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dc.contributor.authorMonsicha Pongpomen_US
dc.contributor.authorThira Sirisanthanaen_US
dc.contributor.authorNongnuch Vanittanakomen_US
dc.date.accessioned2018-09-10T03:21:06Z-
dc.date.available2018-09-10T03:21:06Z-
dc.date.issued2009-12-03en_US
dc.identifier.issn14602709en_US
dc.identifier.issn13693786en_US
dc.identifier.other2-s2.0-70749124150en_US
dc.identifier.other10.1080/13693780802484875en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70749124150&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59755-
dc.description.abstractWe previously reported a nested PCR assay for specific identification of 18S ribosomal DNA of Penicillium marneffei. In this study, the assay was used to detect the DNA of P. marneffei in serum samples. Sensitivity of the test was 4 pg/l and 0.4 fg/l when the cycle numbers used for nested reactions were 15 and 30, respectively. Twenty four out of 35 sera (68.6%) collected from patients with culture confirmed penicilliosis marneffei were positive, while normal healthy and non-P. marneffei infected HIV-positive sera were negative. The results suggested that the assay could be applied for the diagnosis of infections due to P. marneffei. © 2009 ISHAM.en_US
dc.subjectMedicineen_US
dc.subjectVeterinaryen_US
dc.titleApplication of nested PCR to detect Penicillium marneffei in serum samplesen_US
dc.typeJournalen_US
article.title.sourcetitleMedical Mycologyen_US
article.volume47en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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