Regulation of the epithelial sodium channel by N4WBP5A, a novel Nedd4/Nedd4-2-interacting protein (Q28564648)

31 January 2017

title

Regulation of the epithelial sodium channel by N4WBP5A, a novel Nedd4/Nedd4-2-interacting protein (English)

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31 January 2017

Brian Degger

4

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Sharad Kumar

object named as

Sharad Kumar

8

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Daniela Riccardi

object named as

Daniela Riccardi

5

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Linda M. Shearwin

2

object named as

Linda M. Shearwin-Whyatt

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31 January 2017

author name string

Angelos-Aristeidis Konstas

1

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31 January 2017

Andrew B. Fotia

3

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31 January 2017

David I. Cook

6

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31 January 2017

Christoph Korbmacher

7

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31 January 2017

language of work or name

English

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publication date

16 August 2002

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Journal of Biological Chemistry

31 January 2017

published in

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31 January 2017

volume

277

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31 January 2017

issue

33

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31 January 2017

page(s)

29406–29416

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Epithelial sodium channels: function, structure, and regulation

31 January 2017

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Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

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Cell surface expression of the epithelial Na channel and a mutant causing Liddle syndrome: a quantitative approach

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A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system

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Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel

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Mutations causing Liddle syndrome reduce sodium-dependent downregulation of the epithelial sodium channel in the Xenopus oocyte expression system.

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The Activity of the Epithelial Sodium Channel Is Regulated by Clathrin-mediated Endocytosis

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All three WW domains of murine Nedd4 are involved in the regulation of epithelial sodium channels by intracellular Na+

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A novel mouse Nedd4 protein suppresses the activity of the epithelial Na+ channel

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N4WBP5, a potential target for ubiquitination by the Nedd4 family of proteins, is a novel Golgi-associated protein

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Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits

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cAMP stimulates CFTR-like Cl- channels and inhibits amiloride-sensitive Na+ channels in mouse CCD cells

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21 January 2018

Identifiers

DOI

10.1074/JBC.M203018200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017