[HTML][HTML] An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis
E Harris, M Easter, J Ren, S Krick, J Barnes, SM Rowe - Plos one, 2023 - journals.plos.org
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis
E Harris, M Easter, J Ren, S Krick, J Barnes… - PLoS …, 2023 - ui.adsabs.harvard.edu
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis.
E Harris, M Easter, J Ren, S Krick, J Barnes, SM Rowe - Plos one, 2023 - europepmc.org
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis.
E Harris, M Easter, J Ren, S Krick, J Barnes… - PLoS …, 2023 - search.ebscohost.com
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
[HTML][HTML] An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis
E Harris, M Easter, J Ren, S Krick, J Barnes… - PLOS ONE, 2023 - ncbi.nlm.nih.gov
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis
E Harris, M Easter, J Ren, S Krick, J Barnes… - PloS …, 2023 - pubmed.ncbi.nlm.nih.gov
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis.
E Harris, M Easter, J Ren, S Krick, J Barnes, SM Rowe - Plos one, 2023 - europepmc.org
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …