Works matching AU Kass, Robert S.

Results: 36

Decreased Density of Ito in Left Ventricular Myocytes from German Shepherd Dogs with Inherited Arrhythmias.

Published in:

Journal of Cardiovascular Electrophysiology, 1997, v. 8, n. 8, p. 872, doi. 10.1111/j.1540-8167.1997.tb00848.x

By:

Freeman, Lisa C.;
Pacioretty, Linda M.;
Moise, N. Sydney;
Kass, Robert S.;
Gilmour Jr., Robert F.

Publication type:

Article

Divergent regulation of KCNQ1/E1 by targeted recruitment of protein kinase A to distinct sites on the channel complex.

Published in:

eLife, 2023, p. 1, doi. 10.7554/eLife.83466

By:

Xinle Zou;
Shanmugam, Sri Karthika;
Kanner, Scott A.;
Sampson, Kevin J.;
Kass, Robert S.;
Colecraft, Henry M.

Publication type:

Article

Molecular basis of ranolazine block of LQT-3 mutant sodium channels: evidence for site of action.

Published in:

2006

By:

Fredj, Sandra;
Sampson, Kevin J.;
Huajun Liu;
Kass, Robert S.;
Liu, Huajun

Publication type:

journal article

An Integrative Data Science Pipeline to Identify Novel Drug Interactions that Prolong the QT Interval.

Published in:

2016

By:

Lorberbaum, Tal;
Sampson, Kevin;
Woosley, Raymond;
Kass, Robert;
Tatonetti, Nicholas;
Sampson, Kevin J;
Woosley, Raymond L;
Kass, Robert S;
Tatonetti, Nicholas P

Publication type:

journal article

A Computational Model to Predict the Effects of Class I Anti-Arrhythmic Drugs on Ventricular Rhythms.

Published in:

Science Translational Medicine, 2011, v. 3, n. 98, p. 1, doi. 10.1126/scitranslmed.3002588

By:

Moreno, Jonathan D.;
Zhu, Z. Iris;
Pei-Chi Yang;
Bankston, John R.;
Mao-Tsuen Jeng;
Chaoyi Kang;
Lianguo Wang;
Bayer, Jason D.;
Christini, David J.;
Trayanova, Natalia A.;
Ripplinger, Crystal M.;
Kass, Robert S.;
Clancy, Colleen E.

Publication type:

Article

Regulation of IKs Potassium Current by Isoproterenol in Adult Cardiomyocytes Requires Type 9 Adenylyl Cyclase.

Published in:

Cells (2073-4409), 2019, v. 8, n. 9, p. 981, doi. 10.3390/cells8090981

By:

Li, Yong;
Hof, Thomas;
Baldwin, Tanya A.;
Chen, Lei;
Kass, Robert S.;
Dessauer, Carmen W.

Publication type:

Article

Two small-molecule activators share similar effector sites in the KCNQ1 channel pore but have distinct effects on voltage sensor movements.

Published in:

Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.903050

By:

Lei Chen;
Peng, Gary;
Comollo, Thomas W.;
Xinle Zou;
Sampson, Kevin J.;
Larsson, H. Peter;
Kass, Robert S.

Publication type:

Article

Location, location, regulation: a novel role for β-spectrin in the heart.

Published in:

2010

By:

Sampson, Kevin J.;
Kass, Robert S.

Publication type:

journal article

Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.

Published in:

2008

By:

Lehnart, Stephan E.;
Mongillo, Marco;
Bellinger, Andrew;
Lindegger, Nicolas;
Bi-Xing Chen;
Hsueh, William;
Reiken, Steven;
Wronska, Anetta;
Drew, Liam J.;
Ward, Chris W.;
Lederer, W. J.;
Kass, Robert S.;
Morley, Gregory;
Marks, Andrew R.;
Chen, Bi-Xing

Publication type:

journal article

Long QT syndrome: from channels to cardiac arrhythmias.

Published in:

2005

By:

Moss, Arthur J.;
Kass, Robert S.

Publication type:

journal article

The channelopathies: novel insights into molecular and genetic mechanisms of human disease.

Published in:

Journal of Clinical Investigation, 2005, v. 115, n. 8, p. 1986, doi. 10.1172/JCI26011

By:

Kass, Robert S.

Publication type:

Article

The Impact of Heterozygous KCNK3 Mutations Associated With Pulmonary Arterial Hypertension on Channel Function and Pharmacological Recovery.

