Targeting ion channels in cystic fibrosis-Reference-Cited by-同舟云学术

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Targeting ion channels in cystic fibrosis

Published:2015-09 Issue:5 Volume:14 Page:561-570
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Mall Marcus A.,Galietta Luis J.V.

Funder

German Research Foundation

German Ministry for Education and Research

Ministero della Salute

Telethon Foundation

Fondazione Italiana Fibrosi Cistica

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference134 articles.

1. CFTR function and prospects for therapy;Riordan;Annu Rev Biochem,2008

2. CFTR: cystic fibrosis and beyond;Mall;Eur Respir J,2014

3. Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease;Matsui;Cell,1998

4. Airway surface dehydration in cystic fibrosis: pathogenesis and therapy;Boucher;Annu Rev Med,2007

5. Mucus clearance as a primary innate defense mechanism for mammalian airways;Knowles;J Clin Invest,2002

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