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Publications by Eric Bruckert
Elevated CETP Activity Improves Plasma Cholesterol Efflux Capacity From Human Macrophages in Women
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
LDL-apheresis Depletes apoE-HDL and Pre-Β1-HDL in Familial Hypercholesterolemia: Relevance to Atheroprotection
Journal of Lipid Research
Biochemistry
Endocrinology
Cell Biology
Residual Macrovascular Risk in 2013: What Have We Learned?
Cardiovascular Diabetology
Internal Medicine
Cardiology
Endocrinology
Cardiovascular Medicine
Metabolism
Diabetes
Impact of LDL Apheresis on Atheroprotective Reverse Cholesterol Transport Pathway in Familial Hypercholesterolemia
Journal of Lipid Research
Biochemistry
Endocrinology
Cell Biology
Usefulness of the Genetic Risk Score to Identify Phenocopies in Families With Familial Hypercholesterolemia?
European Journal of Human Genetics
Genetics
Lipoprotein-Apheresis in Familial Hypercholesterolemia: Long-Term Patient Compliance in a French Cohort
Atherosclerosis
Cardiovascular Medicine
Cardiology
Low-Density Lipoprotein Receptor-Deficient Hepatocytes Differentiated From Induced Pluripotent Stem Cells Allow Familial Hypercholesterolemia Modeling, CRISPR/Cas-mediated Genetic Correction, and Productive Hepatitis C Virus Infection
Stem Cell Research and Therapy
Genetics
Cell Biology
Molecular Biology
Biochemistry
Medicine
Molecular Medicine
Clinical and Biochemical Features of Different Molecular Etiologies of Familial Chylomicronemia
Journal of Clinical Lipidology
Internal Medicine
Nutrition
Cardiology
Endocrinology
Cardiovascular Medicine
Dietetics
Metabolism
Diabetes
Lifestyle Intervention Enhances High-Density Lipoprotein Function Among Patients With Metabolic Syndrome Only at Normal Low-Density Lipoprotein Cholesterol Plasma Levels
Journal of Clinical Lipidology
Internal Medicine
Nutrition
Cardiology
Endocrinology
Cardiovascular Medicine
Dietetics
Metabolism
Diabetes
Molecular Analysis and Intestinal Expression of SAR1 Genes and Proteins in Anderson's Disease (Chylomicron Retention Disease)
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
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