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G Assmann

Showing results (391-400 of 495) with videos related to

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Biochemical and Biophysical Research Communications|February 13, 2001
Genomic sequence and structure of the human ABCG1 (ABC8) geneS Lorkowski, S Rust, T Engel, et al.
Circulation|August 18, 1999
Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhoodU Nowak-Göttl, R Junker, M Hartmeier, et al.
Journal of Lipid Research|June 1, 1997
A natural apolipoprotein A-I variant, apoA-I (L141R)Pisa, interferes with the formation of alpha-high density lipoproteins (HDL) but not with the formation of pre beta 1-HDL and influences efflux of cholesterol into plasmaR Miccoli, Y Zhu, U Daum, et al.
Circulation|November 5, 1999
Coronary heart disease: reducing the risk: a worldwide view. International Task Force for the Prevention of Coronary Heart DiseaseG Assmann, R Carmena, P Cullen, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 8, 1999
Hypochromic red cells and reticulocyte haemglobin content as markers of iron-deficient erythropoiesis in patients undergoing chronic haemodialysisP Cullen, J Söffker, M Höpfl, et al.
The Journal of Clinical Investigation|July 15, 1996
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)J A Kuivenhoven, H Weibusch, P H Pritchard, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Plasminogen activator inhibitor-1 4G/5G-polymorphism and factor V Q506 mutation are not associated with myocardial infarction in young menR Junker, J Heinrich, H Schulte, et al.
Circulation|March 18, 1997
Low-density lipoproteins inhibit the Na+/H+ antiport in human platelets. A novel mechanism enhancing platelet activity in hypercholesterolemiaJ R Nofer, M Tepel, B Kehrel, et al.
Human Mutation|January 1, 1996
Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT geneJ S Owen, H Wiebusch, P Cullen, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 5, 2000
Transforming growth factor beta and coronary artery diseaseH Reinecke, M Erren, J O Schurek, et al.
Pageof 50

Showing results (391-400 of 495) with videos related to

Sort By:
Pageof 50
Biochemical and Biophysical Research Communications|February 13, 2001
Genomic sequence and structure of the human ABCG1 (ABC8) geneS Lorkowski, S Rust, T Engel, et al.
Circulation|August 18, 1999
Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhoodU Nowak-Göttl, R Junker, M Hartmeier, et al.
Journal of Lipid Research|June 1, 1997
A natural apolipoprotein A-I variant, apoA-I (L141R)Pisa, interferes with the formation of alpha-high density lipoproteins (HDL) but not with the formation of pre beta 1-HDL and influences efflux of cholesterol into plasmaR Miccoli, Y Zhu, U Daum, et al.
Circulation|November 5, 1999
Coronary heart disease: reducing the risk: a worldwide view. International Task Force for the Prevention of Coronary Heart DiseaseG Assmann, R Carmena, P Cullen, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 8, 1999
Hypochromic red cells and reticulocyte haemglobin content as markers of iron-deficient erythropoiesis in patients undergoing chronic haemodialysisP Cullen, J Söffker, M Höpfl, et al.
The Journal of Clinical Investigation|July 15, 1996
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)J A Kuivenhoven, H Weibusch, P H Pritchard, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Plasminogen activator inhibitor-1 4G/5G-polymorphism and factor V Q506 mutation are not associated with myocardial infarction in young menR Junker, J Heinrich, H Schulte, et al.
Circulation|March 18, 1997
Low-density lipoproteins inhibit the Na+/H+ antiport in human platelets. A novel mechanism enhancing platelet activity in hypercholesterolemiaJ R Nofer, M Tepel, B Kehrel, et al.
Human Mutation|January 1, 1996
Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT geneJ S Owen, H Wiebusch, P Cullen, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 5, 2000
Transforming growth factor beta and coronary artery diseaseH Reinecke, M Erren, J O Schurek, et al.
Pageof 50