(Q46135689)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19570891%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

title

Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes (English)

1 reference

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1 February 2020

1

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1 February 2020

Dina Simkin

2

1 reference

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1 February 2020

author name string

N Arrighi

3

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1 February 2020

F Chapon

4

1 reference

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1 February 2020

M M Larroque

5

1 reference

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1 February 2020

S Vicart

6

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1 February 2020

D Sternberg

7

1 reference

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1 February 2020

B Fontaine

8

1 reference

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1 February 2020

J Barhanin

9

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1 February 2020

C Desnuelle

10

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1 February 2020

S Bendahhou

11

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1 February 2020

publication date

1 July 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19570891%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Physiology - Cell Physiology

1 February 2020

published in

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1 February 2020

volume

297

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1 February 2020

issue

4

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1 February 2020

page(s)

C876-85

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MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis

1 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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In vivo and in vitro functional characterization of Andersen's syndrome mutations.

21 January 2018

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Cable properties of external intercostal muscle fibres from myotonic and nonmyotonic goats

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties

21 January 2018

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Human myoblast fusion requires expression of functional inward rectifier Kir2.1 channels

21 January 2018

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Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

21 January 2018

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Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).

21 January 2018

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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

21 January 2018

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A calcium channel mutation causing hypokalemic periodic paralysis

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

The skeletal muscle chloride channel in dominant and recessive human myotonia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

Crystal structure of the potassium channel KirBac1.1 in the closed state

21 January 2018

1 reference

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Role of an inward rectifier K+ current and of hyperpolarization in human myoblast fusion

21 January 2018

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Inward rectifiers in the heart: an update on I(K1).

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

An improved colorimetric assay for cell proliferation and viability utilizing the tetrazolium salt XTT.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

KV2.1 K+ channels underlie major voltage-gated K+ outward current in H9c2 myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00519.2008