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  1. Artificial cationic peptides that increase nuclease resistance of siRNA without disturbing RNAi activity
  2. Enhancement of the affinity of 2′-O-Me-oligonucleotides for complementary RNA by incorporating a stereoregulated boranophosphate backbone
  3. Synthesis of oligodiaminomannoses and analysis of their RNA duplex binding properties and their potential application as siRNA-based drugs