TargetFinder: a software for antisense oligonucleotide target site selection based on MAST and secondary structures of target mRNA.
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[1] Randall R. Sakai,et al. Mapping of RNA accessible sites for antisense experiments with oligonucleotide libraries , 1998, Nature Biotechnology.
[2] Sverdrup,et al. Antisense oligonucleotides: a systematic high-throughput approach to target validation and gene function determination. , 1999, Drug discovery today.
[3] S. Crooke,et al. An overview of progress in antisense therapeutics. , 1998, Antisense & nucleic acid drug development.
[4] D. Ecker,et al. Implication of RNA structure on antisense oligonucleotide hybridization kinetics. , 1992, Biochemistry.
[5] Claes Wahlestedt,et al. mRNA accessible site tagging (MAST): a novel high throughput method for selecting effective antisense oligonucleotides. , 2003, Nucleic acids research.
[6] S. Freier,et al. Effects of RNA secondary structure on cellular antisense activity. , 2000, Nucleic acids research.
[7] C. A. Stein,et al. Keeping the biotechnology of antisense in context , 1999, Nature Biotechnology.
[8] G Sczakiel,et al. Theoretical and experimental approaches to design effective antisense oligonucleotides. , 2000, Frontiers in bioscience : a journal and virtual library.
[9] Michael Zuker,et al. Mfold web server for nucleic acid folding and hybridization prediction , 2003, Nucleic Acids Res..