Matthew R. Markovetz

Marsico Lung Institute / CF Center

BIOGRAPHY

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PUBLICATIONS

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

INSTITUTIONS

The University of North Carolina at Chapel Hill

JOVE ARTICLES

Jason A. Wykoff¹,

Kendall M. Shaffer¹,

Kenza C. Araba¹,

Matthew R. Markovetz¹,

Jérémy Patarin²,

Matthieu Robert de Saint Vincent²,

Scott H. Donaldson^1,3,

Camille Ehre^1,4

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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