index - Repeat Expansions & Myotonic Dystrophy (REDs)

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