Defects of Secretion in Cystic Fibrosis - Advances in Experimental Medicine and Biology - Carsten Shultz - Livros - Springer-Verlag New York Inc. - 9780387230764 - 10 de fevereiro de 2005
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Carsten Shultz
Defects of Secretion in Cystic Fibrosis - Advances in Experimental Medicine and Biology 2005 edition

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Providing information on cystic fibrosis, this work is of interest to molecular biologists, physiologists, scientists working in pharmaceutical research and drug development, physicians and researchers in cystic fibrosis and related diseases.

Marc Notes: Includes bibliographical references and index. Table of Contents: Contributing Authors.- Preface.- Acknowledgments.- Outside Neurons/Inside Epithelia: Novel Activation of CFTR Cl- and HCO3-Conductances.- Role of CFTR and other Ion Channels In Cystic Fibrosis.- Ion Channels in the Apical mEmbrane: Role of Electrical Coupling on Transepithelial Transport.- Ion channels in secretory granules of the pancreas: Molecular identification and their role in regulated secretion.- Epithelial Transport and Intracellular Trafficking: Physiology and Pathophysiology.- Kinases, Cell Volume, and the Regulation of Chloride Channels.- The CLCAs: Proteins with Ion Channel, Cell Adhesion and Tumor Suppressor Functions.- Is Intervention in Inositol Phosphate Signaling a Useful Therapeutic Option for Cystic Fibrosis?- An Inositol Phosphate Analog, INO-4995, Normalizes Electrophysiology in CF Airway Epithelia.- Vitamin C and Flavonoids Potentiate CFTR Cl Transport in Human Airway Epithelia.- Airway Glycoconjugates Secreted in Cystic Fibrosis and Severe Chronic Airway Inflammation Relationship with Pseudomonas aeruginosa.- Biosynthesis and Secretion of Mucins, Especially the MUC2 MUCIN, in Relation to Cystic Fibrosis.- Index.

Mídia Livros     Hardcover Book   (Livro com lombada e capa dura)
Lançado 10 de fevereiro de 2005
ISBN13 9780387230764
Editoras Springer-Verlag New York Inc.
Páginas 179
Dimensões 170 × 244 × 12 mm   ·   458 g
Idioma Inglês  
Editor Schultz, Carsten

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