Select Publications
Journal articles
2023, 'Development of a robust induced pluripotent stem cell atrial cardiomyocyte differentiation protocol to model atrial arrhythmia', Stem Cell Research and Therapy, 14, http://dx.doi.org/10.1186/s13287-023-03405-5
,2023, 'Action Potential Morphology Accurately Predicts Proarrhythmic Risk for Drugs with Potential to Prolong Cardiac Repolarization', Circulation: Arrhythmia and Electrophysiology, 16, pp. 399 - 410, http://dx.doi.org/10.1161/CIRCEP.122.011574
,2023, 'Using many different voltage protocols to characterise discrepancy in mathematical ion channel models', Biophysical journal, 122, http://dx.doi.org/10.1016/j.bpj.2022.11.1415
,2022, 'Pathophysiological metabolic changes associated with disease modify the proarrhythmic risk profile of drugs with potential to prolong repolarisation', British Journal of Pharmacology, 179, pp. 2631 - 2646, http://dx.doi.org/10.1111/bph.15757
,2021, 'Co-expression of calcium and hERG potassium channels reduces the incidence of proarrhythmic events', Cardiovascular Research, 117, pp. 2216 - 2227, http://dx.doi.org/10.1093/cvr/cvaa280
,2021, 'Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-Throughput automated patch clamp electrophysiology', Biology Methods and Protocols, 6, pp. 1 - 9, http://dx.doi.org/10.1093/biomethods/bpab003
,2021, 'Functional Analysis of a Novel Heterozygous Variant in CASQ2 as a Distinct Cause of Catecholaminergic Polymorphic Ventricular Tachycardia', Heart, Lung and Circulation, 30, pp. S96 - S96, http://dx.doi.org/10.1016/j.hlc.2021.06.016
,2021, 'HeterozygousKCNH2variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology', , http://dx.doi.org/10.1101/2021.02.02.427891
,2020, 'Pharmacological activation of I
2020, 'High-throughput phenotyping of heteromeric human ether-à-go-go-related gene potassium channel variants can discriminate pathogenic from rare benign variants', Heart Rhythm, 17, pp. 492 - 500, http://dx.doi.org/10.1016/j.hrthm.2019.09.020
,2019, 'Protocol-dependent differences in IC
2018, 'Novel Pre–Clinical Risk Prediction of Acquired Long QT Syndrome', Heart, Lung and Circulation, 27, pp. S180 - S180, http://dx.doi.org/10.1016/j.hlc.2018.06.309
,2018, 'Pharmacological Activation of hERG Potassium Channels in Congenital Long QT Syndrome 2: Activator Compound ICA-105574 and its Effects on Mutant hERG Potassium Channels in Long QT Syndrome 2', Heart, Lung and Circulation, 27, pp. S61 - S61, http://dx.doi.org/10.1016/j.hlc.2018.06.039
,2017, 'The S1 helix critically regulates the finely tuned gating of Kv11.1 channels', Journal of Biological Chemistry, 292, pp. 7688 - 7705, http://dx.doi.org/10.1074/jbc.M117.779298
,2017, 'Recent advances in understanding and prevention of sudden cardiac death', F1000Research, 6, http://dx.doi.org/10.12688/f1000research.11855.1
,2016, 'Computational cardiology and risk stratification for sudden cardiac death: one of the grand challenges for cardiology in the 21st century', Journal of Physiology, 594, pp. 6893 - 6908, http://dx.doi.org/10.1113/JP272015
,2016, 'Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes', Journal of Molecular and Cellular Cardiology, 100, pp. 25 - 34, http://dx.doi.org/10.1016/j.yjmcc.2016.09.011
,2016, 'Tyrosine residues from the s4-s5 linker of kv11.1 channels are critical for slow deactivation', Journal of Biological Chemistry, 291, pp. 17293 - 17302, http://dx.doi.org/10.1074/jbc.M116.729392
,2016, 'Rescue of protein expression defects may not be enough to abolish the pro-arrhythmic phenotype of long QT type 2 mutations', Journal of Physiology, 594, pp. 4031 - 4049, http://dx.doi.org/10.1113/JP271805
,2016, 'Segmental differences in upregulated apical potassium channels in Mammalian colon during potassium adaptation', American Journal of Physiology - Gastrointestinal and Liver Physiology, 311, pp. G785 - G793, http://dx.doi.org/10.1152/ajpgi.00181.2015
,2016, 'TECRL: Connecting sequence to consequence for a new sudden cardiac death gene', EMBO Molecular Medicine, 8, pp. 1364 - 1365, http://dx.doi.org/10.15252/emmm.201606967
