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dc.contributor.authorCohen, Kevin
dc.contributor.authorNazik, Hasan
dc.contributor.authorBanaei, Niaz
dc.contributor.authorChoudhary, Varun
dc.contributor.authorStevens, David A.
dc.contributor.authorMoss, Richard B.
dc.contributor.authorKarna, Vyshnavi
dc.contributor.authorClemons, Karl V.
dc.date.accessioned2021-03-04T13:17:04Z
dc.date.available2021-03-04T13:17:04Z
dc.identifier.citationNazik H., Moss R. B. , Karna V., Clemons K. V. , Banaei N., Cohen K., Choudhary V., Stevens D. A. , "Are Cystic Fibrosis Aspergillus fumigatus Isolates Different? Intermicrobial Interactions with Pseudomonas", MYCOPATHOLOGIA, cilt.182, ss.315-318, 2017
dc.identifier.issn0301-486X
dc.identifier.othervv_1032021
dc.identifier.otherav_7b95a1d7-a2be-4547-9cb1-5ec7ca5415e1
dc.identifier.urihttp://hdl.handle.net/20.500.12627/84598
dc.identifier.urihttps://doi.org/10.1007/s11046-016-0087-3
dc.description.abstractPseudomonas aeruginosa and Aspergillus fumigatus are the leading bacterial and fungal pathogens in cystic fibrosis (CF). We have shown that Af biofilms are susceptible to Pseudomonas, particularly CF phenotypes. Those studies were performed with a reference virulent non-CF Aspergillus. Pseudomonas resident in CF airways undergo profound genetic and phenotypic adaptations to the abnormal environment. Studies have also indicated Aspergillus from CF patients have unexpected profiles of antifungal susceptibility. This would suggest that Aspergillus isolates from CF patients may be different or altered from other clinical isolates. It is important to know whether Aspergillus may also be altered, as a result of that CF environment, in susceptibility to Pseudomonas. CF Aspergillus proved not different in that susceptibility.
dc.language.isoeng
dc.subjectMikoloji
dc.subjectBitki Koruma
dc.subjectFitopatoloji
dc.subjectZiraat
dc.subjectTarımsal Bilimler
dc.subjectTarım ve Çevre Bilimleri (AGE)
dc.subjectBitki ve Hayvan Bilimleri
dc.subjectMİKOLOJİ
dc.titleAre Cystic Fibrosis Aspergillus fumigatus Isolates Different? Intermicrobial Interactions with Pseudomonas
dc.typeMakale
dc.relation.journalMYCOPATHOLOGIA
dc.contributor.departmentStanford University , ,
dc.identifier.volume182
dc.identifier.startpage315
dc.identifier.endpage318
dc.contributor.firstauthorID241925


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