Drug Susceptibilities of Isolates of Varicella-Zoster Virus in a Clinical Study of Oral Brovavir

Author:

Machida Haruhiko1,Nishitani Makiko1

Affiliation:

1. Biology Laboratory; R&D Division, Yamasa Shoyu Co., Ltd.; Choshi Chiba 288

Publisher

Wiley

Subject

Virology,Immunology,Microbiology

Reference11 articles.

1. Inhibitory effects of selected antiviral compounds on newly isolated clinical varicella-zoster virus strains;Baba;Tohoku J. Exp. Med.,1984

2. Virus drug-resistance: mechanism and consequences;Larder;Antiviral Res.,1984

3. Antiherprsviral and anticellular effects of 1-β-arabinofuranosyl-E-5-(2-halogenovinyl)uracils;Machida;Antimicrob. Agents Chemother.,1981

4. Inhibitory effects of antiherpesviral thymidine analogs against varicella-zoster virus;Machida;Antimicrob. Agents Chemother.,1982

5. Bromovinyl-arabinosyluracil (BV-araU): antiviral activity and pharmacology;Machida,1985

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3. S;Hagers Handbuch der Pharmazeutischen Praxis;1999

4. Sorivudine and 5‐fluorouracil; a clinically significant drug‐drug interaction due to inhibition of dihydropyrimidine dehydrogenase;British Journal of Clinical Pharmacology;1998-07

5. Enzymatic Synthesis of 2′-O-acyl Prodrugs of 1-(β-D-arabinofuranosyl)-5(E)-(2-bromovinyl)uracil and of 2′-O-acyl-araU, -araC and -araA;Antiviral Chemistry and Chemotherapy;1998-02

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