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http://purl.uniprot.org/citations/18562585http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18562585http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18562585http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18562585http://www.w3.org/2000/01/rdf-schema#comment"Sequence analysis of the endoproteolytic cleavage site within the hemagglutinin (HA) precursor protein HA(0) is fundamental for studies of the molecular biology of influenza A viruses, in particular, for molecular pathotyping of subtype H5 and H7 isolates. A current problem for routine diagnostics is the emergence of new strains of the H5 or H7 subtype or even other subtypes which escape detection by commonly used reverse transcription-PCR (RT-PCR) protocols. Here, the first pan-HA (PanHA) RT-PCR assay targeting the HA(0) cleavage site of influenza A viruses of all 16 HA subtypes is reported. The assay was assessed in comparison to H5 and H7 subtype-specific RT-PCRs for the HA(0) cleavage site and a real-time RT-PCR detecting the M gene. A panel of 92 influenza A viruses was used for validation. Sequence data for influenza A viruses from 32 allantoic fluid samples and 11 diagnostic swab samples of all 16 HA subtypes were generated by direct sequencing of the PanHA RT-PCR products. The results demonstrate that the new PanHA RT-PCR assay--followed by cycle sequencing--can complement existing methods and strengthen the reliability of influenza A virus diagnostics, allowing both molecular pathotyping (H5 and H7) and subtyping (non-H5 or -H7) within a single approach."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.org/dc/terms/identifier"doi:10.1128/JCM.00466-08"xsd:string
http://purl.uniprot.org/citations/18562585http://purl.org/dc/terms/identifier"doi:10.1128/jcm.00466-08"xsd:string
http://purl.uniprot.org/citations/18562585http://purl.org/dc/terms/identifier"doi:10.1128/jcm.00466-08"xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Hoffmann B."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Hoffmann B."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Hoffmann B."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Beer M."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Beer M."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Beer M."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Grund C."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Grund C."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Grund C."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Gall A."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Gall A."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Gall A."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Harder T."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Harder T."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/author"Harder T."xsd:string
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18562585http://purl.uniprot.org/core/date"2008"xsd:gYear