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