Failure of the Cystic Fibrosis Transmembrane Conductance Regulator to Conduct ATP von Reddy, M. M., Quinton, P. M., Haws, C., Wine, J. J., Grygorczyk, R., Tabcharani, J. A., Hanrahan, J. W., Gunderson, K. L., Kopito, R. R.

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Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites von Chang, X.B., Tabcharani, J.A., Hou, Y.X., Jensen, T.J., Kartner, N., Alon, N., Hanrahan, J.W., Riordan, J.R.

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Low‐conductance chloride channel activated by cAMP in the epithelial cell line T84 von Tabcharani, J.A., Low, W., Elie, D., Hanrahan, J.W.

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CFTR channels expressed in CHO cells do not have detectable ATP conductance von Grygorczyk, R, Tabcharani, J A, Hanrahan, J W

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The CFTR chloride channel: nucleotide interactions and temperature-dependent gating von Mathews, C J, Tabcharani, J A, Hanrahan, J W

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Inhibition of an outwardly rectifying anion channel by HEPES and related buffers von HANRAHAN, J. W, TABCHARANI, J. A

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Phosphorylation-regulated Cl- channel in CHO cells stably expressing the cystic fibrosis gene von Tabcharani, J A, Chang, X B, Riordan, J R, Hanrahan, J W

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Multi-ion pore behaviour in the CFTR chloride channel von Tabcharani, Joseph A, Rommens, Johanna M, Hou, Yue-Xian, Chang, Xiu-Bao, Tsui, Lap-Chee, Riordan, John R, Hanrahan, John W

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Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions von Linsdell, P, Tabcharani, J A, Rommens, J M, Hou, Y X, Chang, X B, Tsui, L C, Riordan, J R, Hanrahan, J W

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Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels von Tabcharani, J A, Linsdell, P, Hanrahan, J W

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The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation von Tabcharani, J.A., Chang, X.B., Riordan, J.R., Hanrahan, J.W.

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Bicarbonate permeability of the outwardly rectifying anion channel von TABCHARANI, J. A, JENSEN, T. J, RIORDAN, J. R, HANRAHAN, J. W

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Multi-Ion mechanism for ion permeation and block in the cystic fibrosis transmembrane conductance regulator chloride channel von Linsdell, P, Tabcharani, J A, Hanrahan, J W

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Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel von Mathews, Ceri J., Tabcharani, Joseph A., Chang, Xiu‐Bao, Jensen, Timothy J., Riordan, John R., Hanrahan, John W.

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On the activation of outwardly rectifying anion channels in excised patches von Tabcharani, J. A., Hanrahan, J. W.

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cAMP-dependent Protein Kinase-mediated Phosphorylation of Cystic Fibrosis Transmembrane Conductance Regulator Residue Ser-753 and Its Role in Channel Activation (∗) von Seibert, Fabian S., Tabcharani, Joseph A., Chang, Xiu-Bao, Dulhanty, Ann M., Mathews, Ceri, Hanrahan, John W., Riordan, John R.

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Regulation of an inwardly rectifying K channel in the T84 epithelial cell line by calcium, nucleotides and kinases von Tabcharani, J A, Boucher, A, Eng, J W, Hanrahan, J W

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Basolateral K channel activated by carbachol in the epithelial cell line T84 von Tabcharani, J A, Harris, R A, Boucher, A, Eng, J W, Hanrahan, J W

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Transformed sweat gland and nasal epithelial cell lines from control and cystic fibrosis individuals von Buchanan, J A, Yeger, H, Tabcharani, J A, Jensen, T J, Auerbach, W, Hanrahan, J W, Riodan, J R, Buchwald, M

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Cystic Fibrosis Transmembrane Conductance Regulator and Adenosine Triphosphate von Abraham, Edward H., Okunieff, Paul, Scala, Stefania, Vos, Petra, Michiel J. S. Oosterveld, Chen, Allan Y., Shrivastav, Brij, Guidotti, Guido, Reddy, M. M., Quinton, P. M., Haws, C., Wine, J. J., Grygorczyk, R., Tabcharani, J. A., Hanrahan, J. W., Gunderson, K. L., Kopito, R. R., Grygorczyk, Ryszard, Hanrahan, John W.

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