Fecal Human β-Defensin 2 in Children with Cystic Fibrosis: Is There a Diminished Intestinal Innate Immune Response?-Reference-Cited by-同舟云学术

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Fecal Human β-Defensin 2 in Children with Cystic Fibrosis: Is There a Diminished Intestinal Innate Immune Response?

Published:2015-08-14 Issue:10 Volume:60 Page:2946-2952
ISSN:0163-2116
Container-title:Digestive Diseases and Sciences
language:en
Short-container-title:Dig Dis Sci

Author:

Ooi Chee Y.,Pang Tamara,Leach Steven T.,Katz Tamarah,Day Andrew S.,Jaffe Adam

Funder

The Cystic Fibrosis Australia Research Trust Grant

The Royal Australasian College of Physicians Research and Education Foundation Award

Publisher

Springer Science and Business Media LLC

Subject

Gastroenterology,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s10620-015-3842-2.pdf

Reference42 articles.

1. Riordan JR, Rommens JM, Kerem B, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245:1066–1073.

2. Quinton PM. Chloride impermeability in cystic fibrosis. Nature. 1983;301:421–422.

3. Stutts MJ, Canessa CM, Olsen JC, et al. CFTR as a cAMP-dependent regulator of sodium channels. Science. 1995;269:847–850.

4. Garcia MA, Yang N, Quinton PM. Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion. J Clin Invest. 2009;119:2613–2622.

5. Brennan S. Innate immune activation and cystic fibrosis. Paediatr Respir Rev. 2008;9:271–280.

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