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Robert Tarran

Showing results (101-110 of 143) with videos related to

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American Journal of Physiology. Lung Cellular and Molecular Physiology|April 22, 2017
Flavored e-cigarette liquids reduce proliferation and viability in the CALU3 airway epithelial cell lineTemperance R Rowell, Steven L Reeber, Shernita L Lee, et al.
The Journal of Clinical Investigation|November 27, 2008
17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epitheliaRay D Coakley, Hengrui Sun, Lucy A Clunes, et al.
The European Respiratory Journal|September 8, 2018
SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydrationMegan J Webster, Boris Reidel, Chong D Tan, et al.
Biochemistry|May 5, 2016
Structural Features Essential to the Antimicrobial Functions of Human SPLUNC1William G Walton, Saira Ahmad, Michael S Little, et al.
The Laryngoscope|August 3, 2013
RGS21, a regulator of taste and mucociliary clearance?Adam J Kimple, Alaina L Garland, Staci P Cohen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 17, 2012
Identification of SPLUNC1's ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airwaysCarey A Hobbs, Maxime G Blanchard, Stephan Kellenberger, et al.
American Journal of Respiratory Cell and Molecular Biology|March 28, 2008
A2B adenosine receptors regulate the mucus clearance component of the lung's innate defense systemBrett M Rollins, Mellisa Burn, Ray D Coakley, et al.
The Journal of Physiology|November 18, 2015
Hypercapnia modulates cAMP signalling and cystic fibrosis transmembrane conductance regulator-dependent anion and fluid secretion in airway epitheliaMark J Turner, Vinciane Saint-Criq, Waseema Patel, et al.
American Journal of Respiratory and Critical Care Medicine|November 4, 2017
Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway EpitheliaLubna H Abdullah, Raymond Coakley, Megan J Webster, et al.
American Journal of Respiratory and Critical Care Medicine|May 9, 2017
SPX-101 Is a Novel Epithelial Sodium Channel-targeted Therapeutic for Cystic Fibrosis That Restores Mucus TransportDavid W Scott, Matthew P Walker, Juliana Sesma, et al.
Pageof 15

Showing results (101-110 of 143) with videos related to

Sort By:
Pageof 15
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 22, 2017
Flavored e-cigarette liquids reduce proliferation and viability in the CALU3 airway epithelial cell lineTemperance R Rowell, Steven L Reeber, Shernita L Lee, et al.
The Journal of Clinical Investigation|November 27, 2008
17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epitheliaRay D Coakley, Hengrui Sun, Lucy A Clunes, et al.
The European Respiratory Journal|September 8, 2018
SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydrationMegan J Webster, Boris Reidel, Chong D Tan, et al.
Biochemistry|May 5, 2016
Structural Features Essential to the Antimicrobial Functions of Human SPLUNC1William G Walton, Saira Ahmad, Michael S Little, et al.
The Laryngoscope|August 3, 2013
RGS21, a regulator of taste and mucociliary clearance?Adam J Kimple, Alaina L Garland, Staci P Cohen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 17, 2012
Identification of SPLUNC1's ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airwaysCarey A Hobbs, Maxime G Blanchard, Stephan Kellenberger, et al.
American Journal of Respiratory Cell and Molecular Biology|March 28, 2008
A2B adenosine receptors regulate the mucus clearance component of the lung's innate defense systemBrett M Rollins, Mellisa Burn, Ray D Coakley, et al.
The Journal of Physiology|November 18, 2015
Hypercapnia modulates cAMP signalling and cystic fibrosis transmembrane conductance regulator-dependent anion and fluid secretion in airway epitheliaMark J Turner, Vinciane Saint-Criq, Waseema Patel, et al.
American Journal of Respiratory and Critical Care Medicine|November 4, 2017
Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway EpitheliaLubna H Abdullah, Raymond Coakley, Megan J Webster, et al.
American Journal of Respiratory and Critical Care Medicine|May 9, 2017
SPX-101 Is a Novel Epithelial Sodium Channel-targeted Therapeutic for Cystic Fibrosis That Restores Mucus TransportDavid W Scott, Matthew P Walker, Juliana Sesma, et al.
Pageof 15