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Revista Latinoamericana de Hipertension(5)
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Association between +45t>g adiponectin polymorphism gene and type 2 diabetes mellitus and metabolic syndrome in a venezuelan population [version 1; peer review: 2 approved, 1 approved with reservations]
ArticleAbstract: Background: Adiponectin (ADIPOQ) is a hormone primarily synthesized by adipocytes and encoded by thePalabras claves:ADIPOQ gene, DNA, Metabolic syndrome, polymorphism, Type 2 Diabetes mellitusAutores:Carem Prieto, D'addosio R., Hoedebecke K., Medina M.T., Mujica E., Parra M., Rodriguez J.E., Sánchez M.P., Valencia E., Valmore Bermúdez, Vergara K., Villalobos E.Fuentes:scopusAssociation between apoliprotein E gene polymorphism and hypercholesterolemic phenotype in maracaibo, Zulia State, Venezuela
ArticleAbstract: Apoliprotein (Apo) E gene polymorphisms have been associated with high plasma lipids levels and cardPalabras claves:ApoE, Cardiovascular disease, hypercholesterolemia, Lipids profile, polymorphismsAutores:Arráiz N., Carem Prieto, Escalona C., Reyes F., Rondón N., Sánchez M.P., Sanz E., Valmore Bermúdez, Velasco M.Fuentes:scopusAssociation 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:scopusAllelic variant UCP3-55CT gene in obese individuals with and without anthropometric and metabolic alterations in Maracaibo municipality, Zulia state
ArticleAbstract: Background: The accumulation of body fat has a genetic basis. Given the importance of UCP3 in the rePalabras claves:-55C/T variant, Anthropometric abnormalities, Metabolic abnormalities, obesity, Rs1800849, UCP3Autores:Arráiz N., Camacho M., Carem Prieto, Joselyn Zula, Levy A., Marcucci R., Marín E., Mújica A., Mujica E., Rojas-Quintero J., Urdaneta B., Valmore Bermúdez, Vivas M.Fuentes:googlescopusFTO gene: Historic background and its relationship with chronic-degenerative diseases
ArticleAbstract: Alterations in the development of attention and behavioral organization can configure clinical diagnPalabras claves:Attention, dopamine, obesity, RISK FACTORS, TDAHAutores:Añez-Ramos R., Carem Prieto, Dávila L.C.A., González-Casanova J.E., Guette L.S., Guillén-Burgos H.F., Kusmar I., Maritza Torres, Martínez M.S., Rina Ortiz, Rojas E.R., Rojas-Gómez D.M., Rojas-Quintero J., Roque W., Salazar-Vílchez J., Valmore Bermúdez, Wilson SigüenciaFuentes:scopusDyslipidemia: Genetics, lipoprotein lipase and hindiii polymorphism
ReviewAbstract: The direct link between lipid metabolism alterations and the increase of cardiovascular risk are welPalabras claves:Coronary artery disease, dyslipidemia, HindIII, Lipoprotein Lipase, polymorphismsAutores:Cano-Ponce C., Carem Prieto, D’Addosio R., Garicano C.M.D., Hoedebecke K., Martínez M.S., Martínez N.G., Nava T.N., Parra S.M., Pérez A., Rojas E.R., Rojas M.P., Rojas-Quintero J., Salazar-Vílchez J., Valmore Bermúdez, Vicuña P.M.Fuentes: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:googlescopusNovel mutations identification in exon 4 of LDLR gene in patients with moderate hypercholesterolemia in a venezuelan population
ArticleAbstract: Familial hypercholesterolemia (FH) is an autosomal dominant disease characterized by increase in lowPalabras claves:Coronary artery disease, Familial hypercholesterolemia, Frameshift mutations, LDL-receptor, PCR-SSCPAutores:Arráiz N., Borjas L., Carem Prieto, Mujica E., Reyes F., Reyna-Villasmil N., Rondón N., Solís E., Valmore Bermúdez, Velasco M.Fuentes:googlescopusMelanocortin-4 receptor (MC4R) gene allelic variants and its impact on obese phenotype expression
ArticleAbstract: Obesity is a public health problem worldwide, due to its association with other morbidities such asPalabras claves:Allelic variants, body mass index, MC4R, Melanocortin receptor, obesityAutores:Amell A., Arráiz N., Camacho M., Carem Prieto, González M.C., Gonzalez R., Levy A., Marcucci R., Mujica E., Rojas-Quintero J., Sánchez M.P., Sofía M., Urdaneta B., Valmore BermúdezFuentes:scopus