Loading...
Derniers dépôts
Nombre de documents
793
Nombre de notices
1 384
widget_cloud
Myopathies
Treatment
Actin
Myotonic dystrophy type 1
Spinal muscular atrophy
Animals
Satellite cell
CTG repeat contractions
Lamin A/C LMNA gene
Myoblasts
Biomarkers
Biomarker
ALS
Fabry disease
Congenital muscular dystrophy
Cancer
Cytokines
Myotonic Dystrophy type 1
Congenital myopathy
PABPN1
Myositis
Duchenne muscular dystrophy
Myotonic dystrophy
Muscle
Brain
Long read sequencing
Aged
Trinucleotide repeat expansion
Regeneration
Muscle regeneration
Transgenic mouse model
Heart failure
Mechanotransduction
Mouse model
Satellite cells
Astrocyte
Aging
Muscular dystrophy
Autoimmunity
AAV
Transcriptomics
Rare neuromuscular diseases
Neuromuscular disease
Autoantibodies
CMS
Humans
DMD
Myasthenia gravis
Myopathy
Dermatomyositis
COVID-19
Lamin A/C
Autophagy
Glutamate
LMNA
Heart
Inflammation
Amyotrophic lateral sclerosis
Thérapie génique
Myotonic Dystrophy
Dilated cardiomyopathy
Therapy
CRISPRi
MBNL
Becker muscular dystrophy
Laminopathies
Genotype phenotype correlation
Laminopathie
Autoimmune diseases
Cell therapy
Thymus
LMNA gene
Cardiomyopathy
Myasthenia Gravis MG
Cytoskeleton
Mice
RNA interference
Myogenesis
Gene therapy
Laminopathy
Errance diagnostique
Male
Fibrosis
OPMD
Neuromuscular diseases
Antisense oligonucleotides
Nuclear envelope
Skeletal muscle
RNA biology
Alternative splicing
FSHD
Outcome measures
Centronuclear myopathy
Dystrophin
Neuromuscular junction
Rare diseases
Motoneuron
Exercise
Dynamin 2
Calcium