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A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
(Blackwell Science, 1999-05-01)
We assessed the effect of a recently described mutation in the MTHFR gene (1298 A --> C) on the risk of deep venous thrombosis (DVT) by determining its prevalence in 190 patients with verified DVT and in age-, race- and ...
A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
(Blackwell Science, 1999-05-01)
We assessed the effect of a recently described mutation in the MTHFR gene (1298 A --> C) on the risk of deep venous thrombosis (DVT) by determining its prevalence in 190 patients with verified DVT and in age-, race- and ...
Síndrome metabólico en relación a poliquistosis ovárica y mutación MTHFR: Caso clínico
(Gaceta Médica de Costa Rica, vol. 7, n. 2, julio-diciembre, 2005, 2005)
El síndrome metabólico es una agrupación de factores de riesgo, asociados a la resistencia a la insulina; que predicen la aparición de enfermedad cardiovascular y diabetes. Asimismo se reconoce a la poliquistosis ovárica ...
Síndrome metabólico en relación a poliquistosis ovárica y mutación MTHFR: Caso clínico
(Gaceta Médica de Costa Rica, vol. 7, n. 2, julio-diciembre, 2005, 2005)
El síndrome metabólico es una agrupación de factores de riesgo, asociados a la resistencia a la insulina; que predicen la aparición de enfermedad cardiovascular y diabetes. Asimismo se reconoce a la poliquistosis ovárica ...
Associação do carcinoma epidermóide oral com os polimorfismos MTHFR C677T, MTHFR A1298C e CBS 844ins68 na população do Espírito Santo
(Universidade Federal do Espírito SantoBRPrograma de Pós-Graduação em BiotecnologiaUFESMestrado em Biotecnologia, 2013-09-18)
Associação do carcinoma epidermóide oral com os polimorfismos MTHFR C677T, MTHFR A1298C e CBS 844ins68 na população do Espírito Santo
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil
(BIOMED CENTRAL LTD, 2011)
Background/Aim: Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in particular the C677T (Ala222Val) polymorphism were recently associated to steatosis and fibrosis. We analyzed the frequency ...
Nonsyndromic orofacial clefts in Chile: LINE-1 methylation and MTHFR variants
(Future Medicine, 2020)
Aim: To evaluate the risk of nonsyndromic orofacial clefts (NSOFCs) associated with LINE-1 methylation, as a marker of global DNA methylation, and the effect of MTHFR functional variants on this variable. Patients & methods: ...
Nonsyndromic orofacial clefts in Chile: LINE-1 methylation and MTHFR variants
(2020)
Aim: To evaluate the risk of nonsyndromic orofacial clefts (NSOFCs) associated with LINE-1 methylation, as a marker of global DNA methylation, and the effect of MTHFR functional variants on this variable. Patients & methods: ...
The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease
(Associação Brasileira de Divulgação Científica, 2006-10-01)
Sickle cell disease (SCD) is one of the most common inherited diseases in the world and the patients present notorious clinical heterogeneity. It is known that patients with SCD present activation of the blood coagulation ...
Frequency of 677C -> T and 1298A -> C polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in Turner syndrome individuals
(Sociedade Brasileira de Genética, 2006)