Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.

Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.

Podrobná bibliografie
Hlavní autoři:	Padmanabhan, S, Wallace, C, Munroe, P, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Lathrop, M, Caulfield, M, Dominiczak, A, Connell, J
Médium:	Conference item
Vydáno:	2005

Podobné jednotky

Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study
Autor: Padmanabhan, S, a další
Vydáno: (2005)

Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study.
Autor: Padmanabhan, S, a další
Vydáno: (2006)

No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study.
Autor: Knight, J, a další
Vydáno: (2001)

Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.
Autor: Munroe, P, a další
Vydáno: (2005)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study
Autor: Wallace, C, a další
Vydáno: (2005)

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study
Autor: Wallace, C, a další
Vydáno: (2005)

Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study
Autor: Padmanabhan, S, a další
Vydáno: (2006)

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

Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study
Autor: Padmanabhan, S, a další
Vydáno: (2007)

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
Autor: Wallace, C, a další
Vydáno: (2006)

No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study
Autor: Newhouse, S, a další
Vydáno: (2004)

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

Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study.
Autor: Munroe, P, a další
Vydáno: (2000)

Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study
Autor: Padmanabhan, S, a další
Vydáno: (2007)

A new tool for checks of data precision within the MRC British genetics of hypertension study
Autor: Caulfield, M, a další
Vydáno: (2000)

The MRC British Genetics of Hypertension Study - Genome-wide screen results
Autor: Caulfield, M, a další
Vydáno: (2002)

Genomewide linkage analysis for loci affecting electrocardiographic LV mass
Autor: Padmanabhan, S, a další
Vydáno: (2006)

Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
Autor: Newhouse, S, a další
Vydáno: (2007)

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

WNK1 - functional analyses of variants associated with blood pressure and essential hypertension
Autor: Hoti, M, a další
Vydáno: (2008)

WNK1-functional analyses of variants associated with blood pressure and essential hypertension
Autor: Hoti, M, a další
Vydáno: (2008)

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
Autor: Bell, J, a další
Vydáno: (2006)

Association between variants of the human GSTM gene family and hypertension
Autor: Delles, C, a další
Vydáno: (2006)

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension
Autor: Tzenova Bell, J, a další
Vydáno: (2006)

Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension
Autor: Delles, C, a další
Vydáno: (2006)

Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes
Autor: Newhouse, S, a další
Vydáno: (2007)

Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians.
Autor: Alvarez-Madrazo, S, a další
Vydáno: (2010)

Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.
Autor: Marçano, A, a další
Vydáno: (2007)

Glutathione S-transferase variants and hypertension.
Autor: Delles, C, a další
Vydáno: (2008)

Genome-wide mapping of human loci for essential hypertension.
Autor: Caulfield, M, a další
Vydáno: (2003)

Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension.
Autor: Alvarez-Madrazo, S, a další
Vydáno: (2013)

Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
Autor: Brown, M, a další
Vydáno: (2008)

Common polymorphisms in the CYP11B1 and CYP11B2 genes: Evidence for a digenic influence on hypertension
Autor: Alvarez-Madrazo, S, a další
Vydáno: (2013)

The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource
Autor: Munroe, P, a další
Vydáno: (2004)

High glucose and low lactate: a metabolic signature of hypertension in human serum?
Autor: Huq, S, a další
Vydáno: (2008)

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.
Autor: Julier, C, a další
Vydáno: (1997)

A pharmacogenetic approach to blood pressure in Lyon hypertensive rats. A chromosome 2 locus influences the response to a calcium antagonist.
Autor: Vincent, M, a další
Vydáno: (1997)

Variants and haplotypes of the angiotensinogen gene are associated with hypertension in the Caerphilly Prospective Study
Autor: Xue, M, a další
Vydáno: (2005)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension
Autor: Mayosi, B, a další
Vydáno: (2008)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension.
Autor: Mayosi, B, a další
Vydáno: (2008)