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However, to date, oligonucleotide therapeutics are still facing some technological obstacles, such as how to achieve efficient oligonucleotide delivery to target organs or tissues, how to overcome off-target interactions [4952], and how to address the sequence- and chemistry-dependent toxicity and saturation of endogenous RNA processing pathways [53, 54]

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coli glyceraldehyde-3-phosphate dehydrogenase and isocitrate lysase, respectively (Anjem and Imlay, 2012), and 1020 M 1 s 1 for assorted eukaryotic tyrosine phosphatases (Denu and Tanner, 1998)

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