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  1. ...integration provides a saturated profile of target activity in Schizosaccharomyces pombe. Genome Res 20: 239–248. doi:10.1101/gr.099648.109 ↵Harris MA, Lock A, Bahler J, Oliver SG, Wood V. 2013. FYPO: the fission yeast phenotype ontology. Bioinformatics 29: 1671–1678. doi:10.1093/bioinformatics/btt266...
  2. ...relevant cell signaling. Exponentially growing S. pombe cells were treated with 10 mM caffeine for 15 min (Fig. 6B), which elicits a cellular response similar to nitrogen starvation (Rallis and Bahler 2013). Gene expression and splicing profiles were quantified by nRNA-seq and cytoplasmic mRNA-seq in three...
  3. ...for gene regulation and proper Pol II activity. Histone marks (H3K4me3, H3K9ac, H3K27me3) reveal no narrow peaks but broad domains along gene bodies, whereas intergenic regions are devoid of nucleosomes. Our data implicate H3K4me3 levels inside ORFs to be the main factor associated with gene expression...
  4. ...was performed with TRIzol (Invitrogen). The total RNA samples were snap-frozen in liquid nitrogen and stored at −80°C. RNA samples were quantified and evaluated for quality and using the Bioanalyzer 2100 (Agilent Technologies). Five micrograms of total RNA was isolated from each sample. Two biological...
  5. .... 2014). In contrast to thewell-establishedDhh1 repressing functions, we and others have found that Dhh1 activates translation of viral RNA s. By using amodel system that allows the replication of the plant Brome mosaic virus (BMV) in yeast, we have previously shown that Dhh1 depletion dramatically...
  6. ...hotspots occur most often at most transcriptional promoters and associated nucleosome-depleted regions (NDRs) (Pan et al. 2011), while in fission yeast and mice, DSB hotspots are generally much farther apart and are infrequently promoter associated (Cromie et al. 2007; Smagulova et al. 2011). Hotspots...
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