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Defects of Secretion in Cystic Fibrosis

Overview of attention for book
Cover of 'Defects of Secretion in Cystic Fibrosis'

Table of Contents

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    Book Overview
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    Chapter 1 Outside neurons/inside epithelia: Novel activation of CFTR CL- and HCO3 - conductances
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    Chapter 2 Role of CFTR and Other Ion Channels in Cystic Fibrosis
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    Chapter 3 Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport
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    Chapter 4 Ion Channels in Secretory Granules of the Pancreas: Molecular Identification and Their Role in Regulated Secretion
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    Chapter 5 Epithelial Transport and Intracellular Trafficking: Physiology and Pathophysiology
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    Chapter 6 Kinases, Cell Volume, and the Regulation of Chloride Channels
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    Chapter 7 The CLCAs: Proteins with Ion Channel, Cell Adhesion and Tumor Suppressor Functions
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    Chapter 8 Is Intervention in Inositol Phosphate Signaling a Useful Therapeutic Option for Cystic Fibrosis?
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    Chapter 9 An Inositol Phosphate Analog, INO-4995, Normalizes Electrophysiology in CF Airway Epithelia
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    Chapter 10 Vitamin C and Flavonoids Potentiate CFTR Cl Transport in Human Airway Epithelia
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    Chapter 11 Airway Glycoconjugates Secreted in Cystic Fibrosis and Severe Chronic Airway Inflammation Relationship with Pseudomonas aeruginosa
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    Chapter 12 Biosynthesis and Secretion of Mucins, Especially the MUC2 Mucin, in Relation to Cystic Fibrosis
Attention for Chapter 3: Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport
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Chapter title
Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport
Chapter number 3
Book title
Defects of Secretion in Cystic Fibrosis
Published by
Springer, Boston, MA, January 2005
DOI 10.1007/0-387-23250-8_3
Book ISBNs
978-0-387-23076-4, 978-0-387-23250-8
Authors

Jean-Daniel Horisberger

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