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