CPC C12N 5/0657 (2013.01) [A61K 45/06 (2013.01); A61P 9/10 (2018.01)] | 6 Claims |
1. A method of producing a transplant composition comprising cardiomyocytes having a ASIC1a−/− phenotype, the method comprising the steps of:
a) genetically modifying stem cells to have a ASIC1a−/− phenotype;
b) differentiating said stem cells having a ASIC1a−/− phenotype to cardiomyocytes, wherein the differentiation is performed in vitro; and
c) admixing said cardiomyocytes with a pharmaceutically acceptable carrier.
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