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