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