Key result
Viral internal ribosome entry sites (IRESes), particularly those of the Dicistroviridae, utilize specific RNA structures to directly recruit ribosomes and bypass canonical translation initiation.
Design
Review
Authors
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Does not alter clinical practice; leaves open therapeutic targeting of viral IRES structures.
Key points are not available for this paper at this time.
Pfingsten et al. (2008) reported a review. Viral internal ribosome entry sites (IRESes), particularly those of the Dicistroviridae, utilize specific RNA structures to directly recruit ribosomes and bypass canonical translation initiation.
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