Searching journal content for articles similar to Luu et al. 23 (12): 2013.

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  1. ...that the different patterns of PTM enrichment between the three LAD clusters could affect their three-dimensional organization within the nucleus. We performed 3D DNA FISH to test whether the association with the nuclear lamina varies between clusters, using Lamin A/C staining to visualize the nuclear periphery (Fig...
  2. ...events detected were likely background noise. Given the proposed role of DNA methylation within gene bodies in exon definition, we looked at inclusion levels of differentially spliced exons and introns in WT seedlings. If mCG was a mark for a region to be included in the final transcript, we would...
  3. ...). The chromatin context also affects TF binding, as many consensus sites may be inaccessible owing to histone-bound heterochromatin (Zhu et al. 2018). Chromatin openness strongly correlates with TF binding potential (Thurman et al. 2012), and DNA methylation and local DNA shape also influence binding (Yin et al...
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  4. ...and Xie 2020). In mice, DNA methylation and histone modifications transmitted from parental germ cells are globally reset in early embryos. However, some modifications are known to persist and play essential roles in later development (Xia and Xie 2020). Such examples include DNA methylation at specific...
  5. ...different Nanopore chemistries using guided hypotheses. This work will facilitate comparison among Nanopore data cohorts derived using different chemistries from large-scale sequencing efforts, such as the NIH CARD Long Read Initiative.DNA methylation is an epigenetic mechanism that most commonly involves...
  6. ...from enriched signals of RNA-seq and H3K36me3, a histone mark for transcription elongation (Fig. 3B). Like in the above analysis of Morton's neuroma data, we again found that RNA-seq reads exhibited a significantly greater bias to exon 6 (vs. exon 1) in the male nerve samples compared with the male...
  7. ...-induced DNA damage (Andrade-Lima et al. 2015; Williamson et al. 2017; Cugusi et al. 2022). In addition, dysregulated transcriptional elongation has been implicated in developmental defects as well as disease and aging (Aoi and Shilatifard 2023; Debès et al. 2023).RNAPII elongation rates not only reflect...
  8. ...(TFs) to specific DNA sequences 36 to either activate or repress target gene expression. This regulation directs crucial cellular processes 37 such as differentiation, proliferation, and responses to environmental stimuli. The emergence of 38 high-throughput sequencing, particularly in transcriptomics...
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  9. ...aging. These include changes in DNA methylation, histone modifications, chromatin remodeling, and noncoding RNAs. Collectively, such alterations disrupt gene regulatory networks, leading to transcriptional dysregulation, loss of cellular homeostasis, and increased vulnerability to age-related diseases...
  10. ...24 0 to 8 hours) integrates over 250 paired transcriptome and proteome measurements. We 25 observe upregulation of known DNA repair proteins as well as a global dynamic response of 26 not yet characterized transcripts and proteins. Using artificial neural networks, we classify 27 different expression...
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