Source: Annual Congress 2008 - Airway cell biology



Rating:

Share or cite this content

Citations should be made in the following way:
F. Gamarra, I. Danzer, C. Kellermann, R. Fischer, A. Bergner, R. M. Huber (Munich, Germany). Culture of nasal epithelial spheroids of cystic fibrosis patients to measure mucociliary function. Eur Respir J 2008; 32: Suppl. 52, 4489

Member's Comments

No comment yet.

Related content which might interest you: Investigation of the status of cystic fibrosis airway epithelial cells Source: Annual Congress 2008 - Multigenic expression analyses: a guide for diagnosis and therapy Year: 2008 Proteomics characterisation of nasal epithelial cells in cystic fibrosis Source: Annual Congress 2009 - New results in molecular pathology and functional genomics of non-neoplastic lung diseases Year: 2009 Ciliary function of the nasal and bronchial epithelium in children with cystic fibrosis Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new basic and clinical physiology research Year: 2012 Ciliary beat frequency in nasal and bronchial epithelial cells in patients with cystic fibrosis Source: Annual Congress 2011 - Cystic fibrosis: new basic, clinical and bacteriological knowledge Year: 2011 Normal nasal mucociliary clearance in CF children: evidence against a CFTR-related defect Source: Eur Respir J 2004; 24: 95-100 Year: 2004 Long-term clearance from small airways in patients with cystic fibrosis Source: Eur Respir J 2005; 25: 317-323 Year: 2005 Comparison of fluid secretion in nasal and bronchial spheroids from CF patients. Source: International Congress 2019 – Understanding lung disease: novel in vitro models Year: 2019 Studying ion transport in cultured epithelial cells Source: Annual Congress 2007 - WS1 - Educational Workshop: epithelial cell biology: culture methods and functional studies Year: 2007 Presence of mucus plugging is predictive of long term lung function in children with cystic fibrosis Source: International Congress 2017 – Cystic fibrosis: monitoring and biomarkers Year: 2017 Novel antiviral properties of azithromycin in cystic fibrosis airway epithelial cells Source: Eur Respir J 2015; 45: 428-439 Year: 2015 Distribution and characterisation of lung mast cells in cystic fibrosis Source: Annual Congress 2009 - Airway inflammation and host defence Year: 2009 Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis Source: Eur Respir J, 57 (1) 1902426; 10.1183/13993003.02426-2019 Year: 2021 Intestinal organoids to model cystic fibrosis Source: Eur Respir J, 54 (1) 1802379; 10.1183/13993003.02379-2018 Year: 2019 Individual treatment of cystic fibrosis by using intestinal organoids Source: International Congress 2015 – Advancing therapies for cystic fibrosis Year: 2015 Bronchial immunoglobulins and epithelial pIgR are upregulated in cystic fibrosis Source: International Congress 2017 – Cystic fibrosis: monitoring and biomarkers Year: 2017 Expansion of small sputum macrophages in cystic fibrosis airways Source: Annual Congress 2008 - Cystic fibrosis: new mechanisms, monitoring and treatment tools Year: 2008