Cidofovir and brincidofovir reduce the pathology caused by systemic infection with human type 5 adenovirus in immunosuppressed Syrian hamsters, while ribavirin is largely ineffective in this model.
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HAdV-C6 Is a More Relevant Challenge Virus than HAdV-C5 for Testing Antiviral Drugs with the Immunosuppressed Syrian Hamster Model.Valganciclovir inhibits human adenovirus replication and pathology in permissive immunosuppressed female and male Syrian hamstersSTAT2 Knockout Syrian Hamsters Support Enhanced Replication and Pathogenicity of Human Adenovirus, Revealing an Important Role of Type I Interferon Response in Viral ControlLow-Level Expression of the E1B 20-Kilodalton Protein by Adenovirus 14p1 Enhances Viral Immunopathogenesis.New drug on the horizon for treating adenovirusDevelopment of Small-Molecule Antivirals for Ebola.Pathology in Permissive Syrian Hamsters after Infection with Species C Human Adenovirus (HAdV-C) Is the Result of Virus Replication: HAdV-C6 Replicates More and Causes More Pathology than HAdV-C5USC-087 protects Syrian hamsters against lethal challenge with human species C adenoviruses.
P2860
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P2860
Cidofovir and brincidofovir reduce the pathology caused by systemic infection with human type 5 adenovirus in immunosuppressed Syrian hamsters, while ribavirin is largely ineffective in this model.
description
2014 nî lūn-bûn
@nan
2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
@zh-my
2014年学术文章
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2014年學術文章
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2014年學術文章
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name
Cidofovir and brincidofovir re ...... ely ineffective in this model.
@en
type
label
Cidofovir and brincidofovir re ...... ely ineffective in this model.
@en
prefLabel
Cidofovir and brincidofovir re ...... ely ineffective in this model.
@en
P2093
P1433
P1476
Cidofovir and brincidofovir re ...... ely ineffective in this model.
@en
P2093
Ann E Tollefson
Baoling Ying
Jacqueline F Spencer
R Mark L Buller
William S M Wold
P356
10.1016/J.ANTIVIRAL.2014.10.005
P50
P577
2014-10-15T00:00:00Z