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Relations between markers of renal function, coronary risk factors and the occurrence and severity of coronary artery disease

Atherosclerosis, 2008-04, Vol.197 (2), p.853-859

2008

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Nitric oxide induces and inhibits apoptosis through different pathways

FEBS letters, 1998-08, Vol.433 (1), p.125-131

1998

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Effect of CYP1A1 MspI polymorphism on cigarette smoking related coronary artery disease and diabetes

Atherosclerosis, 2002-06, Vol.162 (2), p.391-397

2002

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Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

Arteriosclerosis, thrombosis, and vascular biology, 1996-07, Vol.16 (7), p.878

1996

Volltextzugriff (PDF)

Physiology of the normal heart

Medicine (Abingdon. 1995, UK ed.), 2014-08, Vol.42 (8), p.409-412

Wilcken, David E.L

2014

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Physiology of the normal heart

Surgery (Oxford), 2015-02, Vol.33 (2), p.43-46

Wilcken, David E.L

2015

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Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study

Arteriosclerosis, thrombosis, and vascular biology, 2001-12, Vol.21 (12), p.2080

2001

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Relations between plasma asymmetric dimethylarginine (ADMA) and risk factors for coronary disease

Atherosclerosis, 2006-02, Vol.184 (2), p.383-388

2006

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Obesity, Type II diabetes and the Ala54Thr polymorphism of fatty acid binding protein 2 in the Tongan population

Molecular genetics and metabolism, 2003-07, Vol.79 (3), p.183-188

2003

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A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene

Nature medicine, 1996-01, Vol.2 (1), p.41-45

1996

Volltextzugriff (PDF)

Physiology of the normal heart

Surgery (Oxford), 2012, Vol.30 (1), p.1-4

Wilcken, David E.L

2012

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Physiology of the normal heart

Medicine (Abingdon. 1995, UK ed.), 2010, Vol.38 (7), p.336-339

Wilcken, David E.L

2010

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Human cytomegalovirus immediate early proteins upregulate endothelial p53 function

FEBS letters, 2000-06, Vol.474 (2), p.213-216

2000

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Genetic polymorphism of heparan sulfate proteoglycan (Perlecan, HSPG2), lipid profiles and coronary artery disease in the Australian population

Atherosclerosis, 2000, Vol.148 (1), p.125-129

2000

Volltextzugriff (PDF)

Physiology of the normal heart

Surgery (Oxford), 2018-02, Vol.36 (2), p.48-51

Wilcken, David E.L.

2018

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Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population

Atherosclerosis, 1999-09, Vol.146 (1), p.133-140

1999

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Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease : The result of a meta-analysis

Circulation (New York, N.Y.), 1998-12, Vol.98 (23), p.2520-2526

1998

Volltextzugriff (PDF)

Angiotensin-converting enzyme genotype in children and coronary events in their grandparents

Circulation (New York, N.Y.), 1995-03, Vol.91 (6), p.1655-1658

1995

Volltextzugriff (PDF)

Asymmetric dimethylarginine (ADMA) in vascular, renal and hepatic disease and the regulatory role of l-arginine on its metabolism

Molecular genetics and metabolism, 2007-08, Vol.91 (4), p.309-317

2007

Volltextzugriff (PDF)

Genetic contribution of the endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.3147

1997

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Homocysteine and its disulfide derivatives: a suggested consensus terminology

Arteriosclerosis, thrombosis, and vascular biology, 2000-07, Vol.20 (7), p.1704

2000

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Association between an angiotensinogen microsatellite marker in children and coronary events in their grandparents

Circulation (New York, N.Y.), 1996-06, Vol.93 (12), p.2092-2096

1996

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Relationship between homocysteine and superoxide dismutase in homocystinuria: possible relevance to cardiovascular risk

Arteriosclerosis, thrombosis, and vascular biology, 2000-05, Vol.20 (5), p.1199

2000

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Reply to "Cardiovascular disease risk"

Nature medicine, 1996-04, Vol.2 (4), p.366-366

1996

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The Glu-298→Asp (894G→T) mutation at exon 7 of the endothelial nitric oxide synthase gene and coronary artery disease

Journal of molecular medicine (Berlin, Germany), 1999-06, Vol.77 (6), p.511-514

1999

Volltextzugriff (PDF)

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Relations between markers of renal function, coronary risk factors and the occurrence and severity of coronary artery disease

Nitric oxide induces and inhibits apoptosis through different pathways

Effect of CYP1A1 MspI polymorphism on cigarette smoking related coronary artery disease and diabetes

Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

Physiology of the normal heart

Physiology of the normal heart

Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study

Relations between plasma asymmetric dimethylarginine (ADMA) and risk factors for coronary disease

Obesity, Type II diabetes and the Ala54Thr polymorphism of fatty acid binding protein 2 in the Tongan population

A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene

Physiology of the normal heart

Physiology of the normal heart

Human cytomegalovirus immediate early proteins upregulate endothelial p53 function

Genetic polymorphism of heparan sulfate proteoglycan (Perlecan, HSPG2), lipid profiles and coronary artery disease in the Australian population

Physiology of the normal heart

Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease : The result of a meta-analysis

Angiotensin-converting enzyme genotype in children and coronary events in their grandparents

Asymmetric dimethylarginine (ADMA) in vascular, renal and hepatic disease and the regulatory role of l-arginine on its metabolism

Genetic contribution of the endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels

Homocysteine and its disulfide derivatives: a suggested consensus terminology

Association between an angiotensinogen microsatellite marker in children and coronary events in their grandparents

Relationship between homocysteine and superoxide dismutase in homocystinuria: possible relevance to cardiovascular risk

Reply to "Cardiovascular disease risk"

The Glu-298→Asp (894G→T) mutation at exon 7 of the endothelial nitric oxide synthase gene and coronary artery disease

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