Genetic determinants of human hypertension (Q33908754)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Genetic determinants of human hypertension	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

review article

1 reference

stated in

Europe PubMed Central

title

Genetic determinants of human hypertension (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

main subject

hypertension

1 reference

based on heuristic

inferred from title

author name string

Lifton RP

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

language of work or name

English

0 references

publication date

1 September 1995

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

published in

Proceedings of the National Academy of Sciences of the United States of America

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

volume

92

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

issue

19

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

page(s)

8545-8551

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

cites work

A molecular variant of angiotensinogen associated with preeclampsia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Genomic mismatch scanning: a new approach to genetic linkage mapping

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Epithelial sodium channel related to proteins involved in neurodegeneration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Evaluation of the SA locus in human hypertension

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Gene targeting approaches to complex genetic diseases: atherosclerosis and essential hypertension

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

The molecular genetics of human hemoglobins

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Kinetics of the human renin and human substrate reaction

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

A comparison of sib-pair linkage tests for disease susceptibility loci

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

A test statistic for the affected-sib-set method

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Hypertension and sodium-lithium countertransport in Utah pedigrees: evidence for major-locus inheritance

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Racial differences in aldosterone excretion and plasma aldosterone concentrations in children

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Hypertension and the genetics of red cell membrane abnormalities.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Commingling and segregation analysis of blood pressure in a French-Canadian population

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Cloning and expression of a cDNA for human cytochrome P-450aldo as related to primary aldosteronism

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Evidence that a single gene with gender- and age-dependent effects influences systolic blood pressure determination in a population-based sample

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Molecular basis of human hypertension: role of angiotensinogen

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Visual pigments and inherited variation in human vision

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Abnormalities of glucocorticoid metabolism and the renin-angiotensin system: a four-corners approach to the identification of genetic determinants of blood pressure

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Sib pair linkage analysis of renin gene haplotypes in human essential hypertension

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

Familial aggregation of blood pressure in 558 adopted children

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

28 July 2018

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

28 July 2018

Linkage of the Angiotensinogen Gene to Essential Hypertension

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=41004

retrieved

29 October 2018

Evidence for HL-A-linked genes in "juvenile" diabetes mellitus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biosynthesis of 18-oxocortisol by aldosterone-producing adrenal tissue

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated urinary excretion of 18-oxocortisol in glucocorticoid-suppressible aldosteronism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for high urinary kallikrein may protect against hypertension in Utah kindreds

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aldosterone synthase cytochrome P-450 expressed in the adrenals of patients with primary aldosteronism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new form of congenital adrenal hyperplasia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7567973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.92.19.8545

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

ADS bibcode

1995PNAS...92.8545L

0 references

PMC publication ID

41004

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

PubMed publication ID

7567973

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7567973

retrieved

29 July 2017

ResearchGate publication ID

15631091

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33908754&oldid=1628094635"