Matches in Nanopublications for { ?s ?p "In platelets, glucose uptake can be stimulated by thrombin or insulin and is primarily mediated by the glucose transporter, GLUT3 [40]. Glucose uptake stimulated by thrombin or insulin is reduced in the presence of the Akt inhibitor, ML-9, suggesting that Akt contributes to glucose uptake in platelets, as it does in skeletal muscle or adipocytes [40]. However, the role of Akt in glucose uptake is not responsible for its role in platelet aggregation, since insulin induces Akt phosphorylation in platelets, but not platelet aggregation." ?g. }
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- _3 value "In platelets, glucose uptake can be stimulated by thrombin or insulin and is primarily mediated by the glucose transporter, GLUT3 [40]. Glucose uptake stimulated by thrombin or insulin is reduced in the presence of the Akt inhibitor, ML-9, suggesting that Akt contributes to glucose uptake in platelets, as it does in skeletal muscle or adipocytes [40]. However, the role of Akt in glucose uptake is not responsible for its role in platelet aggregation, since insulin induces Akt phosphorylation in platelets, but not platelet aggregation." provenance.
- _3 value "In platelets, glucose uptake can be stimulated by thrombin or insulin and is primarily mediated by the glucose transporter, GLUT3 [40]. Glucose uptake stimulated by thrombin or insulin is reduced in the presence of the Akt inhibitor, ML-9, suggesting that Akt contributes to glucose uptake in platelets, as it does in skeletal muscle or adipocytes [40]. However, the role of Akt in glucose uptake is not responsible for its role in platelet aggregation, since insulin induces Akt phosphorylation in platelets, but not platelet aggregation." provenance.