(Q24291252)

potassium ion import across plasma membrane

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

N M Plaster

1

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R Tawil

2

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M Tristani-Firouzi

3

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S Canún

4

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S Bendahhou

5

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A Tsunoda

6

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M R Donaldson

7

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S T Iannaccone

8

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E Brunt

9

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R Barohn

10

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J Clark

11

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F Deymeer

12

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A L George

13

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F A Fish

14

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A Hahn

15

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A Nitu

16

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C Ozdemir

17

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P Serdaroglu

18

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S H Subramony

19

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G Wolfe

20

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Y H Fu

21

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L J Ptácek

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

22

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language of work or name

English

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publication date

18 May 2001

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published in

Cell

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volume

105

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issue

4

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page(s)

511-9

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cites work

1 reference

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7 January 2021

Andersen syndrome autosomal dominant in three generations

1 reference

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7 January 2021

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

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7 January 2021

Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function

1 reference

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7 January 2021

The inward rectifier potassium channel family.

1 reference

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7 January 2021

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis

1 reference

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7 January 2021

Voltage‐gated and inwardly rectifying potassium channels

1 reference

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7 January 2021

Early afterdepolarizations: mechanism of induction and block. A role for L-type Ca2+ current

1 reference

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7 January 2021

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

1 reference

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7 January 2021

Sudden death risk in overt coronary heart disease: the Framingham Study

1 reference

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7 January 2021

Ontogeny of Gene Expression of Kir Channel Subunits in the Rat

1 reference

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7 January 2021

Molecular and cellular mechanisms of cardiac arrhythmias

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Calculation of QTc duration and variability in the presence of sinus arrhythmia

1 reference

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7 January 2021

The exercise test in periodic paralysis

1 reference

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7 January 2021

Molecular cloning and functional expression of a novel brain-specific inward rectifier potassium channel

1 reference

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7 January 2021

Inward rectifier potassium channels

1 reference

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7 January 2021

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

1 reference

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7 January 2021

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

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7 January 2021

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

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7 January 2021

Molecular cloning and expression of a human heart inward rectifier potassium channel

1 reference

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7 January 2021

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

1 reference

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7 January 2021

Insulin acts in hypokalemic periodic paralysis by reducing inward rectifier K+ current

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Skeletal muscle sodium current is reduced in hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Defective slow inactivation of sodium channels contributes to familial periodic paralysis

1 reference

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7 January 2021

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Andersen's syndrome: A distinct periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Diagnostic criteria for the long QT syndrome. An update

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Mutations in the hminK gene cause long QT syndrome and suppress lKs function

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

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

1 reference

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7 January 2021

Regions responsible for the assembly of inwardly rectifying potassium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Kir2.4: a novel K+ inward rectifier channel associated with motoneurons of cranial nerve nuclei

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Voltage‐dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Mapping of the physical interaction between the intracellular domains of an inwardly rectifying potassium channel, Kir6.2

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Circadian variation in the incidence of sudden cardiac death in the Framingham Heart Study population

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

Determination of the subunit stoichiometry of an inwardly rectifying potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900342-7

7 January 2021

10.1016/S0092-8674(01)00342-7

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11371347

1 reference

Consolidated OpenCitations Corpus – April 2017