Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation (Q24306905)

membrane repolarization during atrial cardiac muscle cell action potential

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

7

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Søren-Peter Olesen

8

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Martin Nybo Andersen

Martin N Andersen

4

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Ingrid Christophersen

Ingrid E Christophersen

1

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Morten Salling Olesen

Morten S Olesen

2

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Nicole Schmitt

Nicole Schmitt

11

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Jesper Hastrup Svendsen

Jesper H Svendsen

10

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author name string

Bo Liang

3

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Anders P Larsen

5

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Jonas B Nielsen

6

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Arnljot Tveit

Status of the epidemiology of atrial fibrillation

9

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language of work or name

English

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publication date

May 2013

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published in

European Heart Journal

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volume

34

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issue

20

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page(s)

1517-25

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cites work

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Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring

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New ideas about atrial fibrillation 50 years on.

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Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

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Identity of a novel delayed rectifier current from human heart with a cloned K+ channel current.

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Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

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Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation

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Functional differences in Kv1.5 currents expressed in mammalian cell lines are due to the presence of endogenous Kv beta 2.1 subunits

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Ancillary subunits associated with voltage-dependent K+ channels

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CELLULAR OPEN RESOURCE (COR): current status and future directions.

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QTc: how long is too long?

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Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk

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Polymorphism screening in the cardiac K+ channel gene KCNA5.

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Lone atrial fibrillation: influence of familial disease on gender predilection

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Electrophysiological remodeling in human atrial fibrillation

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Atrial fibrillation begets atrial fibrillation. A study in awake chronically instrumented goats

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High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

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Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

21 January 2018

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Sustained depolarization-induced outward current in human atrial myocytes. Evidence for a novel delayed rectifier K+ current similar to Kv1.5 cloned channel currents

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inferred from DOI database lookup

7 January 2021

based on heuristic

Antisense oligodeoxynucleotides directed against Kv1.5 mRNA specifically inhibit ultrarapid delayed rectifier K+ current in cultured adult human atrial myocytes

1 reference

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