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Derniers dépôts
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Dermatomyositis
Cytoskeleton
Satellite cells
Alternative splicing
Dilated cardiomyopathy
Centronuclear myopathy
Amyotrophic lateral sclerosis
Aging
Fabry disease
Humans
Neuromuscular diseases
Laminopathies
Trinucleotide repeat expansion
DMD
Skeletal muscle
Spinal muscular atrophy
Regeneration
Laminopathie
AAV
Treatment
Glutamate
RNA biology
Neuromuscular disease
Long read sequencing
Antisense oligonucleotides
Errance diagnostique
Animals
Astrocyte
Cell therapy
Actin
Muscular dystrophy
Mechanotransduction
Myotonic Dystrophy
Mouse model
Motoneuron
Cardiomyopathy
Inflammation
ALS
Dynamin 2
Myasthenia gravis
Lamin A/C
Laminopathy
Myogenesis
Exercise
Nuclear envelope
Mice
Lamin A/C LMNA gene
LMNA
Gene therapy
Autophagy
Fibrosis
MBNL
Rare neuromuscular diseases
Myositis
Thérapie génique
Autoimmune diseases
Duchenne muscular dystrophy
Myotonic dystrophy type 1
Heart
LMNA gene
Myoblasts
Muscle
Myotonic Dystrophy type 1
Therapy
Aged
Cytokines
Cancer
Transcriptomics
Biomarker
Myopathies
Male
Becker muscular dystrophy
Heart failure
PABPN1
CRISPRi
Satellite cell
Brain
Myopathy
Congenital muscular dystrophy
Biomarkers
CMS
Muscle regeneration
Thymus
CTG repeat contractions
RNA interference
Myotonic dystrophy
COVID-19
Autoimmunity
Outcome measures
Calcium
Dystrophin
Neuromuscular junction
Congenital myopathy
Autoantibodies
Myasthenia Gravis MG
Rare diseases
OPMD
Genotype phenotype correlation
Transgenic mouse model
FSHD