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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: 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.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: American Thoracic Society 2010
Θέματα:
C. Cystic Fibrosis
Διαθέσιμο Online: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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