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Showing 1–4 of 4 results
Advanced filters: Author: Jeremy D Heidel Clear advanced filters
  • It has previously been shown in mice and non-human primates that systemically delivered short RNA molecules can inhibit gene expression. Here it is shown that a short interfering RNA (siRNA) can be systemically delivered, using nanoparticles, to a solid tumour in humans. The siRNA mediates cleavage of its target mRNA, thereby also reducing levels of the encoded protein. This proof-of-principle study confirms the potential of this technology for treating human disease.

    • Mark E. Davis
    • Jonathan E. Zuckerman
    • Antoni Ribas
    Research
    Nature
    Volume: 464, P: 1067-1070
  • In an effort to develop safer therapeutic agents and to limit unintended side effects, Sabah Oney and her colleagues have designed a set of antidote molecules for a series of aptamers exhibiting anticoagulant activities. These so-called universal antidotes are shown to sequester circulating aptamers and reverse their activity, irrespective of the primary sequence and folded structure of the aptamer.

    • Sabah Oney
    • Ruby T S Lam
    • Bruce A Sullenger
    Research
    Nature Medicine
    Volume: 15, P: 1224-1228