JCI - Citations to Long QT syndrome: from channels to cardiac arrhythmias

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Long QT syndrome: from channels to cardiac arrhythmias

Arthur J. Moss, Robert S. Kass

Arthur J. Moss, Robert S. Kass

Published August 1, 2005
Citation Information: J Clin Invest. 2005;115(8):2018-2024. https://doi.org/10.1172/JCI25537.

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Citations to this article (122)

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Exceptional Seizure-Like Presentation of Torsades De Pointes Kanchan K, Mohamed A, Kumar P	Cureus	2025
Knock-in Kcnh2 rabbit model of long QT syndrome type-2, epilepsy, and sudden death Singh V, Wagner KT, Williams LG, Ryan JM, Keller KR, Mohnkern JD, Gardner RS, Dang LT, Ziobro JM, Wojcikiewicz RJ, Tucker NR, Auerbach DS	Journal of Translational Medicine	2025
Postpartum QT Prolongation in a Long QT Syndrome Type 1 Patient Wiedenmann LC, Ehrlich JR, Goldenberg I	Annals of Noninvasive Electrocardiology	2025
Risk Prediction in Male Adolescents With Congenital Long QT Syndrome: Implications for Sex‐Specific Risk Stratification in Potassium Channel‐Mediated Long QT Syndrome Bjelic M, Goldenberg I, Younis A, Chen AY, Huang DT, Yoruk A, Aktas MK, Rosero S, Cutter K, McNitt S, Sotoodehnia N, Kudenchuk PJ, Rea TD, Arking DE, Zareba W, Ackerman MJ, Goldenberg I	Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease	2024
From genes to clinical management: A comprehensive review of long QT syndrome pathogenesis and treatment Zhu W, Bian X, Lv J	Heart Rhythm O2	2024
Computational analysis of long QT syndrome type 2 and the therapeutic effects of KCNQ1 antibodies. Pan Z, Fu Q, Jiang H, Wei Z, Zhang S	Digital health	2024
Elucidation of ALG10B as a Novel Long QT Syndrome Susceptibility Gene Zhou W, Ye D, Tester DJ, Bains S, Giudicessi JR, Haglund-Turnquist CM, Orland KM, January CT, Eckhardt LL, Maginot KR, Ackerman MJ	Circulation. Genomic and precision medicine	2023
Deciphering the roles of triiodothyronine (T3) and thyroid-stimulating hormone (TSH) on cardiac electrical remodeling in clinical and experimental hypothyroidism Casis O, Echeazarra L, Sáenz-Díez B, Gallego M	Journal of Physiology and Biochemistry	2023
Cardiac Involvement in Classical Organic Acidurias: Clinical Profile and Outcome in a Pediatric Cohort Passantino S, Chiellino S, Girolami F, Zampieri M, Calabri GB, Spaziani G, Bennati E, Porcedda G, Procopio E, Olivotto I, Favilli S	Diagnostics	2023
Low-voltage electrical injuries and the electrocardiogram: is a ‘normal’ electrocardiogram sufficient for safe discharge from care? A systematic review Corrall S, Laws S, Rice A		2023
Polypharmacy, Gender Disparities, and Ethnic and Racial Predispositions in Long QT Syndrome: An In-Depth Review Lima B, Razmjouei S, Bajwa MT, Shahzad Z, Shoewu OA, Ijaz O, Mange P, Khanal S, Gebregiorgis T	Cureus	2023
Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing Fazelifar AF, Pourirahim M, Masoumi T, Biglari A, Maleki M, Kalayinia S	Journal of Arrhythmia	2023
Downregulation of Vascular Hemeoxygenase-1 Leads to Vasculopathy in Systemic Sclerosis R Ross, G Mavria, F Galdo, J Elies	Frontiers in physiology	2022
Exploring mutation specific beta blocker pharmacology of the pathogenic late sodium channel current from patient-specific pluripotent stem cell myocytes derived from long QT syndrome mutation carriers Comollo TW, Zou X, Zhang C, Kesters D, Hof T, Sampson KJ, Kass RS	Channels	2022
Gene mutations in comorbidity of epilepsy and arrhythmia. Yu C, Deng XJ, Xu D	Journal of Neurology	2022
