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Revisiting CFTR Interactions: Old Partners and New Players

International journal of molecular sciences, 2021-12, Vol.22 (24), p.13196

2021

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Pharmacological Rescue of Conditionally Reprogrammed Cystic Fibrosis Bronchial Epithelial Cells

American journal of respiratory cell and molecular biology, 2017-05, Vol.56 (5), p.568-574

2017

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Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration

The FASEB journal, 2012-02, Vol.26 (2), p.533-545

2012

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Small-molecule eRF3a degraders rescue CFTR nonsense mutations by promoting premature termination codon readthrough

The Journal of clinical investigation, 2022-09, Vol.132 (18)

2022

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Impact of Airway Inflammation on the Efficacy of CFTR Modulators

Cells (Basel, Switzerland), 2021-11, Vol.10 (11), p.3260

2021

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Pulmonary Ionocytes: What Are They Transporting and Which Way?

American journal of respiratory and critical care medicine, 2024-09, Vol.210 (6), p.705-707

2024

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Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis

Nature chemical biology, 2010-01, Vol.6 (1), p.25-33

2010

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Airway Epithelial Inflammation In Vitro Augments the Rescue of Mutant CFTR by Current CFTR Modulator Therapies

Frontiers in pharmacology, 2021-03, Vol.12, p.628722-628722

2021

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Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures

American journal of physiology. Lung cellular and molecular physiology, 2010-03, Vol.298 (3), p.L304-L314

2010

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Ion Channel Modulators in Cystic Fibrosis

Chest, 2018-08, Vol.154 (2), p.383-393

2018

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How many SARS-CoV-2 "viroporins" are really ion channels?

Communications biology, 2022-08, Vol.5 (1), p.859-859, Article 859

2022

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Cystic fibrosis airway inflammation enables elexacaftor/tezacaftor/ivacaftor-mediated rescue of N1303K CFTR mutation

ERJ open research, 2024-01, Vol.10 (1), p.746

2024

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A Novel Co-Culture Model Reveals Enhanced CFTR Rescue in Primary Cystic Fibrosis Airway Epithelial Cultures with Persistent Pseudomonas aeruginosa Infection

Cells (Basel, Switzerland), 2023-11, Vol.12 (22), p.2618

2023

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AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosis

PLoS pathogens, 2011-05, Vol.7 (5), p.e1002053-e1002053

2011

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Imaging CFTR protein localization in cultured cells and tissues

Methods in molecular biology (Clifton, N.J.), 2011, Vol.742, p.15

2011

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Role of N-linked oligosaccharides in the biosynthetic processing of the cystic fibrosis membrane conductance regulator

Journal of cell science, 2008-09, Vol.121 (17), p.2814-2823

2008

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The PDZ-binding Chloride Channel ClC-3B Localizes to the Golgi and Associates with Cystic Fibrosis Transmembrane Conductance Regulator-interacting PDZ Proteins

The Journal of biological chemistry, 2003-02, Vol.278 (8), p.6440-6449

2003

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An Expanded Biological Repertoire for Ins(3,4,5,6)P4 through its Modulation of ClC-3 Function

Current biology, 2008-10, Vol.18 (20), p.1600-1605

2008

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Established and novel human translational models to advance cystic fibrosis research, drug discovery, and optimize CFTR-targeting therapeutics

Current opinion in pharmacology, 2022-06, Vol.64, p.102210-102210, Article 102210

2022

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The role of cystic fibrosis transmembrane conductance regulator phenylalanine 508 side chain in ion channel gating

The Journal of physiology, 2006-04, Vol.572 (2), p.347-358

2006

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Protein-O-glycosylation in yeast: protein-specific mannosyltransferases

Glycobiology (Oxford), 1997-06, Vol.7 (4), p.481-486

1997

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Patient-derived cell models for personalized medicine approaches in cystic fibrosis

Journal of cystic fibrosis, 2023-03, Vol.22 (Suppl 1), p.S32-S38

2023

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Recent progress in translational cystic fibrosis research using precision medicine strategies

Journal of cystic fibrosis, 2018-03, Vol.17 (2), p.S52-S60

2018

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Editorial overview – 2022 respiratory issue: Cystic fibrosis pathophysiology, models, and novel therapies

Current opinion in pharmacology, 2022-12, Vol.67, p.102289-102289, Article 102289

2022

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Generation of renewable mouse intestinal epithelial cell monolayers and organoids for functional analyses

BMC cell biology, 2018-08, Vol.19 (1), p.15, Article 15

2018

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Revisiting CFTR Interactions: Old Partners and New Players

Pharmacological Rescue of Conditionally Reprogrammed Cystic Fibrosis Bronchial Epithelial Cells

Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration

Small-molecule eRF3a degraders rescue CFTR nonsense mutations by promoting premature termination codon readthrough

Impact of Airway Inflammation on the Efficacy of CFTR Modulators

Pulmonary Ionocytes: What Are They Transporting and Which Way?

Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis

Airway Epithelial Inflammation In Vitro Augments the Rescue of Mutant CFTR by Current CFTR Modulator Therapies

Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures

Ion Channel Modulators in Cystic Fibrosis

How many SARS-CoV-2 "viroporins" are really ion channels?

Cystic fibrosis airway inflammation enables elexacaftor/tezacaftor/ivacaftor-mediated rescue of N1303K CFTR mutation

A Novel Co-Culture Model Reveals Enhanced CFTR Rescue in Primary Cystic Fibrosis Airway Epithelial Cultures with Persistent Pseudomonas aeruginosa Infection

AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosis

Imaging CFTR protein localization in cultured cells and tissues

Role of N-linked oligosaccharides in the biosynthetic processing of the cystic fibrosis membrane conductance regulator

The PDZ-binding Chloride Channel ClC-3B Localizes to the Golgi and Associates with Cystic Fibrosis Transmembrane Conductance Regulator-interacting PDZ Proteins

An Expanded Biological Repertoire for Ins(3,4,5,6)P4 through its Modulation of ClC-3 Function

Established and novel human translational models to advance cystic fibrosis research, drug discovery, and optimize CFTR-targeting therapeutics

The role of cystic fibrosis transmembrane conductance regulator phenylalanine 508 side chain in ion channel gating

Protein-O-glycosylation in yeast: protein-specific mannosyltransferases

Patient-derived cell models for personalized medicine approaches in cystic fibrosis

Recent progress in translational cystic fibrosis research using precision medicine strategies

Editorial overview – 2022 respiratory issue: Cystic fibrosis pathophysiology, models, and novel therapies

Generation of renewable mouse intestinal epithelial cell monolayers and organoids for functional analyses

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