Benoit Chevalier

Paris, France

Last Updated: 09/26/2026

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Found 25 publications

Beyond Trikafta: new models to assess tissue dependent rescue of N1303K-CFTR.

Beyond Trikafta: new models to assess tissue dependent rescue of N1303K-CFTR.

Journal: Frontiers in pharmacology

Published: July 07, 2025

CFTR correctors potentiate gating mutants causing cystic fibrosis.

CFTR correctors potentiate gating mutants causing cystic fibrosis.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: May 14, 2025

In silico, in vitro and ex vivo characterization of cystic fibrosis transmembrane conductance regulator pathogenic variants localized in the fourth intracellular loop and their rescue by modulators.

In silico, in vitro and ex vivo characterization of cystic fibrosis transmembrane conductance regulator pathogenic variants localized in the fourth intracellular loop and their rescue by modulators.

Journal: British journal of pharmacology

Published: March 14, 2025

Novel gain-of-function mutants identify a critical region within CFTR membrane-spanning domain 2 controlling cAMP-dependent and ATP-independent channel activation.

Novel gain-of-function mutants identify a critical region within CFTR membrane-spanning domain 2 controlling cAMP-dependent and ATP-independent channel activation.

Journal: Cellular and molecular life sciences : CMLS

Published: April 24, 2024

Role of KCNK3 Dysfunction in Dasatinib-associated Pulmonary Arterial Hypertension and Endothelial Cell Dysfunction.

Role of KCNK3 Dysfunction in Dasatinib-associated Pulmonary Arterial Hypertension and Endothelial Cell Dysfunction.

Journal: American journal of respiratory cell and molecular biology

Published: March 28, 2024

Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium.

Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium.

Journal: Frontiers in pharmacology

Published: September 13, 2023

Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells.

Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells.

Journal: Cell reports. Medicine

Published: July 26, 2023

Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children.

Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: April 10, 2023

Theratyping cystic fibrosis patients to guide elexacaftor/tezacaftor/ivacaftor out-of-label prescription.

Theratyping cystic fibrosis patients to guide elexacaftor/tezacaftor/ivacaftor out-of-label prescription.

Journal: The European respiratory journal

Published: January 18, 2023

Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded Mutants.

Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded Mutants.

Journal: International journal of molecular sciences

Published: October 31, 2022

Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance Regulator.

Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance Regulator.

Journal: Journal of molecular biology

Published: September 29, 2022

Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC Transporters.

Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC Transporters.

Journal: International journal of molecular sciences

Published: July 12, 2022

Showing 1-12 of 25

Last Updated: 09/26/2026