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Mots clés
ACETYLCHOLINESTERASE
Myostatin
Muscle
DMSXL mice
Myotonic dystrophy
GSK3
CTG repeat contractions
Animals
Gene editing
Glutamate
Myotonic dystrophy mouse models
Long read sequencing
Glucocorticoids
Central nervous system
Acetylcholinesterase knockout mouse
Brain
CTG repeat instability
Cytoskeleton
Duchenne muscular dystrophy
Mice
CRISPR/Cas9
CONGENITAL MYATHENIC SYNDROME
RNA biology
Gene therapy
Alternative splicing
Astrocyte
Knockout
Thérapie génique
Intermediate filament
Dystrophin
Heart
Acute coronary syndrome
Cell penetrating peptide
CRISPRi
Skeletal muscle
Desmin
Dilated cardiomyopathy
Motoneuron
Centronuclear myopathy
ARN
Neuron
DM1
Expression
CMS
Fibrosis
Antisense oligonucleotide
Cell culture model
Dystrophie myotonique
Genotype phenotype correlation
PacBio
Male
KNOCKOUT MICE
AAV
Heart failure
Myelin
Humans
Oligodendrocyte
Cell model
Oligodendrocytes
Aging
Hypoxia
GABA
Trinucleotide repeat expansion
Myotonic Dystrophy
Endurance training
Myotonic dystrophy type 1
CTG repeats
Acetylcholinesterase deficiency
In vivo
Antisense oligonucleotides
Therapy
Exercice
RNA splicing
Dynamin 2
Muscular dystrophy
Transcriptomics
DMPK
Transgenic mouse
Trinucleotide Repeat Expansion
Exercise
Astrocytes
Diaphragm
Quantitative microdialysis
Brain dysfunction
Myotonic Dystrophy type 1
Gene Therapy
Glial cells
Maximal force
Glucocorticoid-receptor
Myotonic Dystrophy Type 1
Mouse model
RNA interference
Mouse models
MBNL
Autophagy
PCR
BIOLOGIE MOLECULAIRE
Transgenic mouse model
Cardiac muscle
Dystrophie Myotonique