Mutation in murine coronavirus replication protein nsp4 alters assembly of double membrane vesicles.
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Targeting membrane-bound viral RNA synthesis reveals potent inhibition of diverse coronaviruses including the middle East respiratory syndrome virusSARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulumTopology and Membrane Anchoring of the Coronavirus Replication Complex: Not All Hydrophobic Domains of nsp3 and nsp6 Are Membrane SpanningMurine Hepatitis Virus Nonstructural Protein 4 Regulates Virus-Induced Membrane Modifications and Replication Complex FunctionDynamics of coronavirus replication-transcription complexes.Crystal Structure of the C-Terminal Cytoplasmic Domain of Non-Structural Protein 4 from Mouse Hepatitis Virus A59Structure of the C-terminal domain of nsp4 from feline coronavirusHigh-Resolution Analysis of Coronavirus Gene Expression by RNA Sequencing and Ribosome Profiling.Cognitive recovery in the aged rat after stroke and anti-Nogo-A immunotherapy.Mobility and interactions of coronavirus nonstructural protein 4.Coronaviruses post-SARS: update on replication and pathogenesis.The N-terminal region of severe acute respiratory syndrome coronavirus protein 6 induces membrane rearrangement and enhances virus replication.An interaction between the nucleocapsid protein and a component of the replicase-transcriptase complex is crucial for the infectivity of coronavirus genomic RNA.Coronaviruses: an overview of their replication and pathogenesis.NS4B self-interaction through conserved C-terminal elements is required for the establishment of functional hepatitis C virus replication complexes.Mutations across murine hepatitis virus nsp4 alter virus fitness and membrane modifications.RNA-RNA and RNA-protein interactions in coronavirus replication and transcriptionSevere acute respiratory syndrome coronavirus nonstructural proteins 3, 4, and 6 induce double-membrane vesiclesMurine hepatitis virus nsp4 N258T mutants are not temperature-sensitive.Autophagy in viral replication and pathogenesis.Involvement of autophagy in coronavirus replication.Porcine epidemic diarrhea virus ORF3 gene prolongs S-phase, facilitates formation of vesicles and promotes the proliferation of attenuated PEDV.A new cistron in the murine hepatitis virus replicase gene.Extensive coronavirus-induced membrane rearrangements are not a determinant of pathogenicity.Ultrastructural characterization of membranous torovirus replication factories.Detection of nonstructural protein 6 in murine coronavirus-infected cells and analysis of the transmembrane topology by using bioinformatics and molecular approaches.Expression and Cleavage of Middle East Respiratory Syndrome Coronavirus nsp3-4 Polyprotein Induce the Formation of Double-Membrane Vesicles That Mimic Those Associated with Coronaviral RNA Replication.Infectious Bronchitis Virus Nonstructural Protein 4 Alone Induces Membrane Pairing
P2860
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P2860
Mutation in murine coronavirus replication protein nsp4 alters assembly of double membrane vesicles.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Mutation in murine coronavirus ...... y of double membrane vesicles.
@en
Mutation in murine coronavirus ...... y of double membrane vesicles.
@nl
type
label
Mutation in murine coronavirus ...... y of double membrane vesicles.
@en
Mutation in murine coronavirus ...... y of double membrane vesicles.
@nl
prefLabel
Mutation in murine coronavirus ...... y of double membrane vesicles.
@en
Mutation in murine coronavirus ...... y of double membrane vesicles.
@nl
P2093
P2860
P1433
P1476
Mutation in murine coronavirus ...... y of double membrane vesicles.
@en
P2093
Amornrat Kanjanahaluethai
Mark A Clementz
Susan C Baker
Timothy E O'Brien
P2860
P304
P356
10.1016/J.VIROL.2008.01.018
P407
P577
2008-03-04T00:00:00Z