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

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Imrie, H, Mayosi, B, Baker, M, Fraser, R, Davies, E, Ingram, M, Watkins, H, Farrall, M, Connell, J, Keavney, B
التنسيق:	Conference item
منشور في:	2005

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
حسب: Keavney, B, وآخرون
منشور في: (2005)

Genetic variation at the CYP11B locus accounts for heritabilities of aldosterone metabolite (THAIdo) excretion and 11beta-hydroxylase activity
حسب: Freel, M, وآخرون
منشور في: (2006)

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
حسب: Imrie, H, وآخرون
منشور في: (2006)

Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1)
حسب: Imrie, H, وآخرون
منشور في: (2007)

Measured haplotype analysis of the aldosterone synthase gene and heart size (vol 11, pg 395, 2005)
حسب: Mayosi, B, وآخرون
منشور في: (2005)

Measured haplotype analysis of the aldosterone synthase gene and heart size.
حسب: Mayosi, B, وآخرون
منشور في: (2003)

Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy
حسب: Mayosi, B, وآخرون
منشور في: (2002)

Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.
حسب: Barr, M, وآخرون
منشور في: (2007)

11-deoxycortisol positively correlates with T cell immune traits in physiological conditionsResearch in context
حسب: Chunying Peng, وآخرون
منشور في: (2024-01-01)

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

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass.
حسب: Mayosi, B, وآخرون
منشور في: (2002)

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
حسب: Xue Liu, وآخرون
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Best Practice for Identification of Classical 21-Hydroxylase Deficiency Should Include 21 Deoxycortisol Analysis with Appropriate Isomeric Steroid Separation
حسب: Ronda F. Greaves, وآخرون
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Familial and phenotypic associations of the aldosterone Renin ratio.
حسب: Alvarez-Madrazo, S, وآخرون
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ASSOCIATION BETWEEN HSD11B1 POLYMORPHISM AND LEFT VENTRICULAR MASS IN FAMILIES WITH HYPERTENSION
حسب: Rahman, T, وآخرون
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Marked variation in heritability estimates of left ventricular mass depending on modality of measurement
حسب: Nethononda, R, وآخرون
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Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.
حسب: Baker, M, وآخرون
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A rare variant of the leptin (LEP) gene has large effects on blood pressure (BP) and carotid intima-medial thickness (CIMT): Study of 1428 individuals in 248 families
حسب: Imrie, H, وآخرون
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Association between common polymorphisms of the pro-opiomelanocortin (POMC) gene and body fat distribution: A family study
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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.
حسب: Gaukrodger, N, وآخرون
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Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular mass.
حسب: Rahman, T, وآخرون
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Association between the-174G/C polymorphism of the interleukin-6 gene and carotid atherosclerosis: Family study and meta-analysis
حسب: Mayosi, B, وآخرون
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Electrocardiographic markers of cardiac hypertrophy show greater heritability than echocardiographic left ventricular mass: A family study
حسب: Mayosi, B, وآخرون
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Heritability of haemodynamics in the ascending aorta
حسب: McGurk, KA, وآخرون
منشور في: (2020)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension
حسب: Mayosi, B, وآخرون
منشور في: (2008)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension.
حسب: Mayosi, B, وآخرون
منشور في: (2008)

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.
حسب: Mayosi, B, وآخرون
منشور في: (2005)

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.
حسب: Keavney, B, وآخرون
منشور في: (2000)

Method Development and Clinical Utility for Simultaneous Measurement of 21-Deoxycortisol, 17-Hydroxyprogesterone, Cortisol, and Cortisone Levels in Human Plasma Using UHPLC-MS/MS
حسب: Syed N. Alvi, وآخرون
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Primary Aldosteronism: A Series of 11 Cases
حسب: Abhranil Dhar, وآخرون
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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
حسب: Rahman, T, وآخرون
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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.
حسب: Baker, M, وآخرون
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Clinical Characteristics of Aldosterone- and Cortisol-Coproducing Adrenal Adenoma in Primary Aldosteronism
حسب: Lu Tang, وآخرون
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Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome
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Treatment of Nonclassic 11-Hydroxylase Deficiency with Ashwagandha Root
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Bilateral Adrenocortical Masses Producing Aldosterone and Cortisol Independently
حسب: Seung-Eun Lee, وآخرون
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GENETIC POLYMORPHISMS LINKED TO CORONARY ARTERY DISEASE ARE NOT ASSOCIATED WITH CAROTID ARTERY INTIMA-MEDIA THICKNESS, LEFT VENTRICULAR SIZE, OR INTERMEDIATE RISK PHENOTYPES
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Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.
حسب: Cunnington, MS, وآخرون
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Double somatic mutations in CTNNB1 and GNA11 in an aldosterone-producing adenoma
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Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes.
حسب: Palomino-Doza, J, وآخرون
منشور في: (2008)

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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