Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis (Q24295040)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074522%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074522%20AND%20SRC:MED&resulttype=core&format=json

Potassium inwardly rectifying channel subfamily J member 18

16 January 2020

main subject

1 reference

hypokalemic periodic paralysis

GOA release 2020-03-11

1 reference

1

1 reference

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16 January 2020

Mui Cheng Liang

8

1 reference

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16 January 2020

Rui M. B. Maciel

13

1 reference

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16 January 2020

author name string

Magnus R Dias da Silva

2

1 reference

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16 January 2020

Tuck Wah Soong

3

1 reference

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16 January 2020

Bertrand Fontaine

4

1 reference

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16 January 2020

Matt R Donaldson

5

1 reference

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16 January 2020

Annie W C Kung

6

1 reference

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16 January 2020

Wallaya Jongjaroenprasert

7

1 reference

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16 January 2020

Daphne H C Khoo

9

1 reference

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16 January 2020

Jin Seng Cheah

10

1 reference

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16 January 2020

Su Chin Ho

11

1 reference

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16 January 2020

Harold S Bernstein

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074522%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Robert H Brown

14

1 reference

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16 January 2020

Louis J Ptácek

15

1 reference

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16 January 2020

language of work or name

English

0 references

publication date

1 January 2010

1 reference

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16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074522%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

140

1 reference

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16 January 2020

issue

1

1 reference

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16 January 2020

page(s)

88-98

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Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies

16 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Thyroxine signal transduction in liver cells involves phospholipase C and phospholipase D activation. Genomic independent action of thyroid hormone

19 March 2017

1 reference

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Cloning and functional expression of an inwardly rectifying K+ channel from human atrium

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge

19 March 2017

1 reference

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Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins

19 March 2017

1 reference

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A multiprotein trafficking complex composed of SAP97, CASK, Veli, and Mint1 is associated with inward rectifier Kir2 potassium channels

19 March 2017

1 reference

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Channelopathies of inwardly rectifying potassium channels

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

The inwardly rectifying potassium channel subunit Kir2.2v (KCNJN1) maps to 17p11.2-->p11.1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Kir2.2v: a possible negative regulator of the inwardly rectifying K+ channel Kir2.2

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

An assessment of the sequence gaps: unfinished business in a finished human genome

19 March 2017

1 reference

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Mechanisms of thyroid hormone receptor-specific nuclear and extra nuclear actions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Mechanism of rectification in inward-rectifier K+ channels

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Segmental duplications: organization and impact within the current human genome project assembly

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels.

27 September 2017

1 reference

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Thyroid hormone induces activation of mitogen-activated protein kinase in cultured cells

27 September 2017

1 reference

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A novel inward rectifier K+ channel with unique pore properties

27 September 2017

1 reference

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Molecular cloning and functional expression of cDNA encoding a second class of inward rectifier potassium channels in the mouse brain.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Thyrotoxic periodic paralysis. Report of 10 cases and review of electromyographic findings

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

Regions responsible for the assembly of inwardly rectifying potassium channels

27 September 2017

1 reference

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Inward rectifier potassium channels

27 September 2017

1 reference

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Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation.

27 September 2017

1 reference

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[Thyrotoxic hypokalemic periodic paralysis, an endocrine emergency: clinical and genetic features in 25 patients].

30 May 2018

1 reference

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

29 November 2018

1 reference

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Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology.

29 November 2018

1 reference

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Human cardiac inwardly-rectifying K+ channel Kir(2.1b) is inhibited by direct protein kinase C-dependent regulation in human isolated cardiomyocytes and in an expression system

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2885139

A novel sodium channel mutation in a family with hypokalemic periodic paralysis

29 November 2018

1 reference

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Acute onset of hypokalemia and muscular weakness in four hyperthyroid cats

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20074522

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.CELL.2009.12.024

2 references

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16 January 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074522%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

2 references