Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia - Test2 - elhamkhani - TriplyDB

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

http://www.wikidata.org/entity/Q24643127

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Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study Mutations in the SLC2A9 gene cause hyperuricosuria and hyperuricemia in the dog Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum RNAi-based functional profiling of loci from blood lipid genome-wide association studies identifies genes with cholesterol-regulatory function Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study Common variants at 30 loci contribute to polygenic dyslipidemia Association between a literature-based genetic risk score and cardiovascular events in women Biological, clinical and population relevance of 95 loci for blood lipids The genetics of hyperuricaemia and gout Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13 Genome-wide association study of biochemical traits in Korcula Island, Croatia Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk Correlation of GLUT9 Polymorphisms With Gout Risk Renal transport of uric acid: evolving concepts and uncertainties The anatomical distribution of genetic associations.Natural Products Improving Hyperuricemia with Hepatorenal Dual Effects Sortilin, encoded by the cardiovascular risk gene SORT1, and its suggested functions in cardiovascular disease Genome-wide association study identifies multiple loci influencing human serum metabolite levels Vascular biology of eicosanoids and atherogenesis Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey SLC2A9 is a high-capacity urate transporter in humans Serum uric acid and adiposity: deciphering causality using a bidirectional Mendelian randomization approach Clinical and functional characterization of URAT1 variants A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium A HapMap harvest of insights into the genetics of common disease Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: systematic review and meta-analysis of 14,015 stroke cases and pooled analysis of primary biomarker data from up to 60,883 individuals.Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.The genetic architecture of lipoprotein subclasses in Gullah-speaking African American families enriched for type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid levels in the population on the Samoan islands Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.Association of the rs7395662 SNP in the MADD-FOLH1 and several environmental factors with serum lipid levels in the Mulao and Han populations.Distinct and Shared Determinants of Cardiomyocyte Contractility in Multi-Lineage Competent Ethnically Diverse Human iPSCs.

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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

http://www.wikidata.org/entity/Q24643127

description

2008 nî lūn-bûn

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2008 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2008 թվականի հունվարին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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Genome-wide association study ...... : serum urate and dyslipidemia

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J.AJHG.2007.11.001

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American Journal of Human Genetics

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Genome-wide association study ...... : serum urate and dyslipidemia

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Ana Carolina B Marçano

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Cother Hajat

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Feng Zhang

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Kourosh Ahmadi

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Paul Burton

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P2860

Cloning and expression analysis of a novel member of the facilitative glucose transporter family, SLC2A9 (GLUT9)

The human homologue of flamingo, EGFL2, encodes a brain-expressed large cadherin-like protein with epidermal growth factor-like domains, and maps to chromosome 1p13.3-p21.1

p53 downstream target DDA3 is a novel microtubule-associated protein that interacts with end-binding protein EB3 and activates beta-catenin pathway

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

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139-49

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765309

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10.1016/J.AJHG.2007.11.001

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1

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Stephen J. Newhouse

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40219418

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genome-wide association study

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