AbstractBackgroundFor cystic fibrosis (CF) patients there is a lack of good assays of disease activity and response to new therapeutic interventions, including gene therapy. Current measures of airways inflammation severity are insensitive or non-specific.MethodsBronchoalveolar lavage fluid from 39 CF children and 38 respiratory disease controls was obtained at bronchoscopy and analysed by surface enhanced laser desorption ionisation time of flight (SELDI-TOF) mass spectrometry. Recognized proteins were assessed for CF disease specificity. Individual protein identification of specific peaks was performed.Results1277 proteins/peptides, >4 kDa, were detected using 12 different surfaces and binding conditions. 202 proteins/peptides were differ...
Background and aims: Cystic Fibrosis (CF) lung disease is characterized by progressively declining l...
Monitoring clinical disease status in cystic fibrosis frequently requires invasive collection of cli...
To provide a review of the status of biomarkers in cystic fibrosis drug development, including regul...
AbstractBackgroundFor cystic fibrosis (CF) patients there is a lack of good assays of disease activi...
Cystic fibrosis (CF) lung disease is characterised by early airways infection and inflammation, chr...
OBJECTIVES: The aim of this work was to establish protein profiles in serum and nasal epithelial cel...
BackgroundProteomics can reveal molecular pathways of disease and provide translational perspectives...
Sputum biomarkers hold promise as a direct measure of inflammation within the cystic fibrosis (CF) l...
AbstractBackgroundThe focus of this study was to characterize a novel biomarker for cystic fibrosis ...
Cystic Fibrosis (CF) lung disease is characterized by high levels of cytokines and chemokines in the...
Complementary 2D-PAGE and ‘shotgun’ LC–MS/MS approaches were combined to identify medium and low-abu...
<div><p>Rationale</p><p>Monitoring clinical disease status in cystic fibrosis frequently requires in...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Cystic fibrosis (CF) lung disease is nowadays appreciated as a complex trait, characterised by dysfu...
AbstractBackgroundAdequate monitoring of cystic fibrosis lung disease is difficult. CF exacerbation ...
Background and aims: Cystic Fibrosis (CF) lung disease is characterized by progressively declining l...
Monitoring clinical disease status in cystic fibrosis frequently requires invasive collection of cli...
To provide a review of the status of biomarkers in cystic fibrosis drug development, including regul...
AbstractBackgroundFor cystic fibrosis (CF) patients there is a lack of good assays of disease activi...
Cystic fibrosis (CF) lung disease is characterised by early airways infection and inflammation, chr...
OBJECTIVES: The aim of this work was to establish protein profiles in serum and nasal epithelial cel...
BackgroundProteomics can reveal molecular pathways of disease and provide translational perspectives...
Sputum biomarkers hold promise as a direct measure of inflammation within the cystic fibrosis (CF) l...
AbstractBackgroundThe focus of this study was to characterize a novel biomarker for cystic fibrosis ...
Cystic Fibrosis (CF) lung disease is characterized by high levels of cytokines and chemokines in the...
Complementary 2D-PAGE and ‘shotgun’ LC–MS/MS approaches were combined to identify medium and low-abu...
<div><p>Rationale</p><p>Monitoring clinical disease status in cystic fibrosis frequently requires in...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Cystic fibrosis (CF) lung disease is nowadays appreciated as a complex trait, characterised by dysfu...
AbstractBackgroundAdequate monitoring of cystic fibrosis lung disease is difficult. CF exacerbation ...
Background and aims: Cystic Fibrosis (CF) lung disease is characterized by progressively declining l...
Monitoring clinical disease status in cystic fibrosis frequently requires invasive collection of cli...
To provide a review of the status of biomarkers in cystic fibrosis drug development, including regul...