Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants-Reference-Cited by-同舟云学术

Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants

Published:2008-01 Issue:1 Volume:7 Page:44-53
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Mosler Katharina,Coraux Christelle,Fragaki Konstantina,Zahm Jean-Marie,Bajolet Odile,Bessaci-Kabouya Katia,Puchelle Edith,Abély Michel,Mauran Pierre

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference47 articles.

1. Nasal epithelial brushing: a valuable method to study airway epithelial cells in CF and non-CF infants;Mosler;J Cyst Fibros,2006

2. Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia;Kreda;Mol Biol Cell,2005

3. Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings;Bronsveld;J Clin Invest,2001

4. Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation;Sermet-Gaudelus;Pediatr Res,2002

5. CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium;Dupuit;J Clin Invest,1995

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