index - Repeat Expansions & Myotonic Dystrophy (REDs) Accéder directement au contenu

Dernières publications

Chiffres clés

132 Publications avec texte intégral

Open Access

52 %

Mots clés

CRISPRi Maximal force Heart Mice Desmin Gene editing Animals Male Myotonic Dystrophy Type 1 DMPK Glutamate Mouse model Humans Glucocorticoid-receptor GSK3␤ Motoneuron Oligodendrocytes Trinucleotide Repeat Expansion Myotonic dystrophy PacBio Myostatin Transcriptomics Dystrophin Antisense oligonucleotides Dynamin 2 CMS Transgenic mouse RNA biology PCR Central nervous system Myelin Aging Myotonic Dystrophy Astrocytes Centronuclear myopathy Trinucleotide repeat expansion Oligodendrocyte Heart failure Brain Astrocyte Skeletal muscle Antisense oligonucleotide Alternative splicing Brain dysfunction MBNL Long read sequencing GABA Exercise Duchenne muscular dystrophy ARN Genotype phenotype correlation Cell culture model ACETYLCHOLINESTERASE DMSXL mice Lc3 BIOLOGIE MOLECULAIRE Gene therapy Diaphragm Hypoxia Mouse models Myotonic Dystrophy type 1 Acute coronary syndrome CTG repeat contractions Knockout Myotonic dystrophy type 1 KNOCKOUT MICE Glucocorticoids Cytoskeleton AAV Neuron Thérapie génique Autophagy Gene Therapy Muscular dystrophy Dystrophie Myotonique Intermediate filament Muscle Glial cells Dystrophie myotonique Exercice Expression CTG repeat instability In vivo CONGENITAL MYATHENIC SYNDROME Acetylcholinesterase deficiency Transgenic mouse model RNA splicing Dilated cardiomyopathy CRISPR/Cas9 Acetylcholinesterase knockout mouse Cell penetrating peptide Fibrosis RNA interference CTG repeats Myotonic dystrophy mouse models Cardiac muscle Therapy Cell model DM1 Quantitative microdialysis