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Using the CRISPR-Cas9 gene editing system, UT Southwestern researchers corrected mutations responsible for a common inherited heart condition called dilated cardiomyopathy (DCM) in human cells and a mouse model of the disease.

Takahiko nishiyamaRoberta welchEric olsonRhonda bassel dubyEmily hendersonHamon centerResearch on cardiac birth defectsDrug administrationWillie nelson professorship in stem cell researchScience translational medicineMolecular biologyNobel prizeIndustry focusPogue distinguished chairCardiac birth defectsDistinguished chair