Jeffrey J. Wine

Stanford University, Palo Alto, CA 
cystic fibrosis
"Jeffrey Wine"
Mean distance: 13.16 (cluster 6)
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Vaidyanathan S, Salahudeen AA, Sellers ZM, et al. (2019) High-Efficiency, Selection-free Gene Repair in Airway Stem Cells from Cystic Fibrosis Patients Rescues CFTR Function in Differentiated Epithelia. Cell Stem Cell
Kim J, Farahmand M, Dunn C, et al. (2018) Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults. Scientific Reports. 8: 16233
Sellers ZM, Illek B, Figueira MF, et al. (2017) Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease. Plos One. 12: e0189894
Kim J, Davies Z, Dunn C, et al. (2017) Ivacaftor restores CFTR-dependent sweat gland fluid secretion in cystic fibrosis subjects with S945L alleles. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
Wine JJ, Hansson GC, König P, et al. (2017) Progress in understanding mucus abnormalities in cystic fibrosis airways. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
Joo NS, Jeong JH, Cho HJ, et al. (2016) Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel. Scientific Reports. 6: 36806
Kim J, Farahmand M, Dunn C, et al. (2016) Evaporimeter and Bubble-Imaging Measures of Sweat Gland Secretion Rates. Plos One. 11: e0165254
Joo NS, Krouse ME, Choi JY, et al. (2016) Inhibition of airway surface fluid absorption by cholinergic stimulation. Scientific Reports. 6: 20735
Jeong JH, Hwang PH, Cho DY, et al. (2015) Secretion rates of human nasal submucosal glands from patients with chronic rhinosinusitis or cystic fibrosis. American Journal of Rhinology & Allergy. 29: 334-8
Widdicombe JH, Wine JJ. (2015) Airway Gland Structure and Function. Physiological Reviews. 95: 1241-319
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