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Gary L. Wright

Researcher at East Tennessee State University

Publications -  86
Citations -  2225

Gary L. Wright is an academic researcher from East Tennessee State University. The author has contributed to research in topics: Calcium & Actin. The author has an hindex of 25, co-authored 86 publications receiving 2070 citations. Previous affiliations of Gary L. Wright include University of Missouri & Medical University of South Carolina.

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Erythropoietin receptor expression in adult rat cardiomyocytes is associated with an acute cardioprotective effect for recombinant erythropoietin during ischemia-reperfusion injury.

TL;DR: Experiments revealed that the rapid cardioprotective effect of EPO during ischemia‐reperfusion injury was associated with preservation of ATP levels in the ischemic myocardium.
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Mechanisms of erythropoietin-mediated cardioprotection during ischemia-reperfusion injury: role of protein kinase C and phosphatidylinositol 3-kinase signaling

TL;DR: It is shown that postischemia EPO treatment at the onset of reperfusion significantly improved recovery of LVDP and reduced infarct size and EPO‐mediated cardioprotection by EPO required the PI3K pathway but was not affected by inhibition of PKC at the time ofEPO treatment.
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VEGF stimulation of mitochondrial biogenesis: requirement of AKT3 kinase

TL;DR: A subtle but significant, abnormal mitochondrial phenotype is observed in the brain tissue of AKT3 knockout mice, suggesting that Akt3 is important in coordinating mitochondrial biogenesis with growth factor‐induced increases in cellular energy demands.
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Endotoxin stress-response in cardiomyocytes: NF-κB activation and tumor necrosis factor-α expression

TL;DR: The intracellular events leading to its production by heart cells are largely unknown and TNF-α is implicated in numerous cardiac pathologies, but its role in these pathologies is largely unknown.
OtherDOI

C1q/TNF‐Related Protein 3 (CTRP3) Function and Regulation

TL;DR: A comprehensive overview of the research concerning the expression, regulation, and physiological function of CTRP3 is provided, highlighting profound biological potency of this adipokine family.