Designing and analysis of a potent bi-functional aptamers that inhibit protease and helicase activities of HCV NS3.

Nucleic acids symposium series (2004)

Volumn , Issue 48, 2004, Pages 195-196

  Umehara, Takuya ^a   Fukuda, Kotaro ^a   Nishikawa, Fumiko ^a   Sekiya, Satoru ^a   Kohara, Michinori ^a   Hasegawa, Tsunemi ^a   Nishikawa, Satoshi ^a  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVIRUS AGENT; APTAMER; NS3 PROTEIN, HEPATITIS C VIRUS; PROTEINASE; PROTEINASE INHIBITOR; RNA HELICASE; VIRUS PROTEIN;

ARTICLE; DRUG ANTAGONISM; DRUG DESIGN; DRUG EFFECT; ENZYMOLOGY; HEPATITIS C VIRUS; IC 50; METABOLISM; PROTEIN BINDING;

ANTIVIRAL AGENTS; APTAMERS, NUCLEOTIDE; DRUG DESIGN; ENDOPEPTIDASES; HEPACIVIRUS; INHIBITORY CONCENTRATION 50; PROTEASE INHIBITORS; PROTEIN BINDING; RNA HELICASES; VIRAL NONSTRUCTURAL PROTEINS;

EID: 36048973544     PISSN: None     EISSN: 17468272     Source Type: Journal    
DOI: None     Document Type: Article

References (0)