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Potent antisense oligonucleotides to the human multidrug resistance-1 mRNA are rationally selected by mapping RNA-accessible sites with oligonucleotide libraries.

Antisense oligonucleotides can vary significantly and unpredictably in their ability to inhibit protein synthesis. Libraries of chimeric oligonucleotides and RNase H were used to cleave and thereby locate sites on human multidrug resistance-1 RNA transcripts that are relatively accessible to oligonu...

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Detalhes bibliográficos
Main Authors: Ho, S P, Britton, D H, Stone, B A, Behrens, D L, Leffet, L M, Hobbs, F W, Miller, J A, Trainor, G L
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC145867/
https://ncbi.nlm.nih.gov/pubmed/8657572
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