Loading...
Derniers dépôts
Nombre de documents
791
Nombre de notices
1 380
widget_cloud
AAV
Autophagy
Regeneration
Myasthenia Gravis MG
Lamin A/C
Dynamin 2
CRISPRi
Calcium
Dystrophin
Transgenic mouse model
Dermatomyositis
Gene therapy
Rare neuromuscular diseases
ALS
Myopathy
Transcriptomics
Laminopathies
Muscle
Lamin A/C LMNA gene
Therapy
Myositis
Autoimmunity
Fibrosis
Centronuclear myopathy
Neuromuscular junction
Fabry disease
Humans
Biomarker
Aged
Diagnosis
Autoimmune diseases
RNA interference
Cardiomyopathy
Cell therapy
Heart failure
Aging
Myasthenia gravis
Glutamate
Actin
Myotonic Dystrophy
Muscular dystrophy
Treatment
Myoblasts
Thymus
Rare diseases
Antisense oligonucleotides
PABPN1
Satellite cells
Myopathies
CMS
Genotype phenotype correlation
Laminopathy
Inflammation
DMD
Nuclear envelope
OPMD
FSHD
Outcome measures
Myotonic dystrophy type 1
LMNA gene
Trinucleotide repeat expansion
Duchenne muscular dystrophy
Long read sequencing
Mouse model
Amyotrophic lateral sclerosis
Skeletal muscle
Myotonic Dystrophy type 1
COVID-19
Exercise
Errance diagnostique
Cytokines
Satellite cell
Cancer
Congenital myopathy
Motoneuron
Male
Becker muscular dystrophy
Dilated cardiomyopathy
Myotonic dystrophy
MBNL
Neuromuscular disease
Cytoskeleton
Heart
Congenital muscular dystrophy
Brain
Neuromuscular diseases
Autoantibodies
Alternative splicing
Mechanotransduction
Animals
Astrocyte
LMNA
Thérapie génique
CTG repeat contractions
Muscle regeneration
Myogenesis
Clinical trials
RNA biology
Biomarkers
Laminopathie