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