Multiple genes for essential-hypertension susceptibility on chromosome 1q. - Wikidata - wikimedia - TriplyDB

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

http://www.wikidata.org/entity/Q35616722

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Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan Variations in DNA elucidate molecular networks that cause disease Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study Fcγ receptors and ligands and cardiovascular disease Genome-wide association study of blood pressure and hypertension From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.PDGF-dependent regulation of regulator of G protein signaling-5 expression and vascular smooth muscle cell functionality.Detecting gene-by-smoking interactions in a genome-wide association study of early-onset coronary heart disease using random forests.Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships Genetic architecture of complex traits predisposing to nephropathy: hypertension.Genetic analysis of blood pressure in 8 mouse intercross populations Is There a Role for Genomics in the Management of Hypertension?Blood pressure response to potassium supplementation is associated with genetic variation in endothelin 1 and interactions with E selectin in rural Chinese.SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension.Common variants at ten loci modulate the QT interval duration in the QTSCD Study.Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study Association of SELE genotypes/haplotypes with sE-selectin levels in Taiwanese individuals: interactive effect of MMP9 level.Mendelian Inheritance in Man and its online version, OMIM Refined mapping of the renal failure RF-3 quantitative trait locus.A polymorphic 3'UTR element in ATP1B1 regulates alternative polyadenylation and is associated with blood pressure Regulator of G-protein signaling-5 is a marker of hepatic stellate cells and expression mediates response to liver injury P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans.Regulator of G-Protein Signaling 5 Reduces HeyA8 Ovarian Cancer Cell Proliferation and Extends Survival in a Murine Tumor Model.Genetic analysis of albuminuria in collaborative cross and multiple mouse intercross populations.PPARγ regulates resistance vessel tone through a mechanism involving RGS5-mediated control of protein kinase C and BKCa channel activity.Generation and characterization of rgs5 mutant mice.Rgs5 targeting leads to chronic low blood pressure and a lean body habitus.Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites.Genes for blood pressure: an opportunity to understand hypertension Pharmacogenomic association of nonsynonymous SNPs in SIGLEC12, A1BG, and the selectin region and cardiovascular outcomes.Hereditary determinants of human hypertension: strategies in the setting of genetic complexity.Genetic effect on blood pressure is modulated by age: the Hypertension Genetic Epidemiology Network Study.Pathogenesis of essential hypertension: historical paradigms and modern insights.Association of ATP1B1, RGS5 and SELE polymorphisms with hypertension and blood pressure in African-Americans.Adrenergic signaling polymorphisms and their impact on cardiovascular disease.Between candidate genes and whole genomes: time for alternative approaches in blood pressure genetics.E-selectin gene polymorphism (A561C) and essential hypertension. Meta-analysis in the Chinese population.Antihypertensive effects of peroxisome proliferator-activated receptor-β/δ activation.Recent Advances in the Genetics of Hypertension.

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P2860

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

http://www.wikidata.org/entity/Q35616722

description

2006 nî lūn-bûn

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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2006年论文

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2006年论文

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name

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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type

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Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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American Journal of Human Genetics

P1476

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

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P2093

Alan B Weder

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Amy Luke

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Aravinda Chakravarti

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D C Rao

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James Dae Ok Kim

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Marnie R Layton

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Morna A Ikeda

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Richard S Cooper

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Steve C Hunt

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Xin Liu

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P2860

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Molecular cloning and sequence analysis of human Na,K-ATPase beta-subunit

The structure of haplotype blocks in the human genome

Haploview: analysis and visualization of LD and haplotype maps

Differential gene expression during capillary morphogenesis in 3D collagen matrices: regulated expression of genes involved in basement membrane matrix assembly, cell cycle progression, cellular differentiation and G-protein signaling

Human hypertension caused by mutations in WNK kinases

Global burden of hypertension: analysis of worldwide data

Cellular regulation of RGS proteins: modulators and integrators of G protein signaling

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics.

The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.

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10.1086/510918

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Eric Boerwinkle

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