Molecular mechanisms of human hypertension (Q32138445)

6 July 2017

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title

Molecular mechanisms of human hypertension (English)

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6 July 2017

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R P Lifton

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6 July 2017

A G Gharavi

series ordinal

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6 July 2017

D S Geller

series ordinal

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6 July 2017

language of work or name

English

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publication date

1 February 2001

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6 July 2017

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6 July 2017

volume

104

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6 July 2017

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6 July 2017

page(s)

545-556

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

6 July 2017

cites work

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Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

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7 January 2021

A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Role of gammaENaC subunit in lung liquid clearance and electrolyte balance in newborn mice. Insights into perinatal adaptation and pseudohypoaldosteronism

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7 January 2021

Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension

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7 January 2021

Relationship between clinical severity of disease and hemodynamic patterns in essential hypertension

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7 January 2021

Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes

1 reference

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7 January 2021

The adrenogenital syndrome

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7 January 2021

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

1 reference

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7 January 2021

Prevalence of Hypertension in the US Adult Population : Results From the Third National Health and Nutrition Examination Survey, 1988-1991

1 reference

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7 January 2021

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Seven lessons from two candidate genes in human essential hypertension: angiotensinogen and epithelial sodium channel

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7 January 2021

Understanding hypertension through genetic manipulation in mice

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7 January 2021

A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension

1 reference

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7 January 2021

The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results

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7 January 2021

Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Salt-sensitive hypertension in endothelin-B receptor-deficient rats

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy

1 reference

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7 January 2021

High incidence of primary aldosteronism in 199 patients referred with hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects

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https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats

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https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

QTL influencing blood pressure maps to the region of PPH1 on chromosome 2q31-34 in Old Order Amish

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Hypertension in mice lacking the gene for endothelial nitric oxide synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Point mutation causing a single amino acid substitution in the hormone binding domain of the glucocorticoid receptor in familial glucocorticoid resistance

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Molecular basis of human hypertension: role of angiotensinogen

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

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

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

A novel mouse Nedd4 protein suppresses the activity of the epithelial Na+ channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Elevated systolic blood pressure as a cardiovascular risk factor

1 reference

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7 January 2021

Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

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7 January 2021

Molecular genetics of human blood pressure variation

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Environmental and genetic sources of familial aggregation of blood pressure in Tecumseh, Michigan

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Molecular genetics of human hypertension.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21

1 reference

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7 January 2021

MRC trial of treatment of mild hypertension: principal results. Medical Research Council Working Party

1 reference

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7 January 2021

Congenitally defective aldosterone biosynthesis in humans: the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients

1 reference

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7 January 2021

Trends in the prevalence of hypertension, antihypertensive therapy, and left ventricular hypertrophy from 1950 to 1989.

1 reference

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7 January 2021

Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Angiotensinogen gene polymorphisms M235T/T174M: no excess transmission to hypertensive Chinese

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

eNOS mediates L-arginine-induced inhibition of thick ascending limb chloride flux

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Genetic analysis of inherited hypertension in the rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Cardiovascular risk factors in a french canadian population: Resolution of genetic and familial environmental effects on blood pressure using twins, adoptees, and extensive information on environmental correlates

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

The future of genetic studies of complex human diseases

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https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Targeted disruption of the mouse beta1-adrenergic receptor gene: developmental and cardiovascular effects

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Elevated blood pressures in mice lacking endothelial nitric oxide synthase.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

The Activity of the Epithelial Sodium Channel Is Regulated by Clathrin-mediated Endocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

M235T angiotensinogen gene polymorphism and cardiovascular renal risk.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900241-0

7 January 2021

10.1016/S0092-8674(01)00241-0

Identifiers

DOI

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6 July 2017

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