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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
(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
(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: ...
Prevalencia de la mutación c677t en la enzima MTHFR en adultos del Valle Central de Costa Rica
(2005-11)
En Costa Rica la enfermedad cardiovascular (ECV) representa la primera causa de muerte desde la década de 1970 razón por la cual el estudio de los factores de riesgo asociados a esta patología resulta de gran importancia. ...
Prevalencia de la mutación c677t en la enzima MTHFR en adultos del Valle Central de Costa Rica
(2005-11)
En Costa Rica la enfermedad cardiovascular (ECV) representa la primera causa de muerte desde la década de 1970 razón por la cual el estudio de los factores de riesgo asociados a esta patología resulta de gran importancia. ...