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