Jeffrey J. Wine
Affiliations: | Stanford University, Palo Alto, CA |
Area:
cystic fibrosisGoogle:
"Jeffrey Wine"Mean distance: 13.16 (cluster 6) | S | N | B | C | P |
Children
Sign in to add trainee| John Y. Kuwada | grad student | Stanford | |
| Mark R. Plummer | grad student | Stanford | |
| Heinrich Reichert | post-doc | Stanford | |
| Karen A. Sigvardt | post-doc | Stanford | |
| Masakazu Takahata | post-doc | Stanford | |
| David J. Brayden | post-doc | 1989-1991 | Stanford (BME Tree) |
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Publications
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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 |