The various Sendai virus C proteins are not functionally equivalent and exert both positive and negative effects on viral RNA accumulation during the course of infection.
about
Sendai virus Y proteins are initiated by a ribosomal shuntSendai virus C proteins must interact directly with cellular components to interfere with interferon actionSendai virus C proteins counteract the interferon-mediated induction of an antiviral stateComparison of predicted amino acid sequences of measles virus strains in the Edmonston vaccine lineage.Inhibition of STAT 1 phosphorylation by human parainfluenza virus type 3 C protein.Y2, the smallest of the Sendai virus C proteins, is fully capable of both counteracting the antiviral action of interferons and inhibiting viral RNA synthesis.Human parainfluenza virus type 4 is incapable of evading the interferon-induced antiviral effectThe amino-terminal half of Sendai virus C protein is not responsible for either counteracting the antiviral action of interferons or down-regulating viral RNA synthesisThe amino-terminal extensions of the longer Sendai virus C proteins modulate pY701-Stat1 and bulk Stat1 levels independently of interferon signaling.Attenuated and protease-profile modified sendai virus vectors as a new tool for virotherapy of solid tumors.Expression of the Sendai (murine parainfluenza) virus C protein alleviates restriction of measles virus growth in mouse cells.The M2-2 protein of human respiratory syncytial virus is a regulatory factor involved in the balance between RNA replication and transcriptionSuppression of the Sendai virus M protein through a novel short interfering RNA approach inhibits viral particle production but does not affect viral RNA synthesisA 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.A novel human parainfluenza virus type 1 (HPIV1) with separated P and C genes is useful for generating C gene mutants for evaluation as live-attenuated virus vaccine candidates.Sendai virus targets inflammatory responses, as well as the interferon-induced antiviral state, in a multifaceted manner.Rinderpest viruses lacking the C and V proteins show specific defects in growth and transcription of viral RNAs.Longer and shorter forms of Sendai virus C proteins play different roles in modulating the cellular antiviral response.Loss of Sendai virus C protein leads to accumulation of RIG-I immunostimulatory defective interfering RNA.Targeting of the Sendai virus C protein to the plasma membrane via a peptide-only membrane anchor.
P2860
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P2860
The various Sendai virus C proteins are not functionally equivalent and exert both positive and negative effects on viral RNA accumulation during the course of infection.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հուլիսին 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
The various Sendai virus C pro ...... uring the course of infection.
@ast
The various Sendai virus C pro ...... uring the course of infection.
@en
type
label
The various Sendai virus C pro ...... uring the course of infection.
@ast
The various Sendai virus C pro ...... uring the course of infection.
@en
prefLabel
The various Sendai virus C pro ...... uring the course of infection.
@ast
The various Sendai virus C pro ...... uring the course of infection.
@en
P2093
P2860
P1433
P1476
The various Sendai virus C pro ...... during the course of infection
@en
P2093
P2860
P304
P577
1998-07-01T00:00:00Z