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Page 1
Human Genetics of Cardiac Arrhythmias.
Schulze-Bahr E, Dittmann S. Schulze-Bahr E, et al. Adv Exp Med Biol. 2024;1441:1033-1055. doi: 10.1007/978-3-031-44087-8_66. Adv Exp Med Biol. 2024. PMID: 38884768 Review.
Molecular mechanisms of inherited ventricular arrhythmias.
Wichter T, Schulze-Bahr E, Eckardt L, Paul M, Levkau B, Meyborg M, Schäfers M, Haverkamp W, Breithardt G. Wichter T, et al. Herz. 2002 Dec;27(8):712-39. doi: 10.1007/s00059-002-2436-x. Herz. 2002. PMID: 12574890 Review.
Susceptibility genes & modifiers for cardiac arrhythmias.
Schulze-Bahr E. Schulze-Bahr E. Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):289-300. doi: 10.1016/j.pbiomolbio.2009.01.008. Epub 2009 Jan 29. Prog Biophys Mol Biol. 2008. PMID: 19351519 Free article. Review.
Coxsackievirus B3 modulates cardiac ion channels.
Steinke K, Sachse F, Ettischer N, Strutz-Seebohm N, Henrion U, Rohrbeck M, Klosowski R, Wolters D, Brunner S, Franz WM, Pott L, Munoz C, Kandolf R, Schulze-Bahr E, Lang F, Klingel K, Seebohm G. Steinke K, et al. FASEB J. 2013 Oct;27(10):4108-21. doi: 10.1096/fj.13-230193. Epub 2013 Jun 27. FASEB J. 2013. PMID: 23825229
A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome.
Zumhagen S, Veldkamp MW, Stallmeyer B, Baartscheer A, Eckardt L, Paul M, Remme CA, Bhuiyan ZA, Bezzina CR, Schulze-Bahr E. Zumhagen S, et al. PLoS One. 2013 Jun 28;8(6):e67963. doi: 10.1371/journal.pone.0067963. Print 2013. PLoS One. 2013. PMID: 23840796 Free PMC article.
TASK-1 and TASK-3 may form heterodimers in human atrial cardiomyocytes.
Rinné S, Kiper AK, Schlichthörl G, Dittmann S, Netter MF, Limberg SH, Silbernagel N, Zuzarte M, Moosdorf R, Wulf H, Schulze-Bahr E, Rolfes C, Decher N. Rinné S, et al. J Mol Cell Cardiol. 2015 Apr;81:71-80. doi: 10.1016/j.yjmcc.2015.01.017. Epub 2015 Feb 2. J Mol Cell Cardiol. 2015. PMID: 25655935
216 results