Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene. - Wikidata - awgldk - TriplyDB

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

http://www.wikidata.org/entity/Q30947195

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Gender differences in genetic risk profiles for cardiovascular disease Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability Genetic variation among world populations: inferences from 100 Alu insertion polymorphisms Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia Curcumin and its derivatives: their application in neuropharmacology and neuroscience in the 21st century Apolipoprotein E and apolipoprotein E receptors: normal biology and roles in Alzheimer disease Mild cognitive impairment: diagnosis, longitudinal course, and emerging treatments Accessing genetic variation: genotyping single nucleotide polymorphisms Human DNA sequence variation in a 6.6-kb region containing the melanocortin 1 receptor promoter Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium "Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.Mining genetic epidemiology data with Bayesian networks application to APOE gene variation and plasma lipid levels.Mining genetic epidemiology data with Bayesian networks I: Bayesian networks and example application (plasma apoE levels).New Algorithm and Software (BNOmics) for Inferring and Visualizing Bayesian Networks from Heterogeneous Big Biological and Genetic Data.Simultaneous genotyping of indels and SNPs by mass spectroscopy.GERBIL: Genotype resolution and block identification using likelihood.Primary genetic investigation of a hyperlipidemia model: molecular characteristics and variants of the apolipoprotein E gene in Mongolian gerbil.Context-dependent associations between variation in risk of ischemic heart disease and variation in the 5' promoter region of the apolipoprotein E gene in Danish women.A novel method combining linkage disequilibrium information and imputed functional knowledge for tagSNP selection.Sequence variation and linkage disequilibrium in the human T-cell receptor beta (TCRB) locus Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion.Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.Contribution of regulatory and structural variations in APOE to predicting dyslipidemia.Application of industrial scale genomics to discovery of therapeutic targets in heart failure.The role of apolipoprotein E in Alzheimer's disease.Analysis and exploration of the use of rule-based algorithms and consensus methods for the inferral of haplotypes.Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks.The common polymorphism of apolipoprotein E: geographical aspects and new pathophysiological relations.Haplotypes and the systematic analysis of genetic variation in genes and genomes.Genetic variation and pharmacogenomics: concepts, facts, and challenges.Will haplotype maps be useful for finding genes?Subsets of SNPs define rare genotype classes that predict ischemic heart disease.Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism.Variation in 5' promoter region of the APOE gene contributes to predicting ischemic heart disease (IHD) in the population at large: the Copenhagen City Heart Study Alzheimer's disease models and functional genomics-How many needles are there in the haystack?Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes.Genetic variation and atherosclerosis.Apolipoprotein E-promoter single-nucleotide polymorphisms affect the phenotype of primary open-angle glaucoma and demonstrate interaction with the myocilin gene.DNA sequence variation in a 3.7-kb noncoding sequence 5' of the CYP1A2 gene: implications for human population history and natural selection.Diet and age interactions with regards to cholesterol regulation and brain pathogenesis.

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Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

http://www.wikidata.org/entity/Q30947195

description

2000 nî lūn-bûn

@nan

2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

@zh-hant

2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

@ast

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

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type

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Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

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Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

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Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

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Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

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Genome Research

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Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.

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A G Clark

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D A Nickerson

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J H Stengård

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K M Weiss

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S L Taylor

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S M Fullerton

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V Salomaa

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P2860

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

Statistical method for testing the neutral mutation hypothesis by DNA polymorphism

High polymorphism at the human melanocortin 1 receptor locus

Drift, admixture, and selection in human evolution: a study with DNA polymorphisms

X chromosome evidence for ancient human histories

Archaic African and Asian lineages in the genetic ancestry of modern humans

Base-calling of automated sequencer traces using phred. II. Error probabilities

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

Consed: a graphical tool for sequence finishing

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10.1101/GR.146900

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10

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10

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Eric Boerwinkle

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274414412

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11042151

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310963

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