Pascal Trouve

Inserm, EFS, UMR 1078, 22 Avenue Camille Desmoulins
Brest, 29200, France

Last Updated: 09/26/2026

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Found 19 publications

p.Phe508del-CFTR Trafficking: A Protein Quality Control Perspective Through UPR, UPS, and Autophagy.

p.Phe508del-CFTR Trafficking: A Protein Quality Control Perspective Through UPR, UPS, and Autophagy.

Journal: International journal of molecular sciences

Published: February 04, 2025

Cystic Fibrosis: A Journey through Time and Hope.

Cystic Fibrosis: A Journey through Time and Hope.

Journal: International journal of molecular sciences

Published: August 14, 2024

The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease (MBTP1) Alleviates the p.Phe508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Defects in Cystic Fibrosis Cells.

The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease (MBTP1) Alleviates the p.Phe508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Defects in Cystic Fibrosis Cells.

Journal: Cells

Published: December 01, 2023

Evaluation of aminopyrrolidine amide to improve chloride transport in CFTR-defective cells.

Evaluation of aminopyrrolidine amide to improve chloride transport in CFTR-defective cells.

Journal: Bioorganic & medicinal chemistry letters

Published: April 19, 2022

Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis.

Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis.

Journal: American journal of human genetics

Published: March 11, 2022

The Interplay between the Unfolded Protein Response, Inflammation and Infection in Cystic Fibrosis.

The Interplay between the Unfolded Protein Response, Inflammation and Infection in Cystic Fibrosis.

Journal: Cells

Published: October 07, 2021

TIMP1 intron 3 retention is a marker of colon cancer progression controlled by hnRNPA1.

TIMP1 intron 3 retention is a marker of colon cancer progression controlled by hnRNPA1.

Journal: Molecular biology reports

Published: September 16, 2019

Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells.

Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells.

Journal: PloS one

Published: April 28, 2017

Calumenin contributes to ER-Ca2+ homeostasis in bronchial epithelial cells expressing WT and F508del mutated CFTR and to F508del-CFTR retention.

Calumenin contributes to ER-Ca2+ homeostasis in bronchial epithelial cells expressing WT and F508del mutated CFTR and to F508del-CFTR retention.

Journal: Cell calcium

Published: January 03, 2017

In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis.

In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis.

Journal: PloS one

Published: September 26, 2016

Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A.

Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A.

Journal: PloS one

Published: August 26, 2015

Function and regulation of TRPM7, as well as intracellular magnesium content, are altered in cells expressing ΔF508-CFTR and G551D-CFTR.

Function and regulation of TRPM7, as well as intracellular magnesium content, are altered in cells expressing ΔF508-CFTR and G551D-CFTR.

Journal: Cellular and molecular life sciences : CMLS

Published: June 08, 2015

Showing 1-12 of 19

Last Updated: 09/26/2026