Mostrando 4 resultados de: 4
Subtipo de publicación
Article(4)
Publisher
Revista Latinoamericana de Hipertension(2)
American Journal of Therapeutics(1)
Medicina Clinica(1)
Objetivos de Desarrollo Sostenible
ODS 3: Salud y bienestar(4)
ODS 17: Alianzas para lograr los objetivos(2)
ODS 2: Hambre cero(2)
3'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:scopusMelanocortin-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: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:googlescopus