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dc.contributor.authorDelia C. Tangen_US
dc.contributor.authorSuthat Fucharoenen_US
dc.contributor.authorIvan Dingen_US
dc.contributor.authorGriffin P. Rodgersen_US
dc.contributor.otherNational Institutes of Health, Bethesdaen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.contributor.otherNational Institute of Diabetes and Digestive and Kidney Diseasesen_US
dc.date.accessioned2018-09-07T09:52:05Z-
dc.date.available2018-09-07T09:52:05Z-
dc.date.issued2001-01-01en_US
dc.identifier.citationJournal of Laboratory and Clinical Medicine. Vol.137, No.4 (2001), 290-295en_US
dc.identifier.issn00222143en_US
dc.identifier.other2-s2.0-0035068071en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035068071&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/26885-
dc.description.abstractThe α-thalassemias are common genetic disorders that arise from reduced synthesis of the α-globin chains. At present, large-scale carrier screening and clinically valuable antenatal detection programs have not been established for the congenital disorder α-thalassemia (α-thal). We have developed a simple nonradioactive polymerase chain reaction (PCR) approach that can detect and differentiate several common α-globin gene deletional α-thals regardless of the break points. When three primer sets wereused - two gene-specific sets for the α1- and α2-globin genes and one set for the β-actin gene (serving as an internal control) - PCR products from genomic DNA were simultaneously amplified and analyzed after coamplification and gel electrophoresis. The number of α-globin genes present in the subjects was determined by the intensity of α1and α2bands normalized with that of β-actin when using densitometry. Our results demonstrate that five common genotypes of deletional α-thal are differentiated by the ratios of α1/β-actin and α2/β-actin. We also examined the feasibility of coupling this allele-specific amplification to a color-complementary assay. This easy and reproducible PCR assay is suitable for identifying α-thal carriers in screenings of large populations and improving genetic counseling.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035068071&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleRapid differentiation of five common α-thalassemia genotypes by polymerase chain reactionen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1067/mlc.2001.113947en_US
Appears in Collections:Scopus 2001-2005

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