Cystic fibrosis: current therapeutic targets and future approaches
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s12967-017-1193-9.pdf
Reference74 articles.
1. Reis FJ, Damaceno N. Cystic fibrosis. J Pediatr. 1998;74(Suppl 1):S76–9.
2. Guggino WB, Banks-Schlegel SP. Macromolecular interaction and ion transport in cystic fibrosis. Am J Respir Crit Care Med. 2004;170:815–20.
3. Johnson LG, Boyles SE, Wilson J, Boucher RC. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells. J Clin Invest. 1995;95:1377–82.
4. Stutts MJ, Canessa CM, Olsen JC, et al. CFTR as a cAMP-dependent regulator of sodium channels. Science. 1995;269:847–50.
5. Cystic fibrosis foundation patient registry: annual data report to the center directors, 2014. https://www.cff.org/2014_CFF_Annual_Data_Report_to_the_Center_Directors.pdf/ . Accessed 11 Mar 2016.
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