Engineered human cardiac tissues for modeling heart diseases Min S, Cho SW	BMB Reports	2022
A calibrated functional patch-clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome Jiang C, Richardson E, Farr J, Hill AP, Ullah R, Kroncke BM, Harrison SM, Thomson KL, Ingles J, Vandenberg JI, Ng CA	The American Journal of Human Genetics	2022
Determinants of trafficking, conduction, and disease within a K+ channel revealed through multiparametric deep mutational scanning Coyote-Maestas W, Nedrud D, He Y, Schmidt D	eLife	2022
Risk Prediction in Women With Congenital Long QT Syndrome Goldenberg I, Bos JM, Yoruk A, Chen AY, Lopes C, Huang DT, Kutyifa V, Younis A, Aktas MK, Z. Rosero S, McNitt S, Sotoodehnia N, Kudenchuk PJ, Rea TD, Arking DE, Scott CG, Briske KA, Sorensen K, J. Ackerman M, Zareba W	Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease	2021
Human‐induced pluripotent stem cell‐derived cardiomyocytes: Cardiovascular properties and metabolism and pharmacokinetics of deuterated mexiletine analogs Gomez\u2010Galeno J, Okolotowicz K, Johnson M, McKeithan WL, Mercola M, Cashman JR	Pharmacology Research & Perspectives	2021
Specific protein kinase C isoform exerts chronic inhibition on the slowly activating delayed-rectifier potassium current by affecting channel trafficking Gou X, Hu T, Gou Y, Li C, Yi M, Jia M	Channels	2021
A novel mutation in KCNH2 yields loss-of-function of hERG potassium channel in long QT syndrome 2. Gu K, Qian D, Qin H, Cui C, Fernando WCHA, Wang D, Wang J, Cao K, Chen M		2021
Structures Illuminate Cardiac Ion Channel Functions in Health and in Long QT Syndrome KR Brewer, G Kuenze, CG Vanoye, AL George, J Meiler, CR Sanders	Frontiers in pharmacology	2020
Cardiac Complications of Propionic and Other Inherited Organic Acidemias KC Park, S Krywawych, E Richard, LR Desviat, P Swietach	Frontiers in Cardiovascular Medicine	2020
Pseudo-colouring an ECG enables lay people to detect QT-interval prolongation regardless of heart rate A Alahmadi, A Davies, M Vigo, C Jay, P Pławiak	PloS one	2020
Long QT and Silver Russell syndrome: First case report in a 9-year-old girl Roses-Noguer F, Martinez-Villar M, Honti F, Edwards M, Till J, Morris-Rosendahl DJ	HeartRhythm Case Reports	2020
Gating and Regulation of KCNQ1 and KCNQ1 + KCNE1 Channel Complexes Wang Y, Eldstrom J, Fedida D	Frontiers in physiology	2020
Protective role of cardiac-specific overexpression of caveolin-3 in cirrhotic cardiomyopathy Kim SY, Kim KH, Schilling JM, Leem J, Dhanani M, Head BP, Roth DM, Zemljic-Harpf AE, Patel HH	AJP Gastrointestinal and Liver Physiology	2020
Heterogeneity of the action potential duration is required for sustained atrial fibrillation Uma Mahesh Avula, Jeffrey Abrams, Alex Katchman, Sergey I. Zakharov, Sergey Mironov, Joseph Bayne, Daniel Roybal, Anirudh K Gorti, Lin Yang, Vivek Iyer, Marc Waase, Deepak Saluja, Edward Ciaccio, Hasan Garan, Andrew R. Marks, Steven O. Marx, Elaine Y. Wan	JCI Insight	2019
Cardiac function modulation depends on the A‐kinase anchoring protein complex YR Zhu, XX Jiang, Y Zheng, J Xiong, D Wei, DM Zhang	Journal of Cellular and Molecular Medicine	2019
Induced pluripotent stem cells for therapy personalization in pediatric patients: Focus on drug-induced adverse events Genova E, Cavion F, Lucafò M, Leo LD, Pelin M, Stocco G, Decorti G	World journal of stem cells	2019
Statin-specific inhibition of Rab-GTPase regulates cPKC-mediated IKs internalization Ronzier E, Parks XX, Qudsi H, Lopes CM	Scientific Reports	2019
Characterization of a novel LQT3 variant with a selective efficacy of mexiletine treatment Kim HJ, Kim BG, Park JE, Ki CS, Huh J, Youm JB, Kang JS, Cho H	Scientific Reports	2019
