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Marsico Lung Institute/CF Center,
Department of Pediatrics
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Cystic fibrosis: an inherited disease affecting mucin-producing organs.
The international journal of biochemistry & cell biology Jul, 2014 | Pubmed ID: 24685676
Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.
The Journal of clinical investigation Jul, 2014 | Pubmed ID: 24892808
Clinical Application of Polysialylated Deoxyribonuclease and Erythropoietin.
Recent patents on drug delivery & formulation , 2018 | Pubmed ID: 30019653
Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties hydration.
The European respiratory journal 02, 2022 | Pubmed ID: 34172469
Biochemical and rheological analysis of human colonic culture mucus reveals similarity to gut mucus.
Biophysical journal 12, 2021 | Pubmed ID: 34695384
SARS-CoV-2 infection of airway cells causes intense viral and cell shedding, two spreading mechanisms affected by IL-13.
Proceedings of the National Academy of Sciences of the United States of America Apr, 2022 | Pubmed ID: 35353667
University of North Carolina at Chapel Hill
The University of North Carolina at Chapel Hill
Kathryn A. Ramsey1,2,
Zachary L. Rushton1,
Camille Ehre1,3
1Marsico Lung Institute/CF Center, University of North Carolina at Chapel Hill,
2Telethon Kids Institute, University of Western Australia,
3Department of Pediatrics, 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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