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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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                <text>Dominio científico: Coronavirus</text>
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          <name>Title</name>
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              <text>Reference gene selection for quantitative real-time PCR analysis in virus infected cells: SARS corona virus, Yellow fever virus, Human Herpesvirus-6, Camelpox virus and Cytomegalovirus infections</text>
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          <name>Creator</name>
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              <text>Müller Marcel A, Bae Hi-Gung, Thulke Stefanie, Radonić Aleksandar, Siegert Wolfgang, Nitsche Andreas</text>
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              <text>Abstract Ten potential reference genes were compared for their use in experiments investigating cellular mRNA expression of virus infected cells. Human cell lines were infected with Cytomegalovirus, Human Herpesvirus-6, Camelpox virus, SARS coronavirus or Yellow fever virus. The expression levels of these genes and the viral replication were determined by real-time PCR. Genes were ranked by the BestKeeper tool, the GeNorm tool and by criteria we reported previously. Ranking lists of the genes tested were tool dependent. However, over all, β-actin is an unsuitable as reference gene, whereas TATA-Box binding protein and peptidyl-prolyl-isomerase A are stable reference genes for expression studies in virus infected cells.</text>
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              <text>2005</text>
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              <text>DOI: 10.1186/1743-422X-2-7</text>
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              <text>Virology Journal</text>
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          <name>Publisher</name>
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              <text>BMC</text>
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          <name>Coverage</name>
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            <elementText elementTextId="6061">
              <text>Infectious and parasitic diseases</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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