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

Nucleic Acids Research

Volumn 24, Issue 10, 1996, Pages 1901-1907

  Ho, Siew Peng ^a   Britton, Dustin H O ^a   Stone, Barry A ^a   Behrens, Davette L ^a   Leffet, Lynn M ^a   Hobbs, Frank W ^a   Miller, Jeff A ^a   Trainor, George L ^a  

^a DUPONT COMPANY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTISENSE OLIGONUCLEOTIDE; GLYCOPROTEIN P; MESSENGER RNA; PROTEIN SYNTHESIS INHIBITOR; RIBONUCLEASE;

ARTICLE; AUTORADIOGRAPHY; CELL CULTURE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG POTENCY; HUMAN; HUMAN CELL; MULTIDRUG RESISTANCE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN SYNTHESIS INHIBITION; RNA BINDING; RNA SEQUENCE; RNA TRANSCRIPTION;

BASE SEQUENCE; GENE LIBRARY; HUMANS; MOLECULAR SEQUENCE DATA; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDES, ANTISENSE; P-GLYCOPROTEIN; RHODAMINES; RIBONUCLEASE H, CALF THYMUS; RNA, MESSENGER; TUMOR CELLS, CULTURED;

EID: 0029938209     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/24.10.1901     Document Type: Article

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