Publications by authors named "France Pietri-Rouxel"

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Early Endosome Disturbance and Endolysosomal Pathway Dysfunction in Duchenne Muscular Dystrophy.
Julie Chassagne, Nathalie Da Silva, Ines Akrouf, Bruno Cadot, Laura Julien, France Pietri-Rouxel

Am J Pathol· September 2025

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Identification of CaVβ1 Isoforms Required for Neuromuscular Junction Formation and Maintenance.
Amélie Vergnol, Aly Bourguiba, Stephanie Bauché, Massiré Traoré, Maxime Gelin, France Pietri-Rouxel

Cells· August 2025

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Long-Term Dystrophin Replacement Therapy in Duchenne Muscular Dystrophy Causes Cardiac Inflammation.
Anne Forand, Sophie Moog, Nathalie Mougenot, Mégane Lemaitre, Caroline Sevoz-Couche, France Pietri-Rouxel

JACC Basic Transl Sci· June 2025

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GDF5 as a rejuvenating treatment for age-related neuromuscular failure.
Massiré Traoré, Chiara Noviello, Amélie Vergnol, Christel Gentil, Marius Halliez, France Pietri-Rouxel

Brain· November 2024

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Progressive cardiomyopathy with intercalated disc disorganization in a rat model of Becker dystrophy.
Valentina Taglietti, Kaouthar Kefi, Busra Mirciloglu, Sultan Bastu, Jean-Daniel Masson, France Pietri-Rouxel

EMBO Rep· November 2024

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[GDF5: a therapeutic candidate for combating sarcopenia].
France Piétri-Rouxel, Sestina Falcone, Massiré Traoré

Med Sci (Paris)· November 2023

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RhoA Is a Crucial Regulator of Myoblast Fusion.
Chiara Noviello, Kassandra Kobon, Voahangy Randrianarison-Huetz, Pascal Maire, France Pietri-Rouxel

Cells· November 2023

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Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy.
Valentina Taglietti, Kaouthar Kefi, Lea Rivera, Oriane Bergiers, Nastasia Cardone, France Pietri-Rouxel

Sci Transl Med· March 2023

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NR1D1 controls skeletal muscle calcium homeostasis through myoregulin repression.
Alexis Boulinguiez, Christian Duhem, Alicia Mayeuf-Louchart, Benoit Pourcet, Yasmine Sebti

JCI Insight· September 2022

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Muscle regeneration affects Adeno Associated Virus 1 mediated transgene transcription.
Amédée Mollard, Cécile Peccate, Anne Forand, Julie Chassagne, Laura Julien

Sci Rep· June 2022

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CD38-NADase is a new major contributor to Duchenne muscular dystrophic phenotype.
Antoine de Zélicourt, Abdallah Fayssoil, Mbarka Dakouane-Giudicelli, Isley De Jesus, Ahmed Karoui

EMBO Mol Med· May 2022

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New Insights in CaVβ Subunits: Role in the Regulation of Gene Expression and Cellular Homeostasis.
Amélie Vergnol, Massiré Traoré, France Pietri-Rouxel, Sestina Falcone

Front Cell Dev Biol· April 2022

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Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis.
Valentina Taglietti, Kaouthar Kefi, Iwona Bronisz-Budzyńska, Busra Mirciloglu, Mathilde Rodrigues, France Pietri-Rouxel

Acta Neuropathol Commun· April 2022

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Pannexin-1 and CaV1.1 show reciprocal interaction during excitation-contraction and excitation-transcription coupling in skeletal muscle.
Francisco Jaque-Fernández, Gonzalo Jorquera, Jennifer Troc-Gajardo, France Pietri-Rouxel, Christel Gentil

J Gen Physiol· December 2021

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The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMD.
Elena Gargaun, Sestina Falcone, Guilhem Solé, Julien Durigneux, Andoni Urtizberea, France Pietri-Rouxel

Biomedicines· February 2021

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Combined Treatment with Peptide-Conjugated Phosphorodiamidate Morpholino Oligomer-PPMO and AAV-U7 Rescues the Severe DMD Phenotype in Mice.
Anne Forand, Antoine Muchir, Nathalie Mougenot, Caroline Sevoz-Couche, Cécile Peccate

Mol Ther Methods Clin Dev· June 2020

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An embryonic CaVβ1 isoform promotes muscle mass maintenance via GDF5 signaling in adult mouse.
Massiré Traoré, Christel Gentil, Chiara Benedetto, Jean-Yves Hogrel, Pierre De la Grange

Sci Transl Med· November 2019

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Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions.
Olivier Delalande, Anne-Elisabeth Molza, Raphael Dos Santos Morais, Angélique Chéron, Émeline Pollet

J Biol Chem· May 2018

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miR-708-5p and miR-34c-5p are involved in nNOS regulation in dystrophic context.
Marine Guilbaud, Christel Gentil, Cécile Peccate, Elena Gargaun, Isabelle Holtzmann

Skelet Muscle· April 2018

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RFX1 and RFX3 Transcription Factors Interact with the D Sequence of Adeno-Associated Virus Inverted Terminal Repeat and Regulate AAV Transduction.
Laura Julien, Julie Chassagne, Cécile Peccate, Stéphanie Lorain, France Piétri-Rouxel

Sci Rep· January 2018

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Delivery is key: lessons learnt from developing splice-switching antisense therapies.
Caroline Godfrey, Lourdes R Desviat, Bård Smedsrød, France Piétri-Rouxel, Michela A Denti

EMBO Mol Med· May 2017

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Functional Characterization and Rescue of a Deep Intronic Mutation in OCRL Gene Responsible for Lowe Syndrome.
John Rendu, Rodrick Montjean, Charles Coutton, Mohnish Suri, Gaetan Chicanne

Hum Mutat· February 2017

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Dystrophin Threshold Level Necessary for Normalization of Neuronal Nitric Oxide Synthase, Inducible Nitric Oxide Synthase, and Ryanodine Receptor-Calcium Release Channel Type 1 Nitrosylation in Golden Retriever Muscular Dystrophy Dystrophinopathy.
Christel Gentil, Caroline Le Guiner, Sestina Falcone, Jean-Yves Hogrel, Cécile Peccate

Hum Gene Ther· September 2016

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Antisense pre-treatment increases gene therapy efficacy in dystrophic muscles.
Cécile Peccate, Amédée Mollard, Maëva Le Hir, Laura Julien, Graham McClorey

Hum Mol Genet· August 2016

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Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy.
Karima Relizani, Etienne Mouisel, Benoit Giannesini, Christophe Hourdé, Ketan Patel

Mol Ther· August 2014

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