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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Main Authors: 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.
格式: Artigo
語言:Inglês
出版: American Thoracic Society 2010
主題:
C. Cystic Fibrosis
在線閱讀: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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