Delta F508-CFTR channels: kinetics, activation by forskolin, and potentiation by xanthines von Haws, C. M, Nepomuceno, I. B, Krouse, M. E, Wakelee, H, Law, T, Xia, Y, Nguyen, H, Wine, J. J

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CFTR channels in immortalized human airway cells von Haws, C, Krouse, M. E, Xia, Y, Gruenert, D. C, Wine, J. J

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Glycerol Reverses the Misfolding Phenotype of the Most Common Cystic Fibrosis Mutation (∗) von Sato, Sachiko, Ward, Cristina L., Krouse, Mauri E., Wine, Jeffrey J., Kopito, Ron R.

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Selection for MDR1/P-glycoprotein enhances swelling-activated K+ and Cl- currents in NIH/3T3 cells von Luckie, D. B, Krouse, M. E, Harper, K. L, Law, T. C, Wine, J. J

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Evidence that CFTR channels can regulate the open duration of other CFTR channels: cooperativity von Krouse, M E, Wine, J J

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Optical method for quantifying rates of mucus secretion from single submucosal glands von Joo, Nam Soo, Wu, Jin V, Krouse, Mauri E, Saenz, Yamil, Wine, Jeffrey J

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Two novel mutations in a cystic fibrosis patient of Chinese origin von WAGNER, J. A, VASSILAKIS, A, YEE, K, MEI LI, HURLOCK, G, KROUSE, M. E, MOSS, R. B, WINE, J. J

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Cystic Fibrosis Gene Expression is not Correlated with Rectifying Cl-Channels von Ward, C. L., Krouse, M. E., Gruenert, D. C., Kopito, R. R., Wine, J. J.

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Lateral amygdaloid nucleus expansion in adult rats is associated with exposure to prenatal stress von Salm, A.K., Pavelko, Michelle, Krouse, E.Marshall, Webster, Wendy, Kraszpulski, Michał, Birkle, Dale L.

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Doxorubicin selection for MDR1/P-glycoprotein reduces swelling-activated K+ and Cl- currents in MES-SA cells von Luckie, D. B, Krouse, M. E, Law, T. C, Sikic, B. I, Wine, J. J

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Peptide cotransmitter potentiates calcium channel activity in crayfish skeletal muscle von Bishop, CA, Krouse, ME, Wine, JJ

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A large anion-selective channel has seven conductance levels von Krouse, Mauri E., Schneider, Gavan T., Gage, Peter W.

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Calcium-stimulated Cl- secretion in Calu-3 human airway cells requires CFTR von Moon, Samina, Singh, Meetpaul, Krouse, Mauri E, Wine, Jeffrey J

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Dissociation of depolarization-activated and swelling-activated Cl- channels von Krouse, M. E, Haws, C. M, Xia, Y, Fang, R. H, Wine, J. J

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Ion channels in normal human and cystic fibrosis sweat gland cells von Krouse, M. E, Hagiwara, G, Chen, J, Lewiston, N. J, Wine, J. J

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Is cystic fibrosis lung disease caused by abnormal ion composition or abnormal volume? von Krouse, M E

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Peptide potentiation of calcium channel activity can be seasonally variable von BISHOP, C. A, KROUSE, M. E, WINE, J. J

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Patch-clamp study of cultured human sweat duct cells: amiloride-blockable Na+ channel von JORIS, L, KROUSE, M. E, HAGIWARA, G, BELL, C. L, WINE, J. J

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Cystic Fibrosis Transmembrane Conductance Regulator Gating Requires Cytosolic Electrolytes von Wu, Jin V., Joo, Nam Soo, Krouse, Mauri E., Wine, Jeffrey J.

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Rates and equilibria for a photoisomerizable antagonist at the acetylcholine receptor of Electrophorus electroplaques von KROUSE, M. E, LESTER, H. A, WASSERMANN, N. H, ERLANGER, B. F

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