A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction.

No abstract is available for this paper.

• Publication year

  1997

• Venue

  Atherosclerosis

• Publication date

  1997-01-03

• Fields of study

  Medicine

• Identifiers
  DOI 10.1016/S0021-9150(96)05977-1PMID 9051203
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• ANÁLISE DA INFLUÊNCIA DO POLIMORFISMO rs1801133 (677C>T) NO GENE MTHFR EM FISSURAS LABIAIS COM OU SEM FISSURA PALATINA NÃO SINDRÔMICAS: ESTUDO DE BASE FAMILIAR E POPULACIONAL PAREADO POR

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• Evidence for an Important Genetic-Environmental Interaction Angiographically Documented Severe Coronary Atherosclerotic Disease: Homocysteine, and Folate in Subjects From Northern Italy With or Without Methylenetetrahydrofolate Reductase C677T Mutation, Plasma

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• Renal Insufficiency in Non-Diabetic Subjects: Relationship of MTHFR C677t Gene Polymorphism and Left Ventricular Hypertrophy

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• Vitamin B12 level in peripheral arterial disease

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• Study on Homocysteine Levels and Methylenetetrahydrofolate Reductase Gene Variant (C677T) in a Population of Buenos Aires City

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• Carrier-state of two or three polymorphic variants of MTHFR, IL-6 and ICAM1 genes increases the risk of coronary artery disease.

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• CHAPTER 9 – Ischemia and Myocardial Infarction: A Post-Genomic Analysis

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• C677T mutation of methylenetetrahydrofolate reductase gene and serum homocysteine levels in Turkish patients with coronary artery disease

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• METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENE C677T POLYMORPHISM IS ASSOCIATED WITH CORONARY ATHEROSCLEROSIS DISEASE IN A SAMPLE OF IRANIAN PATIENTS

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• Equal proportion of adult male and female homozygous for the 677C → T mutation in the methylenetetrahydrofolate reductase polymorphism

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• Elevated plasma homocysteine is positively associated with age independent of C677T mutation of the methylenetetrahydrofolate reductase gene in selected Egyptian subjects

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• Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene.

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• Mutations in the genes regulating methylene tetrahydrofolate reductase (MTHFR C-->T677) and cystathione beta-synthase (CBS G-->A919, CBS T-->c833) are not associated with myocardial infarction in African Americans.

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