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Literature DB >> 23179362

GSTT1 null genotype and risk of coronary heart disease.

Marianne Solhøj Nørskov.

Abstract

Entities: Disease Gene

Mesh：

Substances：
Glutathione Transferase

Year: 2012 PMID： 23179362 DOI： 10.1007/s11033-012-2260-1

Source DB: PubMed Journal: Mol Biol Rep ISSN： 0301-4851 Impact factor: 2.316

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References

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10 in total

1. GSTT1 null genotype contributes to coronary heart disease risk: a meta-analysis.

Authors: Yuming Du; Hongmin Wang; Xin Fu; Rongqing Sun; Yuqian Liu
Journal: Mol Biol Rep Date: 2012-06-24 Impact factor: 2.316

2. Copy number variation in glutathione S-transferases M1 and T1 and ischemic vascular disease: four studies and meta-analyses.

Authors: Marianne S Nørskov; Ruth Frikke-Schmidt; Steffen Loft; Henrik Sillesen; Peer Grande; Børge G Nordestgaard; Anne Tybjaerg-Hansen
Journal: Circ Cardiovasc Genet Date: 2011-05-11

3. Angiotensinogen M235T polymorphism is associated with coronary artery disease severity.

Authors: José R Lanz; Alexandre C Pereira; Pedro A Lemos; Eulogio Martinez; José E Krieger
Journal: Clin Chim Acta Date: 2005-07-19 Impact factor: 3.786

4. Potential risk modifications of GSTT1, GSTM1 and GSTP1 (glutathione-S-transferases) variants and their association to CAD in patients with type-2 diabetes.

Authors: Tharmarajan Ramprasath; Ponniah Senthil Murugan; Ashok Daniel Prabakaran; Pannerselvam Gomathi; Andiappan Rathinavel; Govindan Sadasivam Selvam
Journal: Biochem Biophys Res Commun Date: 2011-02-23 Impact factor: 3.575

5. Glutathione S-transferase gene polymorphism as a susceptibility factor for acute myocardial infarction and smoking in the North Indian population.

Authors: Neha Singh; Nakul Sinha; Sudeep Kumar; Chandra M Pandey; Suraksha Agrawal
Journal: Cardiology Date: 2011-03-10 Impact factor: 1.869

6. Endothelial nitric oxide synthase gene variant modulates the relationship between serum cholesterol levels and blood pressure in the general population: new evidence for a direct effect of lipids in arterial blood pressure.

Authors: A C Pereira; A C Sposito; G F Mota; R S Cunha; F L Herkenhoff; J G Mill; J E Krieger
Journal: Atherosclerosis Date: 2006-01 Impact factor: 5.162

GSTT1 null genotype and risk of coronary heart disease.

1. GSTT1 null genotype contributes to coronary heart disease risk: a meta-analysis.

2. Copy number variation in glutathione S-transferases M1 and T1 and ischemic vascular disease: four studies and meta-analyses.

3. Angiotensinogen M235T polymorphism is associated with coronary artery disease severity.

4. Potential risk modifications of GSTT1, GSTM1 and GSTP1 (glutathione-S-transferases) variants and their association to CAD in patients with type-2 diabetes.

5. Glutathione S-transferase gene polymorphism as a susceptibility factor for acute myocardial infarction and smoking in the North Indian population.

6. Endothelial nitric oxide synthase gene variant modulates the relationship between serum cholesterol levels and blood pressure in the general population: new evidence for a direct effect of lipids in arterial blood pressure.

7. T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian population.

8. DNA repair gene polymorphism is associated with the genetic basis of atherosclerotic coronary artery disease.

9. Association between glutathione S-transferase polymorphisms and triglycerides and HDL-cholesterol.

10. T null and M null genotypes of the glutathione S-transferase gene are risk factor for CAD independent of smoking.