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Association of PPARγ2 GENE Pro12Ala allelic variant with obesity and metabolic syndrome components in a population of Maracaibo
ArticleAbstract: Introduction: In this study the association of rs1801282 allelic variant, g. 68777C G (Pro12Ala) ofPalabras claves:Metabolic syndrome, obesity, PPARγ2, Pro12Ala, Rs1801282Autores:Arráiz N., Carem Prieto, Marcucci R., Marín E., Mújica A., Mujica E., Perez D., Ramos M., Rojas-Quintero J., Sánchez M.P., Urdaneta B., Valmore BermúdezFuentes:scopus3'UTR +62G>A polymorphism of the RETN gene coding resistin and its association with metabolic syndrome components
ArticleAbstract: Background and objective: The polymorphism of the resistin gene (RETN/RSTN) has been associated withPalabras claves:3'UTR 62G/A, Metabolic syndrome, Resistin, RETN, rs3745368Autores:Arráiz N., Carem Prieto, Escalona C., Mújica A., Mujica E., Sánchez M.P., Valmore BermúdezFuentes:scopusMutations in the coding region of dominium of union of apoliprotein B-100: Diagnosis of apoliprotein B familiar defect
ArticleAbstract: Hypercholesterolemia is a risk factor for cardiovascular disease. Alterations in the genes encodingPalabras claves:ApoB-100, Arg3480Pro mutation, Familial defective apolipoprotein B, hypercholesterolemiaAutores:Añez-Ramos R., Arráiz N., Bello L.M., Carem Prieto, Escalona C., González M.C., Joselyn Zula, Mújica A., Mujica E., Pacheco M., Roque W., Toledo A.C., Valmore BermúdezFuentes:googlescopus