Searching journal content for articles similar to Schnall-Levin et al. 21 (9): 1395.

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  1. ...been shown to be the source of new protein coding exons, RNA-binding motifs, and microRNA target sites (Lev-Maor et al. 2003; Zarnack et al. 2013; Petri et al. 2019; Cosby et al. 2021). Our analyses reveal that DNA transposon transcription is more often gene-dependent than retroelement transcription...
  2. ...are more efficient at triggering mRNA degradation. Our study suggests that miRNAs may combine targeting of CDS and 39 UTR to flexibly tune the time scale and magnitude of their post-transcriptional regulatory effects. [Supplemental material is available for this article.] MicroRNAs (miRNAs) are ;21 nt...
  3. ...conserved microRNA species display their signature tissue-specific expression patterns. In addition, we find a large rapidly evolving cluster of microRNAs on platypus chromosome X1, which is unique to monotremes. Platypus and echidna testes contain a robust Piwi-interacting (piRNA) system, which appears...
  4. ...protein mRNAs, potentially through reduced levels of miRNAs that target them. Finally, a group of transcripts bearing 3′ UTR C-rich sequence elements, many of which encode transcription factors, are significantly less stable in iPS cells. Intriguingly, two poly(C)-binding proteins that recognize this type...
  5. ...to proteins, in many cases mediated by their distinct stable and evolutionarily conserved structure. Prominent examples are structural precursors to small microRNAs (miRNAs) (Lagos-Quintana et al. 2001; Lau et al. 2001; Schnall-Levin et al. 2010, 2011), structural meso-sized RNAs (200 or fewer bases...
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