(Q39816254)

14 September 2017

title

Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing (English)

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14 September 2017

7

Rosa Vargas-Poussou

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author name string

Teddy Grand

1

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14 September 2017

David Mordasini

2

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14 September 2017

Sébastien L'Hoste

3

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14 September 2017

Thomas Pennaforte

4

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14 September 2017

Mathieu Genete

5

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14 September 2017

Marie-Jeanne Biyeyeme

6

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14 September 2017

Rosa Vargas-Poussou

7

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14 September 2017

Anne Blanchard

8

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14 September 2017

Jacques Teulon

9

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14 September 2017

Stéphane Lourdel

10

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14 September 2017

language of work or name

English

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publication date

5 August 2009

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14 September 2017

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14 September 2017

volume

76

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14 September 2017

issue

9

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14 September 2017

page(s)

999-1005

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https://scigraph.springernature.com/pub.10.1038/ki.2009.305

14 September 2017

exact match

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cites work

Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Dent Disease with mutations in OCRL1

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Chloride/proton antiporter activity of mammalian CLC proteins ClC-4 and ClC-5.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Voltage-dependent electrogenic chloride/proton exchange by endosomal CLC proteins

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Molecular cloning and characterization of an intracellular chloride channel in the proximal tubule cell line, LLC-PK1.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Intracellular localization of ClC chloride channels and their ability to form hetero-oligomers

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Impaired acidification in early endosomes of ClC-5 deficient proximal tubule

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

The ClC-5 chloride channel knock-out mouse - an animal model for Dent's disease.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Cofilin interacts with ClC-5 and regulates albumin uptake in proximal tubule cell lines.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Regulation of albumin endocytosis by PSD95/Dlg/ZO-1 (PDZ) scaffolds. Interaction of Na+-H+ exchange regulatory factor-2 with ClC-5.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Nedd4-2 functionally interacts with ClC-5: involvement in constitutive albumin endocytosis in proximal tubule cells

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalization.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Functional expression of the human thiazide-sensitive NaCl cotransporter in Madin-Darby canine kidney cells.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

N-glycosylation of the Xenopus laevis ClC-5 protein plays a role in cell surface expression, affecting transport activity at the plasma membrane.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Coexpression of complementary fragments of ClC-5 and restoration of chloride channel function in a Dent's disease mutation.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

ClC-5: role in endocytosis in the proximal tubule.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.305

7 January 2021

Identifiers

DOI

10.1038/KI.2009.305

1 reference

Dimensions Publication ID

14 September 2017

1035776395

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1 reference