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Department of Pediatrics
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Cystic fibrosis transmembrane regulator protein mutations: 'class' opportunity for novel drug innovation.
Paediatric drugs , 2007 | Pubmed ID: 17291132
Lubiprostone activates non-CFTR-dependent respiratory epithelial chloride secretion in cystic fibrosis mice.
American journal of physiology. Lung cellular and molecular physiology Nov, 2008 | Pubmed ID: 18805957
Spiperone, identified through compound screening, activates calcium-dependent chloride secretion in the airway.
American journal of physiology. Cell physiology Jan, 2009 | Pubmed ID: 18987251
An improved simple method of mouse lung intubation.
Journal of applied physiology (Bethesda, Md. : 1985) Mar, 2009 | Pubmed ID: 19150857
Primary snoring and growth failure in a patient with cystic fibrosis.
Respiratory care Dec, 2009 | Pubmed ID: 19961640
Oral antimicrobial use in outpatient cystic fibrosis pulmonary exacerbation management: a single-center experience.
The clinical respiratory journal Jan, 2012 | Pubmed ID: 21595857
Lubiprostone activates CFTR, but not ClC-2, via the prostaglandin receptor (EP(4)).
Biochemical and biophysical research communications Sep, 2012 | Pubmed ID: 22960173
Oregon Health Sciences University
Sandhya Das1,
Kelvin MacDonald2,
Herng-Yu Sucie Chang1,
Wayne Mitzner1
1Department of Environmental Health Sciences, Program in Respiratory Biology and Lung Disease, Johns Hopkins Bloomberg School of Public Health,
2Department of Pediatrics, Oregon Health Sciences University
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