Identification of small molecule compounds that selectively inhibit varicella-zoster virus replication - Wikidata - awgldk - TriplyDB

Identification of small molecule compounds that selectively inhibit varicella-zoster virus replication

Identification of small molecule compounds that selectively inhibit varicella-zoster virus replication

http://www.wikidata.org/entity/Q34471804

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Assembly of the herpes simplex virus capsid: identification of soluble scaffold-portal complexes and their role in formation of portal-containing capsids.Current and potential treatments for ubiquitous but neglected herpesvirus infections Specific inhibition of human cytomegalovirus glycoprotein B-mediated fusion by a novel thiourea small molecule.The varicella-zoster virus portal protein is essential for cleavage and packaging of viral DNA.Herpes simplex virus type 2 UL24 gene is a virulence determinant in murine and guinea pig disease models.Emerging drugs for varicella-zoster virus infections.Identification of a varicella-zoster virus replication inhibitor that blocks capsid assembly by interacting with the floor domain of the major capsid protein.Development of new antivirals for herpesviruses.Non-axial view of the varicella-zoster virus portal protein reveals conserved crown, wing and clip architecture.The Varicella-zoster virus ORF54 gene product encodes the capsid portal protein, pORF54.Intermolecular Complementation between Two Varicella-Zoster Virus pORF30 Terminase Domains Essential for DNA Encapsidation.The varicella-zoster virus genome Role of a mutation in human cytomegalovirus gene UL104 in resistance to benzimidazole ribonucleosides.The Varicella-zoster virus DNA encapsidation genes: Identification and characterization of the putative terminase subunits.Characterization of the Varicella-zoster virus ORF25 gene product: pORF25 interacts with multiple DNA encapsidation proteins.Design and development of antivirals and intervention strategies against human herpesviruses using high-throughput approach.Monitoring prevalence of varicella-zoster virus clades in Germany.Characterization of an anti-varicella-zoster virus compound that targets the portal protein encoded by ORF54.Susceptibilities of several clinical varicella-zoster virus (VZV) isolates and drug-resistant VZV strains to bicyclic furano pyrimidine nucleosides.

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Identification of small molecule compounds that selectively inhibit varicella-zoster virus replication

http://www.wikidata.org/entity/Q34471804

description

2003 nî lūn-bûn

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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի փետրվարին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Identification of small molecu ...... cella-zoster virus replication

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Identification of small molecu ...... cella-zoster virus replication

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Identification of small molecu ...... cella-zoster virus replication

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type

label

Identification of small molecu ...... cella-zoster virus replication

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Identification of small molecu ...... cella-zoster virus replication

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Identification of small molecu ...... cella-zoster virus replication

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prefLabel

Identification of small molecu ...... cella-zoster virus replication

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Identification of small molecu ...... cella-zoster virus replication

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Identification of small molecu ...... cella-zoster virus replication

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JVI.77.4.2349-2358.2003

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Journal of Virology

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Identification of small molecu ...... cella-zoster virus replication

@en

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Adma Ross

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Boris Feld

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Jeanette Fairhurst

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Jeffrey I Cohen

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John O'Connell

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Jonathan D Bloom

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Kevin Curran

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Marja van Zeijl

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Martin DiGrandi

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Robert J Visalli

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P2860

Novel class of thiourea compounds that inhibit herpes simplex virus type 1 DNA cleavage and encapsidation: resistance maps to the UL6 gene.

Varicella-zoster virus

A novel nonnucleoside inhibitor specifically targets cytomegalovirus DNA maturation via the UL89 and UL56 gene products.

Inhibition of human cytomegalovirus DNA maturation by a benzimidazole ribonucleoside is mediated through the UL89 gene product

Resistance of human cytomegalovirus to benzimidazole ribonucleosides maps to two open reading frames: UL89 and UL56

The UL6 gene product forms the portal for entry of DNA into the herpes simplex virus capsid.

Herpes simplex virus DNA cleavage and packaging proteins associate with the procapsid prior to its maturation.

Current pharmacological approaches to the therapy of varicella zoster virus infections: a guide to treatment.

Nucleotide sequences that distinguish Oka vaccine from parental Oka and other varicella-zoster virus isolates.

Novel anti-RSV dianionic dendrimer-like compounds: design, synthesis and biological evaluation.

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2349-2358

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scholarly article

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10.1128/JVI.77.4.2349-2358.2003

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4

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2003-02-01T00:00:00Z

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12551972

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141108

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