Functional Properties of Mixed Cystic Fibrosis and Normal Bronchial Epithelial Cell Cultures-Reference-Cited by-同舟云学术

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Functional Properties of Mixed Cystic Fibrosis and Normal Bronchial Epithelial Cell Cultures

Published:2009-06 Issue:6 Volume:40 Page:717-723
ISSN:1044-1549
Container-title:American Journal of Respiratory Cell and Molecular Biology
language:en
Short-container-title:Am J Respir Cell Mol Biol

Author:

Dannhoffer Luc,Blouquit-Laye Sabine,Regnier Agathe,Chinet Thierry

Publisher

American Thoracic Society

Subject

Cell Biology,Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology

Reference56 articles.

1. Kunzelmann K. The cystic fibrosis transmembrane conductance regulator and its function in epithelial transport.Rev Physiol Biochem Pharmacol1999;137:1–70.

2. Schwiebert EM, Benos DJ, Egan ME, Stutts MJ, Guggino WB. CFTR is a conductance regulator as well as a chloride channel.Physiol Rev1999;79:S145–S166.

3. Molecular insights into the physiology of the ‘thin film’ of airway surface liquid

4. Expression of cystic fibrosis transmembrane conductance regulator in the human distal lung

5. Normal and Cystic Fibrosis Airway Surface Liquid Homeostasis

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