Cystic fibrosis salt/fluid controversy: In the thick of it
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://www.nature.com/articles/nm0801_888.pdf
Reference8 articles.
1. Rosenstein, B.J. What is a cystic fibrosis diagnosis? Clin. Chest Med. 19, 423–441 (1998).
2. Matsui, H. et al. Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease. Cell 95, 1005–1015 (1998).
3. Smith, J.J., Travis, S.M., Greenberg, E.P. & Welsh, M.J. Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid. Cell 85, 229–236 (1996).
4. Tarran, R. et al. The CF salt controversy: in vivo observations and theraputic approaches. Mol. Cell (in the press).
5. Imundo, L., Barasch, J., Prince, A. & Al-Awqati, Q. Cystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surface. Proc. Natl. Acad. Sci. USA 92, 3019–3023 (1995).
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