Loading...
Derniers dépôts
Nombre de documents
772
Nombre de notices
1 376
widget_cloud
Myotonic Dystrophy type 1
Aging
Transgenic mouse model
MBNL
Lamin A/C LMNA gene
CMS
ALS
Transcriptomics
Motoneuron
Errance diagnostique
Treatment
FSHD
LMNA gene
Myoblasts
Cardiomyopathy
Skeletal muscle
Laminopathies
Long read sequencing
Outcome measures
Mechanotransduction
Autoimmune diseases
Male
Clinical trials
Regeneration
Becker muscular dystrophy
Congenital myopathy
Thymus
Exercise
Mouse model
Genotype phenotype correlation
Fabry disease
Heart failure
Actin
Therapy
Cell therapy
Laminopathy
Rare neuromuscular diseases
Biomarkers
Astrocyte
Dystrophin
Centronuclear myopathy
Biomarker
Muscular dystrophy
DMD
Autophagy
Lamin A/C
Myotonic dystrophy type 1
LMNA
Humans
Dynamin 2
Myasthenia Gravis MG
Satellite cell
Autoimmunity
Alternative splicing
Myotonic Dystrophy
Myopathy
Gene therapy
Dermatomyositis
Congenital muscular dystrophy
Neuromuscular disease
Diagnosis
Nuclear envelope
Autoantibodies
Amyotrophic lateral sclerosis
Fibrosis
Rare diseases
Heart
Animals
AAV
CTG repeat contractions
Glutamate
OPMD
Laminopathie
Thérapie génique
Myositis
Myasthenia gravis
Muscle
Brain
Cytoskeleton
Myopathies
Muscle regeneration
CRISPRi
Neuromuscular junction
Cancer
Aged
Trinucleotide repeat expansion
COVID-19
Dilated cardiomyopathy
PABPN1
RNA biology
Duchenne muscular dystrophy
Myogenesis
Inflammation
Calcium
RNA interference
Cytokines
Antisense oligonucleotides
Neuromuscular diseases
Myotonic dystrophy
Satellite cells