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