Loading...
Derniers dépôts
Nombre de documents
775
Nombre de notices
1 374
widget_cloud
Regeneration
Biomarker
Long read sequencing
Lamin A/C LMNA gene
MBNL
RNA interference
Astrocyte
Cytoskeleton
Muscle regeneration
Dilated cardiomyopathy
Transcriptomics
PABPN1
Myopathy
Neuromuscular disease
Therapy
Myoblasts
OPMD
Transgenic mouse model
Brain
Cancer
Autoimmune diseases
Myopathies
Myogenesis
Diagnosis
DMD
Fabry disease
Biomarkers
Nuclear envelope
ALS
Myasthenia Gravis MG
Myotonic dystrophy type 1
CMS
Antisense oligonucleotides
Congenital myopathy
Aged
Dystrophin
LMNA
Inflammation
Exercise
Actin
Satellite cell
Amyotrophic lateral sclerosis
Mechanotransduction
Cardiomyopathy
CRISPRi
Autoantibodies
RNA biology
Cell therapy
Alternative splicing
Neuromuscular junction
Thymus
Laminopathy
Mouse model
Skeletal muscle
Myotonic Dystrophy
Rare diseases
Centronuclear myopathy
Treatment
Dermatomyositis
Satellite cells
Myotonic Dystrophy type 1
Humans
Thérapie génique
Gene therapy
Fibrosis
Outcome measures
Heart
Becker muscular dystrophy
Genotype phenotype correlation
Laminopathies
Rare neuromuscular diseases
Errance diagnostique
Heart failure
CTG repeat contractions
Myositis
Muscle
Lamin A/C
Duchenne muscular dystrophy
Autoimmunity
Trinucleotide repeat expansion
Laminopathie
COVID-19
Autophagy
Clinical trials
Calcium
Congenital muscular dystrophy
Animals
Neuromuscular diseases
Dynamin 2
LMNA gene
AAV
Glutamate
Cytokines
Male
Myasthenia gravis
FSHD
Myotonic dystrophy
Motoneuron
Aging
Muscular dystrophy