Compartmentalization of VP16 in cells infected with recombinant herpes simplex virus expressing VP16-green fluorescent protein fusion proteins.
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The art of cellular communication: tunneling nanotubes bridge the divideApplications of Replicating-Competent Reporter-Expressing Viruses in Diagnostic and Molecular VirologyFluorescent Protein Approaches in Alpha Herpesvirus ResearchCRISPR/Cas9-Mediated Genome Editing of Herpesviruses Limits Productive and Latent InfectionsSpatial and Temporal Resolution of Global Protein Synthesis during HSV Infection Using Bioorthogonal Precursors and Click ChemistryTransient reversal of episome silencing precedes VP16-dependent transcription during reactivation of latent HSV-1 in neuronsA core extended naphtalene diimide G-quadruplex ligand potently inhibits herpes simplex virus 1 replicationCytoskeletal rearrangements and cell extensions induced by the US3 kinase of an alphaherpesvirus are associated with enhanced spread.Coxsackievirus B3-induced cellular protrusions: structural characteristics and functional competenceMembrane nanotubes physically connect T cells over long distances presenting a novel route for HIV-1 transmission.Cytonemes and tunneling nanotubules in cell-cell communication and viral pathogenesis.Characterization of a potent refractory state and persistence of herpes simplex virus 1 in cell culture.Phosphorylation of the VP16 transcriptional activator protein during herpes simplex virus infection and mutational analysis of putative phosphorylation sites.Proteomic analysis of the herpes simplex virus 1 virion protein 16 transactivator protein in infected cellsSelective recruitment of nuclear factors to productively replicating herpes simplex virus genomes.Evidence for the Use of Multiple Mechanisms by Herpes Simplex Virus-1 R7020 to Inhibit Intimal Hyperplasia.Long-distance calls between cells connected by tunneling nanotubules.Live visualization of herpes simplex virus type 1 compartment dynamicsIdentification of a highly conserved, functional nuclear localization signal within the N-terminal region of herpes simplex virus type 1 VP1-2 tegument protein.Nuclear pore composition and gating in herpes simplex virus-infected cellsAlphaherpesvirus US3-mediated reorganization of the actin cytoskeleton is mediated by group A p21-activated kinases.Tunneling nanotubes (TNT) are induced by HIV-infection of macrophages: a potential mechanism for intercellular HIV trafficking.Early events in herpes simplex virus lifecycle with implications for an infection of lifetimeFluorosomes: fluorescent virus-like nanoparticles that represent a convenient tool to visualize receptor-ligand interactions.Cell Cycle-Dependent Expression of Adeno-Associated Virus 2 (AAV2) Rep in Coinfections with Herpes Simplex Virus 1 (HSV-1) Gives Rise to a Mosaic of Cells Replicating either AAV2 or HSV-1.Visualization of herpes simplex virus type 1 virions using fluorescent colors.Visualization of DNA G-quadruplexes in herpes simplex virus 1-infected cells.Quantitative Evaluation of Protein Heterogeneity within Herpes Simplex Virus 1 Particles.Epithelial-mesenchymal transition enhances response to oncolytic herpesviral therapy through nectin-1.Herpes simplex virus type 1 UL14 tegument protein regulates intracellular compartmentalization of major tegument protein VP16The UL14 tegument protein of herpes simplex virus type 1 is required for efficient nuclear transport of the alpha transinducing factor VP16 and viral capsids.Marek's disease virus infection of phagocytes: a de novo in vitro infection model.RNA binding by the herpes simplex virus type 1 nucleocytoplasmic shuttling protein UL47 is mediated by an N-terminal arginine-rich domain that also functions as its nuclear localization signal.The alpha-TIF (VP16) homologue (ETIF) of equine herpesvirus 1 is essential for secondary envelopment and virus egress.Herpes simplex virus tegument protein VP22 contains an internal VP16 interaction domain and a C-terminal domain that are both required for VP22 assembly into the virus particle.Suppression of herpes simplex virus 1 in MDBK cells via the interferon pathway.Genome-wide engineering of an infectious clone of herpes simplex virus type 1 using synthetic genomics assembly methods.Two-color fluorescence analysis of individual virions determines the distribution of the copy number of proteins in herpes simplex virus particles.Multifaceted roles of tunneling nanotubes in intercellular communication.Different modes of herpes simplex virus type 1 spread in brain and skin tissues.
P2860
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P2860
Compartmentalization of VP16 in cells infected with recombinant herpes simplex virus expressing VP16-green fluorescent protein fusion proteins.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Compartmentalization of VP16 i ...... scent protein fusion proteins.
@en
type
label
Compartmentalization of VP16 i ...... scent protein fusion proteins.
@en
prefLabel
Compartmentalization of VP16 i ...... scent protein fusion proteins.
@en
P2093
P2860
P1433
P1476
Compartmentalization of VP16 i ...... escent protein fusion proteins
@en
P2093
Peter O'Hare
Sophie Malcomber
Sylvie La Boissière
P2860
P304
P356
10.1128/JVI.78.15.8002-8014.2004
P407
P50
P577
2004-08-01T00:00:00Z