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