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Sarah E. Ernst

Roy J. and Lucille A. Carver College of Medicine

22

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Early pathogenesis of cystic fibrosis gallbladder disease in a porcine model

2020 Laboratory Investigation
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Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs

2018 Laboratory Investigation
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Airway acidification initiates host defense abnormalities in cystic fibrosis mice

2016 Science
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Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia

2015 Journal of Biological Chemistry
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Medical reversal of chronic rhinosinusitis in a cystic fibrosis patient with ivacaftor

2015 International Forum of Allergy & Rhinology
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Integrin α6β4 identifies human distal lung epithelial progenitor cells with potential as a cell-based therapy for cystic fibrosis lung disease

2013 PLOS ONE
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Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model.

2013 Molecular Therapy
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Multicenter Intestinal Current Measurements in Rectal Biopsies from CF and Non-CF Subjects to Monitor CFTR Function

2013 PLOS ONE
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Loss of Anion Transport without Increased Sodium Absorption Characterizes Newborn Porcine Cystic Fibrosis Airway Epithelia

2010 Cell
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Citations (207)