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