Short QT Syndrome 3

Known as: SQT3 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2005-2017
024620052017

Papers overview

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2017
2017
Gain-of-function mutations in KCNJ2-encoded Kir2.1 channels underlie variant 3 (SQT3) of the short QT syndrome, which is… (More)
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2017
2017
Kir2.1 plays key roles in setting rest membrane potential and modulation of cell excitability. Mutations of Kir2.1, such as D172N… (More)
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2017
2017
A gain-of-function KCNJ2 D172N mutation in KCNJ2-encoded Kir2.1 channels underlies one form of short QT syndrome (SQT3), which is… (More)
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2015
2015
BACKGROUND Short QT syndrome (SQTS) is a rare inheritable arrhythmia, associated with atrial and ventricular fibrillations… (More)
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2013
2013
In the present study we developed a computer models of human ventricular cell and tissue to simulate SQT3 syndrome that is… (More)
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2012
2012
AIMS One form of the short QT syndrome (SQT3) has been linked to the D172N gain-in-function mutation to Kir2.1, which… (More)
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Review
2012
Review
2012
The short QT syndrome (SQTS) is a recently recognized cardiac channelopathy characterized by a shortened QT interval in the… (More)
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2009
2009
Short QT Syndrome (SQTS) is a novel clinical entity characterized by markedly rapid cardiac repolarization and lethal arrhythmias… (More)
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Review
2006
Review
2006
In 2005, one of the major areas of interest in the field of electrophysiology remains ablation of atrial fibrillation (AF… (More)
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Highly Cited
2005
Highly Cited
2005
Short QT syndrome (SQTS) leads to an abbreviated QTc interval and predisposes patients to life-threatening arrhythmias. To date… (More)
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