A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia-Reference-Cited by-同舟云学术

A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia

Published:2019-09-07 Issue:5 Volume:46 Page:457-472
ISSN:1567-567X
Container-title:Journal of Pharmacokinetics and Pharmacodynamics
language:en
Short-container-title:J Pharmacokinet Pharmacodyn

Author:

Serrano Castillo Florencio,Bertrand Carol A.,Myerburg Michael M.,Shapiro Monica E.,Corcoran Timothy E.,Parker Robert S.

Funder

Foundation for the National Institutes of Health

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology

Link

http://link.springer.com/content/pdf/10.1007/s10928-019-09649-0.pdf

Reference67 articles.

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2. Orestein David M, Spahr Jonathan E, Weiner DJ (2012) Cystic fibrosis: a guide for patient and family, 4th edn. Lippincott Williams & Wilkins, Philadelphia

3. Locke LW, Myerburg MM, Weiner DJ et al (2016) Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis lung. Eur Respir J 47:1392–1401. https://doi.org/10.1183/13993003.01880-2015

4. Pilewski JM, Frizzell RA (1999) Role of CFTR in airway disease. Physiol Rev 79:S215–S255

5. Corcoran TE, Thomas KM, Myerburg MM et al (2010) Absorptive clearance of DTPA as an aerosol-based biomarker in the cystic fibrosis airway. Eur Respir J 35:781–786. https://doi.org/10.1183/09031936.00059009

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