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Current Opinion in Pediatrics|May 14, 2005
Novel, mechanism-based therapies for cystic fibrosisRonald C Rubenstein
Frontiers in Pediatrics|January 31, 2014
On preventing the extinction of the physician-scientist in pediatric pulmonologyRonald C Rubenstein, James L Kreindler
Frontiers in Pharmacology|July 24, 2012
Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic FibrosisRebecca A Chanoux, Ronald C Rubenstein
American Journal of Physiology. Cell Physiology|July 11, 2006
Abnormal regulatory interactions of I148T-CFTR and the epithelial Na+ channel in Xenopus oocytesLaurence Suaud, Wusheng Yan, Ronald C Rubenstein
Expert Review of Respiratory Medicine|April 2, 2019
Safety and efficacy of treatment with lumacaftor in combination with ivacaftor in younger patients with cystic fibrosisPi Chun Cheng, Stamatia Alexiou, Ronald C Rubenstein
Journal of Clinical & Translational Endocrinology|November 22, 2017
Patient and parent perceptions of the diagnosis and management of cystic fibrosis-related diabetesKate Millington, Victoria Miller, Ronald C Rubenstein, et al.
American Journal of Physiology. Renal Physiology|September 22, 2005
Differential modulation of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel by protein kinase CdeltaWusheng Yan, Laurence Suaud, Thomas R Kleyman, et al.
The Journal of Biological Chemistry|October 19, 2002
Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytesLaurence Suaud, Marcelo Carattino, Thomas R Kleyman, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 25, 2020
Abnormal glucose tolerance and the 50-gram glucose challenge test in Cystic fibrosisSaba Sheikh, A Russell Localio, Andrea Kelly, et al.
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