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            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Coronavirus</text>
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            <description>An account of the resource</description>
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                <text>Dominio científico: Coronavirus</text>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>Suppression of feline coronavirus replication in vitro by cyclosporin A</text>
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          <name>Creator</name>
          <description>An entity primarily responsible for making the resource</description>
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              <text>Tanaka Yoshikazu, Sato Yuka, Osawa Shuichi, Inoue Mai, Tanaka Satoka, Sasaki Takashi</text>
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          <description>An account of the resource</description>
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              <text>Abstract The feline infectious peritonitis virus (FIPV) is a member of the feline coronavirus family that causes FIP, which is incurable and fatal in cats. Cyclosporin A (CsA), an immunosuppressive agent that targets the nuclear factor pathway of activated T-cells (NF-AT) to bind cellular cyclophilins (CyP), dose-dependently inhibited FIPV replication in vitro. FK506 (an immunosuppressor of the pathway that binds cellular FK506-binding protein (FKBP) but not CyP) did not affect FIPV replication. Neither cell growth nor viability changed in the presence of either CsA or FK506, and these factors did not affect the NF-AT pathway in fcwf-4 cells. Therefore, CsA does not seem to exert inhibitory effects via the NF-AT pathway. In conclusion, CsA inhibited FIPV replication in vitro and further studies are needed to verify the practical value of CsA as an anti-FIPV treatment in vivo.</text>
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              <text>2012</text>
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          <name>Identifier</name>
          <description>An unambiguous reference to the resource within a given context</description>
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              <text>DOI: 10.1186/1297-9716-43-41</text>
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          <name>Source</name>
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              <text>Veterinary Research</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
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              <text>BMC</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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              <text>Veterinary medicine</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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              <text>EN</text>
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