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Select item 86399301.

Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome

Pasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, Nicolas Guex, Jacqueline Chrast, Audrey Putoux, Tipu Sultan, Javeria Raza Alvi, Zia ur Rahman, Faisal Zafar, Nuzhat Rana, Fatima Rahman, Najwa Anwar, Shazia Maqbool, Maha S Zaki, Joseph G Gleeson, David Murphy, Hamid Galehdari, Gholamreza Shariati, Neda Mazaheri, Alireza Sedaghat, SYNAPS Study Group, Gaetan Lesca, Nicolas Chatron, Vincenzo Salpietro, Marilena Christoforou, Henry Houlden, William F Simonds, Thierry Pedrazzini, Reza Maroofian, Alexandre Reymond

J Med Genet. 2021 Dec; 58(12): 815–831. Published online 2020 Nov 10. doi: 10.1136/jmedgenet-2020-107015

PMCID:: PMC8639930

Article PDF–6.3M

Select item 80735452.

A circadian clock in the sinus node mediates day-night rhythms in Hcn4 and heart rate

Alicia D’Souza, Yanwen Wang, Cali Anderson, Annalisa Bucchi, Mirko Baruscotti, Servé Olieslagers, Pietro Mesirca, Anne Berit Johnsen, Svetlana Mastitskaya, Haibo Ni, Yu Zhang, Nicholas Black, Charlotte Cox, Sven Wegner, Beatriz Bano-Otalora, Cheryl Petit, Eleanor Gill, Sunil Jit R.J. Logantha, Halina Dobrzynski, Nick Ashton, George Hart, Rai Zhang, Henggui Zhang, Elizabeth J. Cartwright, Ulrik Wisloff, Matteo E. Mangoni, Paula A. da Costa Martins, Hugh D. Piggins, Dario DiFrancesco, Mark R. Boyett

Heart Rhythm. 2021 May; 18(5): 801–810. doi: 10.1016/j.hrthm.2020.11.026

PMCID:: PMC8073545

Article

Select item 80686103.

Rad-GTPase Contributes to Heart Rate Via L-type Calcium Channel Regulation

Bryana M. Levitan, Brooke M. Ahern, Ajoy Aloysius, Laura Brown, Yuan Wen, Douglas A. Andres, Jonathan Satin

J Mol Cell Cardiol. Author manuscript; available in PMC 2022 May 1.

Published in final edited form as: J Mol Cell Cardiol. 2021 May; 154: 60–69. Published online 2021 Feb 6. doi: 10.1016/j.yjmcc.2021.01.005

PMCID:: PMC8068610

Article PDF–2.1M

Select item 73333354.

Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose

Koichi Kato, Tomoya Ozawa, Seiko Ohno, Yoshihisa Nakagawa, Minoru Horie

BMC Cardiovasc Disord. 2020; 20: 315. Published online 2020 Jul 2. doi: 10.1186/s12872-020-01601-2

PMCID:: PMC7333335

Article PDF–1.8M

Select item 68504205.

Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia

Tommy Dharmawan, Tadashi Nakajima, Seiko Ohno, Takashi Iizuka, Shuntaro Tamura, Yoshiaki Kaneko, Minoru Horie, Masahiko Kurabayashi

Ann Noninvasive Electrocardiol. 2019 May; 24(3): e12623. Published online 2019 Jan 7. doi: 10.1111/anec.12623

PMCID:: PMC6850420

Article PDF–1.3M

Select item 66544586.

Hypertrophic cardiomyopathy complicated by severe bradycardias: A pedigree report

Dao Wen Wang, You Bin Deng

Clin Cardiol. 2002 Feb; 25(2): 76–80. Published online 2006 Dec 5. doi: 10.1002/clc.4950250207

PMCID:: PMC6654458

Summary PDF–294K

Select item 51195537.

