3 results match your criteria: "Campus Univ. de Rabanales[Affiliation]"

Adipobiology for novel therapeutic approaches in metabolic syndrome.

Curr Vasc Pharmacol

November 2013

Department of Cell Biology, Physiology and Immunology, Edificio Severo-Ochoa, Pl. 3, Campus Univ. de Rabanales, University of Cordoba, E-14014 Cordoba, Spain.

Obesity is dramatically increasing virtually worldwide, which has been linked to the rising prevalence of metabolic syndrome. Excess fat accumulation causes severe alterations in adipose tissue function. Actually, adipose tissue is now recognized as a major endocrine and secretory organ that releases a wide variety of signaling molecules (hormones, growth factors, cytokines, chemokines, etc.

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Nutritional, hormonal, and depot-dependent regulation of the expression of the small GTPase Rab18 in rodent adipose tissue.

J Mol Endocrinol

February 2013

Department of Cell Biology, Physiology and Immunology, Instituto Maimónides de Investigación Biomédica de Córdoba, University of Córdoba/Hospital Universitario Reina Sofia, Edificio Severo-Ochoa, Pl. 3, Campus Univ. de Rabanales, E-14014 Córdoba, Spain.

There is increasing evidence that proteins associated with lipid droplets (LDs) play a key role in the coordination of lipid storage and mobilization in adipocytes. The small GTPase, RAB18, has been recently identified as a novel component of the protein coat of LDs and proposed to play a role in both β-adrenergic stimulation of lipolysis and insulin-induced lipogenesis in 3T3-L1 adipocytes. In order to better understand the role of Rab18 in the regulation of lipid metabolism in adipocytes, we evaluated the effects of age, fat location, metabolic status, and hormonal milieu on Rab18 expression in rodent white adipose tissue (WAT).

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Searching for new mathematical growth model approaches for Listeria monocytogenes.

J Food Sci

January 2007

Dept. of Food Science and Technology, Univ. of Cordoba, Campus Univ. de Rabanales, 14014 Córdoba, Spain.

Different secondary modeling approaches for the estimation of Listeria monocytogenes growth rate as a function of temperature (4 to 30 degrees C), citric acid (0% to 0.4% w/v), and ascorbic acid (0% to 0.4% w/v) are presented.

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