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Pharmacological Inhibition of the Ubiquitin Ligase RNF5 Rescues F508del-CFTR in Cystic Fibrosis Airway Epithelia

Cell chemical biology, 2018-07, Vol.25 (7), p.891-905.e8

2018

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In vitro Methods for the Development and Analysis of Human Primary Airway Epithelia

Frontiers in pharmacology, 2018-10, Vol.9, p.1176-1176

2018

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Cytokines induce tight junction disassembly in airway cells via an EGFR-dependent MAPK/ERK1/2-pathway

Laboratory investigation, 2012-08, Vol.92 (8), p.1140-1148

2012

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Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia

International journal of molecular sciences, 2020-02, Vol.21 (4), p.1488

2020

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Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells

Cells (Basel, Switzerland), 2020-09, Vol.9 (9), p.2090

2020

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Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis Mutation

Scientific reports, 2015-07, Vol.5 (1), p.12138, Article 12138

2015

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Functional analysis of acid-activated Cl− channels: Properties and mechanisms of regulation

Biochimica et biophysica acta, 2015-01, Vol.1848 (1), p.105-114

2015

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Anion-Transport Mechanism of a Triazole-Bearing Derivative of Prodigiosine: A Candidate for Cystic Fibrosis Therapy

Frontiers in pharmacology, 2018-08, Vol.9, p.852-852

2018

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The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism

Frontiers in pharmacology, 2018-12, Vol.9, p.1464-1464

2018

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Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin

PloS one, 2015-06, Vol.10 (6), p.e0131775-e0131775

2015

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Dual Activity of Aminoarylthiazoles on the Trafficking and Gating Defects of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Caused by Cystic Fibrosis Mutations

The Journal of biological chemistry, 2011-04, Vol.286 (17), p.15215-15226

2011

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A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree

European journal of human genetics : EJHG, 2013-06, Vol.21 (6), p.613-619

2013

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Thiocyanate Transport in Resting and IL-4-Stimulated Human Bronchial Epithelial Cells: Role of Pendrin and Anion Channels

Journal of Immunology, 2007-04, Vol.178 (8), p.5144-5153

2007

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Increased expression of ATP12A proton pump in cystic fibrosis airways

JCI insight, 2018-10, Vol.3 (20)

2018

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Non-canonical translation start sites in the TMEM16A chloride channel

Biochimica et biophysica acta, 2014-01, Vol.1838 (1), p.89-97

2014

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IL-12 can target human lung adenocarcinoma cells and normal bronchial epithelial cells surrounding tumor lesions

PloS one, 2009-07, Vol.4 (7), p.e6119-e6119

2009

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Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators

The Journal of pharmacology and experimental therapeutics, 2009-09, Vol.330 (3), p.783

2009

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Antihypertensive 1,4-Dihydropyridines as Correctors of the Cystic Fibrosis Transmembrane Conductance Regulator Channel Gating Defect Caused by Cystic Fibrosis Mutations

Molecular pharmacology, 2005-12, Vol.68 (6), p.1736-1746

2005

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IL-4 Is a Potent Modulator of Ion Transport in the Human Bronchial Epithelium In Vitro

The Journal of immunology (1950), 2002-01, Vol.168 (2), p.839-845

2002

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Gelsolin Secretion in Interleukin-4-treated Bronchial Epithelia and in Asthmatic Airways

American journal of respiratory and critical care medicine, 2005-11, Vol.172 (9), p.1090-1096

2005

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CD4+CD25highCD127- regulatory T-cells in COPD: smoke and drugs effect

The World Allergy Organization journal, 2016-01, Vol.9, p.5, Article 5

2016

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TMEM16A, A Membrane Protein Associated with Calcium-Dependent Chloride Channel Activity

Science (American Association for the Advancement of Science), 2008-10, Vol.322 (5901), p.590-594

2008

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SWATH label-free proteomics for cystic fibrosis research

Journal of cystic fibrosis, 2019-07, Vol.18 (4), p.501-506

2019

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TRPV4 and purinergic receptor signalling pathways are separately linked in airway epithelia to CFTR and TMEM16A chloride channels

The Journal of physiology, 2019-12, Vol.597 (24), p.5859-5878

2019

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Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms

The Journal of physiology, 2015-09, Vol.593 (17), p.3829-3848

2015

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Pharmacological Inhibition of the Ubiquitin Ligase RNF5 Rescues F508del-CFTR in Cystic Fibrosis Airway Epithelia

In vitro Methods for the Development and Analysis of Human Primary Airway Epithelia

Cytokines induce tight junction disassembly in airway cells via an EGFR-dependent MAPK/ERK1/2-pathway

Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia

Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells

Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis Mutation

Functional analysis of acid-activated Cl− channels: Properties and mechanisms of regulation

Anion-Transport Mechanism of a Triazole-Bearing Derivative of Prodigiosine: A Candidate for Cystic Fibrosis Therapy

The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism

Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin

Dual Activity of Aminoarylthiazoles on the Trafficking and Gating Defects of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Caused by Cystic Fibrosis Mutations

A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree

Thiocyanate Transport in Resting and IL-4-Stimulated Human Bronchial Epithelial Cells: Role of Pendrin and Anion Channels

Increased expression of ATP12A proton pump in cystic fibrosis airways

Non-canonical translation start sites in the TMEM16A chloride channel

IL-12 can target human lung adenocarcinoma cells and normal bronchial epithelial cells surrounding tumor lesions

Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators

Antihypertensive 1,4-Dihydropyridines as Correctors of the Cystic Fibrosis Transmembrane Conductance Regulator Channel Gating Defect Caused by Cystic Fibrosis Mutations

IL-4 Is a Potent Modulator of Ion Transport in the Human Bronchial Epithelium In Vitro

Gelsolin Secretion in Interleukin-4-treated Bronchial Epithelia and in Asthmatic Airways

CD4+CD25highCD127- regulatory T-cells in COPD: smoke and drugs effect

TMEM16A, A Membrane Protein Associated with Calcium-Dependent Chloride Channel Activity

SWATH label-free proteomics for cystic fibrosis research

TRPV4 and purinergic receptor signalling pathways are separately linked in airway epithelia to CFTR and TMEM16A chloride channels

Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms

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