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American Journal of Respiratory Cell and Molecular Biology|September 10, 2019
Lack of IL-1 Receptor Signaling Reduces Spontaneous Airway Eosinophilia in Juvenile Mice with Muco-Obstructive Lung DiseaseRyan Brown, Michelle Paulsen, Simone Schmidt, et al.
European Journal of Radiology|March 25, 2011
Morphologic and functional scoring of cystic fibrosis lung disease using MRIMonika Eichinger, Daiva-Elzbieta Optazaite, Annette Kopp-Schneider, et al.
The European Respiratory Journal|July 11, 2015
miR-17 overexpression in cystic fibrosis airway epithelial cells decreases interleukin-8 productionIrene K Oglesby, Sebastian F Vencken, Raman Agrawal, et al.
Pflugers Archiv : European Journal of Physiology|June 4, 2018
Expression and function of Anoctamin 1/TMEM16A calcium-activated chloride channels in airways of in vivo mouse models for cystic fibrosis researchAnne Hahn, Johanna J Salomon, Dominik Leitz, et al.
Antioxidants (Basel, Switzerland)|September 28, 2021
Increased Inflammatory Markers Detected in Nasal Lavage Correlate with Paranasal Sinus Abnormalities at MRI in Adolescent Patients with Cystic FibrosisJaehi Chung, Felix Wünnemann, Johanna Salomon, et al.
Respiration; International Review of Thoracic Diseases|April 16, 2023
Survival-Adjusted FEV1 and BMI Percentiles for Patients with Cystic Fibrosis before the Era of Triple CFTR Modulator Therapy in GermanyA Susanne Dittrich, Markus Dumke, Ferdinand Kapl, et al.
The European Respiratory Journal|July 10, 2025
Neutrophil-derived biomarkers in bronchiectasis: identifying a common therapeutic targetJames D Chalmers, Marcus A Mall, Kim G Nielsen, et al.
American Journal of Respiratory and Critical Care Medicine|July 20, 2021
Magnetic Resonance Imaging Detects Progression of Lung Disease and Impact of Newborn Screening in Preschool Children with Cystic FibrosisMirjam Stahl, Eva Steinke, Simon Y Graeber, et al.
American Journal of Respiratory and Critical Care Medicine|April 1, 2014
Lack of neutrophil elastase reduces inflammation, mucus hypersecretion, and emphysema, but not mucus obstruction, in mice with cystic fibrosis-like lung diseaseStefanie Gehrig, Julia Duerr, Michael Weitnauer, et al.
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