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Myotonic dystrophy type 1 (DM1) is a dominantly inherited disease that affects multiple organ systems. Cardiac dysfunction is the second leading cause of death in DM1. We quantified gene expression in heart tissue from a heart-specific DM1 mouse model (EpA960/MCM) which inducibly expresses human DMP...
ORGANISM(S): Mus musculus 
Cell Delivery Agent as Drug. A Multitarget Agent Delivers an Antisense Oligonucleotide for Synergistic Activity in Myotonic Dystrophy Type 1
Cellular plasticity balances the metabolic and proliferation dynamics of a regenerating liver
Dysregulated RNA splicing induces regeneration failure in alcohol-associated liver disease
PTBP1 mediates Sertoli cell actin cytoskeleton organization through regulating alternative splicing of actin regulators
PTBP1 controls intestinal epithelial regeneration through post-transcriptional regulation of gene expression
Overexpression of the non-muscle RBFOX2 isoform triggers cardiac conduction defects in myotonic dystrophy
Lipid Droplet-Associated Hydrolase Mobilizes Oxysterol Stores and Inhibits Atheroma Growth and Progression
ESRP2-miR122 axis regulates postnatal onset of polyploidization
Single-cell transcriptomic analysis reveals unique cell types and patterns of gene expression in the frog corneal epithelium.
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