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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 15, 2024
Self-reported chronic therapy use after 24-weeks of follow-up by participants who completed the simplify randomized, controlled trial
Alex H Gifford, Katherine Odem-Davis, Margaret Kloster, et al.
Pediatric Research
|
May 6, 2010
Extracorporeal membrane oxygenation causes loss of intestinal epithelial barrier in the newborn piglet
Ashish R Kurundkar, Cheryl R Killingsworth, R Britt McIlwain, et al.
Plos One
|
August 8, 2013
Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation
Steven M Rowe, Bo Liu, Aubrey Hill, et al.
Physical Review Letters
|
October 15, 2008
Spin waves and quantum criticality in the frustrated XY pyrochlore antiferromagnet Er2Ti2O7
J P C Ruff, J P Clancy, A Bourque, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 8, 2025
TGF-β induces excessive pulmonary IL-6 secretion in cystic fibrosis via PI3K
Grace Scharf, Cynthia R Davidson, Vladimir Ustiyan, et al.
The Journal of Biological Chemistry
|
January 1, 2004
Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry
Akos Zsembery, James A Fortenberry, Lihua Liang, et al.
Biochemistry
|
November 12, 2003
Activation of chloride secretion in cystic fibrosis cells and tissues by the substituted imidazole SRI 2931
Julie R Jones, Erik M Schwiebert, Michael D DuVall, et al.
Pulmonary Pharmacology & Therapeutics
|
March 16, 2010
DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers
S M Rowe, L C Pyle, A Jurkevante, et al.
Neuromuscular Disorders : NMD
|
January 26, 2015
Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease
Laura E Case, Carl Bjartmar, Claire Morgan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 25, 2019
Utilizing centralized biorepository samples for biomarkers of cystic fibrosis lung disease severity
Scott D Sagel, Brandie D Wagner, Assem Ziady, et al.
Page
of 23
Search research articles
Search
Showing results (171-180 of 226) with videos related to
Sort By:
Page
of 23
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 15, 2024
Self-reported chronic therapy use after 24-weeks of follow-up by participants who completed the simplify randomized, controlled trial
Alex H Gifford, Katherine Odem-Davis, Margaret Kloster, et al.
Pediatric Research
|
May 6, 2010
Extracorporeal membrane oxygenation causes loss of intestinal epithelial barrier in the newborn piglet
Ashish R Kurundkar, Cheryl R Killingsworth, R Britt McIlwain, et al.
Plos One
|
August 8, 2013
Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation
Steven M Rowe, Bo Liu, Aubrey Hill, et al.
Physical Review Letters
|
October 15, 2008
Spin waves and quantum criticality in the frustrated XY pyrochlore antiferromagnet Er2Ti2O7
J P C Ruff, J P Clancy, A Bourque, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 8, 2025
TGF-β induces excessive pulmonary IL-6 secretion in cystic fibrosis via PI3K
Grace Scharf, Cynthia R Davidson, Vladimir Ustiyan, et al.
The Journal of Biological Chemistry
|
January 1, 2004
Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry
Akos Zsembery, James A Fortenberry, Lihua Liang, et al.
Biochemistry
|
November 12, 2003
Activation of chloride secretion in cystic fibrosis cells and tissues by the substituted imidazole SRI 2931
Julie R Jones, Erik M Schwiebert, Michael D DuVall, et al.
Pulmonary Pharmacology & Therapeutics
|
March 16, 2010
DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers
S M Rowe, L C Pyle, A Jurkevante, et al.
Neuromuscular Disorders : NMD
|
January 26, 2015
Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease
Laura E Case, Carl Bjartmar, Claire Morgan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 25, 2019
Utilizing centralized biorepository samples for biomarkers of cystic fibrosis lung disease severity
Scott D Sagel, Brandie D Wagner, Assem Ziady, et al.
Page
of 23