Aldosterone-related genetic effects in hypertension (Q34028560)

30 July 2017

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title

Aldosterone-related genetic effects in hypertension (English)

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30 July 2017

Warnock DG

1

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30 July 2017

1 June 2000

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Current Hypertension Reports

30 July 2017

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30 July 2017

2

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30 July 2017

3

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30 July 2017

295-301

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https://scigraph.springernature.com/pub.10.1007/s11906-000-0013-3

30 July 2017

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cites work

Genetic analysis of the beta subunit of the epithelial Na+ channel in essential hypertension

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Genetic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Genotype-phenotype relationships for the renin-angiotensin-aldosterone system in a normal population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Regulation of aldosterone secretion in hypertensive blacks

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Altered adrenal sensitivity to angiotensin II in low-renin essential hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Levels of mineralocorticoids in whites and blacks

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Genetic association of 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

Importance of the renin system in determining blood pressure fall with salt restriction in black and white hypertensives

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-000-0013-3

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

21 January 2018

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12 December 2020

Deficient inactivation of cortisol by 11 beta-hydroxysteroid dehydrogenase in essential hypertension

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12 December 2020

Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome

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12 December 2020

A new polymorphic restriction site in the human 11 beta-hydroxysteroid dehydrogenase type 2 gene

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12 December 2020

Sodium status, corticosteroid metabolism and blood pressure in normal human subjects and in a patient with abnormal salt appetite

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12 December 2020

Mass spectrometry in the diagnosis of steroid-related disorders and in hypertension research

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12 December 2020

Polymorphism in the beta subunit and Na+ transport

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12 December 2020

Loss of protein kinase C inhibition in the beta-T594M variant of the amiloride-sensitive Na+ channel

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12 December 2020

Alterations in aldosterone secretion and metabolism in low renin hypertension

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12 December 2020

Liddle disease caused by a missense mutation of beta subunit of the epithelial sodium channel gene

1 reference

12 December 2020

Evidence of coexisting changes in 11 beta-hydroxysteroid dehydrogenase and 5 beta-reductase activity in subjects with untreated essential hypertension

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12 December 2020

Blood pressure control--special role of the kidneys and body fluids

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12 December 2020

Liddle's disease: abnormal regulation of amiloride-sensitive Na+ channels by beta-subunit mutation

1 reference

12 December 2020

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

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12 December 2020

Grapefruit juice and its flavonoids inhibit 11 beta-hydroxysteroid dehydrogenase

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12 December 2020

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

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12 December 2020

G-proteins modulate amiloride-sensitive sodium channels.

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12 December 2020

Liddle syndrome: an autosomal dominant form of human hypertension

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12 December 2020

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

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12 December 2020

Abnormalities of nasal potential difference measurement in Liddle's syndrome

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12 December 2020

Epithelial Sodium Channel Activity Is Not Increased in Hypertension in Whites

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12 December 2020

Naringin and naringenin are not the primary CYP3A inhibitors in grapefruit juice

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12 December 2020

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

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12 December 2020

Liddle's syndrome, an underrecognized entity: a report of four cases, including the first report in black individuals

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12 December 2020

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

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12 December 2020

Molecular genetics of human blood pressure variation

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12 December 2020

Mineralocorticoid activity of liquorice: 11-beta-hydroxysteroid dehydrogenase deficiency comes of age

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12 December 2020

Genetic disorders of renal electrolyte transport

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12 December 2020

Inappropriate elevation of the aldosterone/plasma renin activity ratio in hypertensive patients with increases of 11-deoxycorticosterone and 18-hydroxy-11-deoxycorticosterone: a subtype of essential hypertension?

1 reference

12 December 2020

T594M mutation in the ENaC beta subunit and low-renin hypertension in blacks

1 reference

12 December 2020

A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system

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12 December 2020

Expression of the amiloride-sensitive sodium channel beta subunit gene in human B lymphocytes

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12 December 2020

A novel variant of the beta-subunit of the amiloride-sensitive sodium channel in African Americans

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12 December 2020

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

1 reference

12 December 2020

Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome.

1 reference

12 December 2020

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

1 reference

12 December 2020

Cure of apparent mineralocorticoid excess by kidney transplantation

1 reference

12 December 2020

Low-renin and nonmodulating essential hypertension

1 reference

12 December 2020

The epithelial sodium channel in hypertension

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

10.1007/S11906-000-0013-3

Identifiers

DOI

1 reference

PubMed ID

10981163

Dimensions Publication ID

30 July 2017

0 references

1 reference

PubMed ID

10981163