(Q34492779)

2 August 2017

1 reference

title

Genetics of the mineralocorticoid system in primary hypertension (English)

1 reference

2 August 2017

Paolo Ferrari

1

0 references

publication date

1 February 2002

1 reference

Current Hypertension Reports

2 August 2017

published in

1 reference

2 August 2017

volume

4

1 reference

2 August 2017

issue

1

1 reference

2 August 2017

page(s)

18-24

1 reference

https://scigraph.springernature.com/pub.10.1007/s11906-002-0048-8

2 August 2017

exact match

0 references

cites work

Aldosterone regulation of gene transcription leading to control of ion transport

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11906-002-0048-8

Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11906-002-0048-8

The steroid receptor superfamily: mechanisms of diversity

21 January 2018

1 reference

12 December 2020

Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase

1 reference

12 December 2020

Point mutations abolish 11 beta-hydroxysteroid dehydrogenase type II activity in three families with the congenital syndrome of apparent mineralocorticoid excess.

1 reference

12 December 2020

A genetic defect resulting in mild low-renin hypertension

1 reference

12 December 2020

Biochemical evidence of aldosterone overproduction and abnormal regulation in normotensive individuals with familial hyperaldosteronism type I

1 reference

12 December 2020

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

1 reference

12 December 2020

The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization

1 reference

12 December 2020

Angiotensin II and potassium regulate human CYP11B2 transcription through common cis-elements

1 reference

12 December 2020

Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess

1 reference

12 December 2020

Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy

1 reference

12 December 2020

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

1 reference

12 December 2020

Variation of phenotype in patients with glucocorticoid remediable aldosteronism

1 reference

12 December 2020

Mineralocorticoid action: target tissue specificity is enzyme, not receptor, mediated

1 reference

12 December 2020

A Syndrome of Apparent Mineralocorticoid Excess Associated with Defects in the Peripheral Metabolism of Cortisol*

1 reference

12 December 2020

Lack of mutations in epithelial sodium channel beta-subunit gene in human subjects with hypertension

1 reference

12 December 2020

Molecular basis of human salt sensitivity: the role of the 11beta-hydroxysteroid dehydrogenase type 2.

1 reference

12 December 2020

Cloning of the 11βHSD type II enzyme from human kidney

1 reference

12 December 2020

A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess

1 reference

12 December 2020

The Effect of Triamterene and Sodium Intake on Renin, Aldosterone, and Erythrocyte Sodium Transport in Liddle’s Syndrome

1 reference

12 December 2020

Control of transcription activation by steroid hormone receptors

1 reference

12 December 2020

Immunohistochemical localization of the 11 beta-hydroxysteroid dehydrogenase type II enzyme in human kidney and placenta

1 reference

12 December 2020

Aldosterone excretion rate and blood pressure in essential hypertension are related to polymorphic differences in the aldosterone synthase gene CYP11B2

1 reference

12 December 2020

Cloning and expression of rat cDNA encoding corticosteroid 11 beta-dehydrogenase

1 reference

12 December 2020

Structural analysis of the 11β-hydroxysteroid dehydrogenase type 2 gene in end-stage renal disease

1 reference

12 December 2020

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2

1 reference

12 December 2020

Mineralocorticoid and glucocorticoid receptor activities distinguished by nonreceptor factors at a composite response element

1 reference

12 December 2020

Brief report: Liddle's syndrome revisited--a disorder of sodium reabsorption in the distal tubule

1 reference

12 December 2020

Cloning and tissue distribution of the human 11 beta-hydroxysteroid dehydrogenase type 2 enzyme

1 reference

12 December 2020

NAD(+)-dependent isoform of 11 beta-hydroxysteroid dehydrogenase. Cloning and characterization of cDNA from sheep kidney.

1 reference

12 December 2020

Heterogeneous hypertension.

1 reference

12 December 2020

Role of steroid 11 beta-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans

1 reference

12 December 2020

Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone

1 reference

12 December 2020

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

1 reference

12 December 2020

Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel

1 reference

12 December 2020

Association of hypertension with T594M mutation in beta subunit of epithelial sodium channels in black people resident in London

1 reference

12 December 2020

Evaluation of the dexamethasone suppression test for the diagnosis of glucocorticoid-remediable aldosteronism

1 reference

12 December 2020

10.1007/S11906-002-0048-8

Identifiers

DOI

1 reference

Dimensions Publication ID

2 August 2017

1039556129

0 references

1 reference