Concepedia

Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells

Sonia Baconnais, Franck Delavoie, Jean‐Marie Zahm, Magali Milliot, Christine Terryn, Nicolas Castillon, Vincent Banchet, Jean Michel, Olivier Danos, Marc Merten

Experimental Cell Research · 2005 · 21 citations · 29 references

DOI

Concepts

References

29

CFTR as a cAMP-Dependent Regulator of Sodium Channels

M. Jackson Stutts, Cecilia M. Canessa, John C. Olsen et al. · Science · 1995 · 1.1K citations

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Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice

Marcus Mall, Barbara R. Grubb, Jack R. Harkema et al. · Nature Medicine · 2004 · 899 citations

, , +12

Submucosal glands are the predominant site of CFTR expression in the human bronchus

John F. Engelhardt, James R. Yankaskas, Stephen A. Ernst et al. · Nature Genetics · 1992 · 649 citations

, , +13

Ion composition of airway surface liquid of patients with cystic fibrosis as compared with normal and disease-control subjects.

Michael R. Knowles, J M Robinson, R E Wood et al. · Journal of Clinical Investigation · 1997 · 297 citations · Full text

, , +7

Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH

Sujatha Jayaraman, Yuanlin Song, L. Vetrivel et al. · Journal of Clinical Investigation · 2001 · 209 citations · Full text

, , +16