Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/113756/1/ppul23243.pd
Molecular techniques have uncovered vast numbers of organisms in the cystic fibrosis (CF) airways, t...
RATIONALE: The underlying defect in the cystic fibrosis (CF) airway leads to defective mucociliar...
Repeated pulmonary exacerbation and progressive lung function decline characterize cystic fibrosis (...
peer-reviewedBackground: Molecular techniques have uncovered vast numbers of organisms in the cysti...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
© The Author(s), 2014. This article is distributed under the terms of the Creative Commons Attributi...
peer-reviewedThe cystic fibrosis (CF) lung harbours a diverse microbiome and reduced diversity in th...
The defective mucociliary clearance due to CFTR malfunctioning causes predisposition to the coloniza...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Infection plays a critical role in the pathogenesis of cystic fibrosis (CF) lung disease. Over the p...
<div><p>Background</p><p>Molecular techniques have uncovered vast numbers of organisms in the cystic...
Cystic fibrosis (CF) is caused by mutations in the CFTR gene that predispose the airway to infection...
peer reviewedThe cystic fibrosis (CF) lung harbours a diverse microbiome and reduced diversity in th...
While much research supports a polymicrobial view of the CF airway, one in which the community is se...
Molecular techniques have uncovered vast numbers of organisms in the cystic fibrosis (CF) airways, t...
RATIONALE: The underlying defect in the cystic fibrosis (CF) airway leads to defective mucociliar...
Repeated pulmonary exacerbation and progressive lung function decline characterize cystic fibrosis (...
peer-reviewedBackground: Molecular techniques have uncovered vast numbers of organisms in the cysti...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
© The Author(s), 2014. This article is distributed under the terms of the Creative Commons Attributi...
peer-reviewedThe cystic fibrosis (CF) lung harbours a diverse microbiome and reduced diversity in th...
The defective mucociliary clearance due to CFTR malfunctioning causes predisposition to the coloniza...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Infection plays a critical role in the pathogenesis of cystic fibrosis (CF) lung disease. Over the p...
<div><p>Background</p><p>Molecular techniques have uncovered vast numbers of organisms in the cystic...
Cystic fibrosis (CF) is caused by mutations in the CFTR gene that predispose the airway to infection...
peer reviewedThe cystic fibrosis (CF) lung harbours a diverse microbiome and reduced diversity in th...
While much research supports a polymicrobial view of the CF airway, one in which the community is se...
Molecular techniques have uncovered vast numbers of organisms in the cystic fibrosis (CF) airways, t...
RATIONALE: The underlying defect in the cystic fibrosis (CF) airway leads to defective mucociliar...
Repeated pulmonary exacerbation and progressive lung function decline characterize cystic fibrosis (...
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