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