Peptidyl-transferase inhibitors have antiviral properties by altering programmed -1 ribosomal frameshifting efficiencies: Development of model systems

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

Volumn 94, Issue 13, 1997, Pages 6606-6611

  Dinman, Jonathan D ^a,b   Ruiz Echevarria, Maria J ^a   Czaplinski, Kevin ^a   Peltz, Stuart W ^a,b,c  

^a RUTGERS ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY   (United States)

^c RUTGERS CANCER INSTITUTE OF NEW JERSEY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANISOMYCIN; CYCLOHEXIMIDE; DNA; DOUBLE STRANDED RNA; HYBRID PROTEIN; HYGROMYCIN; LUCIFERASE; MESSENGER RNA; PAROMOMYCIN; PEPTIDYLTRANSFERASE; SPARSOMYCIN; TRANSFERASE INHIBITOR;

AGAR GEL ELECTROPHORESIS; ANTIVIRAL ACTIVITY; ARTICLE; CELL GROWTH; CONTROLLED STUDY; MODEL; NONHUMAN; PRIORITY JOURNAL; RIBOSOMAL FRAMESHIFTING; RIBOSOME; RNA VIRUS; SACCHAROMYCES CEREVISIAE; TRANSLATION REGULATION; VIRUS ASSEMBLY; VIRUS PARTICLE;

ANISOMYCIN; ANTIVIRAL AGENTS; FRAMESHIFTING, RIBOSOMAL; GENE EXPRESSION REGULATION, VIRAL; PEPTIDYL TRANSFERASES; PROTEIN SYNTHESIS INHIBITORS; RNA VIRUSES; SACCHAROMYCES CEREVISIAE; SPARSOMYCIN;

EUKARYOTA; MAMMALIA; RNA VIRUSES; SACCHAROMYCES CEREVISIAE;

EID: 0030966221     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.13.6606     Document Type: Article

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