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Therefore, drugs can be selected on the basis of the expression pattern of ferroptosis-inducing genes (e.g., SLC7A11, GSH, and GPX) or genes associated with metabolic pathways that affect ferroptosis (e.g., GLUT, PDK4, glutaminase, VDAC, and G6PD)
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Another emerging class of drugs with dual incretin agonistic effects is currently being developed for treating type 2 diabetes patients with chronic kidney disease and NASH
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