Searching journal content for articles similar to Kudron et al. 34 (12): 2319.

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  1. ...of differences in gene regulation across germ layers in Drosophila embryogenesis (Cusanovich et al. 2018b), the generation of an atlas of 85 different clusters of cells from 13 different mouse tissues (Cusanovich et al. 2018a), and the identification of cell types in hippocampal tissue from mice (Sinnamon et al...
  2. ...al. 2005; Potthoff and Olson 2007; Zdobnov et al. 2020), with highly conserved DNA-binding domains (Carlsson and Mahlapuu 2002; Chang et al. 2015).View larger version: In this window In a new window Figure 1. Profiling transcription factor (TF) binding in F1 embryos of Drosophila melanogaster. (A...
  3. ...with the tissue-specific TE-CREs (Fig. 2E). We also found that tissue-specific TE-CREs were associated with tissue bias in gene expression (Fig. 2F), supporting a regulatory effect of TE-CREs.One reason for TE-CREs tending to be specific to the liver rather than the brain (Fig. 2D) could be owing to differences...
  4. ...a classical question in aging biology: Do different tissues age in the same way? Transcriptomic analysis at the bulk tissue level revealed tissue-specific features of aging in several studies (Schumacher et al. 2008; Jonker et al. 2013; Ori et al. 2015; Benayoun et al. 2019). Proteomic analysis of brain...
  5. ...to the regulation of mRNA decay may result from other binding sites for regulatory RNAs and proteins that act in specific contexts.High transcript accumulation is associated with increased mRNA stabilityThroughout C. elegans embryogenesis, many genes accumulate to high transcript levels. Although this requires high...
  6. ...the dynamism of the chromatin landscape across developmental transitions and provides a resource for future investigation into epigenetic regulatory mechanisms in germ cells.Epigenetic mechanisms are essential to correctly establish tissue-specific gene expression programs during development. At the genomic...
  7. ...expression (CV) as a metric, we considered genes in the bottom 20% of CV values to have broad ubiquitous expression and those in the top 20% to have highly regulated expression (e.g., tissue specificity). As found in C. elegans, we observed that promoters of broadly expressed genes in Drosophila...
  8. ...as a transcriptional activator, in part due to its ability to increase chromatin accessibility (Adkins et al. 2006). Like Drosophila GAF, C. elegans EOR-1 is a transcriptional activator in the Ras/ERK signaling pathway that has been suggested to also repress gene expression (Liu et al. 2011a). GAF and EOR-1 are also...
  9. ..., Scc2 in budding yeast), which is required for loading of cohesin onto chromatin (Rollins et al. 2004). Although essential for sister chromatid cohesion, Nipped-B was first identified in Drosophila melanogaster as a result of its function in gene regulation, where it was suggested to facilitate...
  10. ...accessibility, histone modifications, and gene expression in F1 embryos generated from eight Drosophila crosses at three embryonic stages, yielding a comprehensive data set of 240 samples spanning multiple regulatory layers. Genetic variation (allelic imbalance) impacts gene expression more frequently than...
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