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dc.contributor.authorVida Delgado, Rafael Ángeles-ES
dc.date.accessioned2020-02-04T10:39:34Z-
dc.date.available2020-02-04T10:39:34Z-
dc.date.issued01/06/2017es_ES
dc.identifier.issn1569-1993es_ES
dc.identifier.urihttp://hdl.handle.net/11531/44668-
dc.descriptionArtículos en revistases_ES
dc.description.abstractLos análisis basados ​​en el ADN de muestras de vías respiratorias con FQ han desafiado las ideas sobre la etiología de las infecciones por FQ. Dos hallazgos notables son: (1) En la enfermedad pulmonar con FQ temprana, el ADN microbiano en las muestras generalmente deriva de diversas colecciones de microbios no considerados patógenos convencionales de la FQ. (2) En la enfermedad establecida (cuando dominan los patógenos convencionales de la FQ) los patógenos no convencionales son aún identificado, aunque en menor cantidad. Estos hallazgos son complicados porque las muestras de las vías respiratorias transitan por la orofaringe donde los patógenos no convencionales son muy abundantes. Además, los dispositivos de recolección (por ejemplo, broncoscopios) y los reactivos de análisis albergan ADN microbiano.es-ES
dc.description.abstractDNA-based analyses of CF airway samples have challenged ideas about the etiology of CF infections. Two notable findings are:(1) In early CF lung disease, the microbial DNA in samples typically derives from diverse collections of microbes not considered conventional CF pathogens.(2) In established disease (when conventional CF pathogens dominate) non-conventional pathogens are still identified, although in lesser quantities. These findings are complicated because airway samples transit through the oropharynx where non-conventional pathogens are highly abundant. In addition, collection devices (eg bronchoscopes) and analysis reagents harbor microbial DNAen-GB
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoes-ESes_ES
dc.rightsCreative Commons Reconocimiento-NoComercial-SinObraDerivada Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/es_ES
dc.sourceRevista: Journal of Cystic Fibrosis, Periodo: 12, Volumen: 16, Número: , Página inicial: on-line, Página final: on-linees_ES
dc.titleWS03. 7 Coexistence of prey and predator bacteria in cystic fibrosis lung microbiotaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.description.versioninfo:eu-repo/semantics/publishedVersiones_ES
dc.rights.holderes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.keywordsDNA-based analyses of CF airway samples have challenged ideas about the etiology of CF infections. Two notable findings are:(1) In early CF lung disease, the microbial DNA in samples typically derives from diverse collections of microbes not considered conventional CF pathogens.(2) In established disease (when conventional CF pathogens dominate) non-conventional pathogens are still identified, although in lesser quantities. These findings are complicated because airway samples transit through the oropharynx where non-conventional pathogens are highly abundant. In addition, collection devices (eg bronchoscopes) and analysis reagents harbor microbial DNAes-ES
dc.keywordsDNA-based analyses of CF airway samples have challenged ideas about the etiology of CF infections. Two notable findings are:(1) In early CF lung disease, the microbial DNA in samples typically derives from diverse collections of microbes not considered conventional CF pathogens.(2) In established disease (when conventional CF pathogens dominate) non-conventional pathogens are still identified, although in lesser quantities. These findings are complicated because airway samples transit through the oropharynx where non-conventional pathogens are highly abundant. In addition, collection devices (eg bronchoscopes) and analysis reagents harbor microbial DNAen-GB
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