From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. - Wikidata - wikimedia - TriplyDB

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

http://www.wikidata.org/entity/Q30374131

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Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study An integrated approach of comparative genomics and heritability analysis of pig and human on obesity trait: evidence for candidate genes on human chromosome 2 Renal dopaminergic system: Pathophysiological implications and clinical perspectives Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Mechanisms for blood pressure lowering and metabolic effects of thiazide and thiazide-like diuretics The thiazide-sensitive Na+-Cl- cotransporter: molecular biology, functional properties, and regulation by WNKs STK39 polymorphism is associated with essential hypertension: a systematic review and meta-analysis Domain-Swapping Switch Point in Ste20 Protein Kinase SPAK Protein Kinases and Parkinson's Disease Epithelial sodium transport and its control by aldosterone: the story of our internal environment revisited A genome-wide association study of hypertension and blood pressure in African Americans Genome-wide association study of blood pressure and hypertension Non-synonymous single-nucleotide polymorphisms associated with blood pressure and hypertension.Salt sensitivity of blood pressure is associated with polymorphisms in the sodium-bicarbonate cotransporter Dopamine and G protein-coupled receptor kinase 4 in the kidney: role in blood pressure regulation.A statistical method for region-based meta-analysis of genome-wide association studies in genetically diverse populations.Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression.Synopsis and data synthesis of genetic association studies in hypertension for the adrenergic receptor family genes: the CUMAGAS-HYPERT database.Rare mutations in renal sodium and potassium transporter genes exhibit impaired transport function.PedHunter 2.0 and its usage to characterize the founder structure of the Old Order Amish of Lancaster County.Extent and distribution of linkage disequilibrium in the Old Order Amish.Mining the pre-diagnostic antibody repertoire of TgMMTV-neu mice to identify autoantibodies useful for the early detection of human breast cancer.Multivariate generalized multifactor dimensionality reduction to detect gene-gene interactions Recent advances in genetics of the spontaneously hypertensive rat.Interactive contribution of serine/threonine kinase 39 gene multiple polymorphisms to hypertension among northeastern Han Chinese.Genetic architecture of complex traits predisposing to nephropathy: hypertension.An Exploration of Gene-Gene Interactions and Their Effects on Hypertension Parkinson's disease-implicated kinases in the brain; insights into disease pathogenesis.Genome-wide association studies: contribution of genomics to understanding blood pressure and essential hypertension Genome-wide case/control studies in hypertension: only the 'tip of the iceberg'.The genetics of obesity and the metabolic syndrome.Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension.Signaling mechanisms that link salt retention to hypertension: endogenous ouabain, the Na(+) pump, the Na(+)/Ca(2+) exchanger and TRPC proteins.Lack of association between polymorphisms in STK39, a putative thiazide response gene, and blood pressure response to hydrochlorothiazide Integrated statistical and pathway approach to next-generation sequencing analysis: a family-based study of hypertension.Practical investigation of the performance of robust logistic regression to predict the genetic risk of hypertension.Extracellular water and blood pressure in adults with growth hormone (GH) deficiency: a genotype-phenotype association study.Blood pressure and human genetic variation in the general population.A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.

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From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

http://www.wikidata.org/entity/Q30374131

description

2008 nî lūn-bûn

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2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2008 թվականի դեկտեմբերին 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年论文

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P2860

Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.

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

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

A common allele on chromosome 9 associated with coronary heart disease

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

HLA and mate choice in humans

Haploview: analysis and visualization of LD and haplotype maps

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