Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator von PIND, S, RIORDAN, J. R, WILLIAMS, D. B

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The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected... von LUKACS, G. L, XIU-BAO CHANG, BEAR, C, KARTNER, N, MOHAMED, A, RIORDAN, J. R, GRINSTEIN, S

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Inhibition of epithelial Na + currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator von Kunzelmann, K, Kiser, G.L, Schreiber, R, Riordan, J.R

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Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum von Seibert, F.S., Chang, X.-B., Aleksandrov, A.A., Clarke, D.M., Hanrahan, J.W., Riordan, J.R.

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Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion von XIU-BAO CHANG, YUE-XIAN HOU, JENSEN, T. J, RIORDAN, J. R

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Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP von Lukacs, G.L., Mohamed, A., Kartner, N., Chang, X.B., Riordan, J.R., Grinstein, S.

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Synthetic and natural opiates interact with P-glycoprotein in multidrug-resistant cells von CALLAGHAN, R, RIORDAN, J. 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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Identification of Mutations in Regions Corresponding to the Two Putative Nucleotide (ATP)-Binding Folds of the Cystic Fibrosis Gene von Kerem, Bat-sheva, Zielenski, Julian, Markiewicz, Danuta, Bozon, Dominique, Gazit, Ephraim, Yahav, Jacob, Kennedy, Dara, Riordan, John R., Collins, Francis S., Rommens, Johanna M., Tsui, Lap-Chee

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Forefronts in Nephrology: The molecular basis of renal cystic disease von Riordan, J.R.

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Forefronts in Nephrology: The molecular basis of renal cystic disease: II. Abnormal Transport By Epithelial Cells: CFTR: Cloning, mutations and functions von Riordan, J.R.

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CFTR is a monomer: biochemical and functional evidence von Chen, J-H, Chang, X-B, Aleksandrov, A A, Riordan, J R

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Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene von BEAR, C. E, DUGUAY, F, NAISMITH, A. L, KARTNER, N, HANRAHAN, J. W, RIORDAN, J. R

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Cystic fibrosis-type mutational analysis in the ATP-binding cassette transporter signature of human P-glycoprotein MDR1 von HOOOF, T, DEMMER, A, HADAM, M. R, RIORDAN, J. R, TÜMMLER, B

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The cystic fibrosis transmembrane regulator is present and functional in endosomes. Role as a determinant of endosomal pH von LUKACS, GL, CHANG, XB, KARTNER, N, ROTSTEIN, OD, RIORDAN, GRINSTEIN, S

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Regulation of CFTR expression and function during differentiation of intestinal epithelial cells von Sood, R., Bear, C., Auerbach, W., Reyes, E., Jensen, T., Kartner, N., Riordan, J.R., Buchwald, M.

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Intracellular localization of GDP- l-fucose: Glycoprotein and CMP-sialic acid: Apolipoprotein glycosyltransferases in rat and pork livers von Munro, J.Ronald, Narasimhan, Saroja, Wetmore, Steve, Riordan, J.R., Schachter, Harry

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Purification of P-glycoprotein from plasma membrane vesicles of Chinese hamster ovary cell mutants with reduced colchicine permeability von Riordan, J R, Ling, V

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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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Induction of expression of the cystic fibrosis transmembrane conductance regulator von BREUER, W, KARTNER, N, RIORDAN, J. R, CABANTCHIK, Z. I

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