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Identification of Halophilic Microbes in Lung Fibrotic Tissue by Oligotyping

Idiopathic pulmonary fibrosis (IPF) is an incurable disease with poor prognosis and unknown etiology. The poor clinical outcome is associated with enhanced microbial burden in bronchoalveolar lavage fluid from IPF patients. However, whether microbes from the respiratory tract fluid cause the disease...

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Detalles Bibliográficos
Autores principales: D’Alessandro-Gabazza, Corina N., Méndez-García, Celia, Hataji, Osamu, Westergaard, Sara, Watanabe, Fumiaki, Yasuma, Taro, Toda, Masaaki, Fujimoto, Hajime, Nishihama, Kota, Fujiwara, Kentaro, Taguchi, Osamu, Kobayashi, Tetsu, Mackie, Roderick I., Cann, Isaac, Gabazza, Esteban C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127444/
https://www.ncbi.nlm.nih.gov/pubmed/30233503
http://dx.doi.org/10.3389/fmicb.2018.01892

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