(Q40196949)

18 September 2017

An andersen-Tawil syndrome mutation in Kir2.1 (V302M) alters the G-loop cytoplasmic K+ conduction pathway (English)

1 reference

18 September 2017

Andersen-Tawil syndrome

1 reference

Donghui Ma

1

1 reference

18 September 2017

Xiang D Tang

series ordinal

2

1 reference

18 September 2017

Terry B Rogers

series ordinal

3

1 reference

18 September 2017

Paul A Welling

series ordinal

4

1 reference

18 September 2017

language of work or name

English

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publication date

13 December 2006

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Journal of Biological Chemistry

18 September 2017

9

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based on heuristic

inferred from page(s)

published in

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18 September 2017

282

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18 September 2017

8

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18 September 2017

5781-5789

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Andersen's syndrome: A distinct periodic paralysis

18 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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/10.1074%2FJBC.M608776200

Inward rectification and implications for cardiac excitability

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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/10.1074%2FJBC.M608776200

Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

A glutamate residue at the C terminus regulates activity of inward rectifier K+ channels: implication for Andersen's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Structural basis of inward rectification: cytoplasmic pore of the G protein-gated inward rectifier GIRK1 at 1.8 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Functional roles of charged amino acid residues on the wall of the cytoplasmic pore of Kir2.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

The mechanism of inward rectification of potassium channels: "long-pore plugging" by cytoplasmic polyamines

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Structural determinants of PIP(2) regulation of inward rectifier K(ATP) channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Andersen's syndrome mutation effects on the structure and assembly of the cytoplasmic domains of Kir2.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Role of ER export signals in controlling surface potassium channel numbers

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

A mutation linked with Bartter's syndrome locks Kir 1.1a (ROMK1) channels in a closed state

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

A phosphorylation-dependent export structure in ROMK (Kir 1.1) channel overrides an endoplasmic reticulum localization signal

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Reactive oxygen species impair Slo1 BK channel function by altering cysteine-mediated calcium sensing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Assembly and Trafficking of a Multiprotein ROMK (Kir 1.1) Channel Complex by PDZ Interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Primary structure and functional expression of a mouse inward rectifier potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Characteristic interactions with phosphatidylinositol 4,5-bisphosphate determine regulation of kir channels by diverse modulators

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Carboxy-terminal determinants of conductance in inward-rectifier K channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

The kinetic and physical basis of K(ATP) channel gating: toward a unified molecular understanding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Coupling Gbetagamma-dependent activation to channel opening via pore elements in inwardly rectifying potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

Yeast screen for constitutively active mutant G protein-activated potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608776200

21 January 2018

Identifiers

DOI

10.1074/JBC.M608776200

1 reference

18 September 2017

1 reference