(Q77159547)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

review article

1 reference

title

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

author name string

D B Simon

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

R P Lifton

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

publication date

1 August 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Cell Biology

3 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

page(s)

450-454

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

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

3 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Bartter's syndrome: the unsolved puzzle

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

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/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

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%2FS0955-0674%2898%2980057-4

7 January 2021

Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Gitelman’s syndrome is genetically distinct from other forms of Bartter’s syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

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%2FS0955-0674%2898%2980057-4

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/10.1016%2FS0955-0674%2898%2980057-4

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%2FS0955-0674%2898%2980057-4

7 January 2021

Renal potassium channels and their regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Renal potassium channels: an overview

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Cloning and expression of an inwardly rectifying ATP-regulated potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Phosphorylation of the ATP-sensitive, inwardly rectifying K+ channel, ROMK, by cyclic AMP-dependent protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published e

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

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%2FS0955-0674%2898%2980057-4

7 January 2021

Two highly homologous members of the ClC chloride channel family in both rat and human kidney

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Chloride channels: an emerging molecular picture

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980057-4

7 January 2021

10.1016/S0955-0674(98)80057-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9719864%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

1 reference