Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion

Библиографические подробности
Главные авторы:	Imrie, H, Mayosi, B, Baker, M, Fraser, R, Davies, E, Ingram, M, Watkins, H, Farrall, M, Connell, J, Keavney, B
Формат:	Conference item
Опубликовано:	2005

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
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Genetic variation at the CYP11B locus accounts for heritabilities of aldosterone metabolite (THAIdo) excretion and 11beta-hydroxylase activity
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Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
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Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1)
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Measured haplotype analysis of the aldosterone synthase gene and heart size (vol 11, pg 395, 2005)
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Measured haplotype analysis of the aldosterone synthase gene and heart size.
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Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy
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Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
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11-deoxycortisol positively correlates with T cell immune traits in physiological conditionsResearch in context
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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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Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass.
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Gender-Specific Independent and Combined Effects of the Cortisol-to-Cortisone Ratio and 11-Deoxycortisol on Prediabetes and Type 2 Diabetes Mellitus: From the Henan Rural Cohort Study
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Familial and phenotypic associations of the aldosterone Renin ratio.
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ASSOCIATION BETWEEN HSD11B1 POLYMORPHISM AND LEFT VENTRICULAR MASS IN FAMILIES WITH HYPERTENSION
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A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.
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Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular mass.
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Electrocardiographic markers of cardiac hypertrophy show greater heritability than echocardiographic left ventricular mass: A family study
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Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension
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Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension.
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Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis.
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Plasma C-reactive protein (CRP), a novel cardiovascular risk factor, shows high heritability but no association with the-174 G/C polymorphism of the interleukin-6 (IL-6) gene in human families.
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Cell foundry with high product specificity and catalytic activity for 21-deoxycortisol biotransformation
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The C-532T polymorphism of the angiotensinogen (AGT) gene is associated with arterial stiffness: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension
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The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: a possible explanation for heterogeneity in genetic association studies of AGT and hypertension.
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Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion

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