Published in:

Journal of the American Heart Association, 2017, v. 6, n. 9, p. 1, doi. 10.1161/JAHA.117.006465

By:

Bohnen, Michael S.;
Roman-Campos, Danilo;
Terrenoire, Cecile;
Jnani, Jack;
Sampson, Kevin J.;
Chung, Wendy K.;
Kass, Robert S.

Publication type:

Article

Adrenergic regulation of a key cardiac potassium channel can contribute to atrial fibrillation: evidence from an IKs transgenic mouse.

Published in:

Journal of Physiology, 2008, v. 586, n. 2, p. 627, doi. 10.1113/jphysiol.2007.141333

By:

Sampson, Kevin J.;
Terrenoire, Cecile;
Cervantes, Daniel O.;
Kaba, Riyaz A.;
Peters, Nicholas S.;
Kass, Robert S.

Publication type:

Article

IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubules.

Published in:

Cardiovascular Research, 2008, v. 79, n. 3, p. 427, doi. 10.1093/cvr/cvn085

By:

Nicolas, Céline S.;
Park, Kyu-Ho;
Harchi, Aziza El;
Camonis, Jacques;
Kass, Robert S.;
Escande, Denis;
Mérot, Jean;
Loussouarn, Gildas;
Bouffant, Françoise Le;
Baro, Isabelle

Publication type:

Article

The roles of ion channels in an inherited heart disease: molecular genetics of the long QT syndrome.

Published in:

Cardiovascular Research, 1996, v. 32, n. 3, p. 443, doi. 10.1016/S0008-6363(96)00122-8

By:

Kass, Robert S.;
Davies, Michael P.

Publication type:

Article

Role of Sodium Channels in Propagation in Heart Muscle: How Subtle Genetic Alterations Result in Major Arrhythmic Disorders.

Published in:

Journal of Cardiovascular Electrophysiology, 2007, v. 18, n. 8, p. 900, doi. 10.1111/j.1540-8167.2007.00838.x

By:

TERRENOIRE, CECILE;
SIMHAEE, DANIEL;
KASS, ROBERT S.

Publication type:

Article

Sodium Channel Inactivation in Heart: A Novel Role of the Carboxy-Terminal Domain.

Published in:

Journal of Cardiovascular Electrophysiology, 2006, v. 17, p. S21, doi. 10.1111/j.1540-8167.2006.00381.x

By:

KASS, ROBERT S.

Publication type:

Article

A Novel mutation L619F in the cardiac Na+ channel SCN5A associated with long‐QT syndrome (LQT3): a role for the I‐II linker in inactivation gatingCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #607(2002) onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/607.pdf

Published in:

Human Mutation, 2003, v. 21, n. 5, p. 552, doi. 10.1002/humu.9136

By:

Xander H.T. Wehrens;
Tom Rossenbacker;
Roselie J. Jongbloed;
Marc Gewillig;
Hein Heidbüchel;
Pieter A. Doevendans;
Marc A. Vos;
Hein J.J. Wellens;
Robert S. Kass

Publication type:

Article

A Novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #607(2002) online http://www.interscience.wiley.com/humanmutation/pdf/mutation/607.pdf)

Published in:

Human Mutation, 2003, v. 21, n. 5, p. 552, doi. 10.1002/humu.9136

By:

Xander H.T. Wehrens;
Tom Rossenbacker;
Roselie J. Jongbloed;
Marc Gewillig;
Hein Heidbüchel;
Pieter A. Doevendans;
Marc A. Vos;
Hein J.J. Wellens;
Robert S. Kass

Publication type:

Article

Deranged sodium to sudden death.

Published in:

Journal of Physiology, 2015, v. 593, n. 6, p. 1331, doi. 10.1113/jphysiol.2014.281204

By:

Clancy, Colleen E.;
Chen‐Izu, Ye;
Bers, Donald M.;
Belardinelli, Luiz;
Boyden, Penelope A.;
Csernoch, Laszlo;
Despa, Sanda;
Fermini, Bernard;
Hool, Livia C.;
Izu, Leighton;
Kass, Robert S.;
Lederer, W. Jonathan;
Louch, William E.;
Maack, Christoph;
Matiazzi, Alicia;
Qu, Zhilin;
Rajamani, Sridharan;
Rippinger, Crystal M.;
Sejersted, Ole M.;
O'Rourke, Brian

Publication type:

Article

Biophysical properties of slow potassium channels in human embryonic stem cell derived cardiomyocytes implicate subunit stoichiometry.

