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