Three of the four nucleocapsid proteins of Marburg virus, NP, VP35, and L, are sufficient to mediate replication and transcription of Marburg virus-specific monocistronic minigenomes.
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Nucleocapsid formation and RNA synthesis of Marburg virus is dependent on two coiled coil motifs in the nucleoproteinDRBP76 associates with Ebola virus VP35 and suppresses viral polymerase functionMutual antagonism between the Ebola virus VP35 protein and the RIG-I activator PACT determines infection outcomeEbola virus protein VP35 impairs the function of interferon regulatory factor-activating kinases IKKepsilon and TBK-1Marburg Virus Reverse Genetics SystemsInteraction with Tsg101 is necessary for the efficient transport and release of nucleocapsids in marburg virus-infected cellsStructural basis for Marburg virus VP35-mediated immune evasion mechanismsA PPxY motif within the VP40 protein of Ebola virus interacts physically and functionally with a ubiquitin ligase: implications for filovirus buddingA small stem-loop structure of the Ebola virus trailer is essential for replication and interacts with heat-shock protein A8Structural Insight into Nucleoprotein Conformation Change Chaperoned by VP35 peptide in Marburg virus.A coevolution analysis for identifying protein-protein interactions by Fourier transformComparison of the transcription and replication strategies of marburg virus and Ebola virus by using artificial replication systemsEstablishment of fruit bat cells (Rousettus aegyptiacus) as a model system for the investigation of filoviral infectionRNA polymerase I-driven minigenome system for Ebola viruses.Role of protein phosphatase 1 in dephosphorylation of Ebola virus VP30 protein and its targeting for the inhibition of viral transcription.Structural dissection of Ebola virus and its assembly determinants using cryo-electron tomographyRescue of recombinant Marburg virus from cDNA is dependent on nucleocapsid protein VP30The spatio-temporal distribution dynamics of Ebola virus proteins and RNA in infected cellsEbola virus VP30-mediated transcription is regulated by RNA secondary structure formation.Filovirus replication and transcription.VP35 knockdown inhibits Ebola virus amplification and protects against lethal infection in miceDetermination of specific antibody responses to the six species of ebola and Marburg viruses by multiplexed protein microarraysAnalysis of the highly diverse gene borders in Ebola virus reveals a distinct mechanism of transcriptional regulation.Ebolavirus VP35 is a multifunctional virulence factor.Reverse genetic generation of recombinant Zaire Ebola viruses containing disrupted IRF-3 inhibitory domains results in attenuated virus growth in vitro and higher levels of IRF-3 activation without inhibiting viral transcription or replication.Key genomic changes necessary for an in vivo lethal mouse marburgvirus variant selection process.Sequence variability in viral genome non-coding regions likely contribute to observed differences in viral replication amongst MARV strainsThe Ebola virus VP35 protein inhibits activation of interferon regulatory factor 3.Recombinant Marburg virus expressing EGFP allows rapid screening of virus growth and real-time visualization of virus spread.Innate immune evasion by filovirusesAssembly of the Ebola Virus Nucleoprotein from a Chaperoned VP35 ComplexHighly conserved regions in Ebola virus RNA dependent RNA polymerase may be act as a universal novel peptide vaccine target: a computational approachThe Ebola virus ribonucleoprotein complex: a novel VP30-L interaction identifiedA cell-based high-throughput approach to identify inhibitors of influenza A virus.Inclusion bodies are a site of ebolavirus replicationForty-five years of Marburg virus research.Transcriptional Regulation in Ebola Virus: Effects of Gene Border Structure and Regulatory Elements on Gene Expression and Polymerase Scanning Behavior.Minigenomes, transcription and replication competent virus-like particles and beyond: reverse genetics systems for filoviruses and other negative stranded hemorrhagic fever virusesThe Ebola virus matrix protein deeply penetrates the plasma membrane: an important step in viral egress.DNA topoisomerase 1 facilitates the transcription and replication of the Ebola virus genome.
P2860
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P2860
Three of the four nucleocapsid proteins of Marburg virus, NP, VP35, and L, are sufficient to mediate replication and transcription of Marburg virus-specific monocistronic minigenomes.
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին 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
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@ast
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@en
type
label
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@ast
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@en
prefLabel
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@ast
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@en
P2093
P2860
P1433
P1476
Three of the four nucleocapsid ...... fic monocistronic minigenomes.
@en
P2093
B Lötfering
E Mühlberger
P2860
P304
P577
1998-11-01T00:00:00Z