Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1)

Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1)

Bibliographic Details
Main Authors:	Imrie, H, Freel, M, Mayosi, B, Davies, E, Fraser, R, Ingram, M, Cordell, H, Avery, P, Farrall, M, Watkins, H, Connell, J, Keavney, B
Format:	Conference item
Published:	2007

Similar Items

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
by: Imrie, H, et al.
Published: (2006)

Genetic variation at the CYP11B locus accounts for heritabilities of aldosterone metabolite (THAIdo) excretion and 11beta-hydroxylase activity
by: Freel, M, et al.
Published: (2006)

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion
by: Imrie, H, et al.
Published: (2005)

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
by: Keavney, B, et al.
Published: (2005)

Measured haplotype analysis of the aldosterone synthase gene and heart size (vol 11, pg 395, 2005)
by: Mayosi, B, et al.
Published: (2005)

Molecular and Epigenetic Control of Aldosterone Synthase, CYP11B2 and 11-Hydroxylase, CYP11B1
by: Yoshimichi Takeda, et al.
Published: (2023-03-01)

Measured haplotype analysis of the aldosterone synthase gene and heart size.
by: Mayosi, B, et al.
Published: (2003)

Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy
by: Mayosi, B, et al.
Published: (2002)

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

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

Familial and phenotypic associations of the aldosterone Renin ratio.
by: Alvarez-Madrazo, S, et al.
Published: (2009)

ASSOCIATION BETWEEN HSD11B1 POLYMORPHISM AND LEFT VENTRICULAR MASS IN FAMILIES WITH HYPERTENSION
by: Rahman, T, et al.
Published: (2009)

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.
by: Gaukrodger, N, et al.
Published: (2005)

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
by: Imrie, H, et al.
Published: (2005)

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.
by: Baker, M, et al.
Published: (2005)

Association between common polymorphisms of the pro-opiomelanocortin (POMC) gene and body fat distribution: A family study
by: Baker, M, et al.
Published: (2005)

Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular mass.
by: Rahman, T, et al.
Published: (2011)

Association between the-174G/C polymorphism of the interleukin-6 gene and carotid atherosclerosis: Family study and meta-analysis
by: Mayosi, B, et al.
Published: (2005)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension
by: Mayosi, B, et al.
Published: (2008)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension.
by: Mayosi, B, et al.
Published: (2008)

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

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

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.
by: Mayosi, B, et al.
Published: (2005)

Clinical significance of CYP11B2 immunostaining in unilateral primary aldosteronism
by: Marianna Viukari, et al.
Published: (2024-01-01)

The Role of the CYP11B2 Promoter Polymorphism in the Diagnosis of Primary Aldosteronism
by: Łukasz Żukowski, et al.
Published: (2020-05-01)

Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study
by: Padmanabhan, S, et al.
Published: (2007)

11β-hydroxylase deficiency caused by a novel CYP11B1 variant: A case report
by: Hossam A Aldosari, et al.
Published: (2023-01-01)

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.
by: Baker, M, et al.
Published: (2007)

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
by: Rahman, T, et al.
Published: (2007)

Case Report: A combination of chimeric CYP11B2/CYP11B1 and a novel p.Val68Gly CYP11B1 variant causing 11β-Hydroxylase deficiency in a Chinese patient
by: Jialin Li, et al.
Published: (2023-11-01)

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

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass.
by: Mayosi, B, et al.
Published: (2002)

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.
by: Cunnington, MS, et al.
Published: (2009)

GENETIC POLYMORPHISMS LINKED TO CORONARY ARTERY DISEASE ARE NOT ASSOCIATED WITH CAROTID ARTERY INTIMA-MEDIA THICKNESS, LEFT VENTRICULAR SIZE, OR INTERMEDIATE RISK PHENOTYPES
by: Cunnington, MS, et al.
Published: (2009)

Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes.
by: Palomino-Doza, J, et al.
Published: (2008)

Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency
by: Mark R. Garrelfs, et al.
Published: (2024-03-01)

Association of aldosterone synthase (CYP11B2) -344 T/C polymorphism with diabetic nephropathy: A meta-analysis
by: Haiyan Xu, et al.
Published: (2016-03-01)

Primary Aldosteronism: A Series of 11 Cases
by: Abhranil Dhar, et al.
Published: (2023-09-01)

Common variation in the CD36 (fatty acid translocase) gene is associated with left-ventricular mass.
by: Hall, D, et al.
Published: (2011)

Marked variation in heritability estimates of left ventricular mass depending on modality of measurement
by: Nethononda, R, et al.
Published: (2019)