(Q43744651)

English

Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families

scientific article published on 9 January 2007

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Andersen-Tawil syndrome

1 reference

based on heuristic

inferred from title

author name string

Byung-Ok Choi

1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Joonki Kim

2

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Bum Chun Suh

3

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Jin Seok Yu

4

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Il Nam Sunwoo

5

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Song Ja Kim

6

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Gwang Hoon Kim

7

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Ki Wha Chung

8

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

publication date

9 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

52

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

280-283

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Channelopathies: Kir2.1 mutations jeopardize many cell functions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of inwardly rectifying K+ channels by distinct PtdIns(4,5)P2 interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of the subunit stoichiometry of an inwardly rectifying potassium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Andersen's syndrome: A distinct periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct activation of inward rectifier potassium channels by PIP2 and its stabilization by Gbetagamma

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17211524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-006-0100-7

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q43744651&oldid=2206235532"