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The liver remains a central part of not only the energy expenditure component of glucagon, but of also mediating systemic metabolic parameters including risk for insulin insensitivity, atherosclerosis, hyperlipidemia, and other attributes leading to progressive systems deterioration

PPAR- ligands may influence the activity of the reninangiotensin system by transcriptional regulation at both the mediator and receptor levels, in addition to lowering blood glucose levels

Cloning and identification of tissue-specific expression of KCNN4 splice variants in rat colon

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These events are typically dose-dependent and occur most often during treatment initiation or dose escalation

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