Searching journal content for articles similar to Wang et al. 26 (11): 1544.

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  1. ...response and inappropriate repair. In the budding yeast Saccharomyces cerevisiae, these include Rap1 and its cofactors Rif1/Rif2, which are bound to double-stranded DNA (dsDNA) in numbers roughly proportional to TL (Marcand et al. 1997; Levy and Blackburn 2004). In addition, owing to the incomplete...
  2. ..., Chovanec M. 2007. DNA interstrand cross-link repair in 523 saccharomyces cerevisiae. FEMS Microbiol Rev 31: 109–33. 524 Li X, Heyer W-D. 2008. Homologous recombination in DNA repair and DNA damage 525 tolerance. Cell Res 18: 99–113. 526 Li Z, Pearlman AH, Hsieh P. 2016. DNA mismatch repair and the DNA...
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  3. ...sample originating from a 10-cm dish).Total RNA was extracted using TRIzol according to the manufacturer's instructions with an additional chloroform cleanup prior to isopropanol precipitation. For U2OS samples, 20 μg of total RNA were spiked in with 0.2 μg of yeast spike-ins (Saccharomyces cerevisiae W...
  4. ...yeast Saccharomyces cerevisiae before human domestication remain poorly understood. Taiwan is regarded as part of this yeast's geographic birthplace, where the most divergent natural lineage was discovered. Here, we extensively sampled the broadleaf forests across this continental island to probe...
  5. ...et al. 2020). In this study, we explore the transitions in and out of quiescence in budding yeast, aiming to understand how the adapts to environmental changes.Saccharomyces cerevisiae undergoes a number of metabolic transitions, favoring glucose fermentation in rich medium and activating alternative...
  6. ...(Saccharomyces cerevisiae) nucleosome (White et al. 2001). Although C4 atoms in most cytosine bases had zero SASA, a subset had a non-zero SASAC4 (Supplemental Fig. S10A), indicating that there are significant differences in C4 solvent accessibility depending upon the location of the cytosine base within...
  7. ...-validating approaches to measure absolute nucleosome occupancy across the Saccharomyces cerevisiae via restriction enzymes and DNA methyltransferases. The resulting high-resolution (9-bp) map shows uniform absolute occupancies. Most nucleosome positions are occupied in most cells: 97% of all nucleosomes called...
  8. .... The second approach consisted in generating a “superaccuracy” RNA basecalling model (“SUP” model) (see Supplemental Table S1), based on the latest CTC-CRF (bonito) DNA model architecture, achieving 96% accuracy for DNA basecalling, which we reasoned should show increased basecalling accuracy for RNA (see...
  9. ...in response to various environmental stimuli in a classic model organism Saccharomyces cerevisiae has not been systematically investigated. In this study, we generated quantitative maps of transcription start sites (TSSs) at a single-nucleotide resolution for S. cerevisiae grown in nine different conditions...
  10. ...transferExperimental evidence has indicated that mtDNA escape is independent of RNA intermediates in yeast (Shafer et al. 1999), and plastid-to-nucleus transfer of DNA in plants can occur without the elimination of introns (Fuentes et al. 2012) or RNA editing sites (Sheppard et al. 2011). Further, an RNA...
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