(Q34071229)

30 July 2017

1 reference

title

In vivo role of CLC chloride channels in the kidney (English)

1 reference

30 July 2017

Uchida S

1

1 reference

30 July 2017

publication date

1 November 2000

1 reference

American Journal of Physiology - Renal Physiology

30 July 2017

published in

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30 July 2017

volume

279

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30 July 2017

issue

5

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30 July 2017

page(s)

F802-8

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Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis

30 July 2017

cites work

1 reference

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ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family

21 January 2018

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Evidence for the intracellular location of chloride channel (ClC)-type proteins: co-localization of ClC-6a and ClC-6c with the sarco/endoplasmic-reticulum Ca2+ pump SERCA2b

21 January 2018

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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

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Molecular identification of a volume-regulated chloride channel

21 January 2018

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

21 January 2018

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The yeast CLC chloride channel functions in cation homeostasis

21 January 2018

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The GEF1 gene of Saccharomyces cerevisiae encodes an integral membrane protein; mutations in which have effects on respiration and iron-limited growth

21 January 2018

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

21 January 2018

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A family of putative chloride channels from Arabidopsis and functional complementation of a yeast strain with a CLC gene disruption

21 January 2018

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Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.

21 January 2018

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Sodium chloride, urea, and water transport in the thin ascending limb of Henle. Generation of osmotic gradients by passive diffusion of solutes

21 January 2018

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

21 January 2018

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Identification of an acid-activated Cl(-) channel from human skeletal muscles

21 January 2018

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Stable and functional expression of the CIC-3 chloride channel in somatic cell lines

21 January 2018

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Cloning and expression of a protein kinase C-regulated chloride channel abundantly expressed in rat brain neuronal cells

21 January 2018

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

21 January 2018

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Complete genomic structure of the CLCN6 and CLCN7 putative chloride channel genes(1).

21 January 2018

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Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

21 January 2018

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A common molecular basis for three inherited kidney stone diseases

21 January 2018

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Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)

21 January 2018

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Diet-dependent hypercalciuria in transgenic mice with reduced CLC5 chloride channel expression.

21 January 2018

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

21 January 2018

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Molecular cloning of CLC chloride channels in Oreochromis mossambicus and their functional complementation of yeast CLC gene mutant.

21 January 2018

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Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria

21 January 2018

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The swelling-activated chloride channel ClC-2, the chloride channel ClC-3, and ClC-5, a chloride channel mutated in kidney stone disease, are expressed in distinct subpopulations of renal epithelial cells

21 January 2018

1 reference

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Disruption of clh-1, a chloride channel gene, results in a wider body of Caenorhabditis elegans

21 January 2018

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CLC chloride channels in Caenorhabditis elegans

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.2000.279.5.F802

Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.2000.279.5.F802

Cloning, tissue distribution, and intrarenal localization of ClC chloride channels in human kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.2000.279.5.F802

A chloride channel widely expressed in epithelial and non-epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.2000.279.5.F802

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

21 January 2018

1 reference

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Localization and induction by dehydration of ClC-K chloride channels in the rat kidney.

21 January 2018

1 reference

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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/10.1152%2FAJPRENAL.2000.279.5.F802

10.1152/AJPRENAL.2000.279.5.F802

21 January 2018

Identifiers

DOI

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1 reference