Different Antiviral Potencies of BV-araU and Related Nucleoside Analogues against Herpes Simplex Virus Type 1 in Human Cell Lines and Vero Cells
Author:
Affiliation:
1. Biology Laboratory, R & D Division; Yamasa Shoyu Co., Ltd.; Choshi Chiba 288 Japan
2. Division of Microbiology; Asahikawa Medical College; Asahikawa Hokkaido 078-11 Japan
3. Public Health Research Institute of Kobe City; Kobe Hyogo 650 Japan
Publisher
Wiley
Subject
Virology,Immunology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1348-0421.1991.tb01618.x/fullpdf
Reference18 articles.
1. Role of viral ribonucleotide reductase in the increase of dTTP pool size in herpes simplex virus-infected Vero cells;Daikoku;J. Gen. Virol.,1991
2. Comparative efficacy of antiherpes drugs in different cell lines;De Clercq;Antimicrob. Agents Chemother.,1982
3. Structure-activity analysis of antagonism of the feedback inhibition of thymidine kinase;Fischer;Biochem. Pharmacol.,1988
4. Antiviral activities of some newer 2′-fluoro-5-substituted arabinosylpyrimidine nucleosides,1985
5. Influence of cells and virus multiplicity on the inhibition of herpesviruses with acycloguanosine;Harmenberg;Intervirology,1980
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