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