Effect of Ischemic Preconditioning and Postconditioning on Exosome-Rich Fraction microRNA Levels, in Relation with Electrophysiological Parameters and Ventricular Arrhythmia in Experimental Closed-Chest Reperfused Myocardial Infarction Spannbauer A, Traxler D, Lukovic D, Zlabinger K, Winkler J, Gugerell A, Ferdinandy P, Hausenloy DJ, Pavo N, Emmert MY, Hoerstrup SP, Jakab A, Gyöngyösi M, Riesenhuber M	International journal of molecular sciences	2019
Development of a High-Throughput Flow Cytometry Assay to Monitor Defective Trafficking and Rescue of Long QT2 Mutant hERG Channels SA Kanner, A Jain, HM Colecraft	Frontiers in physiology	2018
Mutations in voltage-gated L-type calcium channel: implications in cardiac arrhythmia Q Zhang, J Chen, Y Qin, J Wang, L Zhou	Channels (Austin, Tex.)	2018
Autonomic Regulation and Ventricular Arrhythmias L Meng, K Shivkumar, O Ajijola	Current Treatment Options in Cardiovascular Medicine	2018
Abnormal Repolarization Duration During Everyday Emotional Arousal in Long QT Syndrome and Coronary Artery Disease Lane RD, Reis HT, Hsu CH, Kern KB, Couderc JP, Moss AJ, Zareba W	The American Journal of Medicine	2018
Doxorubicin induces caspase-mediated proteolysis of KV7.1 Strigli A, Raab C, Hessler S, Huth T, Schuldt AJ, Alzheimer C, Friedrich T, Burridge PW, Luedde M, Schwake M	Communications biology	2018
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Polymorphisms/Mutations in A-Kinase Anchoring Proteins (AKAPs): Role in the Cardiovascular System Suryavanshi SV, Jadhav SM, McConnell BK	Journal of Cardiovascular Development and Disease	2018
The Impact of CRISPR/Cas9 Technology on Cardiac Research: From Disease Modelling to Therapeutic Approaches BM Motta, PP Pramstaller, AA Hicks, A Rossini	Stem Cells International	2017
Human pluripotent stem cell models of cardiac disease: from mechanisms to therapies KO Brandão, VA Tabel, DE Atsma, CL Mummery, RP Davis	Disease models & mechanisms	2017
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Computational design of membrane proteins using RosettaMembrane Duran AM, Meiler J	Protein science : a publication of the Protein Society	2017
The Association between QT Interval Components and Sudden Cardiac Death: The Atherosclerosis Risk In Communities Study O'Neal WT, Singleton MJ, Roberts JD, Tereshchenko LG, Sotoodehnia N, Chen LY, Marcus GM, Soliman EZ	Circulation. Arrhythmia and electrophysiology	2017
Trigger vs. Substrate: Multi-Dimensional Modulation of QT-Prolongation Associated Arrhythmic Dynamics by a hERG Channel Activator Colman MA, Perez Alday EA, Holden AV, Benson AP	Frontiers in physiology	2017
The effects of zoledronic acid on ECG: a prospective study on patients with bone metastatic cancer Demirtas D, Bilir C, Demirtas AO, Engin H	Clinical Cases in Mineral and Bone Metabolism	2017
A novel transgenic rabbit model with reduced repolarization reserve: long QT syndrome caused by a dominant-negative mutation of the KCNE1 gene: LQT5 transgenic rabbits P Major, I Baczkó, L Hiripi, KE Odening, V Juhász, Z Kohajda, A Horváth, G Seprényi, M Kovács, L Virág, N Jost, J Prorok, B Ördög, Z Doleschall, S Nattel, A Varró, Z Bősze	British Journal of Pharmacology	2016
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Migration of PIP2 lipids on voltage-gated potassium channel surface influences channel deactivation Chen L, Zhang Q, Qiu Y, Li Z, Chen Z, Jiang H, Li Y, Yang H	Scientific Reports	2015
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The Long and the Short of It: Seizures Induce Cardiac Remodeling and Arrhythmia Smith BN, Delisle BP	Epilepsy Currents	2015
