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

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	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
التنسيق:	Journal article
منشور في:	2007

مواد مشابهة

Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
حسب: Newhouse, S, وآخرون
منشور في: (2007)

No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study
حسب: Newhouse, S, وآخرون
منشور في: (2004)

WNK1 - functional analyses of variants associated with blood pressure and essential hypertension
حسب: Hoti, M, وآخرون
منشور في: (2008)

WNK1-functional analyses of variants associated with blood pressure and essential hypertension
حسب: Hoti, M, وآخرون
منشور في: (2008)

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
حسب: Newhouse, S, وآخرون
منشور في: (2005)

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
حسب: Wallace, C, وآخرون
منشور في: (2006)

Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study.
حسب: Munroe, P, وآخرون
منشور في: (2006)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study
حسب: Wallace, C, وآخرون
منشور في: (2005)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study
حسب: Wallace, C, وآخرون
منشور في: (2005)

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
حسب: Newhouse, S, وآخرون
منشور في: (2009)

Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.
حسب: Munroe, P, وآخرون
منشور في: (2005)

Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
حسب: Brown, M, وآخرون
منشور في: (2008)

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
حسب: Stephen Newhouse, وآخرون
منشور في: (2009-01-01)

Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study.
حسب: Padmanabhan, S, وآخرون
منشور في: (2006)

Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.
حسب: Padmanabhan, S, وآخرون
منشور في: (2005)

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
حسب: Bell, J, وآخرون
منشور في: (2006)

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension
حسب: Tzenova Bell, J, وآخرون
منشور في: (2006)

Genomewide linkage analysis for loci affecting electrocardiographic LV mass
حسب: Padmanabhan, S, وآخرون
منشور في: (2006)

Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study
حسب: Padmanabhan, S, وآخرون
منشور في: (2005)

Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.
حسب: Marçano, A, وآخرون
منشور في: (2007)

Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study
حسب: Padmanabhan, S, وآخرون
منشور في: (2007)

Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study
حسب: Padmanabhan, S, وآخرون
منشور في: (2006)

Discovery of novel genes for serum urate and low-density lipoprotein cholesterol - Two biomarkers of cardiovascular disease
حسب: Wallace, C, وآخرون
منشور في: (2007)

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
حسب: Wallace, C, وآخرون
منشور في: (2008)

Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension
حسب: Delles, C, وآخرون
منشور في: (2006)

Association between variants of the human GSTM gene family and hypertension
حسب: Delles, C, وآخرون
منشور في: (2006)

A new tool for checks of data precision within the MRC British genetics of hypertension study
حسب: Caulfield, M, وآخرون
منشور في: (2000)

Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study
حسب: Padmanabhan, S, وآخرون
منشور في: (2007)

The MRC British Genetics of Hypertension Study - Genome-wide screen results
حسب: Caulfield, M, وآخرون
منشور في: (2002)

Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study.
حسب: Munroe, P, وآخرون
منشور في: (2000)

Genome-wide mapping of human loci for essential hypertension.
حسب: Caulfield, M, وآخرون
منشور في: (2003)

Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study.
حسب: Freel, E, وآخرون
منشور في: (2007)

No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study.
حسب: Knight, J, وآخرون
منشور في: (2001)

Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians.
حسب: Alvarez-Madrazo, S, وآخرون
منشور في: (2010)

The Post-Translational Modification Networking in WNK-Centric Hypertension Regulation and Electrolyte Homeostasis
حسب: Shiuan-Chen Lin, وآخرون
منشور في: (2022-09-01)

The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource
حسب: Munroe, P, وآخرون
منشور في: (2004)

Glutathione S-transferase variants and hypertension.
حسب: Delles, C, وآخرون
منشور في: (2008)

Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension.
حسب: Alvarez-Madrazo, S, وآخرون
منشور في: (2013)

Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array.
حسب: Sober, S, وآخرون
منشور في: (2009)

Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
حسب: Barr, M, وآخرون
منشور في: (2007)