Searching journal content for articles similar to Vandevyver et al. 5 (2): 195.

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  1. ...) Numbers of genes with different numbers of the identified PAS.We performed RNA 3′ end-seq (QuantSeq 3′ mRNA-seq, Lexogen) on four cell lines, including K562, HepG2, THLE2, and SNU398, to comprehensively characterize the expressed/used PAS in these four samples, respectively. To avoid internal primming...
  2. ...to revolutionize scientific discoveries in RNA biology through the comprehensive identification and quantification of full-length mRNA isoforms. Despite great promise, challenges remain in the widespread implementation of LRS technologies for RNA-based applications, including concerns about low coverage, high...
  3. ...Corresponding author: jmurr@pennmedicine.upenn.eduAbstractDuring embryonic development, cells undergo dynamic changes in gene expression that are required for appropriate cell fate specification. Although both transcription and mRNA degradation contribute to gene expression dynamics, patterns of mRNA decay...
  4. ...of RNA, University of California Santa Cruz, Santa Cruz, California 95064, USA ↵3 These authors contributed equally to this work. Corresponding author: jsanfor2@ucsc.eduAbstractAlternative splicing (AS) alters the cis-regulatory landscape of mRNA isoforms, leading to transcripts with distinct...
  5. ...by amplification of cDNA in which a dNTP analog was incorporated using the mRNA Selective PCR Kit (TAKARA) as described in Washietl et al. (2007). Aliquots (two of 12.5 mL) of up to 4700 independent amplification reactions were pooled together respecting the tissue origin and purified with the QIAquick PCR...
  6. ...initiation, tRNA processing, mRNA processing, and regulation of RNA polII transcription, as well as pathways related to immune system and response to cytokine (Supplemental Fig. S8B; Supplemental Table S1). Significantly down-regulated transcripts are enriched for ribosomal proteins, protein ubiquitination...
  7. ..., Lianne Boeglin2, Sudha Chivukula2, Anusha Dias2, Tod Strugnell2, Fernando Ulloa Montoya3, Vikram Agarwal2, Ziv Bar-Joseph1 and Sven Jager1 1Digital R&D, Sanofi, Cambridge, Massachusetts 02141, USA; 2mRNA Center of Excellence, Sanofi, Waltham, Massachusetts 02451, USA; 3mRNA Center of Excellence, Sanofi...
  8. ...Genomics Institute, University of California at Santa Cruz, Santa Cruz, California 95064, USA ↵4 Present address: Molecular Engineering and Sciences Institute, University of Washington, Seattle, WA 98105, USA Corresponding author: jarriber@ucsc.eduAbstractPremature stop codon–containing mRNAs can produce...
  9. ...-optimal probabilistic RNA-seq quantification. Nat Biotechnol 34: 525–527. ↵Bregman A, Avraham-Kelbert M, Barkai O, Duek L, Guterman A, Choder M. 2011. Promoter elements regulate cytoplasmic mRNA decay. Cell 147: 1473–1483. ↵Carey LB, van Dijk D, Sloot PMA, Kaandorp JA, Segal E. 2013. Promoter sequence determines...
  10. ...directly using qualitative RT-PCR methods that allow qualitative detection of specific viral mRNAs, as in the cases of HIV-1 (13-1s) and HBV infections. (16,17) Third, because PCR amplification supplies templates pure enough to be an- alyzed directly using standard sequenc- ing protocols, this method...
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