Abstract
The properties of the 31-mer 10-23 DNA enzyme and its analog with the terminal 3"-3" internucleotide linkage, which are complementary to an mRNA region of the multi-drug resistance gene MDR1, were investigated. DNA enzymes can selectively cleave RNA with high efficiency in a catalytic mode as exemplified by a synthetic 18-mer fragment of MDR1 mRNA.
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Kuznetsova, M.A., Repkova, M.N., Fokina, A.A. et al. 10-23 DNA enzymes for targeting MDR1 mRNA. Russian Chemical Bulletin 51, 1190–1193 (2002). https://doi.org/10.1023/A:1020936110045
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DOI: https://doi.org/10.1023/A:1020936110045