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