Lymphocytes in cystic fibrosis lung disease: a tale of two immunities
Author:
Affiliation:
1. Department of Pediatrics, Stanford University, CA, USA
Publisher
Oxford University Press (OUP)
Subject
Immunology,Immunology and Allergy
Link
https://academic.oup.com/cei/article-pdf/135/3/358/42145769/j.1365-2249.2003.02389.x.pdf
Reference43 articles.
1. Mucus clearance as a primary innate defense mechanism for mammalian airways;Knowles;J Clin Invest,2002
2. Update on pathogenesis of cystic fibrosis lung disease;Donaldson;Curr Opin Pulm Med,2003
3. State of the art: why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection?;Chmiel;Respir Res,2003
4. Transcriptional adaptation to cystic fibrosis transmembrane conductance regulator deficiency;Xu;J Biol Chem,2003
5. Modifier genes in cystic fibrosis lung disease;Merlo;J Lab Clin Med,2003
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