FRET-based assay using a three-way junction DNA substrate to identify inhibitors of human cytomegalovirus pUL89 endonuclease activity-Reference-Cited by-同舟云学术

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FRET-based assay using a three-way junction DNA substrate to identify inhibitors of human cytomegalovirus pUL89 endonuclease activity

Published:2019-01 Issue: Volume:127 Page:29-37
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Wang Yan,Geraghty Robert J.^ORCID

Funder

University of Minnesota

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference50 articles.

1. Suramin inhibits Zika virus replication by interfering with virus attachment and release of infectious particles;Albulescu;Antivir. Res.,2017

2. Drug targets in cytomegalovirus infection;Andrei;Infect. Disord. Drug Targets,2009

3. Selective inhibition of human cytomegalovirus replication by naphthalenedisulfonic acid derivatives;Baba;Antivir. Res.,1993

4. Herpes simplex virus capsid assembly and DNA packaging: a present and future antiviral drug target;Baines;Trends Microbiol.,2011

5. Clinical and biologic aspects of human cytomegalovirus resistance to antiviral drugs;Baldanti;Hum. Immunol.,2004

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1. Anti-HCMV activity by an irreversible p97 inhibitor LC-1310;Medicinal Chemistry Research;2021-01-09

2. Recent applications of FRET-based multiplexed techniques;TrAC Trends in Analytical Chemistry;2020-02

3. Application of fluorescence resonance energy transfer to bioprinting;TrAC Trends in Analytical Chemistry;2020-01

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