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Long QT Syndrome (LQTS) is a genetic disorder that causes prolongation of cardiac repolarization, observed as an elongation between the Q and T waves observed on an electrocardiogram. The lengthening of these waves can cause unexpected and life threatening arrhythmias. Current therapies for the LQTS are limited to ?-blockers and left cardiac sympathetic denervation which prevent fatal arrhythmia and Implantable Cardiac-Defibrillators (ICD) which terminate arrhythmia. However, these therapies often need to be used in combination, and impact negatively the quality of life of the patients. So far, no therapy actually restores normal repolarization and shortens the QT interval. Recently a compound, 2-MMB, has been reported to rescue LQTS on zebrafishes by correcting the repolarization defect. However, no therapeutic target has been identified yet for this compound, and the mechanism of action remains unknown. The purpose of that project is to identify the therapeutic target of 2-MMB.
Andreea Schmitzer
Thryv Therapeutics
Life Sciences
Health and Related Sciences & Technology; Biotechnology; Pharmaceuticals
Université de Montréal
Accelerate
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