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