Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
about
Cyclooxygenase-2 inhibitor blocks the production of West Nile virus-induced neuroinflammatory markers in astrocytes.Epigenetic changes mediated by microRNA miR29 activate cyclooxygenase 2 and lambda-1 interferon production during viral infection.Differential COX-2 induction by viral and bacterial PAMPs: Consequences for cytokine and interferon responses and implications for anti-viral COX-2 directed therapies.Prostaglandin E2 As a Modulator of Viral Infections.Inhibition of viral protein translation by indomethacin in vesicular stomatitis virus infection: role of eIF2α kinase PKR.COX-2 induction during murine gammaherpesvirus 68 infection leads to enhancement of viral gene expression.
P2860
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
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
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@en
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@nl
type
label
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@en
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@nl
prefLabel
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@en
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@nl
P1476
Selective inhibition of COX-2 is beneficial to mice infected intranasally with VSV.
@en
P2093
Andrew Restivo
Nannan Chen
P304
P356
10.1016/S0090-6980(01)00185-X
P577
2002-02-01T00:00:00Z