Searching journal content for articles similar to Bénitière et al. 35 (3): 446.

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  1. ...modulate ribosome occupancy—many of these differences lie close to start codons and upstreamORFs. Our results reveal a new level of gene expression variation among humans and indicate that genetic variants can cause changes in protein levels through effects on translation. [Supplemental material...
  2. ...RNAs lack the 5′ TOP motif but that 5′ UTR features distinguish two functionally and translationally distinct subsets of MTOR-sensitive mRNAs: (1) mRNAs with short 5′ UTRs enriched for mitochondrial functions, which require EIF4E but are less EIF4A1-sensitive; and (2) long 5′ UTR mRNAs encoding...
  3. .... We did not notice any selectivity in the region occupied by the upstream ribosome or at the boundary between the ribosomes. These findings fit the model that the leading ribosome defined the pause site (with preference for specific codons) and an upstream ribosome colliding sequence independently...
  4. ...at each exonic position in the 10 HMs are compared in Figure 2F. The region from position 2 to ∼15 shows great variation among HMs as expected since this stretch overlaps the distinctive six-base substitutions they contain. That is, if two mutations are within about 6 nt, they may be creating an entirely...
  5. ...points and the assessment of the directionality to the gene components allowed us to categorize the impact of genomic rearrangements to gene structures into four categories (Supplemental Glossary; Supplemental Fig. 2A): fusion genes (FG), in which two distinct RefSeq genes are fused together in the same...
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