(Q24317311)

GOA release 2020-03-11

excretion

1 reference

GOA release 2020-03-11

6

R. Stone

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9326936

19 November 2024

author name string

D. B. Simon

1

1 reference

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19 November 2024

R. S. Bindra

2

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19 November 2024

T. A. Mansfield

3

1 reference

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19 November 2024

C. Nelson-Williams

4

1 reference

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19 November 2024

E. Mendonca

5

1 reference

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19 November 2024

S. Schurman

7

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19 November 2024

A. Nayir

8

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19 November 2024

H. Alpay

9

1 reference

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19 November 2024

A. Bakkaloglu

10

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19 November 2024

J. Rodriguez-Soriano

11

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19 November 2024

J. M. Morales

12

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19 November 2024

S. A. Sanjad

13

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19 November 2024

C. M. Taylor

14

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19 November 2024

D. Pilz

15

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19 November 2024

A. Brem

16

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19 November 2024

H. Trachtman

17

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19 November 2024

W. Griswold

18

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19 November 2024

G. A. Richard

19

1 reference

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19 November 2024

E. John

20

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19 November 2024

R. P. Lifton

21

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full work available at URL

19 November 2024

language of work or name

English

0 references

publication date

October 1997

0 references

http://www.nature.com/articles/ng1097-171

1 reference

http://www.nature.com/articles/ng1097-171.pdf

19 November 2024

file format

Portable Document Format

1 reference

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

19 November 2024

0 references

17

0 references

issue

2

0 references

page(s)

171-8

0 references

cites work

1 reference

Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization

20 April 2017

1 reference

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

20 April 2017

1 reference

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

20 April 2017

1 reference

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

20 April 2017

1 reference

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

20 April 2017

1 reference

A common molecular basis for three inherited kidney stone diseases

20 April 2017

1 reference

The 1993-94 Généthon human genetic linkage map

20 April 2017

1 reference

Molecular genetics of human blood pressure variation

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

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%2FNG1097-171

7 January 2021

Hypercalciuric Bartter syndrome: resolution of nephrocalcinosis with indomethacin

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

7 January 2021

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

7 January 2021

Sodium and potassium ion pump in kidney tubules

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

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/10.1038%2FNG1097-171

7 January 2021

Chloride channels: an emerging molecular picture

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

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%2FNG1097-171

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%2FNG1097-171

7 January 2021

Properties of the basolateral membrane of the cortical thick ascending limb of Henle's loop of rabbit kidney. A model for secondary active chloride transport

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

7 January 2021

The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

7 January 2021

Molecular genetics of inherited variation in human color vision

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

7 January 2021

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-171

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%2FNG1097-171

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%2FNG1097-171

7 January 2021

American Journal of Physiology

9

272

F678

A Vandewalle

1995

1 reference