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