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