Longer and shorter forms of Sendai virus C proteins play different roles in modulating the cellular antiviral response.
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Cytopathogenesis of Sendai virus in well-differentiated primary pediatric bronchial epithelial cells.Conserved charged amino acids within Sendai virus C protein play multiple roles in the evasion of innate immune responsesRinderpest virus phosphoprotein gene is a major determinant of species-specific pathogenicityAntagonism to human BST-2/tetherin by Sendai virus glycoproteins.STAT2 acts as a host range determinant for species-specific paramyxovirus interferon antagonism and simian virus 5 replication.The amino-terminal half of Sendai virus C protein is not responsible for either counteracting the antiviral action of interferons or down-regulating viral RNA synthesisRoles of nonstructural protein nsP2 and Alpha/Beta interferons in determining the outcome of Sindbis virus infection.Ambisense sendai viruses are inherently unstable but are useful to study viral RNA synthesis.The amino-terminal extensions of the longer Sendai virus C proteins modulate pY701-Stat1 and bulk Stat1 levels independently of interferon signaling.Passage of a Sendai virus recombinant in embryonated chicken eggs leads to markedly rapid accumulation of U-to-C transitions in a limited region of the viral genomeParamyxovirus accessory proteins as interferon antagonists.Clustered basic amino acids of the small sendai virus C protein Y1 are critical to its RAN GTPase-mediated nuclear localization.Viruses and the type I interferon antiviral system: induction and evasion.Defective viral genomes arising in vivo provide critical danger signals for the triggering of lung antiviral immunityEvolution and structural organization of the C proteins of paramyxovirinae.Characterization of the amino acid residues of sendai virus C protein that are critically involved in its interferon antagonism and RNA synthesis down-regulation.Expression of the Sendai (murine parainfluenza) virus C protein alleviates restriction of measles virus growth in mouse cells.Antagonism of innate immunity by paramyxovirus accessory proteins.Overproduction of double-stranded RNA in vesicular stomatitis virus-infected cells activates a constitutive cell-type-specific antiviral responseImportance of the anti-interferon capacity of Sendai virus C protein for pathogenicity in mice.VIGOR extended to annotate genomes for additional 12 different viruses.A short peptide at the amino terminus of the Sendai virus C protein acts as an independent element that induces STAT1 instability.Human parainfluenza virus type 1 C proteins are nonessential proteins that inhibit the host interferon and apoptotic responses and are required for efficient replication in nonhuman primates.Sendai virus C protein plays a role in restricting PKR activation by limiting the generation of intracellular double-stranded RNA.Virus growth and antibody responses following respiratory tract infection of ferrets and mice with WT and P/V mutants of the paramyxovirus Simian Virus 5.Sendai virus targets inflammatory responses, as well as the interferon-induced antiviral state, in a multifaceted manner.The STAT2 activation process is a crucial target of Sendai virus C protein for the blockade of alpha interferon signalingRespiratory syncytial virus (RSV) nonstructural (NS) proteins as host range determinants: a chimeric bovine RSV with NS genes from human RSV is attenuated in interferon-competent bovine cells.Nipah virus V and W proteins have a common STAT1-binding domain yet inhibit STAT1 activation from the cytoplasmic and nuclear compartments, respectivelyA Kaposi's sarcoma-associated herpesvirus protein that forms inhibitory complexes with type I interferon receptor subunits, Jak and STAT proteins, and blocks interferon-mediated signal transduction.Sendai virus C protein impairs both phosphorylation and dephosphorylation processes of Stat1.Inhibition of the gamma interferon response by a Sendai virus C protein mutant with no STAT1-binding ability.Proteolytic processing and translation initiation: two independent mechanisms for the expression of the Sendai virus Y proteins.
P2860
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P2860
Longer and shorter forms of Sendai virus C proteins play different roles in modulating the cellular antiviral response.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Longer and shorter forms of Se ...... e cellular antiviral response.
@en
Longer and shorter forms of Se ...... e cellular antiviral response.
@nl
type
label
Longer and shorter forms of Se ...... e cellular antiviral response.
@en
Longer and shorter forms of Se ...... e cellular antiviral response.
@nl
prefLabel
Longer and shorter forms of Se ...... e cellular antiviral response.
@en
Longer and shorter forms of Se ...... e cellular antiviral response.
@nl
P2093
P2860
P1433
P1476
Longer and shorter forms of Se ...... e cellular antiviral response.
@en
P2093
P2860
P304
P356
10.1128/JVI.75.15.6800-6807.2001
P407
P577
2001-08-01T00:00:00Z