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Clinical Genetics
|
October 31, 2001
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease
S M Clee, O Loubser, J Collins, et al.
International Journal of Cardiology
|
October 2, 2001
Molecular genetics and gene expression in atherosclerosis
P A Doevendans, W Jukema, W Spiering, et al.
Journal of Lipid Research
|
February 1, 1997
The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes
J A Kuivenhoven, H Pritchard, J Hill, et al.
Journal of Medical Genetics
|
August 1, 1994
Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana
S Tuzgöl, S M Bijvoet, T Bruin, et al.
Biochemical Society Transactions
|
May 1, 1993
Phenotypic variation of mutations in the human lipoprotein-lipase gene
M R Hayden, J J Kastelein, H Funke, et al.
Atherosclerosis
|
March 24, 2000
Paraoxonase gene polymorphisms are associated with carotid arterial wall thickness in subjects with familial hypercholesterolemia
F R Leus, M E Wittekoek, J Prins, et al.
Atherosclerosis. Supplements
|
November 15, 2003
Silent ischaemia in familial hypercholesterolemia
Olivier S Descamps, Antoine de Meester, Paul Cheron, et al.
Annals of Human Genetics
|
March 14, 2001
Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci
D M Hallman, B E Groenemeijer, J W Jukema, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 20, 1998
Increased oxidizability of low-density lipoproteins in hypothyroidism
T Diekman, P N Demacker, J J Kastelein, et al.
The Netherlands Journal of Medicine
|
October 2, 2001
Genetic and metabolic factors predicting risk of cardiovascular disease in familial hypercholesterolemia
T J Smilde, S van Wissen, H Wollersheim, et al.
Page
of 19
Search research articles
Search
Showing results (21-30 of 184) with videos related to
Sort By:
Page
of 19
Clinical Genetics
|
October 31, 2001
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease
S M Clee, O Loubser, J Collins, et al.
International Journal of Cardiology
|
October 2, 2001
Molecular genetics and gene expression in atherosclerosis
P A Doevendans, W Jukema, W Spiering, et al.
Journal of Lipid Research
|
February 1, 1997
The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes
J A Kuivenhoven, H Pritchard, J Hill, et al.
Journal of Medical Genetics
|
August 1, 1994
Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana
S Tuzgöl, S M Bijvoet, T Bruin, et al.
Biochemical Society Transactions
|
May 1, 1993
Phenotypic variation of mutations in the human lipoprotein-lipase gene
M R Hayden, J J Kastelein, H Funke, et al.
Atherosclerosis
|
March 24, 2000
Paraoxonase gene polymorphisms are associated with carotid arterial wall thickness in subjects with familial hypercholesterolemia
F R Leus, M E Wittekoek, J Prins, et al.
Atherosclerosis. Supplements
|
November 15, 2003
Silent ischaemia in familial hypercholesterolemia
Olivier S Descamps, Antoine de Meester, Paul Cheron, et al.
Annals of Human Genetics
|
March 14, 2001
Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci
D M Hallman, B E Groenemeijer, J W Jukema, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 20, 1998
Increased oxidizability of low-density lipoproteins in hypothyroidism
T Diekman, P N Demacker, J J Kastelein, et al.
The Netherlands Journal of Medicine
|
October 2, 2001
Genetic and metabolic factors predicting risk of cardiovascular disease in familial hypercholesterolemia
T J Smilde, S van Wissen, H Wollersheim, et al.
Page
of 19