PhD - Georgia Inst of Tech
BS, Physics, University of Missouri, Columbia, Missouri
We use genetically engineered mouse models, cell culture systems, patient samples, and direct patient investigation to solve problems surrounding pulmonary vascular disease and pulmonary fibrosis. We have created mouse models of different heritable PAH mutations, including BMPR2, CAV1, and KCNK3, and have learned a great deal about the molecular etiology of PAH from them. We are currently studying the role of heritable mutations in regulation of vasculogenesis and cell-cell junctions, metabolism, and interaction between pulmonary vascular cells and circulating inflammatory cells, as well as examining mechanisms of right heart adaptation and failure.