Evidence that herpes simplex virus VP16 is required for viral egress downstream of the initial envelopment event.
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High-level expression of Marek's disease virus glycoprotein C is detrimental to virus growth in vitroMolecular biology of pseudorabies virus: impact on neurovirology and veterinary medicine.Determination of interactions between tegument proteins of herpes simplex virus type 1The herpes simplex virus ICP0 RING finger domain inhibits IRF3- and IRF7-mediated activation of interferon-stimulated genesHerpes simplex virus virion host shutoff protein is stimulated by translation initiation factors eIF4B and eIF4HAssociation of the herpes simplex virus type 1 Us11 gene product with the cellular kinesin light-chain-related protein PAT1 results in the redistribution of both polypeptidesHSV-1 tegument protein and the development of its genome editing technologyTegument Assembly and Secondary Envelopment of AlphaherpesvirusesEvasion of host antiviral innate immunity by HSV-1, an updateEffects of charged cluster mutations on the function of herpes simplex virus type 1 UL34 protein.Identification and characterization of the pseudorabies virus tegument proteins UL46 and UL47: role for UL47 in virion morphogenesis in the cytoplasm.The herpes simplex virus type 1 vhs-UL41 gene secures viral replication by temporarily evading apoptotic cellular response to infection: Vhs-UL41 activity might require interactions with elements of cellular mRNA degradation machinery.Nelfinavir inhibits maturation and export of herpes simplex virus 1.The major determinant for addition of tegument protein pUL48 (VP16) to capsids in herpes simplex virus type 1 is the presence of the major tegument protein pUL36 (VP1/2)Herpes simplex virus type 1 UL51 protein is involved in maturation and egress of virus particles.Herpes simplex virus triggers and then disarms a host antiviral response.A null mutation in the gene encoding the herpes simplex virus type 1 UL37 polypeptide abrogates virus maturation.Microtubule reorganization during herpes simplex virus type 1 infection facilitates the nuclear localization of VP22, a major virion tegument proteinAntagonistic determinants controlling replicative and latent states of human cytomegalovirus infectionSorting and transport of alpha herpesviruses in axons.Human cytomegalovirus UL47 tegument protein functions after entry and before immediate-early gene expressionCharacterization of Marek's disease virus serotype 1 (MDV-1) deletion mutants that lack UL46 to UL49 genes: MDV-1 UL49, encoding VP22, is indispensable for virus growth.Sequential localization of two herpes simplex virus tegument proteins to punctate nuclear dots adjacent to ICP0 domainsRoles for herpes simplex virus type 1 UL34 and US3 proteins in disrupting the nuclear lamina during herpes simplex virus type 1 egress.Herpesvirus assembly and egressVaricella-zoster virus open reading frame 10 is a virulence determinant in skin cells but not in T cells in vivoICP0 is not required for efficient stress-induced reactivation of herpes simplex virus type 1 from cultured quiescently infected neuronal cells.Cultured corneas show dendritic spread and restrict herpes simplex virus infection that is not observed with cultured corneal cells.Psittacid herpesvirus 1 and infectious laryngotracheitis virus: Comparative genome sequence analysis of two avian alphaherpesviruses.A single amino acid substitution in herpes simplex virus type 1 VP16 inhibits binding to the virion host shutoff protein and is incompatible with virus growth.The synergistic effect of IFN-alpha and IFN-gamma against HSV-2 replication in Vero cells is not interfered by the plant antiviral 1-cinnamoyl-3, 11-dihydroxymeliacarpin.Physical interaction between envelope glycoproteins E and M of pseudorabies virus and the major tegument protein UL49.Structural analysis of herpes simplex virus by optical super-resolution imaging.Herpes simplex virus glycoproteins gD and gE/gI serve essential but redundant functions during acquisition of the virion envelope in the cytoplasm.Functional characterization of Kaposi's sarcoma-associated herpesvirus ORF45 by bacterial artificial chromosome-based mutagenesis.Cytoplasmic residues of herpes simplex virus glycoprotein gE required for secondary envelopment and binding of tegument proteins VP22 and UL11 to gE and gDAnalysis of the interaction between the essential herpes simplex virus 1 tegument proteins VP16 and VP1/2.Marek's disease virus expresses multiple UL44 (gC) variants through mRNA splicing that are all required for efficient horizontal transmission.Live visualization of herpes simplex virus type 1 compartment dynamicsNovel Structure and Unexpected RNA-Binding Ability of the C-Terminal Domain of Herpes Simplex Virus 1 Tegument Protein UL21.
P2860
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P2860
Evidence that herpes simplex virus VP16 is required for viral egress downstream of the initial envelopment event.
description
2000 nî lūn-bûn
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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Evidence that herpes simplex v ...... the initial envelopment event.
@ast
Evidence that herpes simplex v ...... the initial envelopment event.
@en
type
label
Evidence that herpes simplex v ...... the initial envelopment event.
@ast
Evidence that herpes simplex v ...... the initial envelopment event.
@en
prefLabel
Evidence that herpes simplex v ...... the initial envelopment event.
@ast
Evidence that herpes simplex v ...... the initial envelopment event.
@en
P2093
P2860
P1433
P1476
Evidence that herpes simplex v ...... the initial envelopment event.
@en
P2093
P2860
P304
P356
10.1128/JVI.74.14.6287-6299.2000
P577
2000-07-01T00:00:00Z