Congenital tracheal malformation in cystic fibrosis transmembrane conductance regulator-deficient mice

In cystic fibrosis (CF) patients, the major alteration in pulmonary function is due to peripheral airway obstruction. In the present study, we investigated the possibility that alterations in the extrathoracic airways, particularly in the trachea that expresses high levels of CFTR (CF transmembrane...

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Detalhes bibliográficos
Main Authors: Bonvin, Elise, Le Rouzic, Philippe, Bernaudin, Jean-François, Cottart, Charles-Henry, Vandebrouck, Clarisse, Crié, Antoine, Leal, Teresinha, Clement, Annick, Bonora, Monique
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2008
Assuntos:
Respiratory
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2538793/
https://ncbi.nlm.nih.gov/pubmed/18450781
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2008.150763
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