Publications by authors named "Maxime Jacoupy"

Claim this Profile
E
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders.
Antonio Atalaia, Dagmar Wandrei, Nawel Lalout, Rachel Thompson, Adrian Tassoni, Maxime Jacoupy

Orphanet J Rare Dis· February 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4.
Livia Parodi, Mathieu Barbier, Maxime Jacoupy, Claire Pujol, François-Xavier Lejeune

Genet Med· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25.
Mathieu Barbier, Melanie Bahlo, Alessandra Pennisi, Maxime Jacoupy, Rick M Tankard

Ann Neurol· July 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.
Marie Coutelier, Maxime Jacoupy, Alexandre Janer, Flore Renaud, Nicolas Auger

Brain· May 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Monitoring the Mitochondrial Presequence Import Pathway In Living Mammalian Cells with a New Molecular Biosensor.
Maxime Jacoupy, Emeline Hamon-Keromen, Olga Corti

Methods Mol Biol· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PINK1/Parkin-Dependent Mitochondrial Surveillance: From Pleiotropy to Parkinson's Disease.
Francois Mouton-Liger, Maxime Jacoupy, Jean-Christophe Corvol, Olga Corti

Front Mol Neurosci· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Suzanne Lesage, Valérie Drouet, Elisa Majounie, Vincent Deramecourt, Maxime Jacoupy

Am J Hum Genet· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia.
Marie Coutelier, Cyril Goizet, Alexandra Durr, Florence Habarou, Sara Morais, Maxime Jacoupy

Brain· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The TOMM machinery is a molecular switch in PINK1 and PARK2/PARKIN-dependent mitochondrial clearance.
Giulia Bertolin, Rosa Ferrando-Miguel, Maxime Jacoupy, Sabine Traver, Karl Grenier

Autophagy· November 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis