Two mechanisms for human immunodeficiency virus type 1 inhibition by N-terminal modifications of RANTES

Antimicrobial Agents and Chemotherapy

Volumn 47, Issue 2, 2003, Pages 509-517

  Pastore, Cristina ^a   Picchio, Gastón R ^a   Galimi, Francesco ^b,d   Fish, Richard ^c   Hartley, Oliver ^c   Offord, Robin E ^c   Mosier, Donald E ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^c UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^d UNIVERSITY OF SASSARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; CHEMOKINE; CHEMOKINE RECEPTOR CCR5; RANTES; SERINE;

AMINO ACID SUBSTITUTION; AMINO TERMINAL SEQUENCE; ANTIVIRAL ACTIVITY; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DRUG MECHANISM; DRUG POTENCY; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; INTERNALIZATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN MODIFICATION; PROTEIN PHOSPHORYLATION; PROTEIN VARIANT; RECEPTOR BINDING; RECEPTOR BLOCKING; VIRUS INHIBITION;

ANTI-HIV AGENTS; HELA CELLS; HIV INFECTIONS; HIV-1; HUMANS; RANTES; RECEPTORS, CCR5; VIRUS REPLICATION;

EID: 0037311452     PISSN: 00664804     EISSN: None     Source Type: Journal    
DOI: 10.1128/AAC.47.2.509-517.2003     Document Type: Article

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