U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from MedGen

Items: 1 to 20 of 207

1.
Sevoflurane prolonged the QTc interval and increased transmural dispersion of repolarization in a patient with long QT syndrome 3: a case report
Atsuhiro Kitaura, Shinichi Nakao, Shinichi Hamasaki, Kei Houri, Takatoshi Tsujimoto, Seishi Kimura, Mayuka Matsushima
JA Clin Rep. 2017 Dec; 3: 29. Published online 2017 May 18. doi: 10.1186/s40981-017-0093-6
PMCID:
PMC5804612
ArticlePDF–936K
2.
Characterization of N-terminally mutated cardiac Na+ channels associated with long QT syndrome 3 and Brugada syndrome
Christian Gütter, Klaus Benndorf, Thomas Zimmer
Front Physiol. 2013; 4: 153. Prepublished online 2013 May 19. Published online 2013 Jun 26. doi: 10.3389/fphys.2013.00153
PMCID:
PMC3693076
ArticlePDF–2.4M
3.
Effects of L-type Ca2+ channel antagonism on ventricular arrhythmogenesis in murine hearts containing a modification in the Scn5a gene modelling human long QT syndrome 3
Glyn Thomas, Iman S Gurung, Matthew J Killeen, Parvez Hakim, Catharine A Goddard, Martyn P Mahaut-Smith, William H Colledge, Andrew A Grace, Christopher L-H Huang
J Physiol. 2007 Jan 1; 578(Pt 1): 85–97. Published online 2006 Nov 16. doi: 10.1113/jphysiol.2006.121921
PMCID:
PMC2075124
ArticlePDF–347K
4.
Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes
Dries A. M. Feyen, Wesley L. McKeithan, Arne A. N. Bruyneel, Sean Spiering, Larissa Hörmann, Bärbel Ulmer, Hui Zhang, Francesca Briganti, Michaela Schweizer, Bence Hegyi, Zhandi Liao, Risto-Pekka Pölönen, Kenneth S. Ginsburg, Chi Keung Lam, Ricardo Serrano, Christine Wahlquist, Alexander Kreymerman, Michelle Vu, Prashila L. Amatya, Charlotta S. Behrens, Sara Ranjbarvaziri, Renee G. C. Maas, Matthew Greenhaw, Daniel Bernstein, Joseph C. Wu, Donald M. Bers, Thomas Eschenhagen, Christian M. Metallo, Mark Mercola
Cell Rep. Author manuscript; available in PMC 2020 Aug 19.
Published in final edited form as: Cell Rep. 2020 Jul 21; 32(3): 107925. doi: 10.1016/j.celrep.2020.107925
PMCID:
PMC7437654
ArticlePDF–1.5M
5.
Differential calcium sensitivity in NaV1.5 mixed syndrome mutants
Mena Abdelsayed, Alban‐Elouen Baruteau, Karen Gibbs, Shubhayan Sanatani, Andrew D. Krahn, Vincent Probst, Peter C. Ruben
J Physiol. 2017 Sep 15; 595(18): 6165–6186. Published online 2017 Aug 20. doi: 10.1113/JP274536
PMCID:
PMC5599485
ArticlePDF–1.9M
6.
Ranolazine and late cardiac sodium current – a therapeutic target for angina, arrhythmia and more?
Jonathan C Makielski, Carmen R Valdivia
Br J Pharmacol. 2006 May; 148(1): 4–6. Published online 2006 Mar 6. doi: 10.1038/sj.bjp.0706713
PMCID:
PMC1617040
ArticlePDF–98K
7.
Using Ribonucleoprotein-based CRISPR/Cas9 to Edit Single Nucleotide on Human Induced Pluripotent Stem Cells to Model Type 3 Long QT Syndrome (SCN5A±)
Ning Ge, Min Liu, Rui Li, Nicholas M. Allen, Joseph Galvin, Sanbing Shen, Timothy O’Brien, Terence W. Prendiville
Stem Cell Rev Rep. 2023; 19(8): 2774–2789. Published online 2023 Aug 31. doi: 10.1007/s12015-023-10602-5
PMCID:
PMC10661835
ArticlePDF–1.9M
8.
Genetic variant annotation scores in congenital long QT syndrome
Arwa Younis, Christopher Bodurian, Dan E. Arking, Nicola Luigi Bragazzi, Chadi Tabaja, Wojciech Zareba, Scott McNitt, Mehmet K. Aktas, Bronislava Polonsky, Coeli M. Lopes, Nona Sotoodehnia, Peter J. Kudenchuk, Ilan Goldenberg
Ann Noninvasive Electrocardiol. 2023 Sep; 28(5): e13080. Published online 2023 Aug 11. doi: 10.1111/anec.13080
PMCID:
PMC10475886
ArticlePDF–3.0M
9.
Beneficial effects of chronic mexiletine treatment in a human model of SCN5A overlap syndrome
Giovanna Nasilli, Loukia Yiangou, Chiara Palandri, Elisabetta Cerbai, Richard P Davis, Arie O Verkerk, Simona Casini, Carol Ann Remme
Europace. 2023 Jun; 25(6): euad154. Published online 2023 Jun 27. doi: 10.1093/europace/euad154
