Identifying functional metabolic shifts in heart failure with the integration of omics data and a cardiomyocyte-specific, genome-scale model
B. V. Dougherty, K. D. Rawls, G. L. Kolling, K. C. Vinnakota, A. Wallqvist, J. A. Papin
This study uses a cardiomyocyte-specific genome-scale model to identify common metabolic shifts in heart failure across omics datasets, finding decreased NO and Neu5Ac synthesis as common markers.
bioRxiv · Jul 20, 2020Bioengineering