Publications by authors named "Alexandre Mejat"

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Basket trials in rare diseases: a systematic review of current practices, methodological challenges, and future directions.
Wael Khazen, Solange Corriol-Rohou, Teresinha Evangelista, Arnauld Valent, Sarah Abbas, Alexandre Mejat

Orphanet J Rare Dis· November 2025

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The European Neuromuscular Centre has celebrated its 30th anniversary!
Alexandra Breukel, Raffaella Willmann, Kate Adcock, Alexandre Méjat, Ingeborg Meijer

Neuromuscul Disord· March 2023

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MorphoScript: a dedicated analysis to assess the morphology and contractile structures of cardiomyocytes derived from stem cells.
Tess Homan, Hélène Delanoë-Ayari, Albano C Meli, Olivier Cazorla, Csilla Gergely, Alexandre Mejat

Bioinformatics· November 2021

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Understanding European patient expectations towards current therapeutic development in spinal muscular atrophy.
Nicole Gusset, Caroline Stalens, Eva Stumpe, Lori Klouvi, Alexandre Mejat

Neuromuscul Disord· May 2021

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Deciphering DSC2 arrhythmogenic cardiomyopathy electrical instability: From ion channels to ECG and tailored drug therapy.
Adrien Moreau, Jean-Baptiste Reisqs, Helene Delanoe-Ayari, Marion Pierre, Alexandre Janin, Alexandre Mejat

Clin Transl Med· March 2021

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"Be an ambassador for change that you would like to see": a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscular disease.
Anna Ambrosini, Ros Quinlivan, Valeria A Sansone, Ingeborg Meijer, Guus Schrijvers, Alexandre Mejat

Orphanet J Rare Dis· June 2019

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SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.
Alexandre Janin, Delphine Bauer, Francesca Ratti, Camille Valla, Anne Bertrand

Sci Rep· April 2018

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Nuclear envelopathies: a complex LINC between nuclear envelope and pathology.
Alexandre Janin, Delphine Bauer, Francesca Ratti, Gilles Millat, Alexandre Méjat

Orphanet J Rare Dis· August 2017

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PAK1 and CtBP1 Regulate the Coupling of Neuronal Activity to Muscle Chromatin and Gene Expression.
Jean-Luc Thomas, Vincent Moncollin, Aymeric Ravel-Chapuis, Carmen Valente, Daniela Corda

Mol Cell Biol· December 2015

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Histone deacetylase 6 is a FoxO transcription factor-dependent effector in skeletal muscle atrophy.
Francesca Ratti, Francis Ramond, Vincent Moncollin, Thomas Simonet, Giulia Milan

J Biol Chem· February 2015

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The Tomato/GFP-FLP/FRT method for live imaging of mosaic adult Drosophila photoreceptor cells.
Pierre Dourlen, Clemence Levet, Alexandre Mejat, Alexis Gambis, Bertrand Mollereau

J Vis Exp· September 2013

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LINC complexes in health and disease.
Alexandre Méjat, Tom Misteli

Nucleus· June 2012

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Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy.
Alexandre Méjat, Valérie Decostre, Juan Li, Laure Renou, Akanchha Kesari

J Cell Biol· January 2009

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Calcineurin-NFAT signaling, together with GABP and peroxisome PGC-1{alpha}, drives utrophin gene expression at the neuromuscular junction.
Lindsay M Angus, Joe V Chakkalakal, Alexandre Méjat, Joe K Eibl, Guy Bélanger

Am J Physiol Cell Physiol· October 2005

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Histone deacetylase 9 couples neuronal activity to muscle chromatin acetylation and gene expression.
Alexandre Méjat, Francis Ramond, Rhonda Bassel-Duby, Saadi Khochbin, Eric N Olson

Nat Neurosci· March 2005

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14-3-3 gamma associates with muscle specific kinase and regulates synaptic gene transcription at vertebrate neuromuscular synapse.
Laure Strochlic, Annie Cartaud, Alexandre Mejat, Régis Grailhe, Laurent Schaeffer

Proc Natl Acad Sci U S A· December 2004

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Synapse-specific gene expression at the neuromuscular junction.
Alexandre Méjat, Aymeric Ravel-Chapuis, Marie Vandromme, Laurent Schaeffer

Ann N Y Acad Sci· September 2003

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