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dc.contributor.authorYang, Yun-Liangen_US
dc.contributor.authorWang, Chih-Weien_US
dc.contributor.authorChen, Chiung-Tonyen_US
dc.contributor.authorWang, Min-Hsienen_US
dc.contributor.authorHsiao, Chin-Fuen_US
dc.contributor.authorLo, Hsiu Junyen_US
dc.date.accessioned2014-12-08T15:09:55Z-
dc.date.available2014-12-08T15:09:55Z-
dc.date.issued2009-03-01en_US
dc.identifier.issn0953-7562en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.mycres.2008.11.016en_US
dc.identifier.urihttp://hdl.handle.net/11536/7580-
dc.description.abstractAlthough Candida albicans cph1/cph1 efg1/efg1 mutant cells are not lethal to mice, they proliferated in infected mice instead of simply being cleared by the host immune system. Here, we have shown that the cph1/cph1 efg1/efg1 mutant partially protects mice from systemic infections by the lethal wild-type Candida albicans cells. Our results further indicate that a second dose of the cph1/cph1 efg1/efg1 mutant did not boost the degree of protection. (c) 2008 The British Mycological Society. Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectCandida albicansen_US
dc.subjectMouse modelen_US
dc.subjectProtectionen_US
dc.subjectVirulenceen_US
dc.titleNon-lethal Candida albicans cph1/cph1 efg1/efg1 mutant partially protects mice from systemic infections by lethal wild-type cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.mycres.2008.11.016en_US
dc.identifier.journalMYCOLOGICAL RESEARCHen_US
dc.citation.volume113en_US
dc.citation.issueen_US
dc.citation.spage388en_US
dc.citation.epage390en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000264693700011-
dc.citation.woscount3-
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