Loading...
Derniers dépôts
Nombre de documents
Nombre de notices
1 375
widget_cloud
Genotype phenotype correlation
PABPN1
Myositis
Cell therapy
Rare neuromuscular diseases
Myotonic dystrophy type 1
Duchenne muscular dystrophy
CMS
Laminopathy
AAV
Lamin A/C LMNA gene
Amyotrophic lateral sclerosis
Male
Myasthenia Gravis MG
Actin
Treatment
Antisense oligonucleotides
RNA interference
Gene therapy
Transgenic mouse model
DMD
Nuclear envelope
Heart failure
Clinical trials
Diagnosis
OPMD
Autoimmune diseases
Satellite cells
Skeletal muscle
Becker muscular dystrophy
Therapy
Calcium
CTG repeat contractions
Errance diagnostique
Rare diseases
RNA biology
Myotonic Dystrophy type 1
LMNA
Autophagy
Long read sequencing
Inflammation
Myogenesis
FSHD
Myopathies
ALS
Cancer
Biomarker
Laminopathie
LMNA gene
Thymus
Fabry disease
Myoblasts
Cytokines
Humans
Astrocyte
Muscle
Biomarkers
Neuromuscular disease
Brain
Muscular dystrophy
MBNL
Animals
Motoneuron
Myotonic Dystrophy
Trinucleotide repeat expansion
Congenital myopathy
Cardiomyopathy
Regeneration
Autoimmunity
Autoantibodies
Outcome measures
Mechanotransduction
Mouse model
Glutamate
Dystrophin
Laminopathies
Dilated cardiomyopathy
Exercise
Fibrosis
CRISPRi
Aging
Alternative splicing
Muscle regeneration
Myopathy
Satellite cell
Centronuclear myopathy
Dermatomyositis
Cytoskeleton
Heart
Thérapie génique
Neuromuscular junction
Congenital muscular dystrophy
Neuromuscular diseases
Dynamin 2
Myotonic dystrophy
Aged
Transcriptomics
Lamin A/C
COVID-19
Myasthenia gravis