Nuclear domain 10, the site of DNA virus transcription and replication.
about
Nuclear structure in normal and Bloom syndrome cellsBovine papillomavirus E1 protein is sumoylated by the host cell Ubc9 proteinRegulation of p53 activity in nuclear bodies by a specific PML isoformCommon properties of nuclear body protein SP100 and TIF1alpha chromatin factor: role of SUMO modificationSp100 interacts with ETS-1 and stimulates its transcriptional activityPML contributes to a cellular mechanism of repression of herpes simplex virus type 1 infection that is inactivated by ICP0Evidence for a role of the cellular ND10 protein PML in mediating intrinsic immunity against human cytomegalovirus infectionsViral immediate-early proteins abrogate the modification by SUMO-1 of PML and Sp100 proteins, correlating with nuclear body disruptionCarboxy terminus of human herpesvirus 8 latency-associated nuclear antigen mediates dimerization, transcriptional repression, and targeting to nuclear bodies.Functional architecture in the cell nucleusInactivating a cellular intrinsic immune defense mediated by Daxx is the mechanism through which the human cytomegalovirus pp71 protein stimulates viral immediate-early gene expressionRNA-templated replication of hepatitis delta virus: genomic and antigenomic RNAs associate with different nuclear bodiesEpstein-Barr virus (EBV) SM protein induces and recruits cellular Sp110b to stabilize mRNAs and enhance EBV lytic gene expressionEstablishment of papillomavirus infection is enhanced by promyelocytic leukemia protein (PML) expressionFormation of nuclear foci of the herpes simplex virus type 1 regulatory protein ICP4 at early times of infection: localization, dynamics, recruitment of ICP27, and evidence for the de novo induction of ND10-like complexesThe herpes simplex virus ICP0 RING finger domain inhibits IRF3- and IRF7-mediated activation of interferon-stimulated genesCurrent understanding of the mechanism of HPV infectionCovalent modification of the homeodomain-interacting protein kinase 2 (HIPK2) by the ubiquitin-like protein SUMO-1PML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1The potential link between PML NBs and ICP0 in regulating lytic and latent infection of HSV-1Differential sub-nuclear distribution of hypoxia-inducible factors (HIF)-1 and -2 alpha impacts on their stability and mobility.CREB-binding protein (CBP)/p300 and RNA polymerase II colocalize in transcriptionally active domains in the nucleusThe transcriptional role of PML and the nuclear bodyPromyelocytic leukemia protein PML inhibits Nur77-mediated transcription through specific functional interactionsTelomeric DNA mediates de novo PML body formationKaposi's sarcoma-associated herpesvirus K-Rta exhibits SUMO-targeting ubiquitin ligase (STUbL) like activity and is essential for viral reactivationAdenovirus type 5 early region 1B 55K oncoprotein-dependent degradation of cellular factor Daxx is required for efficient transformation of primary rodent cellsp53 binding protein 1 (53BP1) is an early participant in the cellular response to DNA double-strand breaksND10 components relocate to sites associated with herpes simplex virus type 1 nucleoprotein complexes during virus infection.Herpesviruses carrying a Brainbow cassette reveal replication and expression of limited numbers of incoming genomesVisualization by live-cell microscopy of disruption of ND10 during herpes simplex virus type 1 infection.Nuclear heat shock response and novel nuclear domain 10 reorganization in respiratory syncytial virus-infected a549 cells identified by high-resolution two-dimensional gel electrophoresisICP0 induces the accumulation of colocalizing conjugated ubiquitin.Relocalization of the Mre11-Rad50-Nbs1 complex by the adenovirus E4 ORF3 protein is required for viral replicationElimination of ie1 significantly attenuates murine cytomegalovirus virulence but does not alter replicative capacity in cell cultureAnalysis of HCF, the cellular cofactor of VP16, in herpes simplex virus-infected cells.Herpes simplex virus ICP0 mutants are hypersensitive to interferonH-1 parvovirus-associated replication bodies: a distinct virus-induced nuclear structure.In vivo accumulation of cyclin A and cellular replication factors in autonomous parvovirus minute virus of mice-associated replication bodies.Interactions of herpes simplex virus type 1 with ND10 and recruitment of PML to replication compartments.
P2860
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P2860
Nuclear domain 10, the site of DNA virus transcription and replication.
description
1998 nî lūn-bûn
@nan
1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Nuclear domain 10, the site of DNA virus transcription and replication.
@ast
Nuclear domain 10, the site of DNA virus transcription and replication.
@en
Nuclear domain 10, the site of DNA virus transcription and replication.
@nl
type
label
Nuclear domain 10, the site of DNA virus transcription and replication.
@ast
Nuclear domain 10, the site of DNA virus transcription and replication.
@en
Nuclear domain 10, the site of DNA virus transcription and replication.
@nl
prefLabel
Nuclear domain 10, the site of DNA virus transcription and replication.
@ast
Nuclear domain 10, the site of DNA virus transcription and replication.
@en
Nuclear domain 10, the site of DNA virus transcription and replication.
@nl
P2860
P1433
P1476
Nuclear domain 10, the site of DNA virus transcription and replication.
@en
P2093
P2860
P304
P356
10.1002/(SICI)1521-1878(199808)20:8<660::AID-BIES9>3.0.CO;2-M
P407
P577
1998-08-01T00:00:00Z