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Jeffrey J Wine

Showing results (1-10 of 58) with videos related to

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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 defectsJeffrey 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 systemJeffrey 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 mutationsJeffrey 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 activityJeffrey J Wine
Science Translational Medicine|April 30, 2010
The development of lung disease in cystic fibrosis pigsJeffrey J Wine
Science (New York, N.Y.)|August 16, 2014
Medicine. Letting go of mucusJeffrey 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 ferretJeffrey J Wine
Nature Medicine|July 2, 2003
Rules of conduct for the cystic fibrosis anion channelJeffrey J Wine
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 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 defectsJeffrey 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 systemJeffrey 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 mutationsJeffrey 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 activityJeffrey J Wine
Science Translational Medicine|April 30, 2010
The development of lung disease in cystic fibrosis pigsJeffrey J Wine
Science (New York, N.Y.)|August 16, 2014
Medicine. Letting go of mucusJeffrey 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 ferretJeffrey J Wine
Nature Medicine|July 2, 2003
Rules of conduct for the cystic fibrosis anion channelJeffrey J Wine
Pageof 6