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

ग्रंथसूची विवरण
मुख्य लेखकों:	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
स्वरूप:	Journal article
प्रकाशित:	2007

समान संसाधन

Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
द्वारा: Newhouse, S, और अन्य
प्रकाशित: (2007)

No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study
द्वारा: Newhouse, S, और अन्य
प्रकाशित: (2004)

WNK1 - functional analyses of variants associated with blood pressure and essential hypertension
द्वारा: Hoti, M, और अन्य
प्रकाशित: (2008)

WNK1-functional analyses of variants associated with blood pressure and essential hypertension
द्वारा: Hoti, M, और अन्य
प्रकाशित: (2008)

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
द्वारा: Newhouse, S, और अन्य
प्रकाशित: (2005)

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
द्वारा: Wallace, C, और अन्य
प्रकाशित: (2006)

Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study.
द्वारा: Munroe, P, और अन्य
प्रकाशित: (2006)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study
द्वारा: Wallace, C, और अन्य
प्रकाशित: (2005)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study
द्वारा: Wallace, C, और अन्य
प्रकाशित: (2005)

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
द्वारा: Newhouse, S, और अन्य
प्रकाशित: (2009)

Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.
द्वारा: Munroe, P, और अन्य
प्रकाशित: (2005)

Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
द्वारा: Brown, M, और अन्य
प्रकाशित: (2008)

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
द्वारा: Stephen Newhouse, और अन्य
प्रकाशित: (2009-01-01)

Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study.
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2006)

Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2005)

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
द्वारा: Bell, J, और अन्य
प्रकाशित: (2006)

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension
द्वारा: Tzenova Bell, J, और अन्य
प्रकाशित: (2006)

Genomewide linkage analysis for loci affecting electrocardiographic LV mass
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2006)

Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2005)

Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.
द्वारा: Marçano, A, और अन्य
प्रकाशित: (2007)

Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2007)

Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2006)

Discovery of novel genes for serum urate and low-density lipoprotein cholesterol - Two biomarkers of cardiovascular disease
द्वारा: Wallace, C, और अन्य
प्रकाशित: (2007)

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
द्वारा: Wallace, C, और अन्य
प्रकाशित: (2008)

Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension
द्वारा: Delles, C, और अन्य
प्रकाशित: (2006)

Association between variants of the human GSTM gene family and hypertension
द्वारा: Delles, C, और अन्य
प्रकाशित: (2006)

A new tool for checks of data precision within the MRC British genetics of hypertension study
द्वारा: Caulfield, M, और अन्य
प्रकाशित: (2000)

Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study
द्वारा: Padmanabhan, S, और अन्य
प्रकाशित: (2007)

The MRC British Genetics of Hypertension Study - Genome-wide screen results
द्वारा: Caulfield, M, और अन्य
प्रकाशित: (2002)

Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study.
द्वारा: Munroe, P, और अन्य
प्रकाशित: (2000)

Genome-wide mapping of human loci for essential hypertension.
द्वारा: Caulfield, M, और अन्य
प्रकाशित: (2003)

Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study.
द्वारा: Freel, E, और अन्य
प्रकाशित: (2007)

No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study.
द्वारा: Knight, J, और अन्य
प्रकाशित: (2001)

Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians.
द्वारा: Alvarez-Madrazo, S, और अन्य
प्रकाशित: (2010)

The Post-Translational Modification Networking in WNK-Centric Hypertension Regulation and Electrolyte Homeostasis
द्वारा: Shiuan-Chen Lin, और अन्य
प्रकाशित: (2022-09-01)

The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource
द्वारा: Munroe, P, और अन्य
प्रकाशित: (2004)

Glutathione S-transferase variants and hypertension.
द्वारा: Delles, C, और अन्य
प्रकाशित: (2008)

Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension.
द्वारा: Alvarez-Madrazo, S, और अन्य
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Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array.
द्वारा: Sober, S, और अन्य
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Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
द्वारा: Barr, M, और अन्य
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