(Q48889584)

16 February 2018

title

Functional and structural analysis of ClC-K chloride channels involved in renal disease. (English)

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16 February 2018

author

Thomas Jentsch

series ordinal

2

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16 February 2018

author name string

Waldegger S

series ordinal

1

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16 February 2018

language of work or name

English

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publication date

1 August 2000

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16 February 2018

Journal of Biological Chemistry

number of pages

7

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based on heuristic

inferred from page(s)

published in

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16 February 2018

volume

275

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16 February 2018

issue

32

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16 February 2018

page(s)

24527-24533

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16 February 2018

The CLC chloride channel family

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Cl- channels in basolateral renal medullary vesicles. X. Cloning of a Cl- channel from rabbit outer medulla

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Expression and targeting to the plasma membrane of xClC-K, a chloride channel specifically expressed in distinct tubule segments of Xenopus laevis kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Localization and functional characterization of rat kidney-specific chloride channel, ClC-K1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Heteromultimeric CLC chloride channels with novel properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Pore-forming segments in voltage-gated chloride channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

A mutation in autosomal dominant myotonia congenita affects pore properties of the muscle chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Transmembrane topology of a CLC chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1.

21 January 2018

1 reference

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Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p

21 January 2018

1 reference

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Expression of human pICln and ClC-6 in Xenopus oocytes induces an identical endogenous chloride conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Mutational analysis demonstrates that ClC-4 and ClC-5 directly mediate plasma membrane currents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Inward rectification in ClC-0 chloride channels caused by mutations in several protein regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Gating of the voltage-dependent chloride channel CIC-0 by the permeant anion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Two physically distinct pores in the dimeric ClC-0 chloride channel.

21 January 2018

1 reference

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Homodimeric architecture of a ClC-type chloride ion channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

The muscle chloride channel ClC-1 has a double-barreled appearance that is differentially affected in dominant and recessive myotonia

21 January 2018

1 reference

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Pore stoichiometry of a voltage-gated chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells

21 January 2018

1 reference

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Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Mechanism of inverted activation of ClC-1 channels caused by a novel myotonia congenita mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

cAMP-activated chloride channel in the basolateral membrane of the thick ascending limb of the mouse kidney.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

Cl- channels in basolateral TAL membranes. XIV. Kinetic properties of a basolateral MTAL Cl- channel.

21 January 2018

1 reference

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Apical extracellular calcium/polyvalent cation-sensing receptor regulates vasopressin-elicited water permeability in rat kidney inner medullary collecting duct

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M001987200

21 January 2018

Identifiers

DOI

10.1074/JBC.M001987200

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16 February 2018

1 reference

16 February 2018