,2015, 'A universal and robust integrated platform for the scalable production of human cardiomyocytes from pluripotent stem cells', Stem Cells Translational Medicine, 4, pp. 1482 - 1494, http://dx.doi.org/10.5966/sctm.2014-0275
,2015, 'Getting to the heart of hERG K+ channel gating', Journal of Physiology, 593, pp. 2575 - 2585, http://dx.doi.org/10.1113/JP270095
,2015, 'Steady-state modulation of voltage-gated K+ channels in rat arterial smooth muscle by cyclic AMP-dependent protein kinase and protein phosphatase 2B', PLoS ONE, 10, http://dx.doi.org/10.1371/journal.pone.0121285
,2014, 'Can many subunits make light work of ion channel inactivation?', Journal of Physiology, 592, pp. 4411 - 4412, http://dx.doi.org/10.1113/jphysiol.2014.281568
,2014, 'Multiple interactions between cytoplasmic domains regulate slow deactivation of Kv11.1 channels', Journal of Biological Chemistry, 289, pp. 25822 - 25832, http://dx.doi.org/10.1074/jbc.M114.558379
,2014, 'Role of the cytoplasmic N-terminal cap and Per-Arnt-Sim (PAS) domain in trafficking and stabilization of Kv11.1 channels', Journal of Biological Chemistry, 289, pp. 13782 - 13791, http://dx.doi.org/10.1074/jbc.M113.531277
,2014, 'Multiscale cardiac modelling reveals the origins of notched T waves in long QT syndrome type 2', Nature Communications, 5, http://dx.doi.org/10.1038/ncomms6069
,2013, 'C-Terminal β9-Strand of the Cyclic Nucleotide-Binding Homology Domain Stabilizes Activated States of Kv11.1 Channels', PLoS ONE, 8, pp. e77032, http://dx.doi.org/10.1371/journal.pone.0077032
,2013, 'Hydrophobic interactions between the voltage sensor and pore mediate inactivation in Kv11.1 channels', Journal of General Physiology, 142, pp. 275 - 288, http://dx.doi.org/10.1085/jgp.201310975
,2012, 'Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels', Journal of General Physiology, 140, pp. 293 - 306, http://dx.doi.org/10.1085/jgp.201110761
,2011, 'Principal role of adenylyl cyclase 6 in K + channel regulation and vasodilator signalling in vascular smooth muscle cells', Cardiovascular Research, 91, pp. 694 - 702, http://dx.doi.org/10.1093/cvr/cvr137
,2010, 'Revealing the structural basis of action of hERG potassium channel activators and blockers', Journal of Physiology, 588, pp. 3157 - 3167, http://dx.doi.org/10.1113/jphysiol.2010.194670
,2009, 'PD-118057 contacts the pore helix of hERG1 channels to attenuate inactivation and enhance K+ conductance', Proceedings of the National Academy of Sciences of the United States of America, 106, pp. 20075 - 20080, http://dx.doi.org/10.1073/pnas.0906597106
,2009, 'Regulation of colonic apical potassium (BK) channels by cAMP and somatostatin', American Journal of Physiology - Gastrointestinal and Liver Physiology, 297, http://dx.doi.org/10.1152/ajpgi.00132.2009
,2008, 'A single amino acid difference between ether-a-go-go-related gene channel subtypes determines differential sensitivity to a small molecule activator', Molecular Pharmacology, 73, pp. 1044 - 1051, http://dx.doi.org/10.1124/mol.107.043018
,2007, 'Structural basis of action for a human ether-a-go-go-related gene 1 potassium channel activator', Proceedings of the National Academy of Sciences of the United States of America, 104, pp. 13827 - 13832, http://dx.doi.org/10.1073/pnas.0703934104
,2007, 'Altered cryptal expression of luminal potassium (BK) channels in ulcerative colitis', Journal of Pathology, 212, pp. 66 - 73, http://dx.doi.org/10.1002/path.2159
,2006, 'Drug binding interactions in the inner cavity of hERG channels: Molecular insights from structure-activity relationships of clofilium and ibutilide analogs', Molecular Pharmacology, 69, pp. 509 - 519, http://dx.doi.org/10.1124/mol.105.016741
,2004, 'The low-potency, voltage-dependent herg blocker propafenone - Molecular determinants and drug trapping', Molecular Pharmacology, 66, pp. 1201 - 1212, http://dx.doi.org/10.1124/mol.104.001743
,2004, 'Structural determinants of HERG channel block by clofilium and ibutilide', Molecular Pharmacology, 66, pp. 240 - 249, http://dx.doi.org/10.1124/mol.104.000117
,2003, 'Molecular determinants of high-affinity drug binding to HERG channels', Current Opinion in Drug Discovery and Development, 6, pp. 667 - 674
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