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Items: 1 to 20 of 137


Rare variants in genes encoding the cardiac sodium channel and associated compounds and their impact on outcome of catheter ablation of atrial fibrillation.

Husser D, Ueberham L, Hindricks G, Büttner P, Ingram C, Weeke P, Shoemaker MB, Adams V, Arya A, Sommer P, Darbar D, Roden DM, Bollmann A.

PLoS One. 2017 Aug 24;12(8):e0183690. doi: 10.1371/journal.pone.0183690. eCollection 2017.


Sudden cardiac death: focus on the genetics of channelopathies and cardiomyopathies.

Magi S, Lariccia V, Maiolino M, Amoroso S, Gratteri S.

J Biomed Sci. 2017 Aug 15;24(1):56. doi: 10.1186/s12929-017-0364-6. Review.


Landscape and variation of novel retroduplications in 26 human populations.

Zhang Y, Li S, Abyzov A, Gerstein MB.

PLoS Comput Biol. 2017 Jun 29;13(6):e1005567. doi: 10.1371/journal.pcbi.1005567. eCollection 2017 Jun.


Microdomain-specific localization of functional ion channels in cardiomyocytes: an emerging concept of local regulation and remodelling.

Balycheva M, Faggian G, Glukhov AV, Gorelik J.

Biophys Rev. 2015 Mar;7(1):43-62. doi: 10.1007/s12551-014-0159-x. Epub 2015 Jan 15.


Genetics and Sinus Node Dysfunction.

Nof E, Glikson M, Antzelevitch C.

J Atr Fibrillation. 2009 Apr 1;1(6):151. doi: 10.4022/jafib.151. eCollection 2009 Apr-May. Review. No abstract available.


Potential Roles of Serum Caveolin-3 Levels in Patients with Atrial Fibrillation.

Sun LY, Qu X, Chen LZ, Zheng GS, Wu XL, Chen XX, Huang WJ, Zhou H.

Front Aging Neurosci. 2017 Apr 4;9:90. doi: 10.3389/fnagi.2017.00090. eCollection 2017.


Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.

Abou Ziki MD, Seidelmann SB, Smith E, Atteya G, Jiang Y, Fernandes RG, Marieb MA, Akar JG, Mani A.

Clin Genet. 2017 Apr 13. doi: 10.1111/cge.13036. [Epub ahead of print]


Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence.

Ioakeimidis NS, Papamitsou T, Meditskou S, Iakovidou-Kritsi Z.

J Biol Res (Thessalon). 2017 Mar 14;24:6. doi: 10.1186/s40709-017-0063-1. eCollection 2017 Dec. Review.


Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances.

Fernández-Falgueras A, Sarquella-Brugada G, Brugada J, Brugada R, Campuzano O.

Biology (Basel). 2017 Jan 29;6(1). pii: E7. doi: 10.3390/biology6010007. Review.


Murine Electrophysiological Models of Cardiac Arrhythmogenesis.

Huang CL.

Physiol Rev. 2017 Jan;97(1):283-409. Review.


Molecular Pathophysiology of Congenital Long QT Syndrome.

Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, Kass RS.

Physiol Rev. 2017 Jan;97(1):89-134. Review.


The Caveolin-3 G56S sequence variant of unknown significance: Muscle biopsy findings and functional cell biological analysis.

Brauers E, Roos A, Kollipara L, Zahedi RP, Beckmann A, Mohanadas N, Bauer H, Häusler M, Thoma S, Kress W, Senderek J, Weis J.

Proteomics Clin Appl. 2017 Jan;11(1-2). doi: 10.1002/prca.201600007. Epub 2016 Nov 14.


PTRF/Cavin-1 Deficiency Causes Cardiac Dysfunction Accompanied by Cardiomyocyte Hypertrophy and Cardiac Fibrosis.

Taniguchi T, Maruyama N, Ogata T, Kasahara T, Nakanishi N, Miyagawa K, Naito D, Hamaoka T, Nishi M, Matoba S, Ueyama T.

PLoS One. 2016 Sep 9;11(9):e0162513. doi: 10.1371/journal.pone.0162513. eCollection 2016.


Cavin4b/Murcb Is Required for Skeletal Muscle Development and Function in Zebrafish.

Housley MP, Njaine B, Ricciardi F, Stone OA, Hölper S, Krüger M, Kostin S, Stainier DY.

PLoS Genet. 2016 Jun 13;12(6):e1006099. doi: 10.1371/journal.pgen.1006099. eCollection 2016 Jun.


IK1-enhanced human-induced pluripotent stem cell-derived cardiomyocytes: an improved cardiomyocyte model to investigate inherited arrhythmia syndromes.

Vaidyanathan R, Markandeya YS, Kamp TJ, Makielski JC, January CT, Eckhardt LL.

Am J Physiol Heart Circ Physiol. 2016 Jun 1;310(11):H1611-21. doi: 10.1152/ajpheart.00481.2015. Epub 2016 Apr 8.


α1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium Current.

Choi JI, Wang C, Thomas MJ, Pitt GS.

PLoS One. 2016 Mar 30;11(3):e0152355. doi: 10.1371/journal.pone.0152355. eCollection 2016.


Electrophysiology and metabolism of caveolin-3-overexpressing mice.

Schilling JM, Horikawa YT, Zemljic-Harpf AE, Vincent KP, Tyan L, Yu JK, McCulloch AD, Balijepalli RC, Patel HH, Roth DM.

Basic Res Cardiol. 2016 May;111(3):28. doi: 10.1007/s00395-016-0542-9. Epub 2016 Mar 29.


Genetics of channelopathies associated with sudden cardiac death.

Campuzano O, Sarquella-Brugada G, Brugada R, Brugada J.

Glob Cardiol Sci Pract. 2015 Oct 13;2015(3):39. doi: 10.5339/gcsp.2015.39. eCollection 2015. Review.


Genetics of inherited primary arrhythmia disorders.

Spears DA, Gollob MH.

Appl Clin Genet. 2015 Sep 18;8:215-33. doi: 10.2147/TACG.S55762. eCollection 2015. Review.


Ion Channels in the Heart.

Bartos DC, Grandi E, Ripplinger CM.

Compr Physiol. 2015 Jul 1;5(3):1423-64. doi: 10.1002/cphy.c140069. Review.

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