Plasma TGF-β1 in pediatric cystic fibrosis: Potential biomarker of lung disease and response to therapy-Reference-Cited by-同舟云学术

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Plasma TGF-β1 in pediatric cystic fibrosis: Potential biomarker of lung disease and response to therapy

Published:2011-02-18 Issue:7 Volume:46 Page:688-695
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr. Pulmonol.

Author:

Harris William T.,Muhlebach Marianne S.,Oster Robert A.,Knowles Michael R.,Clancy J.P.,Noah Terry L.

Funder

Cystic Fibrosis Foundation

NIH/NHLBI

University of North Carolina Medical Alumni Grant

William Aycock Endowment for Cystic Fibrosis Research

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ppul.21430/fullpdf

Reference33 articles.

1. Hutchinson IV. TGF-beta(1) genotype and accelerated decline in lung function of patients with cystic fibrosis;Arkwright;Thorax,2000

2. Genetic modifiers of lung disease in cystic fibrosis;Drumm;N Engl J Med,2005

3. Interactions between secondhand smoke and genes that affect cystic fibrosis lung disease;Collaco;JAMA,2008

4. Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis;Corvol;Pediatr Pulmonol,2008

5. Update on gene modifiers in cystic fibrosis;Collaco;Curr Opin Pulm Med,2008

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