Defects of Secretion in Cystic Fibrosis

1. Outside Neurons/Inside Epithelia: Novel Activation of CFTR Cl- and HCO3 - Conductances
Marsh M. Reddy, Andres Ponce, Paul M. Quinton

2. Role of CFTR and Other Ion Channels in Cystic Fibrosis
Karl Kunzelmann, Tanja Bachhuber, Gabriele Adam, Thilo Voelcker, Bettina Murle, Marcus Mall, Rainer Schreiber

3. Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport
Jean-Daniel Horisberger

4. Ion Channels in Secretory Granules of the Pancreas: Molecular Identification and Their Role in Regulated Secretion
Frank Thévenod

5. Epithelial Transport and Intracellular Trafficking: Physiology and Pathophysiology
Helmut Kipp, Rolf K. H. Kinne

6. Kinases, Cell Volume, and the Regulation of Chloride Channels
Florian Lang, Albrecht Lepple-Wienhues, Ildicko Szabo, Erich Gulbins, Monica Palmada, Sabine Wallisch, Christoph Böhmer, Karin Klingel, Reinhard Kandolf

7. The CLCAs: Proteins with Ion Channel, Cell Adhesion and Tumor Suppressor Functions
Catherine M. Fuller, Gergely Kovacs, Susan J. Anderson, Dale J. Benos

8. Is Intervention in Inositol Phosphate Signaling a Useful Therapeutic Option for Cystic Fibrosis?
Stephen B. Shears, Ling Yang, Sherif Gabriel, Carla M. Pedrosa Ribeiro

9. An Inositol Phosphate Analog, INO-4995, Normalizes Electrophysiology in CF Airway Epithelia
Alexis Traynor-Kaplan, Mark Moody, Carsten Schultz

10. Vitamin C and Flavonoids Potentiate CFTR Cl Transport in Human Airway Epithelia
Horst Fischer, Beate Illek

11. Airway Glycoconjugates Secreted in Cystic Fibrosis and Severe Chronic Airway Inflammation Relationship with Pseudomonas aeruginosa
Philippe Roussel

12. Biosynthesis and Secretion of Mucins, Especially the MUC2 Mucin, in Relation to Cystic Fibrosis
Gunnar C. Hansson, Malin E. V. Johansson, Martin E. Lidell

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Avainsanat: TECHNOLOGY & ENGINEERING / Biomedical TEC059000