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9‐Phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels

British journal of pharmacology, 2008-04, Vol.153 (8), p.1697-1705

2008

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Synthetic deoxynojirimycin derivatives bearing a thiolated, fluorinated or unsaturated N-alkyl chain: identification of potent α-glucosidase and trehalase inhibitors as well as F508del-CFTR correctors

Organic & biomolecular chemistry, 2015-01, Vol.13 (43), p.10734-10744

2015

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Expression and function of cystic fibrosis transmembrane conductance regulator in rat intrapulmonary arteries

The European respiratory journal, 2007-11, Vol.30 (5), p.857-864

2007

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Identification of a novel water-soluble activator of wild-type and F508del CFTR: GPact-11a

The European respiratory journal, 2010-08, Vol.36 (2), p.311-322

2010

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Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the α-glucosidase inhibitor miglustat

FEBS letters, 2006-04, Vol.580 (8), p.2081-2086

2006

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Disruption of CFTR chloride channel alters mechanical properties and cAMP‐dependent Cl− transport of mouse aortic smooth muscle cells

The Journal of physiology, 2005-10, Vol.568 (2), p.483-495

2005

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Regulation of the cystic fibrosis transmembrane conductance regulator channel by beta-adrenergic agonists and vasoactive intestinal peptide in rat smooth muscle cells and its role in vasorelaxation

The Journal of biological chemistry, 2004-05, Vol.279 (20), p.21160-21168

2004

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The cystic fibrosis mutation G1349D within the signature motif LSHGH of NBD2 abolishes the activation of CFTR chloride channels by genistein

Biochemical pharmacology, 2004-06, Vol.67 (12), p.2187-2196

2004

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Synthesis, SAR, Crystal Structure, and Biological Evaluation of Benzoquinoliziniums as Activators of Wild-Type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Channels

Journal of medicinal chemistry, 2004-02, Vol.47 (4), p.962-972

2004

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Syntaxin 8 impairs trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) and inhibits its channel activity

Journal of cell science, 2004-04, Vol.117 (Pt 10), p.1923-1935

2004

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The glycine residues G551 and G1349 within the ATP-binding cassette signature motifs play critical roles in the activation and inhibition of cystic fibrosis transmembrane conductance regulator channels by phloxine B

The Journal of membrane biology, 2006-01, Vol.208 (3), p.203-212

2006

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General anesthetic octanol and related compounds activate wild‐type and delF508 cystic fibrosis chloride channels

British journal of pharmacology, 2004-03, Vol.141 (6), p.905-914

2004

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Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation

American Journal of Physiology: Cell Physiology, 2001-11, Vol.281 (5), p.C1657-C1666

2001

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9‐Phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels

Synthetic deoxynojirimycin derivatives bearing a thiolated, fluorinated or unsaturated N-alkyl chain: identification of potent α-glucosidase and trehalase inhibitors as well as F508del-CFTR correctors

Expression and function of cystic fibrosis transmembrane conductance regulator in rat intrapulmonary arteries

Identification of a novel water-soluble activator of wild-type and F508del CFTR: GPact-11a

Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the α-glucosidase inhibitor miglustat

Disruption of CFTR chloride channel alters mechanical properties and cAMP‐dependent Cl− transport of mouse aortic smooth muscle cells

Regulation of the cystic fibrosis transmembrane conductance regulator channel by beta-adrenergic agonists and vasoactive intestinal peptide in rat smooth muscle cells and its role in vasorelaxation

The cystic fibrosis mutation G1349D within the signature motif LSHGH of NBD2 abolishes the activation of CFTR chloride channels by genistein

Synthesis, SAR, Crystal Structure, and Biological Evaluation of Benzoquinoliziniums as Activators of Wild-Type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Channels

Syntaxin 8 impairs trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) and inhibits its channel activity

The glycine residues G551 and G1349 within the ATP-binding cassette signature motifs play critical roles in the activation and inhibition of cystic fibrosis transmembrane conductance regulator channels by phloxine B

General anesthetic octanol and related compounds activate wild‐type and delF508 cystic fibrosis chloride channels

Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation

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