and novel partners in HepG2 cells...
  6. ...development. Finally, we show that MEDEA performs well on both bulk and single-cell ATAC-seq data. MEDEA is publicly available as part of our Glossary-GENRE suite for motif enrichment analysis.In eukaryotic development, gene transcription happens in precise spatiotemporal patterns that require the specific...
  7. ...shock and non–heat shock HCT116 cells were washed with PBS before fixing with 1% formaldehyde (Sigma-Aldrich 252549) in PBS for 15 min and processing for ChIP-seq.ChIP-exo testing was initially prioritized in K562, MCF-7, and HepG2, using gene expression values (FPKM in RNA-seq) generated from...
  8. ...covering 10 TFs (CTCF, EGR1, FOXA1, FOXA2, GABPA, HNF4A, JUND, NANOG, REST, and TAF1) in 13 cell types (A549, GM12878, H1-hESC, HCT116, HeLa-S3, HepG2, iPSC, IMR-90, K562, liver, MCF-7, PANC-1, PC-3). The ChIP-seq data were downloaded from the ENCODE data portal (https...
  9. ...are prevalent in the We used two orthogonal methods to infer DAP associations across the . The first involved analysis of ENCODE ChIP-seq peaks (208, 129, 312 DAPs in the HepG2, GM12878, K562 cell lines) (Supplemental Table S1). A subset of DAPs was further classified into sequence-specific transcription...
  10. ...SA-exposed HepG2 clones are shown in Figure 5C and Supplemental Figure S12. The mutational signature of duoSA is characterized by strong peaks of T > A mutations with always either an adenine directly 3′ or a thymine directly 5′ of the mutation site. DuoSA-associated mutagenesis showed strong transcriptional...
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