Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes

Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes

Bibliografische gegevens
Hoofdauteurs:	Newhouse, S, Wallace, C, Hoti, M, Burke, B, Marcano, A, Onipinla, A, Dobson, R, Mein, C, Clayton, D, Samani, N, Dominiczak, A, Brown, M, Webster, J, Lathrop, M, Farrall, M, Connell, J, Caulfield, M, Munroe, P
Formaat:	Journal article
Gepubliceerd in:	2007

Gelijkaardige items

Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
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No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study
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WNK1 - functional analyses of variants associated with blood pressure and essential hypertension
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WNK1-functional analyses of variants associated with blood pressure and essential hypertension
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Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
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Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
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Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study.
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Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study
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Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study
door: Wallace, C, et al.
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Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
door: Newhouse, S, et al.
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Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.
door: Munroe, P, et al.
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Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
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Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
door: Stephen Newhouse, et al.
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Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study.
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Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.
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Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
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Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension
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Genomewide linkage analysis for loci affecting electrocardiographic LV mass
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Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study
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Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.
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Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study
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Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study
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Discovery of novel genes for serum urate and low-density lipoprotein cholesterol - Two biomarkers of cardiovascular disease
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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
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Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension
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Association between variants of the human GSTM gene family and hypertension
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A new tool for checks of data precision within the MRC British genetics of hypertension study
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Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study
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The MRC British Genetics of Hypertension Study - Genome-wide screen results
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Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study.
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Genome-wide mapping of human loci for essential hypertension.
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Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study.
door: Freel, E, et al.
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No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study.
door: Knight, J, et al.
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Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians.
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The Post-Translational Modification Networking in WNK-Centric Hypertension Regulation and Electrolyte Homeostasis
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The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource
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Glutathione S-transferase variants and hypertension.
door: Delles, C, et al.
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Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension.
door: Alvarez-Madrazo, S, et al.
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Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array.
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Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
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