Loss of Cystic Fibrosis Transmembrane Conductance Regulator Function Produces Abnormalities in Tracheal Development in Neonatal Pigs and Young Children

Rationale: Although airway abnormalities are common in patients with cystic fibrosis (CF), it is unknown whether they are all secondary to postnatal infection and inflammation, which characterize the disease. Objectives: To learn whether loss of the cystic fibrosis transmembrane conductance regulato...

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Hauptverfasser: Meyerholz, David K., Stoltz, David A., Namati, Eman, Ramachandran, Shyam, Pezzulo, Alejandro A., Smith, Amanda R., Rector, Michael V., Suter, Melissa J., Kao, Simon, McLennan, Geoffrey, Tearney, Guillermo J., Zabner, Joseph, McCray, Paul B., Welsh, Michael J.
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Thoracic Society 2010
Schlagworte:
C. Cystic Fibrosis
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3001264/
https://ncbi.nlm.nih.gov/pubmed/20622026
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201004-0643OC
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