Design, delivery and efficacy testing of therapeutic nucleic acids used to inhibit hepatitis C virus gene expression in vitro and in vivo

doi:10.3748/wjg.v6.i5.626

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Oct 15, 2000 (publication date) through Apr 29, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Oct 15, 2000; 6(5): 626-629
Published online Oct 15, 2000. doi: 10.3748/wjg.v6.i5.626

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Figure 3 Modified hammerhead RZ and HCV target sequence. The G_16.2,C_16.1, A₁₇ recognition site (nts. 346-348), in which cleavage occurs, is marked by an arrow. All nucleotides are 2’-O-ally l-ribonucleotides except G₅, A₆, G₈ and G₁₂ (light gray), which are unmodified ribonucleotides. The position of the A to l exchange (medium gray) and the start AUG of the HCV template are indicated.

Citation: Caselmann WH, Serwe M, Lehmann T, Ludwig J, Sproat BS, Engels JW. Design, delivery and efficacy testing of therapeutic nucleic acids used to inhibit hepatitis C virus gene expression in vitro and in vivo. World J Gastroenterol 2000; 6(5): 626-629
URL: https://www.wjgnet.com/1007-9327/full/v6/i5/626.htm
DOI: https://dx.doi.org/10.3748/wjg.v6.i5.626