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Article

Efficient production of Rift Valley fever virus-like particles: The antiviral protein MxA can inhibit primary transcription of bunyaviruses

20 Jan 2009

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19155037
DOI: 10.1016/j.virol.2008.12.011

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Related research

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Efficient production of Rift Valley fever virus-like particles: The antiviral protein MxA can inhibit primary transcription of bunyavirusesPMID 19155037Read ↗

Inhibition of bunyaviruses, phleboviruses, and hantaviruses by human MxA proteinSemantic proximity Read ↗

Inhibition of Puumala and Tula Hantaviruses in Vero Cells by MxA ProteinSemantic proximity Read ↗

Inhibition of a Large Double-Stranded DNA Virus by MxA ProteinSemantic proximity Read ↗

Targeting the alphavirus virus replication process for antiviral developmentSemantic proximity Read ↗

RNA polymerase I-mediated expression of viral RNA for the rescue of infectious virulent and avirulent Rift Valley fever virusesSemantic proximity Read ↗

Evolution and Antiviral Specificities of Interferon-Induced Mx Proteins of Bats against Ebola, Influenza, and Other RNA VirusesSemantic proximity Read ↗

Antivirally active MxA protein sequesters La Crosse virus nucleocapsid protein into perinuclear complexesSemantic proximity Read ↗

The antiviral GTPase MxB is packaged into virions and binds via its N-terminal domain to alphaherpesvirus capsidsSemantic proximity Read ↗

Reverse genetics technology for Rift Valley fever virus: Current and future applications for the development of therapeutics and vaccinesSemantic proximity Read ↗

Anti-viral mechanism of barramundi Mx against betanodavirus involves the inhibition of viral RNA synthesis through the interference of RdRpSemantic proximity Read ↗

The N-terminal domain of MX1 proteins is essential for their antiviral activity against different families of RNA virusesSemantic proximity Read ↗

The Human Interferon-Induced MxA Protein Inhibits Early Stages of Influenza A Virus Infection by Retaining the Incoming Viral Genome in the CytoplasmSemantic proximity Read ↗

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