Area of research
Surgery · Cancer Research
Research interest
Research interests include microRNA, Biology, Cholesterol, ABCA1, Lipid metabolism, and Inflammation.
Macrophage-Derived 25-Hydroxycholesterol Promotes Vascular Inflammation, Atherogenesis, and Lesion Remodeling
Loss of hepatic miR-33 improves metabolic homeostasis and liver function without altering body weight or atherosclerosis
Absence of ANGPTL4 in adipose tissue improves glucose tolerance and attenuates atherogenesis
Genetic Ablation of miR-33 Increases Food Intake, Enhances Adipose Tissue Expansion, and Promotes Obesity and Insulin Resistance
Inflammatory Ly6Chi monocytes and their conversion to M2 macrophages drive atherosclerosis regression
MicroRNAs and lipid metabolism
Genetic Dissection of the Impact of miR-33a and miR-33b during the Progression of Atherosclerosis
ANGPTL4 deficiency in haematopoietic cells promotes monocyte expansion and atherosclerosis progression
Chronic miR‐29 antagonism promotes favorable plaque remodeling in atherosclerotic mice
MicroRNA-148a regulates LDL receptor and ABCA1 expression to control circulating lipoprotein levels
Akt‐mediated foxo1 inhibition is required for liver regeneration
Genetic Evidence Supports a Major Role for Akt1 in VSMCs During Atherogenesis
Autoregulation of glypican-1 by intronic microRNA-149 fine-tunes the angiogenic response to fibroblast growth factor in human endothelial cells
Control of Cholesterol Metabolism and Plasma High-Density Lipoprotein Levels by microRNA-144
Therapeutic Silencing of MicroRNA-33 Inhibits the Progression of Atherosclerosis in <i>Ldlr</i> <sup>−/−</sup> Mice—Brief Report
MicroRNA 33 Regulates Glucose Metabolism
MicroRNAs and Atherosclerosis
MicroRNA modulation of lipid metabolism and oxidative stress in cardiometabolic diseases
Cardiovascular dysregulation of miR‐17‐92 causes a lethal hypertrophic cardiomyopathy and arrhythmogenesis
MicroRNA Regulation of Cholesterol Metabolism
Gain-of-Function Lipoprotein Lipase Variant rs13702 Modulates Lipid Traits through Disruption of a MicroRNA-410 Seed Site