Combinatorially selected guanosine-quartet structure is a potent inhibitor of human immunodeficiency virus envelope-mediated cell fusion

Proceedings of the National Academy of Sciences of the United States of America

Volumn 91, Issue 4, 1994, Pages 1356-1360

  Wyatt, Jacqueline R ^a   Vickers, Timothy A ^a   Roberson, Joseph L ^b   Buckheit Jr , Robert W ^b   Klimkait, Thomas ^c   Debaets, Elizabeth ^a   Davis, Peter W ^a   Rayner, Bernard ^d   Imbach, J L ^d   Ecker, David J ^a  

^a ISIS PHARMACEUTICALS   (United States)

^b SOUTHERN RESEARCH INSTITUTE   (United States)

^c CIBA GEIGY LTD   (Switzerland)

^d UNIV MONTPELLIER   (France)

Author keywords

gp120; oligonucleotide; phosphorothioate; random libraries; V3 loop

Indexed keywords

ANTIVIRUS AGENT; GLYCOPROTEIN GP 120; GUANOSINE DERIVATIVE; OLIGONUCLEOTIDE; PHOSPHOROTHIOIC ACID DERIVATIVE; TETRAMER; VIRUS ENVELOPE PROTEIN;

ANTIVIRAL ACTIVITY; ARTICLE; CELL FUSION; CONTROLLED STUDY; DRUG SCREENING; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; PRIORITY JOURNAL; PROTEIN BINDING; VIRUS ENVELOPE; VIRUS INHIBITION;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0027983025     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.91.4.1356     Document Type: Article

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