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