Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension

Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension

Bibliográfalaš dieđut
Váldodahkkit:	Delles, C, Marcano, A, Munroe, P, Padmanabhan, S, McClure, J, Brain, N, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Connell, J, Caulfield, M, Dominiczak, A
Materiálatiipa:	Conference item
Almmustuhtton:	2006

Geahča maid

Association between variants of the human GSTM gene family and hypertension
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Glutathione S-transferase variants and hypertension.
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Almmustuhtton: (2008)

The diverse functions of Mu-class Glutathione S-transferase HrGSTm1 during the development of Hyalomma rufipes with a focus on the detoxification metabolism of cyhalothrin
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Deletion polymorphism of glutathione S-transferases genes (GSTT1, GSTM1) in patients with breast cancer in Primorye region
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Urinary albumin excretion in hypertensive siblings 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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Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study
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Aldehyde dehydrogenase 2 (ALDH2) and glutathione S-transferase M1 (GSTM1) polymorphisms in relation to oral cancer risk among Malaysians
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An Updated Meta-Analysis: Risk Conferred by Glutathione S-Transferases (GSTM1 and GSTT1) Polymorphisms to Age-Related Cataract
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Glutathione S-Transferase Mu 1 and Glutathione S-transferase theta 1 Genes Polymorphism and Susceptibility to Chronic Myeloid Leukemia in Erbil-Iraq Kurdistan Region
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A dominance of Mu class glutathione transferases within the equine tapeworm Anoplocephala perfoliata
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Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study.
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CYTOGENETIC EFFECTS OF TICK-BORNE TRANSMITTED CO- OR MONOINFECTIONS DEPENDING ON THE VARIANTS OF GLUTATHIONE-S-TRANSFERASE GENES (GSTM1 OR GSTT1) IN THE PATIENT’S GENOTYPE
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Genomewide linkage analysis for loci affecting electrocardiographic LV mass
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Reduction of MTT by Glutathione S-Transferase
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Impact of the deletion glutathione S-transferase (class Mu) on lung cancer risk among smokers
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Glutathione S-transferase gene deletions in myelodysplasia.
Dahkki: Atoyebi, W, et al.
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Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study.
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Chemotherapy induces breast cancer stem cell enrichment through repression of glutathione S-transferase Mu
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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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Glutathione S-transferase polymorphisms may be associated with risk of oedematous severe childhood malnutrition.
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Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians.
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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.
Dahkki: Knight, J, et al.
Almmustuhtton: (2001)

Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.
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Regulation of Signal Transduction by Glutathione Transferases
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Glutathione transferase P1 is modified by palmitate.
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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.
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A new tool for checks of data precision within the MRC British genetics of hypertension study
Dahkki: Caulfield, M, et al.
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Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes
Dahkki: Newhouse, S, et al.
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Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
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Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study
Dahkki: Padmanabhan, S, et al.
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The MRC British Genetics of Hypertension Study - Genome-wide screen results
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Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
Dahkki: Newhouse, S, et al.
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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.
Dahkki: Newhouse, S, et al.
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Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
Dahkki: Barr, M, et al.
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Insecticide toxicity, glutathione transferases and carboxylesterase activities in the larva of the Aedes mosquito
Dahkki: Shamaan, N.A., et al.
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Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study
Dahkki: Padmanabhan, S, et al.
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Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
Dahkki: Wallace, C, et al.
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