Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage respo
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The Epstein-Barr virus replication protein BBLF2/3 provides an origin-tethering function through interaction with the zinc finger DNA binding protein ZBRK1 and the KAP-1 corepressorThe DNA damage response induced by infection with human cytomegalovirus and other virusesA viral E3 ligase targets RNF8 and RNF168 to control histone ubiquitination and DNA damage responsesChk2 is required for HSV-1 ICP0-mediated G2/M arrest and enhancement of virus growthHuman papillomaviruses activate the ATM DNA damage pathway for viral genome amplification upon differentiationSpatial and Temporal Resolution of Global Protein Synthesis during HSV Infection Using Bioorthogonal Precursors and Click ChemistryThe HSV-1 exonuclease, UL12, stimulates recombination by a single strand annealing mechanismHerpes Simplex Virus Latency: The DNA Repair-Centered Pathway.Inhibition of the herpes simplex virus type 1 DNA polymerase induces hyperphosphorylation of replication protein A and its accumulation at S-phase-specific sites of DNA damage during infection.Herpes simplex virus type I disrupts the ATR-dependent DNA-damage response during lytic infection.Definition of herpes simplex virus type 1 helper activities for adeno-associated virus early replication eventsHomologous recombinational repair factors are recruited and loaded onto the viral DNA genome in Epstein-Barr virus replication compartments.Inhibition of herpes simplex virus type 1 replication by adeno-associated virus rep proteins depends on their combined DNA-binding and ATPase/helicase activities.Contributions of nucleotide excision repair, DNA polymerase eta, and homologous recombination to replication of UV-irradiated herpes simplex virus type 1Transcriptional coactivator HCF-1 couples the histone chaperone Asf1b to HSV-1 DNA replication componentsIdentification of rep-associated factors in herpes simplex virus type 1-induced adeno-associated virus type 2 replication compartments.ATR and ATRIP are recruited to herpes simplex virus type 1 replication compartments even though ATR signaling is disabled.Chromatin at the intersection of viral infection and DNA damageArchitecture of replication compartments formed during Epstein-Barr virus lytic replication.Herpes simplex virus reorganizes the cellular DNA repair and protein quality control machinery.Relocalization of the Mre11-Rad50-Nbs1 complex by the adenovirus E4 ORF3 protein is required for viral replicationHSV-1 ICP0: An E3 Ubiquitin Ligase That Counteracts Host Intrinsic and Innate ImmunityDNA repair proteins affect the lifecycle of herpes simplex virus 1.The intrinsic antiviral defense to incoming HSV-1 genomes includes specific DNA repair proteins and is counteracted by the viral protein ICP0.Processing of lagging-strand intermediates in vitro by herpes simplex virus type 1 DNA polymeraseDengue virus capsid protein binds core histones and inhibits nucleosome formation in human liver cells.Dissection of a novel nuclear localization signal in open reading frame 29 of varicella-zoster virus.Productive replication of human papillomavirus 31 requires DNA repair factor Nbs1.Structure of the herpes simplex virus 1 genome: manipulation of nicks and gaps can abrogate infectivity and alter the cellular DNA damage response.Evidence that herpes simplex virus DNA derived from quiescently infected cells in vitro, and latently infected cells in vivo, is physically damagedNuclear IFI16 induction of IRF-3 signaling during herpesviral infection and degradation of IFI16 by the viral ICP0 proteinInhibition of the ATM/p53 signal transduction pathway by Kaposi's sarcoma-associated herpesvirus interferon regulatory factor 1.Efficient herpes simplex virus 1 replication requires cellular ATR pathway proteinsInsight into the mechanism of inhibition of adeno-associated virus by the Mre11/Rad50/Nbs1 complexHerpes simplex virus type 1 single strand DNA binding protein and helicase/primase complex disable cellular ATR signaling.Nuclear domain 10 of the viral aspect.Herpes simplex virus immediate-early protein ICP0 is targeted by SIAH-1 for proteasomal degradation.DNA mismatch repair proteins are required for efficient herpes simplex virus 1 replicationCharacterization of the uracil-DNA glycosylase activity of Epstein-Barr virus BKRF3 and its role in lytic viral DNA replication.Oncolytic virus-mediated manipulation of DNA damage responses: synergy with chemotherapy in killing glioblastoma stem cells.
P2860
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P2860
Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage respo
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
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
name
Recruitment of cellular recomb ...... uction of the DNA damage respo
@ast
Recruitment of cellular recomb ...... uction of the DNA damage respo
@en
type
label
Recruitment of cellular recomb ...... uction of the DNA damage respo
@ast
Recruitment of cellular recomb ...... uction of the DNA damage respo
@en
prefLabel
Recruitment of cellular recomb ...... uction of the DNA damage respo
@ast
Recruitment of cellular recomb ...... uction of the DNA damage respo
@en
P2860
P1433
P1476
Recruitment of cellular recomb ...... ion of the DNA damage response
@en
P2093
Dianna E Wilkinson
P2860
P304
P356
10.1128/JVI.78.9.4783-4796.2004
P577
2004-05-01T00:00:00Z