PMCID:
PMC10299896
ArticlePDF–1018K
10.
Modeling incomplete penetrance in long QT syndrome type 3 through ion channel heterogeneity: an in silico population study
Jacob A. Miller, Nicolae Moise, Seth H. Weinberg
Am J Physiol Heart Circ Physiol. 2023 Feb 1; 324(2): H179–H197. Published online 2022 Dec 9. doi: 10.1152/ajpheart.00430.2022
PMCID:
PMC10072004
Article
11.
Continuous Bayesian Variant Interpretation Accounts for Incomplete Penetrance among Mendelian Cardiac Channelopathies
Matthew J. O’Neill, Luca Sala, Isabelle Denjoy, Yuko Wada, Krystian Kozek, Lia Crotti, Federica Dagradi, Maria-Christina Kotta, Carla Spazzolini, Antoine Leenhardt, Joe-Elie Salem, Asami Kashiwa, Seiko Ohno, Ran Tao, Dan M. Roden, Minoru Horie, Fabrice Extramiana, Peter J. Schwartz, Brett M. Kroncke
Genet Med. Author manuscript; available in PMC 2024 Mar 1.
Published in final edited form as: Genet Med. 2023 Mar; 25(3): 100355. Published online 2022 Dec 7. doi: 10.1016/j.gim.2022.12.002
PMCID:
PMC9992222
ArticlePDF–1.8M
12.
Same family, same mutation, different ECG
Kürşat Akbuğa, Mustafa Karanfil
Mol Genet Genomic Med. 2023 Jan; 11(1): e2079. Published online 2022 Oct 28. doi: 10.1002/mgg3.2079
PMCID:
PMC9834179
ArticlePDF–1.1M
13.
When the Gates Swing Open Only: Arrhythmia Mutations That Target the Fast Inactivation Gate of Nav1.5
Tamer M. Gamal El-Din
Cells. 2022 Dec; 11(23): 3714. Published online 2022 Nov 22. doi: 10.3390/cells11233714
PMCID:
PMC9735811
ArticlePDF–1.4M
14.
Utility of Provocative Testing in the Diagnosis and Genotyping of Congenital Long QT Syndrome: A Systematic Review and Meta‐Analysis
Ying Yang, Ting‐ting Lv, Si‐yuan Li, Peng Liu, Qing‐gele Gao, Ping Zhang
J Am Heart Assoc. 2022 Jul 19; 11(14): e025246. Published online 2022 Jul 8. doi: 10.1161/JAHA.122.025246
PMCID:
PMC9707831
ArticlePDF–4.1M
15.
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
Thomas W. Comollo, Xinle Zou, Chuangeng Zhang, Divya Kesters, Thomas Hof, Kevin J. Sampson, Robert S. Kass
Channels (Austin) 2022; 16(1): 173–184. Published online 2022 Aug 10. doi: 10.1080/19336950.2022.2106025
PMCID:
PMC9373745
ArticlePDF–2.4M
16.
Diagnostic Lacunae and Implications of an Automated Implantable Cardioverter Defibrillator Implantation in a Child with Type 3 Long QT (LQT3) Syndrome
Madan M Maddali, Pranav S Kandachar, Ismail A Al-Abri, Mohammed I Al-Yamani
Ann Card Anaesth. 2022 Apr-Jun; 25(2): 210–213. Published online 2022 Apr 11. doi: 10.4103/aca.aca_13_21
PMCID:
PMC9244276
ArticlePDF–1.1M
17.
CONGENITAL LONG QT SYNDROME: A SYSTEMATIC REVIEW
Edvard Galić, Petar Bešlić, Paula Kilić, Zrinka Planinić, Ante Pašalić, Iva Galić, Vlado-Vlaho Ćubela, Petar Pekić
Acta Clin Croat. 2021 Dec; 60(4): 739–748. doi: 10.20471/acc.2021.60.04.22
PMCID:
PMC9196236
ArticlePDF–256K
18.
Cardiac sodium channel mutations: Why so many phenotypes?
Man Liu, Kai-Chien Yang, Samuel C. Dudley, Jr.
Curr Top Membr. Author manuscript; available in PMC 2021 Nov 17.
Published in final edited form as: Curr Top Membr. 2016; 78: 513–559. Published online 2016 Mar 14. doi: 10.1016/bs.ctm.2015.12.004
PMCID:
PMC8597931
ArticlePDF–1.9M
19.
NaV1.5 knockout in iPSCs: a novel approach to study NaV1.5 variants in a human cardiomyocyte environment
Marion Pierre, Mohammed Djemai, Hugo Poulin, Mohamed Chahine
Sci Rep. 2021; 11: 17168. Published online 2021 Aug 25. doi: 10.1038/s41598-021-96474-6
PMCID:
PMC8387439
ArticlePDF–7.4M
20.
Elementary mechanisms of calmodulin regulation of NaV1.5 producing divergent arrhythmogenic phenotypes
Po Wei Kang, Nourdine Chakouri, Johanna Diaz, Gordon F. Tomaselli, David T. Yue, Manu Ben-Johny
Proc Natl Acad Sci U S A. 2021 May 25; 118(21): e2025085118. Published online 2021 May 21. doi: 10.1073/pnas.2025085118
PMCID:
PMC8166197
ArticlePDF–2.9M

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center