Aurélie Goyenvalle

Université Paris-Saclay

France

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Research Interests

Cell Biology

40%

Pharmacology

30%

Mouse Genetics

30%

Murine Model

30%

Genome Engineering

30%

Muscular Atrophy

20%

Rna Therapeutics

20%

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Articles11

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

Article Link

Year:

2023

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

Article Link

Year:

2023

Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscle

Article Link

Year:

2023

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

Article Link

Year:

2022

Histone deacetylase inhibitors improve antisense-mediated exon-skipping efficacy in mdx mice.

Article Link

Year:

2022

Abnormal Expression of Synaptic and Extrasynaptic GABAA Receptor Subunits in the Dystrophin-Deficient mdx Mouse

Article Link

Year:

2022

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

Article Link

Year:

2022

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

Article Link

Year:

2022

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

Article Link

Year:

2022

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

Article Link

Year:

2021

Les approches thérapeutiques de modulation de l’épissage

Article Link

Year:

2021

Collaborators7

Willeke van Roon-Mom

Assistant Professor

Leiden University Medical Center

NETHERLANDS

Cyrille Vaillend

Université Paris-Saclay

FRANCE

Falcone Sestina

Sorbonne Université

FRANCE

Nicolas Tournier

Université Paris-Saclay

FRANCE

Pietro Spitali

Assistant Professor

Universitair Medisch Centrum Utrecht

NETHERLANDS

Virginia Arechavala-Gomeza

Ikerbasque Professor

Ikerbasque, Basque Foundation for Science

SPAIN

arnaud mansart

Université Paris-Saclay

FRANCE

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Aurélie Goyenvalle

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Research Interests

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Articles11

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

Collaborators7

Willeke van Roon-Mom

Cyrille Vaillend

Falcone Sestina

Nicolas Tournier

Pietro Spitali

Virginia Arechavala-Gomeza

arnaud mansart

How do I reach out?