Ranolazine for Congenital Long QT Syndrome Type III (LQT3): Experimental and Long-Term Clinical Data

Ehud Chorin, Dan Hu, Charles Antzelevitch, Aviram Hochstadt, Luiz Belardinelli, David Zeltser, Hector Barajas-Martinez, Uri Rozovski, Raphael Rosso, Arnon Adler, Jesaia Benhorin, Sami Viskin

Circ Arrhythm Electrophysiol. Author manuscript; available in PMC 2017 Oct 1.

Published in final edited form as: Circ Arrhythm Electrophysiol. 2016 Oct; 9(10): e004370. doi: 10.1161/CIRCEP.116.004370

PMCID:: PMC5119553

Article PDF–3.8M

Select item 50278128.

Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort study

Hannah E. Steele, Elizabeth Harris, Rita Barresi, Julie Marsh, Anna Beattie, John P. Bourke, Volker Straub, Patrick F. Chinnery

Neurology. 2016 Sep 6; 87(10): 1031–1035. doi: 10.1212/WNL.0000000000003064

PMCID:: PMC5027812

Article PDF–263K

Select item 41515289.

Arrhythmia Phenotype during Fetal Life Suggests LQTS Genotype: Risk Stratification of Perinatal Long QT Syndrome

Bettina F. Cuneo, Susan P. Etheridge, Hitoshi Horigome, Denver Sallee, Anita Moon-Grady, Hsin-Yi Weng, Michael J. Ackerman, D. Woodrow Benson

Circ Arrhythm Electrophysiol. Author manuscript; available in PMC 2014 Oct 1.

Published in final edited form as: Circ Arrhythm Electrophysiol. 2013 Oct; 6(5): 946–951. Published online 2013 Aug 30. doi: 10.1161/CIRCEP.113.000618

PMCID:: PMC4151528

Article PDF–1.4M

Select item 392638610.

Topical timolol for treatment of epistaxis in hereditary haemorrhagic telangiectasia associated with bradycardia: a look at CYP2D6 metabolising variants

Narendranath Epperla, Murray H Brilliant, Humberto Vidaillet

BMJ Case Rep. 2014; 2014: bcr2013203056. Published online 2014 Feb 11. doi: 10.1136/bcr-2013-203056

PMCID:: PMC3926386

Article PDF–656K

Select item 391032711.

Gene dose-dependent atrial arrhythmias, heart block, and brady-cardiomyopathy in mice overexpressing A₃ adenosine receptors

Larissa Fabritz, Paulus Kirchhof, Lisa Fortmüller, John A. Auchampach, Hideo A. Baba, Günter Breithardt, Joachim Neumann, Peter Boknik, Wilhelm Schmitz

Cardiovasc Res. Author manuscript; available in PMC 2014 Feb 3.

Published in final edited form as: Cardiovasc Res. 2004 Jun 1; 62(3): 500–508. doi: 10.1016/j.cardiores.2004.02.004

PMCID:: PMC3910327

Article PDF–1.8M

Select item 333078912.

Altered sinoatrial node function and intra-atrial conduction in murine gain-of-function Scn5a+/ΔKPQ hearts suggest an overlap syndrome

Jingjing Wu, Yanmin Zhang, Xinzhao Zhang, Longxian Cheng, Wim J. Lammers, Andrew A. Grace, James A. Fraser, Henggui Zhang, Christopher L. -H. Huang, Ming Lei

Am J Physiol Heart Circ Physiol. 2012 Apr 1; 302(7): H1510–H1523. Published online 2012 Jan 27. doi: 10.1152/ajpheart.00357.2011

PMCID:: PMC3330789

Article

Select item 328722213.

Popeye domain containing proteins are essential for stress-mediated modulation of cardiac pacemaking in mice

Alexander Froese, Stephanie S. Breher, Christoph Waldeyer, Roland F.R. Schindler, Viacheslav O. Nikolaev, Susanne Rinné, Erhard Wischmeyer, Jan Schlueter, Jan Becher, Subreena Simrick, Franz Vauti, Juliane Kuhtz, Patrick Meister, Sonja Kreissl, Angela Torlopp, Sonja K. Liebig, Sandra Laakmann, Thomas D. Müller, Joachim Neumann, Juliane Stieber, Andreas Ludwig, Sebastian K. Maier, Niels Decher, Hans-Henning Arnold, Paulus Kirchhof, Larissa Fabritz, Thomas Brand

J Clin Invest. 2012 Mar 1; 122(3): 1119–1130. Published online 2012 Feb 22. doi: 10.1172/JCI59410

PMCID:: PMC3287222

Article PDF–1.4M

Select item 327190414.

Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis

Deborah U. Frank, Kandis L. Carter, Kirk R. Thomas, R. Michael Burr, Martijn L. Bakker, William A. Coetzee, Martin Tristani-Firouzi, Michael J. Bamshad, Vincent M. Christoffels, Anne M. Moon

Proc Natl Acad Sci U S A. 2012 Jan 17; 109(3): E154–E163. Published online 2011 Dec 27. doi: 10.1073/pnas.1115165109

PMCID:: PMC3271904

Article PDF–2.2M

Select item 322846315.

Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype

Amanda L. Blasius, Adrienne E. Dubin, Matt J. Petrus, Byung-Kwan Lim, Anna Narezkina, José R. Criado, Derek N. Wills, Yu Xia, Eva Marie Y. Moresco, Cindy Ehlers, Kirk U. Knowlton, Ardem Patapoutian, Bruce Beutler

Proc Natl Acad Sci U S A. 2011 Nov 29; 108(48): 19413–19418. Published online 2011 Nov 15. doi: 10.1073/pnas.1117020108

PMCID:: PMC3228463

Article PDF–1.0M

Select item 313571116.

Rescue and Worsening of Congenital Heart Block-Associated Electrocardiographic Abnormalities in Two Transgenic Mice

Eddy Karnabi, Yongxia Qu, Salvatore Mancarella, Mohamed Boutjdir

J Cardiovasc Electrophysiol. Author manuscript; available in PMC 2012 Aug 1.

Published in final edited form as: J Cardiovasc Electrophysiol. 2011 Aug; 22(8): 922–930. Published online 2011 Feb 25. doi: 10.1111/j.1540-8167.2011.02032.x

PMCID:: PMC3135711

Article PDF–778K

Select item 265938717.

Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na⁺ channel

Y Zhang, T Wang, A Ma, X Zhou, J Gui, H Wan, R Shi, C Huang, A A Grace, C L-H Huang, D Trump, H Zhang, T Zimmer, M Lei

Acta Physiol (Oxf) 2008 Dec; 194(4): 311–323. doi: 10.1111/j.1748-1716.2008.01883.x

PMCID:: PMC2659387

Article PDF–1.0M

Select item 261457518.

Impaired Ca²⁺ homeostasis is associated with atrial fibrillation in the α_1D L-type Ca²⁺ channel KO mouse

Salvatore Mancarella, Yuankun Yue, Eddy Karnabi, Yongxia Qu, Nabil El-Sherif, Mohamed Boutjdir

Am J Physiol Heart Circ Physiol. 2008 Nov; 295(5): H2017–H2024. Published online 2008 Sep 12. doi: 10.1152/ajpheart.00537.2008

PMCID:: PMC2614575

Article

Select item 176750019.

Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death

N Sumitomo, K Harada, M Nagashima, T Yasuda, Y Nakamura, Y Aragaki, A Saito, K Kurosaki, K Jouo, M Koujiro, S Konishi, S Matsuoka, T Oono, S Hayakawa, M Miura, H Ushinohama, T Shibata, I Niimura

Heart. 2003 Jan; 89(1): 66–70. doi: 10.1136/heart.89.1.66

PMCID:: PMC1767500

Article PDF–203K

Select item 173595520.

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients

A Postma, I Denjoy, J Kamblock, M Alders, J Lupoglazoff, G Vaksmann, L Dubosq-Bidot, P Sebillon, M Mannens, P Guicheney, A Wilde

J Med Genet. 2005 Nov; 42(11): 863–870. doi: 10.1136/jmg.2004.028993

PMCID:: PMC1735955

Summary PDF–332K

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