High glucose and low lactate: a metabolic signature of hypertension in human serum?

High glucose and low lactate: a metabolic signature of hypertension in human serum?

Bibliográfalaš dieđut
Váldodahkkit:	Huq, S, Oldapo, M, Wang, Y, Li, J, Loo, R, Braund, P, Tobin, M, Barton, P, Samani, N, Brown, M, Clayton, D, Connell, J, Dominczak, A, Farrall, M, Lathrop, M, Webster, J, Nicholson, J, Caulfield, M, Holmes, E, Munroe, P
Materiálatiipa:	Conference item
Almmustuhtton:	2008

Geahča maid

Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) 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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Almmustuhtton: (2005)

Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension 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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Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study
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Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.
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Genomewide linkage analysis for loci affecting electrocardiographic LV mass
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A new tool for checks of data precision within the MRC British genetics of hypertension study
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Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
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Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study
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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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Analysis of the angiotensinogen gene in the MRC 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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Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
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No association of the WNK1 gene with essential hypertension in the MRC 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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Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension
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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.
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The MRC British Genetics of Hypertension Study - Genome-wide screen results
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Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with 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.
Dahkki: Freel, E, et al.
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Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes
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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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Association between variants of the human GSTM gene family and hypertension
Dahkki: Delles, C, et al.
Almmustuhtton: (2006)

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
Dahkki: Wallace, C, et al.
Almmustuhtton: (2006)

Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study.
Dahkki: Munroe, P, et al.
Almmustuhtton: (2006)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study
Dahkki: Wallace, C, et al.
Almmustuhtton: (2005)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study
Dahkki: Wallace, C, et al.
Almmustuhtton: (2005)

Genome-wide mapping of human loci for essential hypertension.
Dahkki: Caulfield, M, et al.
Almmustuhtton: (2003)

Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians.
Dahkki: Alvarez-Madrazo, S, et al.
Almmustuhtton: (2010)

The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource
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Almmustuhtton: (2004)

Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension.
Dahkki: Alvarez-Madrazo, S, et al.
Almmustuhtton: (2013)

Common polymorphisms in the CYP11B1 and CYP11B2 genes: Evidence for a digenic influence on hypertension
Dahkki: Alvarez-Madrazo, S, et al.
Almmustuhtton: (2013)

Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
Dahkki: Barr, M, et al.
Almmustuhtton: (2007)

Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
Dahkki: Brown, M, et al.
Almmustuhtton: (2008)

Glutathione S-transferase variants and hypertension.
Dahkki: Delles, C, et al.
Almmustuhtton: (2008)

Measured haplotype analysis of the angiotensin-I converting enzyme gene
Dahkki: Keavney, B, et al.
Almmustuhtton: (1999)

Measured haplotype analysis of the angiotensin-I converting enzyme gene.
Dahkki: Keavney, B, et al.
Almmustuhtton: (1998)