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The secret life of CFTR as a calcium‐activated chloride channel

The Journal of physiology, 2013-11, Vol.591 (21), p.5273-5278

2013

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mRNA Delivery: Challenges and Advances through Polymeric Soft Nanoparticles

International journal of molecular sciences, 2024-02, Vol.25 (3), p.1739

2024

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Cholesterol Modulates CFTR Confinement in the Plasma Membrane of Primary Epithelial Cells

Biophysical journal, 2015-07, Vol.109 (1), p.85-94

2015

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Cutting Edge: 1,25-Dihydroxyvitamin D3 Is a Direct Inducer of Antimicrobial Peptide Gene Expression

The Journal of immunology (1950), 2004-09, Vol.173 (5), p.2909-2912

2004

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Pendrin Mediates Bicarbonate Secretion and Enhances Cystic Fibrosis Transmembrane Conductance Regulator Function in Airway Surface Epithelia

American journal of respiratory cell and molecular biology, 2019-06, Vol.60 (6), p.705-716

2019

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Low free drug concentration prevents inhibition of F508del CFTR functional expression by the potentiator VX‐770 (ivacaftor)

British journal of pharmacology, 2016-02, Vol.173 (3), p.459-470

2016

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Macrocycle-stabilization of its interaction with 14-3-3 increases plasma membrane localization and activity of CFTR

Nature communications, 2022-06, Vol.13 (1), p.3586-3586, Article 3586

2022

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Nonspecific binding of common anti-CFTR antibodies in ciliated cells of human airway epithelium

Scientific reports, 2021-12, Vol.11 (1), p.23256-23256, Article 23256

2021

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Hsp70 and DNAJA2 limit CFTR levels through degradation

PloS one, 2019-08, Vol.14 (8), p.e0220984-e0220984

2019

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Phosphodiesterase 8A Regulates CFTR Activity in Airway Epithelial Cells

Cellular physiology and biochemistry, 2021-12, Vol.55 (6), p.784-804

2021

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Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia

Molecular biology of the cell, 2012-11, Vol.23 (21), p.4188-4202

2012

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CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells

Frontiers in physiology, 2021-02, Vol.12, p.619442-619442

2021

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The NSAID glafenine rescues class 2 CFTR mutants via cyclooxygenase 2 inhibition of the arachidonic acid pathway

Scientific reports, 2022-03, Vol.12 (1), p.4595-19, Article 4595

2022

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Lack of CFTR in skeletal muscle predisposes to muscle wasting and diaphragm muscle pump failure in cystic fibrosis mice

PLoS genetics, 2009-07, Vol.5 (7), p.e1000586-e1000586

2009

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Oxygenation as a driving factor in epithelial differentiation at the air-liquid interface

Integrative biology (Cambridge), 2021-03, Vol.13 (3), p.61-72

2021

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The dual phosphodiesterase 3 and 4 inhibitor RPL554 stimulates CFTR and ciliary beating in primary cultures of bronchial epithelia

American journal of physiology. Lung cellular and molecular physiology, 2016-01, Vol.310 (1), p.L59-L70

2016

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Cystic Fibrosis Transmembrane Conductance Regulator Function Is Suppressed in Cigarette Smokers

American journal of respiratory and critical care medicine, 2006-05, Vol.173 (10), p.1139-1144

2006

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Variable Responses to CFTR Correctors in vitro : Estimating the Design Effect in Precision Medicine

Frontiers in pharmacology, 2018-12, Vol.9, p.1490-1490

2018

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Investigating CFTR and KCa3.1 Protein/Protein Interactions

PloS one, 2016-04, Vol.11 (4), p.e0153665-e0153665

2016

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Structural Analog of Sildenafil Identified as a Novel Corrector of the F508del-CFTR Trafficking Defect

Molecular pharmacology, 2008-02, Vol.73 (2), p.478-489

2008

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Treatment With LAU-7b Complements CFTR Modulator Therapy by Improving Lung Physiology and Normalizing Lipid Imbalance Associated With CF Lung Disease

Frontiers in pharmacology, 2022-05, Vol.13, p.876842

2022

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The buffer capacity of airway epithelial secretions

Frontiers in physiology, 2014-06, Vol.5, p.188-188

2014

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PEGylated composite nanoparticles of PLGA and polyethylenimine for safe and efficient delivery of pDNA to lungs

International journal of pharmaceutics, 2017-05, Vol.524 (1-2), p.382-396

2017

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Rescue of Mutant CFTR Trafficking Defect by the Investigational Compound MCG1516A

Cells (Basel, Switzerland), 2022-01, Vol.11 (1), p.136

2022

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The anion transporter SLC26A9 localizes to tight junctions and is degraded by the proteasome when co-expressed with F508del–CFTR

The Journal of biological chemistry, 2019-11, Vol.294 (48), p.18269-18284

2019

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The secret life of CFTR as a calcium‐activated chloride channel

mRNA Delivery: Challenges and Advances through Polymeric Soft Nanoparticles

Cholesterol Modulates CFTR Confinement in the Plasma Membrane of Primary Epithelial Cells

Cutting Edge: 1,25-Dihydroxyvitamin D3 Is a Direct Inducer of Antimicrobial Peptide Gene Expression

Pendrin Mediates Bicarbonate Secretion and Enhances Cystic Fibrosis Transmembrane Conductance Regulator Function in Airway Surface Epithelia

Low free drug concentration prevents inhibition of F508del CFTR functional expression by the potentiator VX‐770 (ivacaftor)

Macrocycle-stabilization of its interaction with 14-3-3 increases plasma membrane localization and activity of CFTR

Nonspecific binding of common anti-CFTR antibodies in ciliated cells of human airway epithelium

Hsp70 and DNAJA2 limit CFTR levels through degradation

Phosphodiesterase 8A Regulates CFTR Activity in Airway Epithelial Cells

Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia

CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells

The NSAID glafenine rescues class 2 CFTR mutants via cyclooxygenase 2 inhibition of the arachidonic acid pathway

Lack of CFTR in skeletal muscle predisposes to muscle wasting and diaphragm muscle pump failure in cystic fibrosis mice

Oxygenation as a driving factor in epithelial differentiation at the air-liquid interface

The dual phosphodiesterase 3 and 4 inhibitor RPL554 stimulates CFTR and ciliary beating in primary cultures of bronchial epithelia

Cystic Fibrosis Transmembrane Conductance Regulator Function Is Suppressed in Cigarette Smokers

Variable Responses to CFTR Correctors in vitro : Estimating the Design Effect in Precision Medicine

Investigating CFTR and KCa3.1 Protein/Protein Interactions

Structural Analog of Sildenafil Identified as a Novel Corrector of the F508del-CFTR Trafficking Defect

Treatment With LAU-7b Complements CFTR Modulator Therapy by Improving Lung Physiology and Normalizing Lipid Imbalance Associated With CF Lung Disease

The buffer capacity of airway epithelial secretions

PEGylated composite nanoparticles of PLGA and polyethylenimine for safe and efficient delivery of pDNA to lungs

Rescue of Mutant CFTR Trafficking Defect by the Investigational Compound MCG1516A

The anion transporter SLC26A9 localizes to tight junctions and is degraded by the proteasome when co-expressed with F508del–CFTR

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