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Novel human bronchial epithelial cell lines for cystic fibrosis research

American journal of physiology. Lung cellular and molecular physiology, 2009-01, Vol.296 (1), p.L82-L91

2009

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PMT gene family: protein O-glycosylation in Saccharomyces cerevisiae is vital

The EMBO journal, 1996-11, Vol.15 (21), p.5752-5759

1996

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366: Airway Obstruction Produces Hypoxia-Dependent Sodium Absorption in Human Airway Epithelial Cells

Journal of cystic fibrosis, 2021-11, Vol.20, p.S173-S174

2021

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309 The CFTR Antibody Distribution Program: Development and production of antibodies for CFTR detection

Journal of cystic fibrosis, 2023-10, Vol.22, p.S155-S155

2023

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339 Effects of Pseudomonas infection on CFTR rescue and epithelial gene expression

Journal of cystic fibrosis, 2024-09, Vol.23, p.S179-S179

2024

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284 Effect of epithelial inflammation on the efficacy of therapeutic oligonucleotides to correct CFTR splice and nonsense mutations

Journal of cystic fibrosis, 2024-09, Vol.23, p.S151-S152

2024

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616: Effects of VX-445 on CFTR channel function and stability

Journal of cystic fibrosis, 2021-11, Vol.20, p.S293

2021

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176 Cystic fibrosis airway inflammation enhances the efficacy of CFTR modulators

Journal of cystic fibrosis, 2023-10, Vol.22, p.S92-S93

2023

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325 Corrector elexacaftor mimics potentiator action by increasing numbers of functional CFTR channels via recovery of rescued inactivated F508del

Journal of cystic fibrosis, 2023-10, Vol.22, p.S162-S162

2023

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311 Active Pseudomonas aeruginosa infection of primary airway epithelia enhances CFTR modulator rescue

Journal of cystic fibrosis, 2023-10, Vol.22, p.S156-S156

2023

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659 Inflammation augments elexacaftor/tezacaftor/ivacaftor-induced cystic fibrosis transmembrane conductance regulator rescue in primary airway epithelia carrying F508del and rare cystic fibrosis transmembrane conductance regulator mutations

Journal of cystic fibrosis, 2022-10, Vol.21, p.S360-S361

2022

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647 Potentiator icenticaftor is superior to ivacaftor in rescuing F508del cystic fibrosis transmembrane conductance regulator and does not destabilize corrected mature protein

Journal of cystic fibrosis, 2022-10, Vol.21, p.S355-S355

2022

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331 CF airway inflammation enhances elexacaftor/tezacaftor/ivacaftormediated rescue of N1303K CFTR

Journal of cystic fibrosis, 2024-09, Vol.23, p.S175-S176

2024

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618: Specific detection of CFTR in airway epithelia

Journal of cystic fibrosis, 2021-11, Vol.20, p.S293-S294

2021

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676 A multicenter approach to optimize and validate a robust cystic fibrosis transmembrane conductance regulator–specific immunolabeling protocol

Journal of cystic fibrosis, 2022-10, Vol.21, p.S370-S370

2022

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423 Novel method for isolation of small airway epithelial cells by bulk enzymatic digestion

Journal of cystic fibrosis, 2022-10, Vol.21, p.S244-S244

2022

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434 In vitro evaluation of TAVT-135, an artificial pan-genotypic chloride ion transporter

Journal of cystic fibrosis, 2022-10, Vol.21, p.S249-S249

2022

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156 Primary pharmacology and toxicology of TAVT-135, a novel chloride ion transporter in development for the treatment of cystic fibrosis

Journal of cystic fibrosis, 2023-10, Vol.22, p.S83-S83

2023

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598: Correction of CF splicing mutations with oligonucleotides

Journal of cystic fibrosis, 2021-11, Vol.20, p.S284-S285

2021

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449 Pathways balancing basal mucin and cystic fibrosis transmembrane conductance regulator–mediated fluid secretion in the human small airway

Journal of cystic fibrosis, 2022-10, Vol.21, p.S257-S258

2022

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WS07.2 A PI3Kγ-peptide promotes Cl− secretion through activation of both CFTR - dependent and independent currents

Journal of cystic fibrosis, 2021, Vol.20, p.S13

2021

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179: Modulator therapy reverses aberrant mucus properties in vitro via hydration

Journal of cystic fibrosis, 2021-11, Vol.20, p.S88-S89

2021

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WS03-3 CFTR malfunction is linked to mucus abnormal properties in cystic fibrosis

Journal of cystic fibrosis, 2019-06, Vol.18, p.S5-S5

2019

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Endocytic Trafficking Routes of Wild Type and ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator

Molecular biology of the cell, 2004-06, Vol.15 (6), p.2684-2696

2004

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Protein O-mannosylation

BBA - General Subjects, 1999-01, Vol.1426 (2), p.297-307

1999

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Novel human bronchial epithelial cell lines for cystic fibrosis research

PMT gene family: protein O-glycosylation in Saccharomyces cerevisiae is vital

366: Airway Obstruction Produces Hypoxia-Dependent Sodium Absorption in Human Airway Epithelial Cells

309 The CFTR Antibody Distribution Program: Development and production of antibodies for CFTR detection

339 Effects of Pseudomonas infection on CFTR rescue and epithelial gene expression

284 Effect of epithelial inflammation on the efficacy of therapeutic oligonucleotides to correct CFTR splice and nonsense mutations

616: Effects of VX-445 on CFTR channel function and stability

176 Cystic fibrosis airway inflammation enhances the efficacy of CFTR modulators

325 Corrector elexacaftor mimics potentiator action by increasing numbers of functional CFTR channels via recovery of rescued inactivated F508del

311 Active Pseudomonas aeruginosa infection of primary airway epithelia enhances CFTR modulator rescue

659 Inflammation augments elexacaftor/tezacaftor/ivacaftor-induced cystic fibrosis transmembrane conductance regulator rescue in primary airway epithelia carrying F508del and rare cystic fibrosis transmembrane conductance regulator mutations

647 Potentiator icenticaftor is superior to ivacaftor in rescuing F508del cystic fibrosis transmembrane conductance regulator and does not destabilize corrected mature protein

331 CF airway inflammation enhances elexacaftor/tezacaftor/ivacaftormediated rescue of N1303K CFTR

618: Specific detection of CFTR in airway epithelia

676 A multicenter approach to optimize and validate a robust cystic fibrosis transmembrane conductance regulator–specific immunolabeling protocol

423 Novel method for isolation of small airway epithelial cells by bulk enzymatic digestion

434 In vitro evaluation of TAVT-135, an artificial pan-genotypic chloride ion transporter

156 Primary pharmacology and toxicology of TAVT-135, a novel chloride ion transporter in development for the treatment of cystic fibrosis

598: Correction of CF splicing mutations with oligonucleotides

449 Pathways balancing basal mucin and cystic fibrosis transmembrane conductance regulator–mediated fluid secretion in the human small airway

WS07.2 A PI3Kγ-peptide promotes Cl− secretion through activation of both CFTR - dependent and independent currents

179: Modulator therapy reverses aberrant mucus properties in vitro via hydration

WS03-3 CFTR malfunction is linked to mucus abnormal properties in cystic fibrosis

Endocytic Trafficking Routes of Wild Type and ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator

Protein O-mannosylation

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