Homologous recombinational repair factors are recruited and loaded onto the viral DNA genome in Epstein-Barr virus replication compartments.
about
Modulation of DNA damage and repair pathways by human tumour virusesThe papillomavirus E1 helicase activates a cellular DNA damage response in viral replication fociFunctional connection between Rad51 and PML in homology-directed repair.Contributions of nucleotide excision repair, DNA polymerase eta, and homologous recombination to replication of UV-irradiated herpes simplex virus type 1Kaposi Sarcoma Herpesvirus (KSHV) Latency-Associated Nuclear Antigen (LANA) recruits components of the MRN (Mre11-Rad50-NBS1) repair complex to modulate an innate immune signaling pathway and viral latencyNoise cancellation: viral fine tuning of the cellular environment for its own genome replication.An E2F1-mediated DNA damage response contributes to the replication of human cytomegalovirus.Productive replication of human papillomavirus 31 requires DNA repair factor Nbs1.Uracil DNA glycosylase BKRF3 contributes to Epstein-Barr virus DNA replication through physical interactions with proteins in viral DNA replication complex.The chromatin remodeling factor SMARCB1 forms a complex with human cytomegalovirus proteins UL114 and UL44Gammaherpesvirus gene expression and DNA synthesis are facilitated by viral protein kinase and histone variant H2AX.Host genetics of Epstein-Barr virus infection, latency and disease.Conserved herpesvirus kinases target the DNA damage response pathway and TIP60 histone acetyltransferase to promote virus replication.Proteomic profiling of the human cytomegalovirus UL35 gene products reveals a role for UL35 in the DNA repair responseUracil DNA glycosylase interacts with the p32 subunit of the replication protein A complex to modulate HIV-1 reverse transcription for optimal virus dissemination.Coordinate regulation of DNA damage and type I interferon responses imposes an antiviral state that attenuates mouse gammaherpesvirus type 68 replication in primary macrophages.Ataxia telangiectasia mutated kinase controls chronic gammaherpesvirus infection.RAD51 and BRCA2 Enhance Oncolytic Adenovirus Type 5 Activity in Ovarian CancerInfection of a Single Cell Line with Distinct Strains of Human Cytomegalovirus Can Result in Large Variations in Virion Production and Facilitate Efficient Screening of Virus Protein Function.SMC1-mediated intra-S-phase arrest facilitates bocavirus DNA replication.Epstein-Barr viral productive amplification reprograms nuclear architecture, DNA replication, and histone deposition.Replication and recombination of herpes simplex virus DNAReplication of Epstein-Barr viral DNA.DNA virus replication compartments.Switching of EBV cycles between latent and lytic states.Regulation of Epstein-Barr virus reactivation from latency.The Ying-Yang of the virus-host interaction: control of the DNA damage response.At a crossroads: human DNA tumor viruses and the host DNA damage response.Modulation of homology-directed repair in T98G glioblastoma cells due to interactions between wildtype p53, Rad51 and HCMV IE1-72.Localization of Double-Strand Break Repair Proteins to Viral Replication Compartments following Lytic Reactivation of Kaposi's Sarcoma-Associated Herpesvirus.Activation of DNA Damage Response Pathways during Lytic Replication of KSHV.Epstein-Barr virus BZLF1 protein impairs accumulation of host DNA damage proteins at damage sites in response to DNA damage.Role of ATM in the formation of the replication compartment during lytic replication of Epstein-Barr virus in nasopharyngeal epithelial cells.Modulation of the DNA damage response during the life cycle of human papillomaviruses.Human papillomaviruses recruit cellular DNA repair and homologous recombination factors to viral replication centers.Stimulation of homology-directed repair at I-SceI-induced DNA breaks during the permissive life cycle of human cytomegalovirus.Spatiotemporally different DNA repair systems participate in Epstein-Barr virus genome maturation.Homologous Recombination Repair Factors Rad51 and BRCA1 Are Necessary for Productive Replication of Human Papillomavirus 31.Bocavirus infection induces a DNA damage response that facilitates viral DNA replication and mediates cell death.Coronavirus infection induces DNA replication stress partly through interaction of its nonstructural protein 13 with the p125 subunit of DNA polymerase δ.
