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