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American Journal of Respiratory and Critical Care Medicine
|
August 16, 2014
Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects
Jeffrey J Wine
American Journal of Physiology. Cell Physiology
|
February 14, 2006
Acid in the airways. Focus on "Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis"
Jeffrey J Wine
Autonomic Neuroscience : Basic & Clinical
|
March 14, 2007
Parasympathetic control of airway submucosal glands: central reflexes and the airway intrinsic nervous system
Jeffrey J Wine
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 15, 2024
Calibrating sweat chloride levels to CFTR activity via ETI effects on CF subjects with one or two F508DEL mutations
Jeffrey J Wine
American Journal of Physiology. Cell Physiology
|
May 18, 2007
The inexhaustible mouse nose. Focus on "olfactory epithelia exhibit progressive functional and morphological defects in CF mice"
Jeffrey J Wine
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 21, 2022
How the sweat gland reveals levels of CFTR activity
Jeffrey J Wine
Science Translational Medicine
|
April 30, 2010
The development of lung disease in cystic fibrosis pigs
Jeffrey J Wine
Science (New York, N.Y.)
|
August 16, 2014
Medicine. Letting go of mucus
Jeffrey J Wine
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 27, 2018
How to live a long and healthy life with cystic fibrosis: Lessons from the CF ferret
Jeffrey J Wine
Nature Medicine
|
July 2, 2003
Rules of conduct for the cystic fibrosis anion channel
Jeffrey J Wine
Page
of 6
Search research articles
Search
Showing results (1-10 of 58) with videos related to
Sort By:
Page
of 6
American Journal of Respiratory and Critical Care Medicine
|
August 16, 2014
Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects
Jeffrey J Wine
American Journal of Physiology. Cell Physiology
|
February 14, 2006
Acid in the airways. Focus on "Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis"
Jeffrey J Wine
Autonomic Neuroscience : Basic & Clinical
|
March 14, 2007
Parasympathetic control of airway submucosal glands: central reflexes and the airway intrinsic nervous system
Jeffrey J Wine
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 15, 2024
Calibrating sweat chloride levels to CFTR activity via ETI effects on CF subjects with one or two F508DEL mutations
Jeffrey J Wine
American Journal of Physiology. Cell Physiology
|
May 18, 2007
The inexhaustible mouse nose. Focus on "olfactory epithelia exhibit progressive functional and morphological defects in CF mice"
Jeffrey J Wine
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 21, 2022
How the sweat gland reveals levels of CFTR activity
Jeffrey J Wine
Science Translational Medicine
|
April 30, 2010
The development of lung disease in cystic fibrosis pigs
Jeffrey J Wine
Science (New York, N.Y.)
|
August 16, 2014
Medicine. Letting go of mucus
Jeffrey J Wine
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 27, 2018
How to live a long and healthy life with cystic fibrosis: Lessons from the CF ferret
Jeffrey J Wine
Nature Medicine
|
July 2, 2003
Rules of conduct for the cystic fibrosis anion channel
Jeffrey J Wine
Page
of 6