HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef. - Wikidata - wikimedia - TriplyDB

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

http://www.wikidata.org/entity/Q30410687

about

Vpu Protein: The Viroporin Encoded by HIV-1 Origin and diversity of human retroviruses Impacts of humanized mouse models on the investigation of HIV-1 infection: illuminating the roles of viral accessory proteins in vivo Evolutionary conflicts between viruses and restriction factors shape immunity Factors determining human-to-human transmissibility of zoonotic pathogens via contact Counteraction of the multifunctional restriction factor tetherin Vpu and BST2: Still Not There Yet?Pandemic HIV-1 Vpu overcomes intrinsic herd immunity mediated by tetherin.Vpu-Mediated Counteraction of Tetherin Is a Major Determinant of HIV-1 Interferon Resistance.Efficient Vpu-Mediated Tetherin Antagonism by an HIV-1 Group O Strain.Efficient SIVcpz replication in human lymphoid tissue requires viral matrix protein adaptation Reacquisition of Nef-mediated tetherin antagonism in a single in vivo passage of HIV-1 through its original chimpanzee host Human tetherin exerts strong selection pressure on the HIV-1 group N Vpu protein.The transmembrane domain of HIV-1 Vpu is sufficient to confer anti-tetherin activity to SIVcpz and SIVgor Vpu proteins: cytoplasmic determinants of Vpu function Non-M variants of human immunodeficiency virus type 1.Tetherin can restrict cell-free and cell-cell transmission of HIV from primary macrophages to T cells.Simian-Human immunodeficiency viruses expressing chimeric subtype B/C Vpu proteins demonstrate the importance of the amino terminal and transmembrane domains in the rate of CD4(+) T cell loss in macaques.Nef proteins of epidemic HIV-1 group O strains antagonize human tetherin.A rare missense variant abrogates the signaling activity of tetherin/BST-2 without affecting its effect on virus release Involvement of a C-terminal motif in the interference of primate lentiviral Vpu proteins with CD1d-mediated antigen presentation.HIV Vpu Interferes with NF-κB Activity but Not with Interferon Regulatory Factor 3.HIV-1 Vpu interference with innate cell-mediated immune mechanisms.Mucosal stromal fibroblasts markedly enhance HIV infection of CD4+ T cells.Construction of a high titer infectious HIV-1 subtype C proviral clone from South Africa.A comparative mutational analysis of HIV-1 Vpu subtypes B and C for the identification of determinants required to counteract BST-2/Tetherin and enhance viral egress.Preservation of tetherin and CD4 counter-activities in circulating Vpu alleles despite extensive sequence variation within HIV-1 infected individuals.The origin and molecular epidemiology of HIV.Enhanced production of enveloped viruses in BST-2-deficient cell lines.Various plus unique: Viral protein U as a plurifunctional protein for HIV-1 replication Ion Channel Activity of Vpu Proteins Is Conserved throughout Evolution of HIV-1 and SIV.The Potency of Nef-Mediated SERINC5 Antagonism Correlates with the Prevalence of Primate Lentiviruses in the Wild.HIV-1 Vpu mediated downregulation of CD155 requires alanine residues 10, 14 and 18 of the transmembrane domain Highlights, predictions, and changes.The KT Jeang Retrovirology prize 2016: Frank Kirchhoff.Inhibiting the Ins and Outs of HIV Replication: Cell-Intrinsic Antiretroviral Restrictions at the Plasma Membrane.Preadaptation of Simian Immunodeficiency Virus SIVsmm Facilitated Env-Mediated Counteraction of Human Tetherin by Human Immunodeficiency Virus Type 2

P2860

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P2860

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

http://www.wikidata.org/entity/Q30410687

description

2011 nî lūn-bûn

@nan

2011 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

@ast

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

@en

type

label

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

@ast

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

@en

prefLabel

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

@ast

HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

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HIV-1 Group P is unable to antagonize human tetherin by Vpu, Env or Nef.

@en

P2093

Daniel Sauter

http://www.w3.org/2001/XMLSchema#string

Greg J Towers

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Ravindra K Gupta

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Sarah J Petit

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P2860

HIV-1 Vpu neutralizes the antiviral factor Tetherin/BST-2 by binding it and directing its beta-TrCP2-dependent degradation

Relaxed phylogenetics and dating with confidence

Species-specific activity of SIV Nef and HIV-1 Vpu in overcoming restriction by tetherin/BST2

Dating the age of the SIV lineages that gave rise to HIV-1 and HIV-2

A new human immunodeficiency virus derived from gorillas

Direct evidence of extensive diversity of HIV-1 in Kinshasa by 1960

Nef-Mediated Suppression of T Cell Activation Was Lost in a Lentiviral Lineage that Gave Rise to HIV-1

Co-localization of HIV-1 Nef with the AP-2 adaptor protein complex correlates with Nef-induced CD4 down-regulation

The molecular population genetics of HIV-1 group O

Identification of amino acid residues in APOBEC3G required for regulation by human immunodeficiency virus type 1 Vif and Virion encapsidation

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1742-4690-8-103

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8

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Frank Kirchhoff

Jean-christophe Plantier

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2011-12-15T00:00:00Z

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51881830

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