Isabelle Richard
Evry, 91000, France
Last Updated: 09/26/2026
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Found 95 publications
Author Correction: Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity.
Journal: NPJ Regenerative medicine
Published: April 14, 2026
Lysosomal damage is a therapeutic target in Duchenne muscular dystrophy.
Journal: Science advances
Published: October 22, 2025
CRISPR-Cas9-mediated upregulation of utrophin ameliorates Duchenne muscular dystrophy.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: October 08, 2025
DAB2 in LGMD R2: a molecular link between disease progression and lipid dysregulation.
Journal: JCI insight
Published: September 09, 2025
A new dystrophin-deficient rat model mirroring exon skipping in patients with DMD exon 45 deletions.
A new dystrophin-deficient rat model mirroring exon skipping in patients with DMD exon 45 deletions.
Journal: Disease models & mechanisms
Published: July 22, 2025
Review: Limb-girdle muscular dystrophies (LGMDs) existing registries and natural history studies: Where do we stand?
Journal: Journal of neuromuscular diseases
Published: July 08, 2025
FAP-CAR-T cells reduce dystrophic muscle fibrosis, improving adeno-associated virus gene transfer efficacy.
Journal: Molecular therapy. Methods & clinical development
Published: April 18, 2025
Transgene-induced cardiotoxicity in high-dose AAV gene transfer.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: March 26, 2025
Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity.
Journal: NPJ Regenerative medicine
Published: March 13, 2025
2024 VCP International Conference: Exploring multi-disciplinary approaches from basic science of valosin containing protein, an AAA+ ATPase protein, to the therapeutic advancement for VCP-associated multisystem proteinopathy.
Journal: Neurobiology of disease
Published: January 25, 2025
Advances and Challenges in Microdystrophin gene therapy for Duchenne Muscular Dystrophy: progress and future directions
Journal: Medecine sciences : M/S
Published: November 18, 2024
In Silico Structural Prediction for the Generation of Novel Performant Midi-Dystrophins Based on Intein-Mediated Dual AAV Approach.
Journal: International journal of molecular sciences
Published: September 04, 2024
Last Updated: 09/26/2026