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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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Roscovitine is a proteostasis regulator that corrects the trafficking defect of F508del‐CFTR by a CDK‐independent mechanism

British journal of pharmacology, 2014-11, Vol.171 (21), p.4831-4849

2014

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N- and C-alkylation of seven-membered iminosugars generates potent glucocerebrosidase inhibitors and F508del-CFTR correctors

Organic & biomolecular chemistry, 2014-11, Vol.12 (44), p.8977-8996

2014

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Maintaining Low Ca2+ Level in the Endoplasmic Reticulum Restores Abnormal Endogenous F508del‐CFTR Trafficking in Airway Epithelial Cells

Traffic (Copenhagen, Denmark), 2006-05, Vol.7 (5), p.562-573

2006

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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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Deficit of osteoprotegerin release by osteoblasts from a patient with cystic fibrosis

The European respiratory journal, 2012-03, Vol.39 (3), p.780-781

2012

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Sildenafil (Viagra) corrects ΔF508-CFTR location in nasal epithelial cells from patients with cystic fibrosis

Thorax, 2005-01, Vol.60 (1), p.55-59

2005

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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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134 Rationale for evaluating (R)-roscovitine (Seliciclib) in patients with cystic fibrosis

Journal of cystic fibrosis, 2015-06, Vol.14, p.S92-S92

2015

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SiRNA glucosidase promotes endogenous F508del-CFTR trafficking

Journal of cystic fibrosis, 2010, Vol.9, p.S15-S15

2010

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SiRNA calnexin promotes endogenous F508del-CFTR trafficking

Journal of cystic fibrosis, 2009-06, Vol.8, p.S19-S19

2009

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Roscovitine: a novel corrector for the functional rescue of F508del-CFTR protein

Journal of cystic fibrosis, 2009, Vol.8, p.S26-S26

2009

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38 Combination of CFTR mutations producing frequent complex alleles with different clinical and functional outcomes

Journal of cystic fibrosis, 2012-06, Vol.11, p.S65-S65

2012

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Identification of TRPC6 as a novel potential target to activate CaCC in human CF airway epithelial cells

Journal of cystic fibrosis, 2010, Vol.9, p.S16-S16

2010

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CL005 - Modèle porcin de culture cellulaire bronchique : étude pharmacologique du CFTR

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-06, Vol.17 (6), p.2-2

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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Calcium homeostasis is abnormal in cystic fibrosis airway epithelial cells but is normalized after rescue of F508del-CFTR

Cell calcium (Edinburgh), 2008-02, Vol.43 (2), p.175-183

2008

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082 CFTR expression and function in rat intrapulmonary arteries

Revue des maladies respiratoires, 2007-11, Vol.24 (9), p.1233-1233

2007

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G622 amino acid has a crucial role in pharmacological activation of CFTR chloride channel by benzo[c]quinolizinium compounds

Journal of cystic fibrosis, 2008-06, Vol.7, p.S18-S18

2008

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Pharmacological characterization of a novel water-soluble activator of F508del-CFTR

Journal of cystic fibrosis, 2009, Vol.8, p.S25-S25

2009

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The Adenovirus chimeric vector Ad5F35/GFP-CFTR efficiently restores the CFTR deficiency in human airway epithelia via apical surface transduction

Journal of cystic fibrosis, 2009, Vol.8, p.S30-S30

2009

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ANTI-INFLAMMATORY EFFECT OF MIGLUSTAT IN BRONCHIAL CELLS

Journal of cystic fibrosis, 2008-07, Vol.7, p.S18-S18

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 correctorsElectronic supplementary information (ESI) available: Copies of 1H, 19F and 13C spectra of all new compounds. See DOI: 10.1039/c5ob01526j

2015-10

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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

Roscovitine is a proteostasis regulator that corrects the trafficking defect of F508del‐CFTR by a CDK‐independent mechanism

N- and C-alkylation of seven-membered iminosugars generates potent glucocerebrosidase inhibitors and F508del-CFTR correctors

Maintaining Low Ca2+ Level in the Endoplasmic Reticulum Restores Abnormal Endogenous F508del‐CFTR Trafficking in Airway Epithelial Cells

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

Deficit of osteoprotegerin release by osteoblasts from a patient with cystic fibrosis

Sildenafil (Viagra) corrects ΔF508-CFTR location in nasal epithelial cells from patients with cystic fibrosis

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

134 Rationale for evaluating (R)-roscovitine (Seliciclib) in patients with cystic fibrosis

SiRNA glucosidase promotes endogenous F508del-CFTR trafficking

SiRNA calnexin promotes endogenous F508del-CFTR trafficking

Roscovitine: a novel corrector for the functional rescue of F508del-CFTR protein

38 Combination of CFTR mutations producing frequent complex alleles with different clinical and functional outcomes

Identification of TRPC6 as a novel potential target to activate CaCC in human CF airway epithelial cells

CL005 - Modèle porcin de culture cellulaire bronchique : étude pharmacologique du CFTR

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

Calcium homeostasis is abnormal in cystic fibrosis airway epithelial cells but is normalized after rescue of F508del-CFTR

082 CFTR expression and function in rat intrapulmonary arteries

G622 amino acid has a crucial role in pharmacological activation of CFTR chloride channel by benzo[c]quinolizinium compounds

Pharmacological characterization of a novel water-soluble activator of F508del-CFTR

The Adenovirus chimeric vector Ad5F35/GFP-CFTR efficiently restores the CFTR deficiency in human airway epithelia via apical surface transduction

ANTI-INFLAMMATORY EFFECT OF MIGLUSTAT IN BRONCHIAL CELLS

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