(Q28239461)

5

0 references

Jesper Hastrup Svendsen

7

Jesper Hastrup Svendsen

0 references

Morten Salling Olesen

Morten Salling Olesen

3

0 references

Nicole Schmitt

Nicole Schmitt

8

0 references

Bo Hjorth Bentzen

Bo Hjorth Bentzen

2

0 references

author name string

Jonas Bille Nielsen

1

0 references

Jens-Peter David

4

0 references

language of work or name

English

0 references

publication date

2014

0 references

published in

Biomarkers in Medicine

1 reference

PubMed

volume

8

0 references

issue

4

0 references

page(s)

557-70

0 references

cites work

From molecule to malady

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Cardiac ion channels in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Current perceptions of the epidemiology of atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Familial aggregation of atrial fibrillation: a study in Danish twins

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

New ideas about atrial fibrillation 50 years on.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Atrial fibrillation: the role of common and rare genetic variants

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks).

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Dynamic partnership between KCNQ1 and KCNE1 and influence on cardiac IKs current amplitude by KCNE2

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNE2 is colocalized with KCNQ1 and KCNE1 in cardiac myocytes and may function as a negative modulator of I(Ks) current amplitude in the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Molecular determinants of cardiac transient outward potassium current (I(to)) expression and regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Functional modulation of the transient outward current Ito by KCNE beta-subunits and regional distribution in human non-failing and failing hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Targeted deletion of kcne2 impairs ventricular repolarization via disruption of I(K,slow1) and I(to,f)

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

KCNE2 and the K (+) channel: the tail wagging the dog

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Kcne2 deletion uncovers its crucial role in thyroid hormone biosynthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Dynamic subunit stoichiometry confers a progressive continuum of pharmacological sensitivity by KCNQ potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137

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

1 reference

https://api.crossref.org/works/10.2217%2FBMM.13.137