Changing the Paradigm – Treating the Basic Defect in Cystic Fibrosis-Reference-Cited by-同舟云学术

Changing the Paradigm – Treating the Basic Defect in Cystic Fibrosis

Published:2015-06-17 Issue:8 Volume:82 Page:727-736
ISSN:0019-5456
Container-title:The Indian Journal of Pediatrics
language:en
Short-container-title:Indian J Pediatr

Author:

Guglani Lokesh

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s12098-015-1786-3.pdf

Reference45 articles.

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2. Cystic Fibrosis Foundation Patient Registry. 2013 Annual Data Report to the Center Directors. Cystic Fibrosis Foundation. 2014.

3. Riordan JR, Rommens JM, Kerem B, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245:1066–73.

4. Collawn JF, Matalon S. CFTR and lung homeostasis. Am J Physiol Lung Cell Mol Physiol. 2014;307:L917–23.

5. Zhang L, Button B, Gabriel SE, et al. CFTR delivery to 25 % of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium. PLoS Biol. 2009;7:e1000155.

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