In Vitro and In Silico Risk Assessment in Acquired Long QT Syndrome: The Devil Is in the Details-Reference-Cited by-同舟云学术

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In Vitro and In Silico Risk Assessment in Acquired Long QT Syndrome: The Devil Is in the Details

Published:2017-11-16 Issue: Volume:8 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

Lee William,Windley Monique J.,Vandenberg Jamie I.,Hill Adam P.

Funder

National Heart Foundation of Australia

National Health and Medical Research Council

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference81 articles.

1. Cellular and ionic mechanism for drug-induced long QT syndrome and effectiveness of verapamil;Aiba;J. Am. Coll. Cardiol.,2005

2. Mechanism of hERG K+ channel blockade by the fluoroquinolone antibiotic moxifloxacin;Alexandrou;Br. J. Pharmacol.,2006

3. Control of cardiac repolarization by phosphoinositide 3-kinase signaling to ion channels;Ballou;Circ. Res.,2015

4. Reverse rate dependency is an intrinsic property of canine cardiac preparations;Bányász;Cardiovasc. Res.,2009

5. Sinusoidal voltage protocols for rapid characterization of ion channel kinetics;Beattie;bioRxiv,2017

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3. The impact of uncertainty in hERG binding mechanism onin silicopredictions of drug-induced proarrhythmic risk;2023-03-15

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