Real-time PCR analysis of trinucleotide repeat allele expansions in the androgen receptor gene

dc.contributor.authorChatzikyriakidou, A.en
dc.contributor.authorYapijakis, C.en
dc.contributor.authorSofikitis, N.en
dc.contributor.authorVassilopoulos, D.en
dc.contributor.authorGeorgiou, I.en
dc.date.accessioned2015-11-24T18:54:56Z
dc.date.available2015-11-24T18:54:56Z
dc.identifier.issn1084-8592-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18777
dc.rightsDefault Licence-
dc.subjectAllelesen
dc.subjectChromosomes, Human, Xen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMuscular Disorders, Atrophic/geneticsen
dc.subjectReceptors, Androgen/*geneticsen
dc.subjectTransition Temperatureen
dc.subject*Trinucleotide Repeat Expansionen
dc.titleReal-time PCR analysis of trinucleotide repeat allele expansions in the androgen receptor geneen
heal.abstractINTRODUCTION: The expansion of specific trinucleotide repeats results in certain genetic disorders. METHOD: Real-time PCR analysis was used to rapidly discriminate between normal and expanded (CAG)(n) alleles in the androgen receptor gene. RESULT: The difference in melting temperature (T(m)) between the most common normal and expanded alleles was approximately 1 degrees C. CONCLUSION: Real-time PCR analysis seems to be a highly reliable and rapid method, which may facilitate the first molecular approach to human trinucleotide repeat disorders.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/16392902-
heal.journalNameMol Diagnen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2005-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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