Amel Saoudi

151 Route De La Rotonde
Saclay, 91400, France

Last Updated: 09/26/2026

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Found 13 publications

Hyperactivity, compulsive-like behaviours, and impaired flexibility in mouse models of Duchenne muscular dystrophy.

Hyperactivity, compulsive-like behaviours, and impaired flexibility in mouse models of Duchenne muscular dystrophy.

Journal: Neurobiology of disease

Published: November 28, 2025

Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse Brain.

Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse Brain.

Journal: Cells

Published: August 06, 2025

Dual AAV gene therapy achieves recovery of hearing and auditory processing in a DFNB16 mouse model.

Dual AAV gene therapy achieves recovery of hearing and auditory processing in a DFNB16 mouse model.

Journal: Clinical and translational medicine

Published: July 11, 2025

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

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

Journal: Molecular therapy. Nucleic acids

Published: June 17, 2025

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

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

Journal: International journal of molecular sciences

Published: January 13, 2025

Levels of Exon-Skipping Are Not Artificially Overestimated Because of the Increased Affinity of Tricyclo-DNA-Modified Antisense Oligonucleotides to the Target DMD Exon.

Levels of Exon-Skipping Are Not Artificially Overestimated Because of the Increased Affinity of Tricyclo-DNA-Modified Antisense Oligonucleotides to the Target DMD Exon.

Journal: Nucleic acid therapeutics

Published: July 24, 2024

Impact of distinct dystrophin gene mutations on behavioral phenotypes of Duchenne muscular dystrophy.

Impact of distinct dystrophin gene mutations on behavioral phenotypes of Duchenne muscular dystrophy.

Journal: Disease models & mechanisms

Published: January 23, 2024

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

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

Journal: Biomedicines

Published: September 19, 2023

Investigating the Impact of Delivery Routes for Exon Skipping Therapies in the CNS of DMD Mouse Models.

Investigating the Impact of Delivery Routes for Exon Skipping Therapies in the CNS of DMD Mouse Models.

Journal: Cells

Published: February 12, 2023

Partial restoration of brain dystrophin by tricyclo-DNA antisense oligonucleotides alleviates emotional deficits in mdx52 mice.

Partial restoration of brain dystrophin by tricyclo-DNA antisense oligonucleotides alleviates emotional deficits in mdx52 mice.

Journal: Molecular therapy. Nucleic acids

Published: October 20, 2022

RNA splicing modulation: Therapeutic progress and perspectives

RNA splicing modulation: Therapeutic progress and perspectives

Journal: Medecine sciences : M/S

Published: June 28, 2021

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

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

Journal: Disease models & mechanisms

Published: March 22, 2021

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Last Updated: 09/26/2026