Searching journal content for articles similar to Sterne-Weiler et al. 23 (10): 1615.

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  1. ...localization, stability, and translational efficiency. To rigorously investigate mRNA isoform-specific ribosome association, we generated subcellular fractionation and sequencing (Frac-seq) libraries using both conventional short reads and long reads from human embryonic stem cells (ESCs) and neural progenitor...
  2. ...the limitations of the methods above. Transcript isoforms in polysome sequencing (TrIP-seq) (Floor and Doudna 2016) and fractionation and high-throughput RNA sequencing (Frac-seq) (Sterne-Weiler et al. 2013) have been used to quantify isoform-level translation by coupling polysome association with short...
  3. ...that may have a function in cell response to Doxo, we designed isoform-specific siRNAs targeting nine IPA isoforms (within their last exon, which is absent in the corresponding LE isoform) that are up-regulated by Doxo in the cytosol and that are up-regulated and/or abundant in polysomes. For eight IPA...
  4. ...reveals isoform-specific recruitment to polyribosomes. Genome Res 23: 1615–1623. ↵Truesdell SS, Mortensen RD, Seo M, Schroeder JC, Lee JH, LeTonqueze O, Vasudevan S. 2012. MicroRNA-mediated mRNA translation activation in quiescent cells and oocytes involves recruitment of a nuclear microRNP. Sci Rep 2...
  5. ...sequences (Wang et al. 2008). Of note, analysis of all junctions (including those in >80% or <20% of transcripts) reveals that 91% fall in the CDS, suggesting that AJs may be somewhat selected against within the CDS. In sum, this analysis identified 3929 genes that express at least two readily detectable m...
  6. ...FU PacBio transcripts by PCR to reveal that an important number of the novel transcripts are technical artifacts of the sequencing approach and that SQANTI quality descriptors can be used to engineer a filtering strategy to remove them. Most novel transcripts in this curated transcriptome are novel...
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