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Determinación de frecuencias genotípicas y alélicas de los polimorfismos genéticos de MTHFR 677C>T (rs1801133) y MTHFR 1298A>C (rs1801131) en niños con leucemia linfoblástica aguda de SOLCA - Loja y SOLCA - Cuenca
(2019-11-09)
Acute lymphoblastic leukemia (ALL) is one of the most frequent oncopathologies in children, occupying the first place among the five types of cancer with the highest incidence in Ecuador. Objective: To determine the genotypic ...
Pollymorphisms in the CBS Gene and Homocysteine, Folate and Vitamin B(12) Levels: Association With Polymorphisms in the MTHFR and MTRR Genes in Brazilian Children
(WILEY-LISS, 2008)
Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR) and cystathionine P-synthase (CBS) genes, involved in the intracellular metabolism of homocysteine (Hcy), can result ...
Polimorfismos em genes envolvidos no metabolismo do ácido fólico e o risco de desenvolvimento da leucemia infantil
(Universidade Federal de PernambucoUFPEBrasilPrograma de Pos Graduacao em Genetica, 2017)
C677T (RS1801133 ) MTHFR gene polymorphism frequency in a colombian population
(Colombia Médica, 2015)
Introduction:
Abnormal levels of the enzyme methylenetetrahydrofolate reductase (MTHFR) are associated with an increased risk of both cardiovascular and cerebrovascular disease and higher concentrations of homocysteine. ...
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil
(2011-08-19)
Abstract
Background/Aim
Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in particular the C677T (Ala222Val) polymorphism were recently associated ...
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil
(2011)
Abstract
Background/Aim
Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in particular the C677T (Ala222Val) polymorphism were recently associated ...
Epistasis between COMT and MTHFR in Maternal-Fetal Dyads Is Associated with Increased Risk for PreeclampsiaEpistasis between COMT and MTHFR in Maternal-Fetal Dyads Is Associated with Increased Risk for Preeclampsia
(2011)
Preeclampsia is a leading cause of perinatal morbidity and mortality. This disorder is thought to be multifactorial in origin, with multiple genes, environmental and social factors, contributing to disease. One proposed ...
C677T and A1298C MTHFR gene polymorphisms and response to fluoropyrimidine-based chemotherapy in Mestizo patients with metastatic colorectal cancer
(2021-06)
Objective: To assess the association between C677T and A1298C methylenetetrahydrofolate reductase (MTHFR) single-nucleotide polymorphisms (SNPs) and response to first-line fluoropyrimidine-based chemotherapy for metastatic ...
EFECTO DE LOS FACTORES DE RIESGO GENÉTICO-AMBIENTALES SOBRE EL GRADO DE ASOCIACIÓN DE LAS VARIANTES MTHFR C677T Y A1298C Y EL AUMENTO EN EL RIESGO DE DEFECTOS DE CIERRE DEL TUBO NEURAL EN RECIÉN NACIDOS
(Biblioteca Digital wdg.biblioUniversidad de Guadalajara, 2021-02-01)
Introducción. Las variantes C677T y A1298C de la enzima 5,10-metilen-tetrahidrofolato reductasa (MTHFR) han sido implicadas como riesgo para defectos de cierre del tubo neural (DCTN). En niños con DCTN, encontramos un solo ...
Association between the MTHFR A1298C polymorphism and increased risk of acute myeloid leukemia in Brazilian children
(Taylor & Francis LtdAbingdonInglaterra, 2006)