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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Hlavní autoři: Bonvin, Elise, Le Rouzic, Philippe, Bernaudin, Jean-François, Cottart, Charles-Henry, Vandebrouck, Clarisse, Crié, Antoine, Leal, Teresinha, Clement, Annick, Bonora, Monique
Médium: Artigo
Jazyk:Inglês
Vydáno: Blackwell Science Inc 2008
Témata:
Respiratory
On-line přístup: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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