Inhibition of Ganciclovir-Susceptible and -Resistant Human Cytomegalovirus Clinical Isolates by the Benzimidazole l -Riboside 1263W94
Author:
Affiliation:
1. Albany Medical College, Albany, New York,1 and
2. GlaxoSmithKline, Research Triangle Park, North Carolina2
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Link
https://journals.asm.org/doi/pdf/10.1128/CDLI.8.6.1279-1281.2001
Reference23 articles.
1. Britt W. J. Alford C. A. Cytomegalovirus P. 2493–2524. Fields virology 3rd ed. Fields B. N. Knipe D. M. Howley P. M. 1996 Lippincott-Raven Publishers Philadelphia Pa
2. Analysis of the UL97 phosphotransferase coding sequence in clinical cytomegalovirus isolates and identification of mutations conferring ganciclovir resistance.;Chou S.;J. Infect. Dis.,1995
3. Frequency of UL97 phosphotransferase mutations related to ganciclovir resistance in clinical cytomegalovirus isolates.;Chou S.;J. Infect. Dis.,1995
4. Development of novel benzimidazole riboside compounds for treatment of cytomegalovirus disease.;Chulay J.;Adv. Exp. Med. Biol.,1999
5. Ganciclovir.;Crumpacker C.;N. Engl. J. Med.,1996
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