Detection and genotyping of herpes simplex virus types 1 and 2 by polymerase chain reaction

dc.contributor.authorLucotte, G.en
dc.contributor.authorBathelier, C.en
dc.contributor.authorLespiaux, V.en
dc.contributor.authorBali, C.en
dc.contributor.authorChampenois, T.en
dc.date.accessioned2015-11-24T19:25:07Z
dc.date.available2015-11-24T19:25:07Z
dc.identifier.issn0890-8508-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/22573
dc.rightsDefault Licence-
dc.subjectBase Sequenceen
dc.subjectDNA Primersen
dc.subjectFemaleen
dc.subjectGenotypeen
dc.subjectHerpes Genitalis/diagnosisen
dc.subjectHerpes Simplex/diagnosisen
dc.subjectHerpesvirus 1, Human/genetics/*isolation & purificationen
dc.subjectHerpesvirus 2, Human/genetics/*isolation & purificationen
dc.subjectHumansen
dc.subjectMolecular Sequence Dataen
dc.subjectPolymerase Chain Reaction/*methodsen
dc.subjectRetrospective Studiesen
dc.subjectSensitivity and Specificityen
dc.subjectSkin/virologyen
dc.subjectVagina/virologyen
dc.titleDetection and genotyping of herpes simplex virus types 1 and 2 by polymerase chain reactionen
heal.abstractA simple and rapid polymerase chain reaction (PCR) procedure was developed for simultaneous detection and typing of herpes simplex virus (HSV) types 1 and 2. It was possible to detect and type HSV using two primers pairs in a simultaneous double PCR reaction, where the type of HSV present was determined on the basis of an ethidium-bromide-stained band after agarose gel electrophoresis. This PCR assay was tested on about 500 clinical specimens.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/8569766-
heal.journalNameMol Cell Probesen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate1995-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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