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