(Q73777204)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326919%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Chloride channels cough up (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326919%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Thakker RV

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326919%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 October 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326919%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326919%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

17

1 reference

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6 November 2019

issue

2

1 reference

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6 November 2019

page(s)

125-127

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng1097-125

6 November 2019

exact match

0 references

cites work

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%2FNG1097-125

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/10.1038%2FNG1097-125

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%2FNG1097-125

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/10.1038%2FNG1097-125

7 January 2021

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

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%2FNG1097-125

7 January 2021

Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

The strychnine-binding subunit of the glycine receptor shows homology with nicotinic acetylcholine receptors

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Sequence and functional expression of the GABA A receptor shows a ligand-gated receptor super-family

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

The skeletal muscle chloride channel in dominant and recessive human myotonia

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Benzodiazepine-induced motor impairment linked to point mutation in cerebellar GABAA receptor.

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-125

7 January 2021

Identifiers

DOI

10.1038/NG1097-125

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326919%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference