Loading...
Derniers dépôts
Nombre de documents
794
Nombre de notices
1 384
widget_cloud
FSHD
Lamin A/C LMNA gene
Rare neuromuscular diseases
Myopathies
OPMD
Neuromuscular diseases
ALS
Errance diagnostique
Aging
LMNA gene
Cell therapy
Transgenic mouse model
Dilated cardiomyopathy
Becker muscular dystrophy
Autoimmunity
LMNA
Aged
Myositis
Treatment
CTG repeat contractions
Mechanotransduction
Transcriptomics
Skeletal muscle
Gene therapy
Muscle regeneration
CMS
Satellite cells
Cytoskeleton
Congenital muscular dystrophy
Inflammation
Dystrophin
Astrocyte
Fabry disease
Cancer
Satellite cell
Mouse model
COVID-19
Neuromuscular junction
Myotonic dystrophy
Myasthenia gravis
Antisense oligonucleotides
Autoantibodies
Myotonic dystrophy type 1
Centronuclear myopathy
Lamin A/C
Glutamate
Myoblasts
Thymus
Dynamin 2
Autoimmune diseases
Neuromuscular disease
Thérapie génique
Calcium
PABPN1
Rare diseases
Cytokines
Heart failure
Outcome measures
Myotonic Dystrophy type 1
Trinucleotide repeat expansion
Brain
Laminopathy
RNA biology
Therapy
RNA interference
CRISPRi
Mice
Long read sequencing
Laminopathies
Genotype phenotype correlation
Actin
Congenital myopathy
Alternative splicing
DMD
Biomarkers
Heart
MBNL
Myasthenia Gravis MG
Fibrosis
Animals
Laminopathie
Spinal muscular atrophy
Muscle
Nuclear envelope
Muscular dystrophy
Motoneuron
Myotonic Dystrophy
Regeneration
Exercise
Autophagy
Myopathy
Cardiomyopathy
Amyotrophic lateral sclerosis
Humans
AAV
Duchenne muscular dystrophy
Dermatomyositis
Male
Biomarker
Myogenesis