Deanna P. Bracy

Fiber type-specific determinants of Vmax for insulin-stimulated muscle glucose uptake in vivo.

Hexokinase II partial knockout impairs exercise-stimulated glucose uptake in oxidative muscles of mice.

Distributed control of glucose uptake by working muscles of conscious mice: roles of transport and phosphorylation.

Quinides of roasted coffee enhance insulin action in conscious rats.

Hexokinase II overexpression improves exercise-stimulated but not insulin-stimulated muscle glucose uptake in high-fat-fed C57BL/6J mice.

AMP kinase-induced skeletal muscle glucose but not long-chain fatty acid uptake is dependent on nitric oxide.

AMPK stimulation increases LCFA but not glucose clearance in cardiac muscle in vivo.

Regulation of insulin-stimulated muscle glucose uptake in the conscious mouse: role of glucose transport is dependent on glucose phosphorylation capacity.

Heart-type fatty acid-binding protein reciprocally regulates glucose and fatty acid utilization during exercise.

Control of exercise-stimulated muscle glucose uptake by GLUT4 is dependent on glucose phosphorylation capacity in the conscious mouse.

Control of muscle glucose uptake: test of the rate-limiting step paradigm in conscious, unrestrained mice.

Hexokinase II protein content is a determinant of exercise endurance capacity in the mouse.

Partial gene deletion of heart-type fatty acid-binding protein limits the severity of dietary-induced insulin resistance.

Considerations in the design of hyperinsulinemic-euglycemic clamps in the conscious mouse.

Chronic treatment with sildenafil improves energy balance and insulin action in high fat-fed conscious mice.

Glucose kinetics and exercise tolerance in mice lacking the GLUT4 glucose transporter.

Phosphorylation barriers to skeletal and cardiac muscle glucose uptakes in high-fat fed mice: studies in mice with a 50% reduction of hexokinase II.

Insulin action in the double incretin receptor knockout mouse.

Metabolic implications of reduced heart-type fatty acid binding protein in insulin resistant cardiac muscle.

The glucagon-like peptide-1 receptor regulates endogenous glucose production and muscle glucose uptake independent of its incretin action.

Skeletal muscle AMP-activated protein kinase is essential for the metabolic response to exercise in vivo.

Endothelial nitric oxide synthase is central to skeletal muscle metabolic regulation and enzymatic signaling during exercise in vivo.

Glucagon-like peptide-1 receptor knockout mice are protected from high-fat diet-induced insulin resistance.