Structure-activity of tetrad-forming oligonucleotides as a potent anti- HIV therapeutic drug

Journal of Biological Chemistry

Volumn 273, Issue 52, 1998, Pages 34992-34999

  Jing, Naijie ^a   Hogan, Michael E ^a,b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b Genometrix Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVIRUS AGENT; T 30695; UNCLASSIFIED DRUG; ZINTEVIR;

ANTIVIRAL ACTIVITY; ARTICLE; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME INHIBITION; HYPOTHESIS; NUCLEAR MAGNETIC RESONANCE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; THERMOSTABILITY; VIRUS INHIBITION; VIRUS REPLICATION;

ANTI-HIV AGENTS; APTAMERS, NUCLEOTIDE; HIV INTEGRASE; HIV INTEGRASE INHIBITORS; INHIBITORY CONCENTRATION 50; MODELS, MOLECULAR; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; NUCLEIC ACID CONFORMATION; OLIGONUCLEOTIDES; POTASSIUM;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0032567432     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.52.34992     Document Type: Article

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