(Q30374131)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

main subject

arterial hypertension

1 reference

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Alan R. Shuldiner

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Carole Ober

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

10

Haiqing Shen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

3

Patrick F McArdle

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

9

Evadnie Rampersaud

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

14

Afshin Parsa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

13

Nanette I Steinle

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

17

Aravinda Chakravarti

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Ying Wang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Jeffrey R O'Connell

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

James B Wade

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Sarah E Dorff

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Sanjiv J Shah

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Xiaolian Shi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Lin Pan

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

James D Kim

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Arohan R Subramanya

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Paul A Welling

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Alan B Weder

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Richard S Cooper

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Yen-Pei C Chang

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

language of work or name

English

0 references

publication date

29 December 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

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

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

106

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

226-231

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

The regulation of salt transport and blood pressure by the WNK-SPAK/OSR1 signalling pathway

19 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

SPAK and OSR1: STE20 kinases involved in the regulation of ion homoeostasis and volume control in mammalian cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

A common allele on chromosome 9 associated with coronary heart disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Alpha1-adrenergic receptors prevent a maladaptive cardiac response to pressure overload

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

WNK1 regulates phosphorylation of cation-chloride-coupled cotransporters via the STE20-related kinases, SPAK and OSR1.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

The WNK1 and WNK4 protein kinases that are mutated in Gordon's hypertension syndrome phosphorylate and activate SPAK and OSR1 protein kinases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Global burden of hypertension: analysis of worldwide data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Haploview: analysis and visualization of LD and haplotype maps

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Human hypertension caused by mutations in WNK kinases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Molecular mechanisms of human hypertension

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

HLA and mate choice in humans

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Association of alpha1A adrenergic receptor gene variants on chromosome 8p21 with human stage 2 hypertension.

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0808358106

Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP).

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0808358106

An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2629209

Use of anti-fluorophore antibody to achieve high-sensitivity immunolocalizations of transporters and ion channels

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19114657

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0808358106

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19114657%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference