(Q24313292)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

author name string

Simon DB

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Hamdan JM

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

DiPietro A

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Sanjad SA

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Lifton RP

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

language of work or name

English

0 references

publication date

1 June 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

page(s)

183-188

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

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

16 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

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/10.1038%2FNG0696-183

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/10.1038%2FNG0696-183

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/10.1038%2FNG0696-183

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Pathogenesis of Bartter's syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Prostaglandins and Bartter's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Resistance to endogenous norepinephrine in Bartter's syndrome: reversion during indomethacin administration.

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Chronic hypomagnesemia and hypokalemia due to renal wasting in siblings.

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Familial hypokalemia-hypomagnesemia or Gitelman's syndrome: a further case

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Growth Characteristics in Patients with Bartter’s Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Bartter's syndrome: the unsolved puzzle

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Hypercalciuric Bartter syndrome: resolution of nephrocalcinosis with indomethacin

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

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/10.1038%2FNG0696-183

7 January 2021

Evidence for a prostaglandin-independent defect in chloride reabsorption in the loop of henle as a proximal cause of Bartter's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Ion transport mechanisms in thick ascending limb of Henle's loop of mammalian nephron

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Cellular mechanism of the action of loop diuretics on the thick ascending limb of Henle's loop

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Alternatively spliced isoforms of the putative renal Na-K-Cl cotransporter are differentially distributed within the rabbit kidney

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Molecular cloning and functional expression of the bumetanide-sensitive Na-K-Cl cotransporter

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Primary structure, functional expression, and chromosomal localization of the bumetanide-sensitive Na-K-Cl cotransporter in human colon

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

A new bacteriophage P1-derived vector for the propagation of large human DNA fragments

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Localization of the renal Na?K?Cl cotransporter gene (Slc 12a1) on mouse Chromosome 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Correction of hypokalemia by magnesium repletion in familial hypokalemic alkalosis with tubulopathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0696-183

7 January 2021

Identifiers

DOI

10.1038/NG0696-183

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8640224%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

16 October 2019

1006663248

0 references

Fatcat ID

release_fvlxoqhhlvhfva64xeenszulgy

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fvlxoqhhlvhfva64xeenszulgy

24 November 2022

mapped directly with Wikidata item

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017