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J Wine

Showing results (1-10 of 150) with videos related to

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Psychological Bulletin|August 1, 1971
Test anxiety and direction of attentionJ Wine
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
Nature Genetics|April 1, 1992
No CFTR: are CF symptoms milder?J J Wine
Science (New York, N.Y.)|June 15, 1979
A readily identifiable neuronJ 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
Experimental Neurology|December 1, 1973
Invertebrate synapse: long-term maintenance of postsynaptic morphology following denervationJ J Wine
Current Biology : CB|December 1, 1995
Cystic fibrosis: How do CFTR mutations cause cystic fibrosis?J J Wine
Current Biology : CB|February 1, 1993
Cystic fibrosis: ion channels and transmembrane transportersJ 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
Pageof 15

Showing results (1-10 of 150) with videos related to

Sort By:
Pageof 15
Psychological Bulletin|August 1, 1971
Test anxiety and direction of attentionJ Wine
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
Nature Genetics|April 1, 1992
No CFTR: are CF symptoms milder?J J Wine
Science (New York, N.Y.)|June 15, 1979
A readily identifiable neuronJ 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
Experimental Neurology|December 1, 1973
Invertebrate synapse: long-term maintenance of postsynaptic morphology following denervationJ J Wine
Current Biology : CB|December 1, 1995
Cystic fibrosis: How do CFTR mutations cause cystic fibrosis?J J Wine
Current Biology : CB|February 1, 1993
Cystic fibrosis: ion channels and transmembrane transportersJ 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
Pageof 15