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