Disruption of KCC2 reveals an essential role of K-Cl cotransport already in early synaptic inhibition (Q28513477)

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8 November 2019

title

Disruption of KCC2 reveals an essential role of K-Cl cotransport already in early synaptic inhibition (English)

2 references

25 January 2017

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Solute carrier family 12, member 5

8 November 2019

main subject

1 reference

GOA release 2020-03-11

author

Valentin Stein

2

1 reference

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8 November 2019

Thomas Jentsch

6

1 reference

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8 November 2019

author name string

C A Hübner

1

1 reference

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8 November 2019

I Hermans-Borgmeyer

3

1 reference

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8 November 2019

T Meyer

4

1 reference

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8 November 2019

K Ballanyi

5

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8 November 2019

language of work or name

English

0 references

publication date

1 May 2001

2 references

25 January 2017

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8 November 2019

2 references

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8 November 2019

volume

30

2 references

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8 November 2019

issue

2

2 references

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8 November 2019

page(s)

515-524

1 reference

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Respiratory network function in the isolated brainstem-spinal cord of newborn rats

8 November 2019

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Perforated-patch recording with gramicidin avoids artifactual changes in intracellular chloride concentration.

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GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis

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Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family

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Failure of spermatogenesis in mouse lines deficient in the Na(+)-K(+)-2Cl(-) cotransporter

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Molecular characterization of a putative K-Cl cotransporter in rat brain. A neuronal-specific isoform

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Partial cloning and characterization of Slc12a2: the gene encoding the secretory Na+-K+-2Cl- cotransporter

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7 January 2021

The K+/Cl- co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation

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7 January 2021

Involvement of GABA and glycine in recurrent inhibition of spinal motoneurons

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7 January 2021

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

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7 January 2021

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

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

1855003

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11395011%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1855003

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1855003