Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene (Q28115562)

3 January 2017

title

Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene (English)

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3 January 2017

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arterial hypertension

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P. M. Stewart

1

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3 January 2017

Z. S. Krozowski

2

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A. Gupta

3

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3 January 2017

D. V. Milford

4

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A. J. Howie

5

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3 January 2017

M. C. Sheppard

6

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C. B. Whorwood

7

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3 January 2017

language of work or name

English

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publication date

13 January 1996

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3 January 2017

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3 January 2017

volume

347

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3 January 2017

issue

8994

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3 January 2017

page(s)

88–91

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

3 January 2017

cites work

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Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor

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7 January 2021

LOCALISATION OF 11β-HYDROXYSTEROID DEHYDROGENASE—TISSUE SPECIFIC PROTECTOR OF THE MINERALOCORTICOID RECEPTOR

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7 January 2021

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

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

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Mineralocorticoid activity of carbenoxolone: contrasting effects of carbenoxolone and liquorice on 11 beta-hydroxysteroid dehydrogenase activity in man.

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New findings in apparent mineralocorticoid excess

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7 January 2021

Syndrome of apparent mineralocorticoid excess. A defect in the cortisol-cortisone shuttle

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Detection of human 11 beta-hydroxysteroid dehydrogenase isoforms using reverse-transcriptase-polymerase chain reaction and localization of the type 2 isoform to renal collecting ducts

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Human placental 11 beta-hydroxysteroid dehydrogenase: evidence for and partial purification of a distinct NAD-dependent isoform

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

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Localization of the gene for human 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) to chromosome band 16q22

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The antinatriuretic and kaliuretic effects of the glucocorticoids corticosterone and cortisol following pretreatment with carbenoxolone sodium (a liquorice derivative) in the adrenalectomized rat

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Dysfunction of placental glucocorticoid barrier: link between fetal environment and adult hypertension?

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

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

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

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

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7 January 2021

10.1016/S0140-6736(96)90211-1

Identifiers

DOI

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