Centre de Recherche en Myologie

Recent papers from Centre de Recherche en Myologie

1. FLNC-related myopathy: a description of 27 patients from 21 unrelated families2026
2. Laminopathies : natural history and risk prediction of heart failureEuropean Heart Journal · 2026
3. Ultrafast Micrometric Laser Structuring of Polymer Surfaces for Highly Organized Skeletal Muscle Tissue ModelingAdvanced Science · 2026
4. LeDucq-funded programme: from pathomechanisms to personalized therapy of cardio-laminopathyEuropean Heart Journal · 2025
5. Genome sequencing improves diagnostic outcomes over panel and exome sequencings in myopathies: findings from the French PFMG2025 initiativeGenome Medicine · 2026
6. Genetic and Pharmacologic Inhibition of Myostatin Restores Muscle Mass in a Dynamin 2 ‐Related Centronuclear Myopathy Mouse ModelJournal of Cachexia Sarcopenia and Muscle · 2026
7. Androgen receptor imprints satellite cell stemness and preserves their reservoir for lifelong regeneration and optimal repairScience Advances · 2026
8. The thymus gland is a target and maintainer of amyotrophic lateral sclerosis pathophysiologyBrain Behavior & Immunity - Health · 2026
9. A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathyEuropean Heart Journal · 2009
10. The actomyosin cortex controls t-tubule remodeling in skeletal muscleScience Advances · 2026
11. Exercise elicits mitonuclear protein imbalance and UPRmt in the liver of mice with obesityJournal of Physiology and Biochemistry · 2026
12. Whole-Body Muscle MRI in Non-5q Spinal Muscular AtrophyNeurology Genetics · 2026
13. Genetic Architecture of Idiopathic Inflammatory Myopathies From Meta‐AnalysesArthritis & Rheumatology · 2024
14. MBNL depletion drives stem cell fusion and immature myonuclear states in myotonic dystrophy type 1Nature Communications · 2026
15. Vimentin bridges scales to convert polarized cell locomotion into coordinated collective migrationMolecular Biology of the Cell · 2026
16. Genetic screening identifies WNT5A/RYK as a determinant of extracellular vesicle fateScience Advances · 2026
17. High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodiesProceedings of the National Academy of Sciences · 2026
18. Comprehensive transcriptomic profiling reveals impaired polyamine metabolism as a contributor to age-related muscle declineiScience · 2026
19. Advanced iPSC-based modeling of LMNA-related congenital muscular dystrophy enables development of genetic therapies for muscle laminopathiesMolecular Therapy · 2026
20. Duchenne muscular dystrophy: from gene to gene-ius therapiesSkeletal Muscle · 2026