Deletion of FoxO1 Leads to Shortening of QRS by Increasing Na+ Channel Activity through Enhanced Expression of both Cardiac NaV1.5 and β3 Subunit B Cai, N Wang, W Mao, T You, Y Lu, X Li, B Ye, F Li, H Xu	Journal of Molecular and Cellular Cardiology	2014
Calcium Transients Closely Reflect Prolonged Action Potentials in iPSC Models of Inherited Cardiac Arrhythmia CI Spencer, S Baba, K Nakamura, EA Hua, MA Sears, C Fu, J Zhang, S Balijepalli, K Tomoda, Y Hayashi, P Lizarraga, J Wojciak, MM Scheinman, K Aalto-Setälä, JC Makielski, CT January, KE Healy, TJ Kamp, S Yamanaka, BR Conklin	Stem Cell Reports	2014
LQT1 mutations in KCNQ1 C-terminus assembly domain suppress IKs using different mechanisms Aromolaran AS, Subramanyam P, Chang DD, Kobertz WR, Colecraft HM	Cardiovascular Research	2014
KCNE1 divides the voltage sensor movement in KCNQ1/KCNE1 channels into two steps Barro-Soria R, Rebolledo S, Liin SI, Perez ME, Sampson KJ, Kass RS, Larsson HP	Nature Communications	2014
Clinical profile of pediatric patients with long QT syndrome masquerading as seizures. Thakkar B, Shukla A, Singh T, Shah S, Bohora S, Shah J, Madan T	The Indian Journal of Pediatrics	2014
Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome DS Auerbach, J Jones, BC Clawson, J Offord, GM Lenk, I Ogiwara, K Yamakawa, MH Meisler, JM Parent, LL Isom	PloS one	2013
Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies PY Hsiao, HC Tien, CP Lo, JM Juang, YH Wang, RJ Sung	The Application of Clinical Genetics	2013
Genomic biomarkers of SUDEP in brain and heart E Glasscock	Epilepsy & Behavior	2013
Single Nucleotide Deletion Mutation of KCNH2 Gene is Responsible for LQT Syndrome in a 3-Generation Korean Family Park JK, Oh YS, Choi JH, Yoon SK	Journal of Korean Medical Science	2013
Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome Boczek NJ, Best JM, Tester DJ, Giudicessi JR, Middha S, Evans JM, Kamp TJ, Ackerman MJ	Circulation. Cardiovascular genetics	2013
Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p Gurrieri F, Zollino M, Oliva A, Pascali V, Orteschi D, Pietrobono R, Camporeale A, Coll Vidal M, Partemi S, Brugada R, Bellocci F, Neri G	European Journal of Human Genetics	2013
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Mouse Models of SCN5A-Related Cardiac Arrhythmias M Derangeon, J Montnach, I Baró, F Charpentier	Frontiers in physiology	2012
Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease CA Martin, GD Matthews, CL Huang	Heart (British Cardiac Society)	2012
Induced pluripotent stem cells used to reveal drug actions in a long QT syndrome family with complex genetics C Terrenoire, K Wang, KW Tung, WK Chung, RH Pass, JT Lu, JC Jean, A Omari, KJ Sampson, DN Kotton, G Keller, RS Kass	The Journal of General Physiology	2012
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Allosteric gating mechanism underlies the flexible gating of KCNQ1 potassium channels Osteen JD, Barro-Soria R, Robey S, Sampson KJ, Kass RS, Larsson HP	Proceedings of the National Academy of Sciences	2012
Mutation and Gender Specific Risk in Type-2 Long QT Syndrome: Implications for Risk Stratification for Life-Threatening Cardiac Events in Patients with Long QT Syndrome Migdalovich D, Moss AJ, Lopes CM, Costa J, Ouellet G, Barsheshet A, McNitt S, Polonsky S, Robinson JL, Zareba W, Ackerman MJ, Benhorin J, Kaufman ES, Platonov PG, Shimizu W, Towbin JA, Vincent GM, Wilde AA, Goldenberg I	Heart rhythm : the official journal of the Heart Rhythm Society	2011
