Critical role for a high-affinity chemokine-binding protein in gamma-herpesvirus-induced lethal meningitis - Wikidata - awgldk - TriplyDB

Critical role for a high-affinity chemokine-binding protein in gamma-herpesvirus-induced lethal meningitis

Critical role for a high-affinity chemokine-binding protein in gamma-herpesvirus-induced lethal meningitis

http://www.wikidata.org/entity/Q39737732

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Gamma-herpesvirus latency requires T cell evasion during episome maintenance Interference of hepatitis C virus RNA replication by short interfering RNAs Dual GPCR and GAG mimicry by the M3 chemokine decoy receptor Inhibition of chemokine-glycosaminoglycan interactions in donor tissue reduces mouse allograft vasculopathy and transplant rejection Identification of candidate gammaherpesvirus 68 genes required for virus replication by signature-tagged transposon mutagenesis.A single CD8+ T cell epitope sets the long-term latent load of a murid herpesvirus Virus-encoded microRNAs facilitate gammaherpesvirus latency and pathogenesis in vivo Pathogenesis of a model gammaherpesvirus in a natural host Characterization of a novel wood mouse virus related to murid herpesvirus 4.Identification of proteins associated with murine gammaherpesvirus 68 virions.Construction and characterization of an infectious murine gammaherpesivrus-68 bacterial artificial chromosome.Murine gammaherpesvirus 68 lacking thymidine kinase shows severe attenuation of lytic cycle replication in vivo but still establishes latency Chemokine binding protein M3 of murine gammaherpesvirus 68 modulates the host response to infection in a natural host Proteomic characterization of murid herpesvirus 4 extracellular virions Selective gene expression of latent murine gammaherpesvirus 68 in B lymphocytes.Gammaherpesvirus infection modulates the temporal and spatial expression of SCGB1A1 (CCSP) and BPIFA1 (SPLUNC1) in the respiratory tract.Retention of anergy and inhibition of antibody responses during acute γ herpesvirus 68 infection Viral strategies for evading antiviral cellular immune responses of the host.A gammaherpesvirus-secreted activator of Vbeta4+ CD8+ T cells regulates chronic infection and immunopathology.The limits of protection by "memory" T cells in Ig-/- mice persistently infected with a gamma-herpesvirus Establishment of B-cell lines latently infected with reactivation-competent murine gammaherpesvirus 68 provides evidence for viral alteration of a DNA damage-signaling cascade.The m4 gene of murine gammaherpesvirus modulates productive and latent infection in vivo.Virtual screening of m3 protein antagonists for finding a model to study the gammaherpesvirus damaged immune system and chemokine related diseases.Pervasive transcription of a herpesvirus genome generates functionally important RNAs.Evasion of adaptive and innate immune response mechanisms by γ-herpesviruses.Rodent herpesvirus Peru encodes a secreted chemokine decoy receptor.Disruption of CCL21-induced chemotaxis in vitro and in vivo by M3, a chemokine-binding protein encoded by murine gammaherpesvirus 68.Effective vaccination against long-term gammaherpesvirus latency.Use of a virus-encoded enzymatic marker reveals that a stable fraction of memory B cells expresses latency-associated nuclear antigen throughout chronic gammaherpesvirus infection.The gammaherpesvirus chemokine binding protein binds to the N terminus of CXCL8.T-cell responses to the M3 immune evasion protein of murid gammaherpesvirus 68 are partially protective and induced with lytic antigen kinetics.An internal ribosome entry site directs translation of the murine gammaherpesvirus 68 MK3 open reading frame.Murine gammaherpesvirus 68 open reading frame 45 plays an essential role during the immediate-early phase of viral replication.Murine gammaherpesvirus 68 glycoprotein 150 does not contribute to latency amplification in vivo.A web interface for easy flexible protein-protein docking with ATTRACT Disruption of Erk-dependent type I interferon induction breaks the myxoma virus species barrier.

P2860

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P2860

Critical role for a high-affinity chemokine-binding protein in gamma-herpesvirus-induced lethal meningitis

http://www.wikidata.org/entity/Q39737732

description

2002 nî lūn-bûn

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2002年の論文

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年學術文章

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2002年學術文章

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2002年學術文章

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name

Critical role for a high-affin ...... irus-induced lethal meningitis

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Critical role for a high-affin ...... rus-induced lethal meningitis.

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type

label

Critical role for a high-affin ...... irus-induced lethal meningitis

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Critical role for a high-affin ...... rus-induced lethal meningitis.

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Critical role for a high-affin ...... irus-induced lethal meningitis

@en

Critical role for a high-affin ...... rus-induced lethal meningitis.

@nl

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P1433

Journal of Clinical Investigation

P1476

Critical role for a high-affin ...... irus-induced lethal meningitis

@en

P2093

Beth Levine

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James E Goldman

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Samuel H Speck

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Sharookh B Kapadia

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Victor van Berkel

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P2860

Complete sequence and genomic analysis of murine gammaherpesvirus 68

Chemokines--chemotactic cytokines that mediate inflammation

A broad spectrum secreted chemokine binding protein encoded by a herpesvirus

Murine gammaherpesvirus 68 encodes a functional regulator of complement activation

Three distinct regions of the murine gammaherpesvirus 68 genome are transcriptionally active in latently infected mice.

Unraveling immunity to gamma-herpesviruses: a new model for understanding the role of immunity in chronic virus infection.

Host and viral genetics of chronic infection: a mouse model of gamma-herpesvirus pathogenesis.

Disruption of the murine gammaherpesvirus 68 M1 open reading frame leads to enhanced reactivation from latency.

Identification of a gammaherpesvirus selective chemokine binding protein that inhibits chemokine action.

Murine gammaherpesvirus 68 cyclin D homologue is required for efficient reactivation from latency.

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905-914

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scholarly article

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10.1172/JCI14358

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7

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109

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Herbert W. "Skip" Virgin

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2002-04-01T00:00:00Z

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11927617

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150927

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