(Q34135261)

31 July 2017

1 reference

title

The genetics of essential hypertension. (English)

1 reference

31 July 2017

K M O'Shaughnessy

1

1 reference

PubMed ID

11167660

31 July 2017

language of work or name

English

0 references

publication date

1 January 2001

1 reference

British Journal of Clinical Pharmacology

31 July 2017

1 reference

31 July 2017

51

1 reference

31 July 2017

1

1 reference

31 July 2017

5-11

1 reference

An extreme-sib-pair genome scan for genes regulating blood pressure

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excess

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Abnormalities of nasal potential difference measurement in Liddle's syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Association of a human G-protein beta3 subunit variant with hypertension

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Association between the angiotensinogen 235T-variant and essential hypertension in whites: a systematic review and methodological appraisal.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Mutation of cytochrome P-45017 alpha gene (CYP17) in a Japanese patient previously reported as having glucocorticoid-responsive hyperaldosteronism: with a review of Japanese patients with mutations of CYP17

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

The causes of essential hypertension

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (type 2) isozyme of 11 beta-hydroxysteroid dehydrogenase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Epithelial sodium channel related to proteins involved in neurodegeneration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

5 July 2018

Linkage and association.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Genetic analysis of blood pressure and sodium balance in spontaneously hypertensive rats

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Heredity and blood pressure

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Molecular basis of human hypertension: role of angiotensinogen

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014421

Evidence-Based Health Policy---Lessons from the Global Burden of Disease Study

5 July 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

Linkage analysis of candidate genes and gene-gene interactions in chinese hypertensive sib pairs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

Linkage of the Angiotensinogen Gene to Essential Hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

Evaluation of the Angiotensinogen Locus in Human Essential Hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01254.X

Linkage of Gordon's syndrome to the long arm of chromosome 17 in a region recently linked to familial essential hypertension

21 January 2018

1 reference

12 December 2020

Susceptibility genes for end-organ damage. New strategies to understand diabetic and hypertensive nephropathy

1 reference

12 December 2020

New genetic concepts in hypertensive cardiovascular disease

1 reference

12 December 2020

Preliminary evidence of linkage of salt sensitivity in black Americans at the beta 2-adrenergic receptor locus

1 reference

12 December 2020

Genetic Analysis of Blood Pressure in Spontaneously Hypertensive Rats

1 reference

12 December 2020

Extreme discordant sib pairs for mapping quantitative trait loci in humans

1 reference

12 December 2020

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

1 reference

12 December 2020

Genomic mismatch scanning identifies human genomic DNA shared identical by descent

1 reference

12 December 2020

The role of alpha-adducin polymorphism in blood pressure and sodium handling regulation may not be excluded by a negative association study

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

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

1 reference

12 December 2020

Glucocorticoid-remediable aldosteronism (GRA): diagnosis, variability of phenotype and regulation of potassium homeostasis

1 reference

12 December 2020

Heredity in hypertension

1 reference

12 December 2020

A search for type 1 diabetes susceptibility genes in families from the United Kingdom

1 reference

12 December 2020

The NATURE of essential hypertension

1 reference

12 December 2020

10.1046/J.1365-2125.2001.01254.X

Identifiers

DOI

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

PubMed ID

11167660