Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. - Wikidata - awgldk - TriplyDB

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.

http://www.wikidata.org/entity/Q34144158

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Gender differences in genetic risk profiles for cardiovascular disease Nucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humans Sequence variability of a human pseudogene Evidence for balancing selection from nucleotide sequence analyses of human G6PD Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.Haplotypic analysis of the TNF locus by association efficiency and entropy Primate aging in the mammalian scheme: the puzzle of extreme variation in brain aging Memory loss in Alzheimer's disease Nucleotide sequence analyses of human complement 6 (C6) gene suggest balancing selection Reconstructing human origins in the genomic era Human-specific derived alleles of CD33 and other genes protect against postreproductive cognitive decline Exercise, APOE genotype, and the evolution of the human lifespan Some evolutionary perspectives on Alzheimer's disease pathogenesis and pathology The apolipoprotein E (APOE) gene appears functionally monomorphic in chimpanzees (Pan troglodytes)Evolution in health and medicine Sackler colloquium: Evolution of the human lifespan and diseases of aging: roles of infection, inflammation, and nutrition Human DNA sequence variation in a 6.6-kb region containing the melanocortin 1 receptor promoter Strong selective sweep associated with a transposon insertion in Drosophila simulans.IQ, educational attainment, memory and plasma lipids: associations with apolipoprotein E genotype in 5995 children.Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.Apolipoprotein E and Sex Bias in Cerebrovascular Aging of Men and Mice.Positive selection of protective variants for type 2 diabetes from the Neolithic onward: a case study in Central Asia.Detecting rare variants for complex traits using family and unrelated data.Selection on alleles affecting human longevity and late-life disease: the example of apolipoprotein E.The helix bundle: a reversible lipid binding motif Global haplotype diversity in the human insulin gene region.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.APOE genotype is associated with oral herpetic lesions but not genital or oral herpes simplex virus shedding.Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome Population genetics of CAPN10 and GPR35: implications for the evolution of type 2 diabetes variants.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.Divergence, demography and gene loss along the human lineage.Hitchhiking mapping: a population-based fine-mapping strategy for adaptive mutations in Drosophilamelanogaster.Genetic variation within the Mx gene of commercially selected chicken lines reveals multiple haplotypes, recombination and a protein under selection pressure.Contribution of regulatory and structural variations in APOE to predicting dyslipidemia.HapScope: a software system for automated and visual analysis of functionally annotated haplotypes.Human arsenic methyltransferase (AS3MT) pharmacogenetics: gene resequencing and functional genomics studies.Frequency of APOE, MTHFR and ACE polymorphisms in the Zambian population Tree scanning: a method for using haplotype trees in phenotype/genotype association studies.Coalescent-based association mapping and fine mapping of complex trait loci.

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P2860

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.

http://www.wikidata.org/entity/Q34144158

description

2000 nî lūn-bûn

@nan

2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի սեպտեմբերին 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

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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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Apolipoprotein E variation at ...... of a major human polymorphism.

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American Journal of Human Genetics

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P2093

A G Clark

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C F Sing

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D A Nickerson

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E Vartiainen

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J H Stengârd

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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

Evidence for variable selective pressures at MC1R

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

A test of neutral molecular evolution based on nucleotide data.

Statistical method for testing the neutral mutation hypothesis by DNA polymorphism

Statistical tests of neutrality of mutations.

Properties of statistical tests of neutrality for DNA polymorphism data.

Mitochondrial portraits of human populations using median networks.

Detection of the signature of natural selection in humans: evidence from the Duffy blood group locus

High polymorphism at the human melanocortin 1 receptor locus

Genetic drift in an infinite population. The pseudohitchhiking model

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881-900

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10.1086/303070

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4

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67

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Eric Boerwinkle

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2000-09-13T00:00:00Z

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12336362

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10986041

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1287893

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