Published in:

Journal of Physiology, 2011, v. 589, n. 24, p. 6093, doi. 10.1113/jphysiol.2011.220863

By:

Wang, Kai;
Terrenoire, Cecile;
Sampson, Kevin J.;
Iyer, Vivek;
Osteen, Jeremiah D.;
Lu, Jonathan;
Keller, Gordon;
Kotton, Darrell N.;
Kass, Robert S.

Publication type:

Article

O-glycosylation of the cardiac IKs complex.

Published in:

Journal of Physiology, 2011, v. 589, n. 15, p. 3721, doi. 10.1113/jphysiol.2011.211284

By:

Chandrasekhar, Kshama D.;
Lvov, Anatoli;
Terrenoire, Cecile;
Gao, Grace Y.;
Kass, Robert S.;
Kobertz, William R.

Publication type:

Article

Potassium Channels as Therapeutic Targets in Pulmonary Arterial Hypertension.

Published in:

Biomolecules (2218-273X), 2022, v. 12, n. 10, p. N.PAG, doi. 10.3390/biom12101341

By:

Redel-Traub, Gabriel;
Sampson, Kevin J.;
Kass, Robert S.;
Bohnen, Michael S.

Publication type:

Article

Autonomous beating rate adaptation in human stem cell-derived cardiomyocytes.

Published in:

Nature Communications, 2016, v. 7, n. 1, p. 10312, doi. 10.1038/ncomms10312

By:

Eng, George;
Lee, Benjamin W.;
Protas, Lev;
Gagliardi, Mark;
Brown, Kristy;
Kass, Robert S.;
Keller, Gordon;
Robinson, Richard B.;
Vunjak-Novakovic, Gordana

Publication type:

Article

KCNE1 divides the voltage sensor movement in KCNQ1/KCNE1 channels into two steps.

Published in:

Nature Communications, 2014, v. 5, n. 4, p. 3750, doi. 10.1038/ncomms4750

By:

Barro-Soria, Rene;
Rebolledo, Santiago;
Liin, Sara I.;
Perez, Marta E.;
Sampson, Kevin J.;
Kass, Robert S.;
Larsson, H. Peter

Publication type:

Article

Measurement and block of potassium channel currents in the heart: Importance of channel type.

Published in:

Drug Development Research, 1990, v. 19, n. 2, p. 115, doi. 10.1002/ddr.430190203

By:

Kass, Robert S.;
Arena, Joseph P.;
Walsh, Kenneth B.

Publication type:

Article

Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.

Published in:

2005

By:

Shushi L;
Kerem B;
Goldmit M;
Peretz A;
Attali B;
Medina A;
Towbin JA;
Kurokawa J;
Kass RS;
Benhorin J;
Shushi, Liat;
Kerem, Batsheva;
Goldmit, Maya;
Peretz, Asher;
Attali, Bernard;
Medina, Aron;
Towbin, Jeffrey A;
Kurokawa, Junko;
Kass, Robert S;
Benhorin, Jesaia

Publication type:

journal article

Clinical, Genetic, and Electrophysiologic Characteristics of a New Pas-Domain HERG Mutation (M124R) Causing Long QT Syndrome.

Published in:

Annals of Noninvasive Electrocardiology, 2005, v. 10, n. 3, p. 334, doi. 10.1111/j.1542-474X.2005.00643.x

By:

Shushi, Liat;
Kerem, Batsheva;
Goldmit, Maya;
Peretz, Asher;
Attali, Bernard;
Medina, Aron;
Towbin, Jeffrey A.;
Kurokawa, Junko;
Kass, Robert S.;
Benhorin, Jesaia

Publication type:

Article

Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.

Published in:

2002

By:

Benhorin, Jesaia;
Moss, Arthur J.;
Bak, Matthew;
Zareba, Wojciech;
Kaufman, Elizabeth S.;
Kerem, Batsheva;
Towbin, Jeffrey A.;
Priori, Silvia;
Kass, Robert S.;
Attali, Bernard;
Brown, Arthur M.;
Ficker, Eckhard

Publication type:

journal article

Calmodulin mutations can underlie the phenotype of long QT syndrome variant 1.

Published in:

Journal of Physiology, 2023, v. 601, n. 17, p. 3695, doi. 10.1113/JP285220

By:

Kass, Robert S.

Publication type:

Article

Perspective on the white paper from the 2022 UC Davis Cardiovascular Research Symposium.

Published in:

Journal of Physiology, 2023, v. 601, n. 13, p. 2543, doi. 10.1113/JP284441

By:

Kass, Robert S.

Publication type:

Article

A-kinase anchoring proteins: different partners, different dance.

