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Marsico Lung Institute / CF Center
Matthew R. Markovetz has not added Biography.
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Pathological mucus and impaired mucus clearance in cystic fibrosis patients result from increased concentration, not altered pH.
The European respiratory journal 12, 2018 | Pubmed ID: 30361244
Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties hydration.
The European respiratory journal 02, 2022 | Pubmed ID: 34172469
Mucus and mucus flake composition and abundance reflect inflammatory and infection status in cystic fibrosis.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society Apr, 2022 | Pubmed ID: 35437233
The University of North Carolina at Chapel Hill
Jason A. Wykoff1,
Kendall M. Shaffer1,
Kenza C. Araba1,
Matthew R. Markovetz1,
Jérémy Patarin2,
Matthieu Robert de Saint Vincent2,
Scott H. Donaldson1,3,
Camille Ehre1,4
1Marsico Lung Institute / CF Center, The University of North Carolina at Chapel Hill,
2, Rheonova,
3Department of Pulmonary and Critical Care Medicine, The University of North Carolina at Chapel Hill,
4Department of Pediatric, Pediatric Pulmonology Division, The University of North Carolina at Chapel Hill
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