Ivacaftor partially corrects airway inflammation in a humanized G551D rat
Animal models have been highly informative for understanding the pathogenesis and progression of cystic fibrosis (CF) lung disease. In particular, the CF rat models recently developed have addressed mechanistic causes of the airway mucus defect characteristic of CF, and how these may change when cys...
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Veröffentlicht in: | American journal of physiology. Lung cellular and molecular physiology 2021-06, Vol.320 (6), p.L1093-L1100 |
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Sprache: | eng |
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