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C-reactive protein and angiographic characteristics of stable and unstable coronary artery disease: Data from the prospective PREVEND cohort

Atherosclerosis, 2008-01, Vol.196 (1), p.372-382

2008

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Pharmacological regulation of cholesterol efflux in human monocyte-derived macrophages in the absence of exogenous cholesterol acceptors

Atherosclerosis, 2005-04, Vol.179 (2), p.229-236

2005

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Lipoprotein distribution and biological variation of 24S- and 27-hydroxycholesterol in healthy volunteers

Atherosclerosis, 2007-09, Vol.194 (1), p.71-78

2007

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High density lipoproteins and reverse cholesterol transport: Lessons from mutations

Atherosclerosis, 1998-04, Vol.137, p.S7-S11

1998

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Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in Tunisia

Atherosclerosis, 2009-04, Vol.203 (2), p.449-453

2009

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DNA polymorphisms of the apolipoprotein B gene in patients with premature coronary artery disease

Atherosclerosis, 1990-05, Vol.82 (1), p.7-17

1990

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The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia

Atherosclerosis, 2002-11, Vol.165 (1), p.127-135

2002

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β-VLDL accumulation in familial dysbetalipoproteinemia is associated with increased exchange or diffusion of chylomicron lipids to apo B-100 containing triglyceride-rich lipoproteins

Atherosclerosis, 1998-06, Vol.138 (2), p.301-312

1998

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Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations

Atherosclerosis, 1998-02, Vol.136 (2), p.247-254

1998

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Atorvastatin increases low-density lipoprotein size and enhances high-density lipoprotein cholesterol concentration in male, but not in female patients with familial hypercholesterolemia

Atherosclerosis, 1999-09, Vol.146 (1), p.167-174

1999

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Molecular genetic analysis of familial hypercholesterolemia: spectrum and regional difference of LDL receptor gene mutations in Japanese population

Atherosclerosis, 2002-12, Vol.165 (2), p.335-342

2002

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Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

Atherosclerosis, 1990, Vol.80 (3), p.235-242

1990

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Increased degradation of low density lipoproteins by mononuclear leukocytes associated with coronary artery disease

Atherosclerosis, 1990-12, Vol.85 (2), p.127-137

1990

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The effect of apolipoprotein E genotype on serum lipoprotein particle response to exercise

Atherosclerosis, 2006-09, Vol.188 (1), p.126-133

2006

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Ciprofibrate therapy normalises the atherogenic low-density lipoprotein subspecies profile in combined hyperlipidemia

Atherosclerosis, 1993-04, Vol.100 (1), p.91-102

1993

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Effect of apolipoprotein E and insulin resistance on VLDL particles in combined hyperlipidemic patients

Atherosclerosis, 1996-10, Vol.126 (2), p.197-205

1996

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The relationship of vitamin D deficiency to statin myopathy

Atherosclerosis, 2011-03, Vol.215 (1), p.23-29

2011

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3-Hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors, atorvastatin and simvastatin, induce apoptosis of vascular smooth muscle cells by downregulation of Bcl-2 expression and Rho A prenylation

Atherosclerosis, 2002-03, Vol.161 (1), p.17-26

2002

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Oxidants and antioxidants in the pathogenesis of atherosclerosis: implications for the oxidized low density lipoprotein hypothesis

Atherosclerosis, 1998-11, Vol.141 (1), p.1-15

Heinecke, Jay W

1998

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A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia

Atherosclerosis, 2003-05, Vol.168 (1), p.1-14

2003

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Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease

Atherosclerosis, 1992-10, Vol.96 (2), p.91-107

1992

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Ability of the LDL receptor from several animal species to recognize the human apo B binding domain: studies with LDL from familial defective apo B-100

Atherosclerosis, 1992-03, Vol.93 (1), p.95-103

1992

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Metabolic modes of action of the statins in the hyperlipoproteinemias

Atherosclerosis, 1998-12, Vol.141 (2), p.203-207

1998

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SC-435, an ileal apical sodium co-dependent bile acid transporter (ASBT) inhibitor lowers plasma cholesterol and reduces atherosclerosis in guinea pigs

Atherosclerosis, 2003-12, Vol.171 (2), p.201-210

2003

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C-reactive protein and angiographic characteristics of stable and unstable coronary artery disease: Data from the prospective PREVEND cohort

Pharmacological regulation of cholesterol efflux in human monocyte-derived macrophages in the absence of exogenous cholesterol acceptors

Lipoprotein distribution and biological variation of 24S- and 27-hydroxycholesterol in healthy volunteers

High density lipoproteins and reverse cholesterol transport: Lessons from mutations

Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in Tunisia

DNA polymorphisms of the apolipoprotein B gene in patients with premature coronary artery disease

The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia

β-VLDL accumulation in familial dysbetalipoproteinemia is associated with increased exchange or diffusion of chylomicron lipids to apo B-100 containing triglyceride-rich lipoproteins

Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations

Atorvastatin increases low-density lipoprotein size and enhances high-density lipoprotein cholesterol concentration in male, but not in female patients with familial hypercholesterolemia

Molecular genetic analysis of familial hypercholesterolemia: spectrum and regional difference of LDL receptor gene mutations in Japanese population

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

Increased degradation of low density lipoproteins by mononuclear leukocytes associated with coronary artery disease

The effect of apolipoprotein E genotype on serum lipoprotein particle response to exercise

Ciprofibrate therapy normalises the atherogenic low-density lipoprotein subspecies profile in combined hyperlipidemia

Effect of apolipoprotein E and insulin resistance on VLDL particles in combined hyperlipidemic patients

Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia

The relationship of vitamin D deficiency to statin myopathy

3-Hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors, atorvastatin and simvastatin, induce apoptosis of vascular smooth muscle cells by downregulation of Bcl-2 expression and Rho A prenylation

Oxidants and antioxidants in the pathogenesis of atherosclerosis: implications for the oxidized low density lipoprotein hypothesis

A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia

Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease

Ability of the LDL receptor from several animal species to recognize the human apo B binding domain: studies with LDL from familial defective apo B-100

Metabolic modes of action of the statins in the hyperlipoproteinemias

SC-435, an ileal apical sodium co-dependent bile acid transporter (ASBT) inhibitor lowers plasma cholesterol and reduces atherosclerosis in guinea pigs

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