Predicting QRS and PR interval prolongations in humans using nonclinical data.

scientific article

Predicting QRS and PR interval prolongations in humans using nonclinical data. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/BPH.13940
P932PMC publication ID5595766
P698PubMed publication ID28675424

P50authorLinnéa BergenholmQ88444495
P2093author name stringT Collins
J Parkinson
M J Chappell
N D Evans
J Mettetal
P2860cites workFlecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansQ24608179
Mouse heart Na+ channels: primary structure and function of two isoforms and alternatively spliced variantsQ28504505
The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligandsQ28603128
The Concise Guide to PHARMACOLOGY 2015/16: Voltage-gated ion channels.Q30488645
Parameter Identifiability of Fundamental Pharmacodynamic ModelsQ30830719
A pharmacokinetic-pharmacodynamic model for the quantitative prediction of dofetilide clinical QT prolongation from human ether-a-go-go-related gene current inhibition dataQ30992286
PKPD modelling of PR and QRS intervals in conscious dogs using standard safety pharmacology dataQ31037653
Animal research: reporting in vivo experiments: the ARRIVE guidelinesQ34116755
The relevance of cellular to clinical electrophysiology in classifying antiarrhythmic actionsQ34534295
How can we improve our understanding of cardiovascular safety liabilities to develop safer medicines?Q35036150
Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug developmentQ35095735
Cardiac Safety Implications of hNav1.5 Blockade and a Framework for Pre-Clinical Evaluation.Q35698299
THE RATIO BETWEEN THE HEART-WEIGHT AND BODY-WEIGHT IN VARIOUS ANIMALS.Q36240881
The promiscuous nature of the cardiac sodium currentQ36731634
Identifying the translational gap in the evaluation of drug-induced QTc interval prolongationQ37369309
Long-term outcomes in individuals with prolonged PR interval or first-degree atrioventricular blockQ37396589
An evaluation of hERG current assay performance: Translating preclinical safety studies to clinical QT prolongationQ37784281
The evaluation and management of drug effects on cardiac conduction (PR and QRS intervals) in clinical developmentQ38093949
L-type CaV1.2 calcium channels: from in vitro findings to in vivo function.Q38175138
The 'overly-sensitive' heart: sodium channel block and QRS interval prolongationQ38464750
On the relationship between block of the cardiac Na⁺ channel and drug-induced prolongation of the QRS complexQ38464799
Pharmacological cardioversion of atrial fibrillation--a double-blind, randomized, placebo-controlled, multicentre, dose-escalation study of AZD1305 given intravenouslyQ38491261
Translational pharmacokinetic-pharmacodynamic modeling of QTc effects in dog and humanQ39438124
Translation of flecainide- and mexiletine-induced cardiac sodium channel inhibition and ventricular conduction slowing from nonclinical models to clinicalQ39613654
Cardiac ion channel safety profiling on the IonWorks Quattro automated patch clamp systemQ39961684
The mechanism of flecainide action in CPVT does not involve a direct effect on RyR2.Q41484309
Implementing guidelines on reporting research using animals (ARRIVE etc.): new requirements for publication in BJP.Q42332476
Experimental design and analysis and their reporting: new guidance for publication in BJP.Q42356330
Detecting drug-induced prolongation of the QRS complex: new insights for cardiac safety assessmentQ42514265
Importance of species selection in arrythmogenic models of Q-T interval prolongationQ42782038
Use of escin as a perforating agent on the IonWorks quattro automated electrophysiology platformQ43777642
Duration of QRS complex in resting electrocardiogram is a predictor of sudden cardiac death in men.Q44375576
Non-invasive telemetric electrocardiogram assessment in conscious beagle dogs.Q45962823
Ionic mechanisms limiting cardiac repolarization reserve in humans compared to dogs.Q46348942
Optimisation and validation of a medium-throughput electrophysiology-based hNav1.5 assay using IonWorks.Q46916241
The role of the anaesthetised guinea-pig in the preclinical cardiac safety evaluation of drug candidate compoundsQ48153495
Predicting changes in cardiac myocyte contractility during early drug discovery with in vitro assays.Q51073087
Voltage-gated Na+ channel transcript patterns in the mammalian heart are species-dependent.Q51731090
Antiarrhythmic agents: modulated receptor applications.Q51794509
Operational models of pharmacological agonism.Q52699226
Effects of flecainide and quinidine on human atrial action potentials. Role of rate-dependence and comparison with guinea pig, rabbit, and dog tissuesQ68339875
The effect of dextro-, levo-, and racemic verapamil on atrioventricular conduction in humansQ70046808
Comparison of intravenous and oral verapamil dosingQ70509532
Mortality following ventricular arrhythmia suppression by encainide, flecainide, and moricizine after myocardial infarction. The original design concept of the Cardiac Arrhythmia Suppression Trial (CAST)Q72580560
Development and validation of a 96-well equilibrium dialysis apparatus for measuring plasma protein bindingQ73311345
Preformulation evaluation of AZD1305, an oxabispidine intended for oral and intravenous treatmentQ84451696
Sensitivity of pharmacokinetic-pharmacodynamic analysis for detecting small magnitudes of QTc prolongation in preclinical safety testingQ86446569
Effects of d,l-verapamil on atrioventricular conduction in relation to its stereoselective first-pass metabolismQ93571513
P433issue19
P407language of work or nameEnglishQ1860
P304page(s)3268-3283
P577publication date2017-08-24
P1433published inBritish Journal of PharmacologyQ919631
P1476titlePredicting QRS and PR interval prolongations in humans using nonclinical data
P478volume174