Search Results - "Pradère, U"

Site-specific conjugation of drug-like fragments to an antimiR scaffold as a strategy to target miRNAs inside RISC by Brunschweiger, A, Gebert, L F R, Lucic, M, Pradère, U, Jahns, H, Berk, C, Hunziker, J, Hall, J

“…We synthesized a miR-122 antimiR library in which drug-like fragments were site-specifically introduced to short 2'-O-methyl-RNAs. At some sites selected…”
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333 Short antisense oligonucleotides antagonize Lin28 and enable pre-let-7 processing and suppression of cell growth in human hepatocarcinoma cells by Roos, M, Civenni, G, Lucic, M, Pavlicek, D, Pradere, U, Towbin, H, Catapano, C.V, Hall, J

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Substrate mimicry: HIV-1 reverse transcriptase recognizes 6-modified-3′-azido-2′,3′-dideoxyguanosine-5′-triphosphates as adenosine analogs by Herman, Brian D., Schinazi, Raymond F., Zhang, Hong-wang, Nettles, James H., Stanton, Richard, Detorio, Mervi, Obikhod, Aleksandr, Pradère, Ugo, Coats, Steven J., Mellors, John W., Sluis-Cremer, Nicolas

“…β-D-3′-Azido-2′,3′-dideoxyguanosine (3′-azido-ddG) is a potent inhibitor of HIV-1 replication with a superior resistance profile to zidovudine. Recently, we…”
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Evaluation of C-5 Substituted Uracil Acyclic Phosphonates as Substrates or Inhibitors for DTMP and UMP–CMP Kinases and Potential Antipox Derivatives by Topalis, Dimitri, Broggi, Julie, Alexandre, Julie A.C., Pradère, Ugo, Roy, Vincent, Berteina-Raboin, Sabine, Agrofoglio, Luigi A, Deville-Bonne, Dominique

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