Modeling human cardiac genetic diseases in the zebrafish: Focus on cardiomyopathies and cohesinopathiesThe zebrafish cohesin protein Sgo1 is required for cardiac function and eye developmentA Heterozygous Mutation in Cardiac Troponin T Promotes Ca2+ Dysregulation and Adult Cardiomyopathy in ZebrafishInflammatory response in hematopoietic stem and progenitor cells triggered by activating SHP2 mutations evokes blood defectsLoss of sdhb in zebrafish larvae recapitulates human paraganglioma characteristicsMUSCLEMOTIONEffective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disordersIstaroxime treatment ameliorates calcium dysregulation in a zebrafish model of phospholamban R14del cardiomyopathyABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9
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Sarah Kamel
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Public - No restriction
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Publiek - Geen beperking
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