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