P2860
Q26825783-5B0758AB-42A1-471E-A0DF-04CC466A0904Q28740852-6ABB51D4-4F45-434B-A276-2FDA410733D9Q31037336-566C88A6-8918-4F34-A877-38107F833629Q33538952-DB030F8A-2EDF-4CAE-A81D-4C3533847A4CQ33632932-A1E0F297-B7CE-49F5-9439-7B127725639AQ33780955-3C7540E3-5FF6-455C-A09A-5EBD8FF36413Q33904045-69C6A6F1-03D5-4B33-AA67-56D73F1D6923Q34057826-D6245534-6130-4741-B0F8-E4E28270BBE6Q34059171-B16FD2E2-0B69-44FD-B403-0E5DA3A7B44EQ34222134-F94607E0-9BE2-439C-9E75-CC771B2C6AB5Q35479323-9485B6E1-CEE5-4236-A643-70FFABC1D6E6Q35532450-0D807152-4FFC-457A-AA47-FF061BBB9505Q35660314-C00905D4-79EB-4FE0-ACE0-584096B97C26Q35665751-068889BE-1134-44ED-8B14-4024F5FF9875Q35986599-FAFFF0F2-F5A4-4661-99F6-0A295AD1F0F4Q36086702-85A7CA34-66AD-4888-8EE6-5705D666FAA6Q36397423-E1D0782C-081F-4E08-9347-F2CC7F7397D1Q36472419-8A594A81-151E-43D5-886C-F753D4190EB7Q36736886-5F1803F9-3F0E-4BE1-886C-1EA94CCD1A4FQ36759739-6EC5AC2F-65C6-42FB-8325-C55C0199226FQ37716502-CEA7664C-A656-4744-9032-E1F8B0698CF0Q37848529-8D9886F2-8E28-4FB8-A85C-2A71EB6771C2Q38071281-06C4F768-8F25-45B3-B318-D4C11D896B5BQ38164528-A9397A9E-FF5A-468B-A3C1-8226E446971FQ38171455-18A8D7E4-9607-4AE9-B67E-1F46743A0B35Q38208532-8581256C-D19A-4557-9655-50B68B1B72D5Q38356270-14F45C3C-6005-4C90-86BD-200C075E812FQ38388893-1DC61120-C6D7-40DD-A481-2FE40C35F1C6Q38562250-BF6294D3-BD31-41A1-95C2-44339D8ACC24Q38693768-5C669CBC-B71C-4440-B40C-BC23F095EA2CQ38865828-624C0AB0-22CC-4792-B6AD-7A944CB8EE80Q38871275-FA005509-402B-464E-8772-D693A927EEDCQ38943928-66CF3844-A2A9-4ED4-A015-429B4DE6B080Q39005827-B4C92E07-BFA4-4D8A-A774-73D374AFD0D1Q39323899-18FB4129-2131-4693-BD4A-D5AEADE27884Q39559207-396BE3C1-D605-4DFF-91AF-75A3E21FB89FQ39559227-CC86B9E5-81B0-472D-8BB9-F63A72A4AE61Q39605249-9A45D328-4A1C-4298-B61F-F49EA43B31F4Q39636146-1E59F201-45EB-4E4A-836B-B10655D38E36Q39707460-FFEBF5AA-2C1E-44E8-B992-4AED3688118F
P2860
Homologous recombinational repair factors are recruited and loaded onto the viral DNA genome in Epstein-Barr virus replication compartments.
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Homologous recombinational rep ...... irus replication compartments.
@ast
Homologous recombinational rep ...... irus replication compartments.
@en
type
label
Homologous recombinational rep ...... irus replication compartments.
@ast
Homologous recombinational rep ...... irus replication compartments.
@en
prefLabel
Homologous recombinational rep ...... irus replication compartments.
@ast
Homologous recombinational rep ...... irus replication compartments.
@en
P2093
P2860
P356
P1433
P1476
Homologous recombinational rep ...... irus replication compartments.
@en
P2093
Ayumi Kudoh
Hiroki Isomura
Sanae Nakayama
Satoko Iwahori
Takayuki Murata
Tatsuya Tsurumi
P2860
P304
P356
10.1128/JVI.00049-09
P577
2009-04-22T00:00:00Z