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Plasma Total Cysteine and Cardiovascular Risk Burden: Action and Interaction

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Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI

(2011) Bas J.M. Peters et al.   ATHEROSCLEROSIS

Hepatic metabolism of retinoids and disease associations

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Racial/Ethnic Variation in the Association of Lipid-Related Genetic Variants With Blood Lipids in the US Adult Population

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Novel mutations in scavenger receptor BI associated with high HDL cholesterol in humans

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Plasma deoxysphingolipids: a novel class of biomarkers for the metabolic syndrome?

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Depletion of Bhmt Elevatessonic hedgehogTranscript Level and Increases β-Cell Number in Zebrafish

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Association between 11 genetic polymorphisms in folate-metabolising genes and head and neck cancer risk

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Common Variants of Homocysteine Metabolism Pathway Genes and Risk of Type 2 Diabetes and Related Traits in Indians

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Weight loss amelioration of non-alcoholic steatohepatitis linked to shifts in hepatic ceramide expression and serum ceramide levels

(2011) Kittichai Promrat et al.   HEPATOLOGY RESEARCH

Genome-wide association study identifies common variants associated with circulating vitamin E levels

(2011) Jacqueline M. Major et al.   HUMAN MOLECULAR GENETICS

Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I

(2011) Annelies Rotthier et al.   HUMAN MUTATION

Deletion of Betaine-HomocysteineS-Methyltransferase in Mice Perturbs Choline and 1-Carbon Metabolism, Resulting in Fatty Liver and Hepatocellular Carcinomas

(2011) Ya-Wen Teng et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Oral l-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1

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Gene Polymorphisms and Low Dietary Intake of Micronutrients in Coronary Artery Disease

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Impairment of the ABCA1 and SR-BI-mediated cholesterol efflux pathways and HDL anti-inflammatory activity in Alzheimer's disease

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The role of zinc in genomic stability

(2011) Razinah Sharif et al.   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS

Genetic Variant of the Scavenger Receptor BI in Humans

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Signaling by vitamin A and retinol-binding protein regulates gene expression to inhibit insulin responses

(2011) D. C. Berry et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Impact of gene variants on sex-specific regulation of human Scavenger receptor class B type 1 (SR-BI) expression in liver and association with lipid levels in a population-based study

(2010) Ornit Chiba-Falek et al.   BMC Medical Genetics

Association of a Functional Polymorphism in the Cholesteryl Ester Transfer Protein (CETP) Gene With Memory Decline and Incidence of Dementia

(2010) Amy E. Sanders   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Newborn Serum Retinoic Acid Level Is Associated With Variants of Genes in the Retinol Metabolism Pathway

(2010) Daniel C Manolescu et al.   PEDIATRIC RESEARCH

Endotoxin activates de novo sphingolipid biosynthesis via nuclear factor kappa B-mediated upregulation of Sptlc2

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Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations

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Relation of plasma homocysteine levels to atherosclerotic vascular disease and inflammation markers in type 2 diabetic patients

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The Molecular Basis of Retinoid Absorption

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