Bruno Cadot
Paris, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 31 publications
GDF5 modulation of MuSC pool as a potential therapeutic benefit for DMD.
Journal: Molecular therapy. Nucleic acids
Published: December 02, 2025
Role of Nuclear Envelope Proteins in the Structure and Function of the Neuromuscular Junction: Focus on Subsynaptic Nuclei.
Journal: Sub-cellular biochemistry
Published: September 26, 2025
Col6a1 knock-in mice provide a promising pre-clinical model for collagen VI-related dystrophies.
Journal: Disease models & mechanisms
Published: April 30, 2025
Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome.
Journal: American journal of human genetics
Published: April 22, 2025
Early Endosome Disturbance and Endolysosomal Pathway Dysfunction in Duchenne Muscular Dystrophy.
Journal: The American journal of pathology
Published: January 10, 2025
GDF5 as a rejuvenating treatment for age-related neuromuscular failure.
Journal: Brain : a journal of neurology
Published: November 22, 2023
Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation.
Journal: eLife
Published: October 12, 2022
Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies.
Journal: Acta neuropathologica communications
Published: June 17, 2022
Reconstituting the Interaction Between Purified Nuclei and Microtubule Network.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: April 27, 2022
Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations.
Journal: Molecular therapy. Nucleic acids
Published: March 28, 2022
Nesprin-1 LINC complexes recruit microtubule cytoskeleton proteins and drive pathology in Lmna-mutant striated muscle.
Journal: Human molecular genetics
Published: December 02, 2021
Last Updated: 09/26/2026