Source: Eur Respir J, 59 (2) 2100185; 10.1183/13993003.00185-2021



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Cameron B. Morrison, Kendall M. Shaffer, Kenza C. Araba, Matthew R. Markovetz, Jason A. Wykoff, Nancy L. Quinney, Shuyu Hao, Martial F. Delion, Alexis L. Flen, Lisa C. Morton, Jimmy Liao, David B. Hill, Mitchell L. Drumm, Wanda K. O'Neal, Mehmet Kesimer, Martina Gentzsch, Camille Ehre. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties via hydration. Eur Respir J, 59 (2) 2100185; 10.1183/13993003.00185-2021

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