Design of a Wearable Sweat Sensor for Diagnosing Cystic Fibrosis in Children
Conference proceeding (May 2013)
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Defects of Secretion in Cystic Fibrosis
Overview of attention for book
Table of Contents
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Altmetric BadgeBook Overview
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Altmetric BadgeChapter 1 Outside neurons/inside epithelia: Novel activation of CFTR CL- and HCO3 - conductances
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Altmetric BadgeChapter 2 Role of CFTR and Other Ion Channels in Cystic Fibrosis
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Altmetric BadgeChapter 3 Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport
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Altmetric BadgeChapter 4 Ion Channels in Secretory Granules of the Pancreas: Molecular Identification and Their Role in Regulated Secretion
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Altmetric BadgeChapter 5 Epithelial Transport and Intracellular Trafficking: Physiology and Pathophysiology
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Altmetric BadgeChapter 6 Kinases, Cell Volume, and the Regulation of Chloride Channels
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Altmetric BadgeChapter 7 The CLCAs: Proteins with Ion Channel, Cell Adhesion and Tumor Suppressor Functions
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Altmetric BadgeChapter 8 Is Intervention in Inositol Phosphate Signaling a Useful Therapeutic Option for Cystic Fibrosis?
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Altmetric BadgeChapter 9 An Inositol Phosphate Analog, INO-4995, Normalizes Electrophysiology in CF Airway Epithelia
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Altmetric BadgeChapter 10 Vitamin C and Flavonoids Potentiate CFTR Cl Transport in Human Airway Epithelia
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Altmetric BadgeChapter 11 Airway Glycoconjugates Secreted in Cystic Fibrosis and Severe Chronic Airway Inflammation Relationship with Pseudomonas aeruginosa
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Altmetric BadgeChapter 12 Biosynthesis and Secretion of Mucins, Especially the MUC2 Mucin, in Relation to Cystic Fibrosis
Attention for Chapter 11:
Airway Glycoconjugates Secreted in Cystic Fibrosis and Severe Chronic Airway Inflammation Relationship with Pseudomonas aeruginosa