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64 IDENTIFICATION AND CHARACTERIZATION OF A HEPATITIS C VIRUS CAPSID ASSEMBLY INHIBITOR

Journal of hepatology, 2011-03, Vol.54, p.S29-S29

2011

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770 REGULATION OF HEPATITIS C VIRUS REPLICATION, VIRUS PRODUCTION AND INFECTIVITY BY BILE ACIDS

Journal of hepatology, 2011-03, Vol.54, p.S310-S310

2011

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752 INHIBITION OF HEPATITS C VIRUS ENTRY BY A PLANT-DERIVED FLAVONE

Journal of hepatology, 2010, Vol.52, p.S293-S293

2010

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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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Hybrid Computing—Where HPC meets grid and Cloud Computing

Future generation computer systems, 2011-05, Vol.27 (5), p.440-453

2011

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A small-molecule inhibitor and degrader of the RNF5 ubiquitin ligase

Molecular biology of the cell, 2022-11, Vol.33 (13), p.ar120-ar120

2022

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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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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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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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CFTR modulator theratyping: Current status, gaps and future directions

Journal of cystic fibrosis, 2019-01, Vol.18 (1), p.22-34

2019

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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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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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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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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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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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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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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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Risk Factors for Mortality and Prolonged Hospitalization in Electric Burn Injuries

Journal of burn care & research, 2021-05, Vol.42 (3), p.505-512

2021

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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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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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Personalised medicine for non-classic cystic fibrosis resulting from rare CFTR mutations

The European respiratory journal, 2020-07, Vol.56 (1), p.2000062

2020

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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), p.1-15

2022

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64 IDENTIFICATION AND CHARACTERIZATION OF A HEPATITIS C VIRUS CAPSID ASSEMBLY INHIBITOR

770 REGULATION OF HEPATITIS C VIRUS REPLICATION, VIRUS PRODUCTION AND INFECTIVITY BY BILE ACIDS

752 INHIBITION OF HEPATITS C VIRUS ENTRY BY A PLANT-DERIVED FLAVONE

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

Hybrid Computing—Where HPC meets grid and Cloud Computing

A small-molecule inhibitor and degrader of the RNF5 ubiquitin ligase

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

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

Novel human bronchial epithelial cell lines for cystic fibrosis research

CFTR modulator theratyping: Current status, gaps and future directions

176 Cystic fibrosis airway inflammation enhances the efficacy of CFTR modulators

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

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

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

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

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

618: Specific detection of CFTR in airway epithelia

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

Risk Factors for Mortality and Prolonged Hospitalization in Electric Burn Injuries

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

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

Personalised medicine for non-classic cystic fibrosis resulting from rare CFTR mutations

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

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