Searching journal content for articles similar to Kim et al. 35 (5): 1108.

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  1. ...contact maps in Kc167 cells contain a few hundred loops that lack CTCF, and their formation does not depend on cohesin (Rowley et al. 2019). Many nonvertebrate organisms, including Caenorhabditis elegans, lack a CTCF homolog (Heger et al. 2012). It is possible that proteins distinct from CTCF are able...
  2. ..., such as enhancers and promoters (Wray 2007; Fairfax et al. 2012; Chen et al. 2016; Cannavò et al. 2017; Abramov et al. 2021; Floc'hlay et al. 2021). However, establishing a mechanistic link between DNA sequence variation and TF binding remains challenging (Deplancke et al. 2016). Sequence variation that disrupts...
  3. ...the complexity of chromatin organization and the nuanced differences in how genomic elements interact within the nucleus (Hyle et al. 2019; Szczepińska et al. 2021; Chakraborty et al. 2023; Spracklin et al. 2023).CTCF/cohesin loopsIn addition to compartments, advancements in -wide chromatin contact mapping have...
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  4. ...satellite sequences (green), and Chromosome 1 BAC sequences (yellow) (Naish et al. 2021). Scale bar, 10 μm. (C) Arabidopsis male meiocyte at pachytene stage immunostained for the SMC3 cohesin (red) and stained for DNA (DAPI; blue) (Lambing et al. 2020). FISH was performed against the CEN178 satellite...
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  5. ...can be driven by alteration of DNA sequence specificity, protein–protein interactions (PPIs), and the expression pattern of the TF-encoding gene. All three parameters contribute to divergence within the Caenorhabditis elegans bHLH TF family (Grove et al. 2009), but it is largely unknown whether...
  6. ...-characterized epigenetic inheritance paradigms, this review will focus on epigenomic insights into the folding of the and thus will not cover DNA modifications or RNAs. Below, we introduce the general methodologies for epigenomic analysis. Then, we discuss the structural organization of the eukaryotic , starting with 3C...
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