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dc.contributor.authorRatikorn Gamngoenen_US
dc.contributor.authorChanyanuch Putimen_US
dc.contributor.authorParichat Saleeen_US
dc.contributor.authorPonrut Phunpaeen_US
dc.contributor.authorBordin Butr-Indren_US
dc.date.accessioned2018-09-05T04:30:40Z-
dc.date.available2018-09-05T04:30:40Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn1873281Xen_US
dc.identifier.issn14729792en_US
dc.identifier.other2-s2.0-85032943312en_US
dc.identifier.other10.1016/j.tube.2017.11.002en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85032943312&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58773-
dc.description.abstract© 2017 Elsevier Ltd Drug resistance to Mycobacterium tuberculosis is a major health problem worldwide. Mycobacterium tuberculosis can progress to be mono-drug resistant or multi-drug resistant by improper treatment. The chemical stress of M. tuberculosis was performed in this study. Rv0559c is an unknown secreted protein. Rv0560c is a putative benzoquinone methyltransferase of M. tuberculosis cell. Rv0559c gene is located downstream of Rv0560c gene. Both genes respond to salicylate stress. Drug susceptible, isoniazid resistant, rifampicin resistant and multi-drug resistant phenotypes of M. tuberculosis clinical isolates were used to determine the expression of Rv0559c and Rv0560c by qRT-PCR. In all of mycobacteria strains there was up-regulation in both genes when stressed with isoniazid. This study determined the expression of both genes, which may play important roles in the drug resistance mechanism of mycobacteria.en_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleA comparison of Rv0559c and Rv0560c expression in drug-resistant Mycobacterium tuberculosis in response to first-line antituberculosis drugsen_US
dc.typeJournalen_US
article.title.sourcetitleTuberculosisen_US
article.volume108en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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