Published in:

Nature Cell Biology, 2005, v. 7, n. 11, p. 1050, doi. 10.1038/ncb1105-1050

By:

Lei Chen;
Kass, Robert S.

Publication type:

Article

Modeling Tissue- and Mutation- Specific Electrophysiological Effects in the Long QT Syndrome: Role of the Purkinje Fiber.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0097720

By:

Iyer, Vivek;
Sampson, Kevin J.;
Kass, Robert S.

Publication type:

Article

Gating mechanisms underlying deactivation slowing by two KCNQ1 atrial fibrillation mutations.

Published in:

Scientific Reports, 2017, p. 45911, doi. 10.1038/srep45911

By:

Peng, Gary;
Barro-Soria, Rene;
Sampson, Kevin J.;
Larsson, H. Peter;
Kass, Robert S.

Publication type:

Article

Purkinje Cells as Sources of Arrhythmias in Long QT Syndrome Type 3.

Published in:

Scientific Reports, 2015, p. 13287, doi. 10.1038/srep13287

By:

Iyer, Vivek;
Roman-Campos, Danilo;
Sampson, Kevin J.;
Kang, Guoxin;
Fishman, Glenn I.;
Kass, Robert S.

Publication type:

Article

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.

Published in:

Channels (19336950), 2022, v. 16, n. 1, p. 173, doi. 10.1080/19336950.2022.2106025

By:

Comollo, Thomas W.;
Zou, Xinle;
Zhang, Chuangeng;
Kesters, Divya;
Hof, Thomas;
Sampson, Kevin J.;
Kass, Robert S.

Publication type:

Article

Works matching AU Kass, Robert S.

Decreased Density of I<sub>to</sub> in Left Ventricular Myocytes from German Shepherd Dogs with Inherited Arrhythmias.

Divergent regulation of KCNQ1/E1 by targeted recruitment of protein kinase A to distinct sites on the channel complex.

Molecular basis of ranolazine block of LQT-3 mutant sodium channels: evidence for site of action.

An Integrative Data Science Pipeline to Identify Novel Drug Interactions that Prolong the QT Interval.

A Computational Model to Predict the Effects of Class I Anti-Arrhythmic Drugs on Ventricular Rhythms.

Regulation of IKs Potassium Current by Isoproterenol in Adult Cardiomyocytes Requires Type 9 Adenylyl Cyclase.

Two small-molecule activators share similar effector sites in the KCNQ1 channel pore but have distinct effects on voltage sensor movements.

Location, location, regulation: a novel role for β-spectrin in the heart.

Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.

Long QT syndrome: from channels to cardiac arrhythmias.

The channelopathies: novel insights into molecular and genetic mechanisms of human disease.

The Impact of Heterozygous KCNK3 Mutations Associated With Pulmonary Arterial Hypertension on Channel Function and Pharmacological Recovery.

Adrenergic regulation of a key cardiac potassium channel can contribute to atrial fibrillation: evidence from an I<sub>Ks</sub> transgenic mouse.

IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubules.

The roles of ion channels in an inherited heart disease: molecular genetics of the long QT syndrome.

Role of Sodium Channels in Propagation in Heart Muscle: How Subtle Genetic Alterations Result in Major Arrhythmic Disorders.

Sodium Channel Inactivation in Heart: A Novel Role of the Carboxy-Terminal Domain.

Deranged sodium to sudden death.

Biophysical properties of slow potassium channels in human embryonic stem cell derived cardiomyocytes implicate subunit stoichiometry.

O-glycosylation of the cardiac I<sub>Ks</sub> complex.

Potassium Channels as Therapeutic Targets in Pulmonary Arterial Hypertension.

Autonomous beating rate adaptation in human stem cell-derived cardiomyocytes.

KCNE1 divides the voltage sensor movement in KCNQ1/KCNE1 channels into two steps.

Measurement and block of potassium channel currents in the heart: Importance of channel type.

Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.

Clinical, Genetic, and Electrophysiologic Characteristics of a New Pas-Domain HERG Mutation (M124R) Causing Long QT Syndrome.

Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.

Calmodulin mutations can underlie the phenotype of long QT syndrome variant 1.

Perspective on the white paper from the 2022 UC Davis Cardiovascular Research Symposium.

A-kinase anchoring proteins: different partners, different dance.

Modeling Tissue- and Mutation- Specific Electrophysiological Effects in the Long QT Syndrome: Role of the Purkinje Fiber.

Gating mechanisms underlying deactivation slowing by two KCNQ1 atrial fibrillation mutations.

Purkinje Cells as Sources of Arrhythmias in Long QT Syndrome Type 3.

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.