Development and evaluation of a host-targeted antiviral that abrogates herpes simplex virus replication through modulation of arginine-associated metabolic pathways-Reference-Cited by-同舟云学术

Development and evaluation of a host-targeted antiviral that abrogates herpes simplex virus replication through modulation of arginine-associated metabolic pathways

Published:2016-08 Issue: Volume:132 Page:13-25
ISSN:0166-3542
Container-title:Antiviral Research
language:en
Short-container-title:Antiviral Research

Author:

Sanchez Maria Dulfary^ORCID,Ochoa Augusto C.,Foster Timothy P.^ORCID

Funder

Louisiana Board of Regents Research Competitiveness Award

Louisiana Board of Regents

Louisiana Vaccine Center

National Institutes of Health

National Center for Research Resources

National Institute of General Medical Sciences

National Institute of Allergy and Infectious Diseases

Louisiana Clinical and Translational Science Center

Publisher

Elsevier BV

Subject

Virology,Pharmacology

Reference69 articles.

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3. Arginine availability, arginase, and the immune response;Bansal;Curr. Opin. Clin. Nutr. Metabolic Care,2003

4. Potent in vivo antiviral activity of the herpes simplex virus primase-helicase inhibitor BAY 57-1293;Betz;Antimicrob. Agents Chemother.,2002

5. Single amino acid substitutions in the HSV-1 helicase protein that confer resistance to the helicase-primase inhibitor BAY 57-1293 are associated with increased or decreased virus growth characteristics in tissue culture;Biswas;Archives Virol.,2007

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