Base Editing, Single-Cell Multiomics, and Cardiac Organoids to Decode Genetic Variants

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Research Objective Develop a high-throughput platform combining iPSC-derived cardiac organoids and CRISPR base editing to functionally assess missense variants in hypertrophic cardiomyopathy. Impact (i) Limited tools for functional interpretation of…

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Allele Prospector: Leveraging human genetic variation to enable therapeutic genome editing in hundreds of disease genes

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Research Objective We are building a foundational platform for developing genome editing technologies that increase patient coverage by 20-40X and can be applied to over 700 genetic diseases in diverse…

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Modified RNA-Based Gene Therapy for Cardiac Regeneration Through Cardiomyocyte Proliferation

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Research Objective Efficacious and safe intramyocardial delivery of modified mRNA encoding cell cycle regulators as a gene therapy for cardiac regeneration through resident cardiomyocyte proliferation. Impact This project would provide…

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