Risk for Life-Threatening Cardiac Events in Patients With Genotype-Confirmed Long-QT Syndrome and Normal-Range Corrected QT Intervals Goldenberg I, Horr S, Moss AJ, Lopes CM, Barsheshet A, McNitt S, Zareba W, Andrews ML, Robinson JL, Locati EH, Ackerman MJ, Benhorin J, Kaufman ES, Napolitano C, Platonov PG, Priori SG, Qi M, Schwartz PJ, Shimizu W, Towbin JA, Vincent GM, Wilde AA, Zhang L	Journal of the American College of Cardiology	2011
Structural heterogeneity promotes triggered activity, reflection and arrhythmogenesis in cardiomyocyte monolayers Auerbach DS, Grzȩda KR, Furspan PB, Sato PY, Mironov S, Jalife J	The Journal of Physiology	2011
Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-QT Syndrome: Genotype-Phenotype Correlations of the KCNQ1(S349W) Mutation Horr S, Goldenberg I, Moss AJ, O-Uchi J, Barsheshet A, Connelly H, Gray DA, Zareba W, Lopes CM	Journal of Cardiovascular Electrophysiology	2011
AMP-activated protein kinase inhibits KCNQ1 channels through regulation of the ubiquitin ligase Nedd4-2 in renal epithelial cells R Alzamora, F Gong, C Rondanino, JK Lee, C Smolak, NM Pastor-Soler, KR Hallows	AJP Renal Physiology	2010
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Absence of the Inhibitory G-Protein Gα i2 Predisposes to Ventricular Cardiac Arrhythmia Z Zuberi, M Nobles, S Sebastian, A Dyson, SY Lim, R Breckenridge, L Birnbaumer, A Tinker	Circulation. Arrhythmia and electrophysiology	2010
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Changes in Ventricular Repolarization Duration During Typical Daily Emotion in Patients With Long QT Syndrome Lane RD, Zareba W, Reis HT, Peterson DR, Moss AJ	Psychosomatic medicine	2010
Spatial and temporal heterogeneities are localized to the right ventricular outflow tract in a heterozygotic Scn5a mouse model Martin CA, Grace AA, Huang CL	American journal of physiology. Heart and circulatory physiology	2010
LQTS Gene LOVD Database Zhang T, Moss A, Cong P, Pan M, Chang B, Zheng L, Fang Q, Zareba W, Robinson J, Lin C, Li Z, Wei J, Zeng Q, Qi M	Human Mutation	2010
Trigger-Specific Risk Factors and Response to Therapy in Type 2 Long QT Syndrome Kim JA, Lopes CM, Moss AJ, McNitt S, Barsheshet A, Robinson JL, Zareba W, Ackerman MJ, Kaufman ES, Towbin JA, Vincent M, Goldenberg I	Heart rhythm : the official journal of the Heart Rhythm Society	2010
Long QT syndrome provoked by induction of general anesthesia -A case report- Kim HT, Lee JH, Park IB, Heo HE, Kim TY, Lee MJ	Korean Journal of Anesthesiology	2010
Characterization of a Binding Site for Anionic Phospholipids on KCNQ1 Thomas AM, Harmer SC, Khambra T, Tinker A	The Journal of biological chemistry	2010
KCNE1 alters the voltage sensor movements necessary to open the KCNQ1 channel gate Osteen JD, Gonzalez C, Sampson KJ, Iyer V, Rebolledo S, Larsson HP, Kass RS	Proceedings of the National Academy of Sciences	2010
The cardiac IKs channel, complex indeed Osteen JD, Sampson KJ, Kass RS	Proceedings of the National Academy of Sciences	2010
Traffic-Related Air Pollution and QT Interval: Modification by Diabetes, Obesity, and Oxidative Stress Gene Polymorphisms in the Normative Aging Study Baja ES, Schwartz JD, Wellenius GA, Coull BA, Zanobetti A, Vokonas PS, Suh HH	Environmental Health Perspectives	2010
Pulmonary surfactant: an immunological perspective ZC Chroneos, Z Sever-Chroneos, VL Shepherd	Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology	2009
Mechanisms of disease pathogenesis in long QT syndrome type 5 SC Harmer, AJ Wilson, R Aldridge, A Tinker	American journal of physiology. Cell physiology	2009
