NS2 is required for efficient translation of viral mRNA in minute virus of mice-infected murine cells.
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Parvovirus minute virus of mice induces a DNA damage response that facilitates viral replicationThe NS2 proteins of parvovirus minute virus of mice are required for efficient nuclear egress of progeny virions in mouse cells.Nuclear export factor CRM1 interacts with nonstructural proteins NS2 from parvovirus minute virus of miceMinute virus of mice NS1 interacts with the SMN protein, and they colocalize in novel nuclear bodies induced by parvovirus infectionPhylogenetic analysis reveals the emergence, evolution and dispersal of carnivore parvoviruses.Complementation for an essential ancillary non-structural protein function across parvovirus genera.Subcellular localization of Aleutian mink disease parvovirus proteins and DNA during permissive infection of Crandell feline kidney cells.Nonstructural proteins NS2 of minute virus of mice associate in vivo with 14-3-3 protein family members.Two parvoviruses that cause different diseases in mink have different transcription patterns: transcription analysis of mink enteritis virus and Aleutian mink disease parvovirus in the same cell lineParvovirus initiation factor PIF: a novel human DNA-binding factor which coordinately recognizes two ACGT motifs.Inhibition of parvovirus minute virus of mice replication by a peptide involved in the oligomerization of nonstructural protein NS1.An in-frame deletion in the NS protein-coding sequence of parvovirus H-1PV efficiently stimulates export and infectivity of progeny virions.Molecular Biology and Epidemiology of Hepatopancreatic parvovirus of Penaeid Shrimp.The cytotoxicity of the autonomous parvovirus minute virus of mice nonstructural proteins in FR3T3 rat cells depends on oncogene expressionProtein species of the parvovirus minute virus of mice strain MVMp: involvement of phosphorylated VP-2 subtypes in viral morphogenesis.Mosquito densonucleosis virus non-structural protein NS2 is necessary for a productive infection.Within-host genetic diversity of endemic and emerging parvoviruses of dogs and catsModulation of minute virus of mice cytotoxic activities through site-directed mutagenesis within the NS coding region.Parvoviral left-end hairpin ears are essential during infection for establishing a functional intranuclear transcription template and for efficient progeny genome encapsidation.Distinct host cell fates for human malignant melanoma targeted by oncolytic rodent parvoviruses.Enhanced cytoplasmic sequestration of the nuclear export receptor CRM1 by NS2 mutations developed in the host regulates parvovirus fitness.Genome replication and postencapsidation functions mapping to the nonstructural gene restrict the host range of a murine parvovirus in human cells.Chimeric and pseudotyped parvoviruses minimize the contamination of recombinant stocks with replication-competent viruses and identify a DNA sequence that restricts parvovirus H-1 in mouse cells.Efficient transactivation of the minute virus of mice P38 promoter requires upstream binding of NS1.Directed integration of minute virus of mice DNA into episomes.Minute Virus of Canines NP1 Protein Governs the Expression of a Subset of Essential Nonstructural Proteins via Its Role in RNA Processing.Mutations in the Non-Structural Protein-Coding Sequence of Protoparvovirus H-1PV Enhance the Fitness of the Virus and Show Key Benefits Regarding the Transduction Efficiency of Derived Vectors.
P2860
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P2860
NS2 is required for efficient translation of viral mRNA in minute virus of mice-infected murine cells.
description
1993 nî lūn-bûn
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1993年の論文
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1993年論文
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1993年論文
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1993年論文
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1993年論文
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NS2 is required for efficient ...... of mice-infected murine cells.
@en
type
label
NS2 is required for efficient ...... of mice-infected murine cells.
@en
prefLabel
NS2 is required for efficient ...... of mice-infected murine cells.
@en
P2093
P2860
P1433
P1476
NS2 is required for efficient ...... of mice-infected murine cells
@en
P2093
P2860
P304
P407
P577
1993-02-01T00:00:00Z