(Q48883925)

16 February 2018

title

Heterogeneous hypertension. (English)

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16 February 2018

main subject

arterial hypertension

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author name string

R D Gordon

series ordinal

1

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16 February 2018

language of work or name

English

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publication date

1 September 1995

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16 February 2018

published in

Nature Genetics

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16 February 2018

volume

11

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16 February 2018

issue

1

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16 February 2018

page(s)

6-9

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16 February 2018

https://scigraph.springernature.com/pub.10.1038/ng0995-6

exact match

0 references

cites work

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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

21 January 2018

1 reference

Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype

21 January 2018

1 reference

Primary aldosteronism--some genetic, morphological, and biochemical aspects of subtypes

21 January 2018

1 reference

Molecular variants in the P450c11AS gene as determinants of aldosterone synthase activity in the Dahl rat model of hypertension.

21 January 2018

1 reference

Aldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1): loss of heterozygosity for polymorphic chromosome 11 deoxyribonucleic acid markers, including the MEN1 locus

21 January 2018

1 reference

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

21 January 2018

1 reference

7 January 2021

Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension

1 reference

7 January 2021

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

1 reference

7 January 2021

Hypertension in a four-year-old child: gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids

1 reference

7 January 2021

The Syndrome of Apparent Mineralocorticoid Excess: Its Association with 1 lβ –Dehydrogenase and 5β –Reductase Deficiency and Some Consequences for Corticosteroid Metabolism*

1 reference

7 January 2021

A new form of the syndrome of apparent mineralocorticoid excess

1 reference

7 January 2021

High incidence of primary aldosteronism in 199 patients referred with hypertension

1 reference

7 January 2021

A new genetic test for familial hyperaldosteronism type I aids in the detection of curable hypertension

1 reference

7 January 2021

Clinical and pathological diversity of primary aldosteronism, including a new familial variety

1 reference

7 January 2021

Familial hyperaldosteronism type II: five families with a new variety of primary aldosteronism

1 reference

7 January 2021

Artificial mutations in P450c11AS (aldosterone synthase) can increase enzymatic activity: a model for low-renin hypertension?

1 reference

7 January 2021

Allelic losses on chromosome band 11q13 in aldosterone-producing adrenal tumors

1 reference

7 January 2021

Steroid 11 beta-hydroxylase deficiency and related disorders

1 reference

7 January 2021

Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency

1 reference

7 January 2021

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0995-6

1 reference

16 February 2018

1 reference

16 February 2018