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Familial long QT syndrome presented as ventricular tachycardia during anesthesia Tran SM, Nobrega RQ, Kammerer WA, Quezado Z	Pediatric Anesthesia	2009
Genotype-Phenotype Aspects of Type-2 Long-QT Syndrome Shimizu W, Moss AJ, Wilde AA, Towbin JA, Ackerman MJ, January CT, Tester DJ, Zareba W, Robinson JL, Qi M, Michael Vincent G, Kaufman ES, Hofman N, Noda T, Kamakura S, Miyamoto Y, Shah S, Amin V, Goldenberg I, Andrews ML, McNitt S	Journal of the American College of Cardiology	2009
The Cardiac IKs Potassium Channel Macromolecular Complex Includes the Phosphodiesterase PDE4D3 Terrenoire C, Houslay MD, Baillie GS, Kass RS	The Journal of biological chemistry	2009
Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade X Cheng, SD Dib-Hajj, L Tyrrell, SG Waxman	Molecular Pain	2008
Antiarrhythmic Benefits of Targeting the Na+/Ca2+ Exchanger Editorial Comment Anumonwo J	Heart rhythm : the official journal of the Heart Rhythm Society	2008
A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope Christé G, Thériault O, Chahine M, Millat G, Rodriguez-Lafrasse C, Rousson R, Deschênes I, Ficker E, Chevalier P	Heart rhythm : the official journal of the Heart Rhythm Society	2008
A novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic response JR Bankston, M Yue, W Chung, M Spyres, RH Pass, E Silver, KJ Sampson, RS Kass	PloS one	2007
QTc and psychopharmacs: are there any differences between monotherapy and polytherapy JC Sumić, V Barić, P Bilić, M Herceg, M Sisek-Sprem, V Jukić	Annals of general psychiatry	2007
Mutation of an A-kinase-anchoring protein causes long-QT syndrome Chen L, Marquardt ML, Tester DJ, Sampson KJ, Ackerman MJ, Kass RS	Proceedings of the National Academy of Sciences	2007
Restitution analysis of alternans and its relationship to arrhythmogenicity in hypokalaemic Langendorff-perfused murine hearts Sabir IN, Li LM, Grace AA, Huang CL		2007
Criteria for arrhythmogenicity in genetically-modified Langendorff-perfused murine hearts modelling the congenital long QT syndrome type 3 and the Brugada syndrome Sabir IN, Li LM, Jones VJ, Goddard CA, Grace AA, Huang CL		2007
Transient alterations in transmural repolarization gradients and arrhythmogenicity in hypokalaemic Langendorff-perfused murine hearts Sabir IN, Killeen MJ, Goddard CA, Thomas G, Gray S, Grace AA, Huang CL	The Journal of Physiology	2007
Long and short QT syndrome B Borchert, T Lawrenz, C Stellbrink	Herzschrittmachertherapie + Elektrophysiologie	2006
Molecular basis of ranolazine block of LQT-3 mutant sodium channels: evidence for site of action S Fredj, KJ Sampson, H Liu, RS Kass	British Journal of Pharmacology	2006
Altered Na+ Channels Promote Pause-Induced Spontaneous Diastolic Activity in Long QT Syndrome Type 3 Myocytes S Fredj, N Lindegger, KJ Sampson, P Carmeliet, RS Kass	Circulation research	2006
[Ventricular tachycardia. Diagnostic spectrum and therapeutic measures]. Lewalter T, Schwab JO, Nickenig G	Der Internist	2006
[Molecular basis of primary electrical heart diseases] E Zitron, EP Scholz, C Kiesecker, M Pirot, S Kathöfer, D Thomas, J Kiehn, HA Katus, R Becker, CA Karle	Herzschrittmachertherapie + Elektrophysiologie	2005
Genetics of acquired long QT syndrome DM Roden, PC Viswanathan	Journal of Clinical Investigation	2005
The channelopathies: novel insights into molecular and genetic mechanisms of human disease RS Kass	Journal of Clinical Investigation	2005
[Primary electrical heart disease in adulthood--electrophysiological findings and therapy]. Schimpf R, Kuschyk J, Veltmann C, Borggrefe M, Wolpert C	Herzschrittmachertherapie & Elektrophysiologie	2005

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