Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59334
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dc.contributor.authorUnthika Chamrasen_US
dc.contributor.authorKanyakan Sukunthamalaen_US
dc.contributor.authorSakorn Pornpraserten_US
dc.date.accessioned2018-09-10T03:13:56Z-
dc.date.available2018-09-10T03:13:56Z-
dc.date.issued2009-12-01en_US
dc.identifier.issn1532432Xen_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-72049083248en_US
dc.identifier.other10.3109/03630260903336560en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=72049083248&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59334-
dc.description.abstractGel electrophoresis and ethidium bromide staining are routine methods in molecular laboratories. However, they are not ideally suited to large scale analyses in clinical laboratories. We used SYTO9 and high resolution melting (HRM) analyses for identification of the common β0-thalassemia (β0-thal) in Southeast Asia including the codons 17 (A>T), 4142 (-TCTT) and 7172 (A) mutations. Multiplex amplification refractory mutation system-polymerase chain reaction (MARMS-PCR) was performed on 102 blood samples that had Hb A2 levels between 3.1 and 9.9. The SYTO9 HRM analysis showed specific characteristic peaks of each investigated type of β0- thal mutation. Results of MARMS-PCR followed by SYTO9 HRM analyses were completely consistent with results of those analyzed by gel electrophoresis. Moreover, the β0-thal 3.5 kb gene deletion could be identified in two samples with Hb A2 levels of >4 by GREEN1 HRM analysis. The SYTO9 and SYBR GREEN1 HRM analysis is simple and rapid. This approach will facilitate laboratory diagnosis and genetic counseling for regions with a high prevalence of β-thal. © Informa UK Ltd.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleSYTO9 and SYBR green1 with high resolution melting analysis for molecular confirmatory testing of the common Southeast Asian β0- thalassemia mutationsen_US
dc.typeJournalen_US
article.title.sourcetitleHemoglobinen_US
article.volume33en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsChiang Mai Neurological Hospitalen_US
Appears in Collections:CMUL: Journal Articles

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