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Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator

The Journal of biological chemistry, 1994-04, Vol.269 (17), p.12784-12788

1994

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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 cells

The Journal of biological chemistry, 1993-10, Vol.268 (29), p.21592-21598

1993

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Inhibition of epithelial Na + currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator

FEBS letters, 1997-01, Vol.400 (3), p.341-344

1997

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Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum

BBA - Biomembranes, 1999-12, Vol.1461 (2), p.275-283

1999

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Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion

The Journal of biological chemistry, 1994-07, Vol.269 (28), p.18572-18575

1994

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Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP

The EMBO journal, 1994-12, Vol.13 (24), p.6076-6086

1994

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Crystallographic and single-particle analyses of native- and nucleotide-bound forms of the cystic fibrosis transmembrane conductance regulator (CFTR) protein

Biochemical Society transactions, 2005-11, Vol.33 (5), p.996

2005

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Crystallographic and single-particle analyses of native- and nucleotide-bound forms of the cystic fibrosis transmembrane conductance regulator (CFTR) protein

Biochemical Society transactions, 2005-11, Vol.33 (Pt 5), p.996-999

2005

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Synthetic and natural opiates interact with P-glycoprotein in multidrug-resistant cells

The Journal of biological chemistry, 1993-07, Vol.268 (21), p.16059-16064

1993

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Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites

The Journal of biological chemistry, 1993-05, Vol.268 (15), p.11304-11311

1993

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Identification of Mutations in Regions Corresponding to the Two Putative Nucleotide (ATP)-Binding Folds of the Cystic Fibrosis Gene

Proceedings of the National Academy of Sciences - PNAS, 1990-11, Vol.87 (21), p.8447-8451

1990

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Forefronts in Nephrology: The molecular basis of renal cystic disease

Kidney international, 1995-03, Vol.47 (3), p.720-720

Riordan, J.R.

1995

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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

Kidney international, 1995-03, Vol.47 (3), p.720-720

Riordan, J.R.

1995

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CFTR is a monomer: biochemical and functional evidence

The Journal of membrane biology, 2002-07, Vol.188 (1), p.55-71

2002

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Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene

The Journal of biological chemistry, 1991-10, Vol.266 (29), p.19142-19145

1991

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Cystic fibrosis-type mutational analysis in the ATP-binding cassette transporter signature of human P-glycoprotein MDR1

The Journal of biological chemistry, 1994-08, Vol.269 (32), p.20575-20583

1994

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The cystic fibrosis transmembrane regulator is present and functional in endosomes. Role as a determinant of endosomal pH

The Journal of biological chemistry, 1992-07, Vol.267 (21), p.14568-14572

1992

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Regulation of CFTR expression and function during differentiation of intestinal epithelial cells

The EMBO journal, 1992-07, Vol.11 (7), p.2487-2494

1992

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Intracellular localization of GDP- l-fucose: Glycoprotein and CMP-sialic acid: Apolipoprotein glycosyltransferases in rat and pork livers

Archives of biochemistry and biophysics, 1975-01, Vol.169 (1), p.269-277

1975

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Purification of P-glycoprotein from plasma membrane vesicles of Chinese hamster ovary cell mutants with reduced colchicine permeability

The Journal of biological chemistry, 1979-12, Vol.254 (24), p.12701-12705

1979

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The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation

Biophysical journal, 1992-04, Vol.62 (1), p.1-4

1992

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Induction of expression of the cystic fibrosis transmembrane conductance regulator

The Journal of biological chemistry, 1992-05, Vol.267 (15), p.10465-10469

1992

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Protein kinase C mediates down-regulation of cystic fibrosis transmembrane conductance regulator levels in epithelial cells

The Journal of biological chemistry, 1993-07, Vol.268 (19), p.13935-13939

1993

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Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA

Trends in genetics, 1989, Vol.5, p.363-363

Riordan, J.R.

1989

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Mutation of Potential Phosphorylation Sites in the Recombinant R Domain of the Cystic Fibrosis Transmembrane Conductance Regulator Has Significant Effects on Domain Conformation

Biochemical and biophysical research communications, 1995-01, Vol.206 (1), p.207-214

1995

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Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator

The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells

Inhibition of epithelial Na + currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator

Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum

Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion

Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP

Crystallographic and single-particle analyses of native- and nucleotide-bound forms of the cystic fibrosis transmembrane conductance regulator (CFTR) protein

Crystallographic and single-particle analyses of native- and nucleotide-bound forms of the cystic fibrosis transmembrane conductance regulator (CFTR) protein

Synthetic and natural opiates interact with P-glycoprotein in multidrug-resistant cells

Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites

Identification of Mutations in Regions Corresponding to the Two Putative Nucleotide (ATP)-Binding Folds of the Cystic Fibrosis Gene

Forefronts in Nephrology: The molecular basis of renal cystic disease

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

CFTR is a monomer: biochemical and functional evidence

Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene

Cystic fibrosis-type mutational analysis in the ATP-binding cassette transporter signature of human P-glycoprotein MDR1

The cystic fibrosis transmembrane regulator is present and functional in endosomes. Role as a determinant of endosomal pH

Regulation of CFTR expression and function during differentiation of intestinal epithelial cells

Intracellular localization of GDP- l-fucose: Glycoprotein and CMP-sialic acid: Apolipoprotein glycosyltransferases in rat and pork livers

Purification of P-glycoprotein from plasma membrane vesicles of Chinese hamster ovary cell mutants with reduced colchicine permeability

The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation

Induction of expression of the cystic fibrosis transmembrane conductance regulator

Protein kinase C mediates down-regulation of cystic fibrosis transmembrane conductance regulator levels in epithelial cells

Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA

Mutation of Potential Phosphorylation Sites in the Recombinant R Domain of the Cystic Fibrosis Transmembrane Conductance Regulator Has Significant Effects on Domain Conformation

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