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dc.contributor.authorUzun, O
dc.contributor.authorKocagoz, S
dc.contributor.authorCetinkaya, Y
dc.contributor.authorArikan, S
dc.contributor.authorUnal, S
dc.date.accessioned2019-12-16T09:19:09Z
dc.date.available2019-12-16T09:19:09Z
dc.date.issued1997
dc.identifier.issn0066-4804
dc.identifier.urihttps://doi.org/10.1128/AAC.41.5.1156
dc.identifier.urihttp://hdl.handle.net/11655/19628
dc.description.abstractThe in vitro activity of LY303366, a new echinocandin derivative, was evaluated with 191 yeast isolates by a broth microdilution method. The MICs at which 50% of the isolates were inhibited were 0.125 mu g/ml for Candida albicans and C. tropicalis, 0.25 mu g/ml for C. krusei, C. kefyr, and C. glabrata, and 2.0 mu g/ml for C. parapsilosis.
dc.language.isoen
dc.publisherAmer Soc Microbiology
dc.relation.isversionof10.1128/AAC.41.5.1156
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMicrobiology
dc.subjectPharmacology & Pharmacy
dc.titleIn Vitro Activity Of A New Echinocandin, Ly303366, Compared With Those Of Amphotericin B And Fluconazole Against Clinical Yeast Isolates
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalAntimicrobial Agents And Chemotherapy
dc.contributor.departmentKimya
dc.identifier.volume41
dc.identifier.issue5
dc.identifier.startpage1156
dc.identifier.endpage1157
dc.description.indexWoS


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