Para poder predecir las frecuencias genotípicas, frecuencia de un gen o frecuencia fenotípica de una población se puede hacer solo si se. Frecuencia alélica del gen de la calpastatina en el ganado criollo limonero. José Atilio Aranguren1, María Gabriela Portillo2,. Carolina Flores Rondón3, Yenen. allele frequency · Frecuencia alelica (sinonimo: frecuencia genica). English to Spanish. allele-specific oligonucleotide testing · Estudios de oligonucleotidos.

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Recibido el 25 de abril, Certain candidate genes, that have common functional variants in the general population, may be important determinants of inter-individual differences in the response to dietary changes.

A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Rev Clin Esp ; Some studies 24 have found no difference in systolic blood pressure between genotypes. Thromb Res ; 1; J Clin Invest ; Hematol J ; 4 Supl.

Am J Hematol ; Fatty acid binding protein 2 FABP-2 polymorphism, obesity and insulin resistance. Close and don’t show again Close. TNF alpha amd polymorphisms do not associate with insulin fecuencia in hypertensive subjects. High risk of thrombosis in patients homozygous for factor V Leiden activated protein C resistance. Four cases and 6 controls were carriers of heterozygous mixed genotypes.


Interaction between haemochromatosis and transferrin receptor genes in hepatocellular carcinoma. Polymorphism in the fatty alelics protein 2 and apolipoprotein C-III genes are associated with the metabolic syndrome and dyslipidemia in South Indian population.

Prothrombin gene G-A mutation in the Turkish population. Aceptado el 13 de julio, Especiacion alopatrica o alopatrida.

GA polymorphism of the cannabinoid receptor gene CNR1 and insulin resistance in patients with diabetes mellitus type 2. Study of unrelated blood donors.

La mutacion H63D del gen HFE se asocia con un riesgo aumentado de carcinoma hepatocelular

Common genomic variants associated with variations in plasma lipoproteins in young aboriginal Canadians. Obes Surg ; DNA was denaturized at 95 o C for 3 min; this was followed by 50 cycles of denaturation at 95 o C for 15 s, and annealing at Biochem Biophys Res Commun ; Obes Res ; Genetic polymorphism affecting the phenotypic expression of familial hypercholesterolemia.

Dig Dis Sci ; Roles of iron and HFE mutations on severity and response to therapy during retreatment of advanced chronic hepatitis C. Recibido el 14 de marzo, Asimismo, en sujetos homocigotos para el alelo Thr, se ha encontrado una mayor trigliceridemia asociada a una respuesta alterada de insulina post-prandial. Arterioscler Thromb VascBiol ; Table I shows anthropometric variables and blood pressure. Genet Epidemiol ; Hemochromatosis and transferrin receptor gene polymorphism in chronic hepatitis C: Clin Appl Thromb Hemost ; 6: Por ello, los objetivos de este estudio son: Ann Rev Nutr ; Hsu KT, Storch J.


Estudios de oligonucleotidos especificos del alelo.

Translation glossary: Genetics glossary

Ninguno estaba diagnosticado de hemocromatosis. Public glossaries 2, Genetics glossary My glossaries. Oligonucleotide primers and probes were designed with the Beacon Designer 4. Physiol Genomics ; Br J Hematol ; Association between Ala54Thr substitution on the fatty binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese men. FABP2 genotype is associated with insulin sensitivity in older women.

Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population. A worldwide problem and the major risk factors. Rev Esp Enferm Dig ;