Cardiac cell modelling of myofibrillar myopathy by AAV-mediated transduction of desmin mutations in human iPSC-derived and neonatal rat cardiomyocytes
ConclusionsOur results indicate that the proposed in vitro model is suitable for the study of the structural defects of desmin-mutated cardiomyocytes.
Source: Archives of Cardiovascular Diseases Supplements - Category: Cardiology Source Type: research
More News: Adenoviruses | Cardiology | Cardiovascular | Genetics | Heart | Perinatology & Neonatology | Stem Cell Therapy | Stem Cells | Study