(Q80193092)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943574%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Mutation analysis of SCNN1B in a family with Liddle's syndrome (English)

1 reference

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29 December 2019

1 reference

Weiqing Wang

1

1 reference

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29 December 2019

Weiwei Zhou

2

1 reference

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29 December 2019

Lei Jiang

3

1 reference

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29 December 2019

Bin Cui

4

1 reference

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29 December 2019

Lei Ye

5

1 reference

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29 December 2019

Tingwei Su

6

1 reference

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29 December 2019

Jiguang Wang

7

1 reference

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29 December 2019

Xiaoying Li

8

1 reference

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29 December 2019

Guang Ning

9

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29 December 2019

publication date

1 June 2006

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29 December 2019

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29 December 2019

volume

29

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29 December 2019

issue

3

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29 December 2019

page(s)

385-390

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https://scigraph.springernature.com/pub.10.1385/endo:29:3:385

29 December 2019

exact match

0 references

cites work

Liddle's syndrome: prospective genetic screening and suppressed aldosterone secretion in an extended kindred

1 reference

12 December 2020

Diagnosis of Liddle syndrome by genetic analysis of beta and gamma subunits of epithelial sodium channel--a report of five affected family members

1 reference

12 December 2020

Liddle's syndrome caused by a novel mutation in the proline-rich PY motif of the epithelial sodium channel beta-subunit

1 reference

12 December 2020

Liddle disease caused by a missense mutation of beta subunit of the epithelial sodium channel gene

1 reference

12 December 2020

A family with Liddle's syndrome caused by a new missense mutation in the beta subunit of the epithelial sodium channel

1 reference

12 December 2020

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

1 reference

12 December 2020

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

1 reference

12 December 2020

A novel epithelial sodium channel beta-subunit mutation associated with hypertensive Liddle syndrome

1 reference

12 December 2020

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

1 reference

12 December 2020

Inhibition of the epithelial Na+ channel by interaction of Nedd4 with a PY motif deleted in Liddle's syndrome.

1 reference

12 December 2020

Identification of a single cytosine base insertion mutation at Arg-597 of the beta subunit of the human epithelial sodium channel in a family with Liddle's disease.

1 reference

12 December 2020

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

1 reference

12 December 2020

Regulation of the epithelial sodium channel by accessory proteins

1 reference

12 December 2020

Two sporadic cases of Liddle's syndrome caused by De novo ENaC mutations

1 reference

12 December 2020

A frameshift mutation of beta subunit of epithelial sodium channel in a case of isolated Liddle syndrome

1 reference

12 December 2020

Structure and regulation of amiloride-sensitive sodium channels

1 reference

12 December 2020

A new mutation, R563Q, of the beta subunit of the epithelial sodium channel associated with low-renin, low-aldosterone hypertension

1 reference

12 December 2020

Effect of subunit composition and Liddle's syndrome mutations on biosynthesis of ENaC

1 reference

12 December 2020

MolTalk--a programming library for protein structures and structure analysis

1 reference

12 December 2020

Epithelial sodium channel related to proteins involved in neurodegeneration

1 reference

12 December 2020

Brief report: Liddle's syndrome revisited--a disorder of sodium reabsorption in the distal tubule

1 reference

12 December 2020

Genetic analysis of the epithelial sodium channel in Liddle's syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

iMolTalk: an interactive, internet-based protein structure analysis server.

1 reference

12 December 2020

Identifiers

DOI

10.1385/ENDO:29:3:385

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943574%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 December 2019

0 references

1 reference