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Aurélie Goyenvalle

Director of Unit - Research director Inserm (DR2)

Université Paris-Saclay

France

Research Interests

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Professors in France Professors in Cell Biology Cell Biology professors in France

Articles (21)

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2026

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2022

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2022

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2022

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2021

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2021

Collaborators (11)

Willeke van Roon-Mom

Assistant Professor

Leiden University Medical Center

NETHERLANDS

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Yoshitsugu Aoki

DIRECTOR

National Center of Neurology and Psychiatry

JAPAN

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Cyrille Vaillend

CNRS Director of Research (DR2)

CNRS Délégation Ile-de-France Sud

FRANCE

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Falcone Sestina

Researcher

INSERM

FRANCE

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Nicolas Tournier

Université Paris-Saclay

FRANCE

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David-Alexandre Trégouët

Team Director / 1st Class INSERM Research Director

INSERM U1219

FRANCE

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Pietro Spitali

Associate Professor - Principal Investigator

Leiden University Medical Center

NETHERLANDS

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Virginia Arechavala-Gomeza

Group Leader

Ikerbasque, Basque Foundation for Science

SPAIN

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Francesco Muntoni

University College London

UNITED KINGDOM

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arnaud mansart

Université de Versailles Saint-Quentin-en-Yvelines

FRANCE

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Beatrice Jaspard-Vinassa

University of Bordeaux

FRANCE

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Aurélie Goyenvalle

Research Interests

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Articles (21)

Givinostat enhances antisense oligonucleotide efficacy in the mdx52 model of Duchenne muscular dystrophy

Efficient Downregulation of Flt-1 Mediated by Splice Switching ASO in Murine Endothelial Cells

Residual Dp71 Expression Is Sufficient to Preserve Retinal Vascular Homeostasis in a Mouse Model of Duchenne Muscular Dystrophy

Beyond muscle: Delivering RNA therapeutics to the CNS in Duchenne muscular dystrophy

Identification and functional validation of intracellular protein partners of phosphorothioate splice-switching oligonucleotides using AP-MS

Duchenne muscular dystrophy: recent insights in brain related comorbidities

Overlapping upstream ORFs ending at c.125 lead to reduced Endoglin, contributing to Hereditary Hemorrhagic Telangiectasia

Ineffective behavioral rescue despite partial brain Dp427 restoration by AAV9-U7-mediated exon 51 skipping in mdx52 mice

Combined 20-Hydroxyecdysone and Antisense-Mediated Exon Skipping Improve Functional Outcomes in a Mouse Model of Duchenne Muscular Dystrophy

Valproic Acid Improves Antisense-Mediated Exon-Skipping Efficacy in mdx Mice

Networking to Optimize Dmd exon 53 Skipping in the Brain of mdx52 Mouse Model

Oligonucleotide Enhancing Compound Increases Tricyclo-DNA Mediated Exon-Skipping Efficacy in the Mdx Mouse Model

Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscle

Considerations in the Preclinical Assessment of the Safety of Antisense Oligonucleotides.

Histone deacetylase inhibitors improve antisense-mediated exon-skipping efficacy in <i>mdx</i> mice.

Abnormal Expression of Synaptic and Extrasynaptic GABA<sub>A</sub> Receptor Subunits in the Dystrophin-Deficient <i>mdx</i> Mouse

Partial Restoration of Brain Dystrophin and Behavioral Deficits by Exon Skipping in the Muscular Dystrophy X‐Linked (mdx) Mouse

Common and Rare 5′UTR Variants Altering Upstream Open Reading Frames in Cardiovascular Genomics

Palmitic acid conjugation enhances potency of tricyclo-DNA splice switching oligonucleotides

Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophy.

Les approches thérapeutiques de modulation de l’épissage

Collaborators (11)

Willeke van Roon-Mom

Yoshitsugu Aoki

Cyrille Vaillend

Falcone Sestina

Nicolas Tournier

David-Alexandre Trégouët

Pietro Spitali

Virginia Arechavala-Gomeza

Francesco Muntoni

arnaud mansart

Beatrice Jaspard-Vinassa

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