(Q34113703)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11840194%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

NEDD4L on human chromosome 18q21 has multiple forms of transcripts and is a homologue of the mouse Nedd4-2 gene (English)

1 reference

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7 December 2019

8

1 reference

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7 December 2019

J. Raymond DePaulo

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11840194%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

author name string

H Chen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11840194%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

C A Ross

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11840194%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

N Wang

3

1 reference

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7 December 2019

Y Huo

4

1 reference

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7 December 2019

D F MacKinnon

5

1 reference

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7 December 2019

J B Potash

6

1 reference

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7 December 2019

S G Simpson

7

1 reference

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7 December 2019

M G McInnis

10

1 reference

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7 December 2019

publication date

1 December 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11840194%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

7 December 2019

published in

1 reference

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7 December 2019

volume

9

1 reference

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7 December 2019

issue

12

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7 December 2019

page(s)

922-930

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Identification of a set of genes with developmentally down-regulated expression in the mouse brain

7 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Prediction of the coding sequences of unidentified human genes. III. The coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

cDNA cloning, expression analysis, and mapping of the mouse Nedd4 gene.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Molecular cloning of Nedd4 from Xenopus laevis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

NPl1, an essential yeast gene involved in induced degradation of Gap1 and Fur4 permeases, encodes the Rsp5 ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Nedd4-like proteins: an emerging family of ubiquitin-protein ligases implicated in diverse cellular functions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Regulation of stability and function of the epithelial Na+ channel (ENaC) by ubiquitination

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Regulation of the cardiac voltage-gated Na+ channel (H1) by the ubiquitin-protein ligase Nedd4.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

The yeast Npi1/Rsp5 ubiquitin ligase lacking its N-terminal C2 domain is competent for ubiquitination but not for subsequent endocytosis of the gap1 permease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Multiple WW domains, but not the C2 domain, are required for inhibition of the epithelial Na+ channel by human Nedd4

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

The C2 domain of the ubiquitin protein ligase Nedd4 mediates Ca2+-dependent plasma membrane localization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Function of WW domains as phosphoserine- or phosphothreonine-binding modules

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Linkage of bipolar affective disorder to chromosome 18 markers in a new pedigree series.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

The Nedd4-like protein KIAA0439 is a potential regulator of the epithelial sodium channel

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Basic local alignment search tool

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

A radiation hybrid map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Consed: a graphical tool for sequence finishing

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Base-calling of automated sequencer traces using phred. II. Error probabilities

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Nedd4 mediates control of an epithelial Na+ channel in salivary duct cells by cytosolic Na+

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Possible Locus on Chromosome 18q Influencing Postural Systolic Blood Pressure Changes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Evidence for a new Graves disease susceptibility locus at chromosome 18q21.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200747

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200747

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11840194%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference