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1 int to evaluate and perhaps develop improved insulin-sensitizing agents.
2 s have demonstrated the potential utility of insulin-sensitizing agents and lipid-lowering therapies
3 estrogen-progestin oral contraceptives, (3) insulin-sensitizing agents, and (4) estrogen-progestin f
5 hese results indicate that treatment with an insulin-sensitizing agent can lead to improvement in bio
6 by thiazolidinediones (TZDs), widely used as insulin-sensitizing agents for the treatment of type 2 d
7 compounds, as well as a subclass of non-TZD insulin-sensitizing agents, have been shown to be peroxi
9 primarily focused on weight loss and use of insulin sensitizing agents, including the thiazolidenedi
12 ce all PPARgamma agonists were orally active insulin-sensitizing agents producing reductions of eleva
17 tazone, like other thiazolidinediones, is an insulin-sensitizing agent that activates the peroxisome
19 ediones, pioglitazone and rosiglitazone, are insulin sensitizing agents, that are licensed for the ma
21 ance that is distinct from commonly utilized insulin-sensitizing agents, the inhibitor promoted insul
24 atment of normal (nondiabetic) pigs with the insulin-sensitizing agent troglitazone improves recovery
26 is and is the molecular target of a class of insulin-sensitizing agents used for the management of ty
27 iazolidinediones (TZDs) are a novel class of insulin-sensitizing agents used in the treatment of NIDD
28 s and then 4 mg twice daily for 8 weeks), an insulin-sensitizing agent, was given to 7 insulin-resist
29 zone) and troglitazone are thiazolidinedione insulin-sensitizing agents, which are undergoing clinica
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