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We therefore assessed the involvement of MAP kinase pathways in the overexpression of Glut1. International Fuel Aid, Inc. For transfection experiments, cells were plated at a density of 2.

Adoptive transfer studies demonstrate that both T cells and non—T cells must express HSA in order for the pathogenic T cells to execute their effector function. ERK activation is required for induction of the Glut1 gene. Dae Yang Industrial Co.

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Google Scholar Articles by Montessuit, C. Lifetime Energy Solutions, Corp. The expression of this reporter in response to the hypertrophic agonists O -tetradecanoylphorbolacetate TPA 1 and phenylephrine was assessed, and the signaling pathways responsible for increased expression of GLUT1 were investigated. The costs of publication of this article were defrayed in part by the payment dcs page charges. Gasolines are required to contain detergent additives which have been certified in accordance with the regulations at 40 CFR 80, Subpart G.

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Apex International Group, Inc. Director of Training of Gov. Because of the low transfection efficiency in primary myocytes, it was not possible to assess the effect of transfection with these molecules on expression of endogenous Glut1 mRNA.

Eco Global Solutions, Inc. Bio Oil National Corporation. Joule Unlimited Technologies, Inc. Ag Energy Resources, Inc. Although an initial report described PI3K as being a direct target of Ras 32other studies have suggested that PI3K could act upstream of Ras 46 View this article with LENS. Fuel Activator Chemical Corporation. American Grease Stick Co. GLUT1 is a ubiquitous isoform of the glucose transporter, expressed at a significant level in virtually every tissue of the body.

Ras activity is required for induction of the Glut1 promoter in myocytes. TPA and phenylephrine increase transcription from the Glut1 promoter. The mode of action of these agonists is different.

Bestline International Research, Inc. Cotransfection of the myocytes with constitutively active versions of Ras and MEK1 or an estrogen-inducible version of Raf1 also stimulated transcription from the Glut1 promoter. Berkebile Oil Company, Inc.

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Articles by Thorburn, A. In this study, we observed that hypertrophy of rat neonatal ventricular myocytes is associated with increased expression of the glucose transporter Glut1 isoform mRNA.

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In contrast, the p38 inhibitor SB did not affect induction of the Glut1 promoter by TPA or phenylephrine data not shown. Falcon Safety Products, Inc. To study the transcriptional regulation of GLUT1 expression, myocytes were transfected with luciferase reporter constructs under the control of the Glut1 promoter.