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Increased Ca2+ content of the sarcoplasmic reticulum provides arrhythmogenic trigger source in swimming-induced rat athlete's heart model.
Gazdag P, Oravecz K, Acsai K, Demeter-Haludka V, Ördög B, Szlovák J, Kohajda Z, Polyák A, Barta BA, Oláh A, Radovits T, Merkely B, Papp JG, Baczkó I, Varró A, Nagy N, Prorok J. Gazdag P, et al. Among authors: ordog b. Sci Rep. 2020 Nov 11;10(1):19596. doi: 10.1038/s41598-020-76496-2. Sci Rep. 2020. PMID: 33177643 Free PMC article.
Ionic mechanisms limiting cardiac repolarization reserve in humans compared to dogs.
Jost N, Virág L, Comtois P, Ordög B, Szuts V, Seprényi G, Bitay M, Kohajda Z, Koncz I, Nagy N, Szél T, Magyar J, Kovács M, Puskás LG, Lengyel C, Wettwer E, Ravens U, Nánási PP, Papp JG, Varró A, Nattel S. Jost N, et al. Among authors: ordog b. J Physiol. 2013 Sep 1;591(17):4189-206. doi: 10.1113/jphysiol.2013.261198. Epub 2013 Jul 22. J Physiol. 2013. PMID: 23878377 Free PMC article.
A novel transgenic rabbit model with reduced repolarization reserve: long QT syndrome caused by a dominant-negative mutation of the KCNE1 gene.
Major P, Baczkó I, Hiripi L, Odening KE, Juhász V, Kohajda Z, Horváth A, Seprényi G, Kovács M, Virág L, Jost N, Prorok J, Ördög B, Doleschall Z, Nattel S, Varró A, Bősze Z. Major P, et al. Among authors: ordog b. Br J Pharmacol. 2016 Jun;173(12):2046-61. doi: 10.1111/bph.13500. Epub 2016 May 19. Br J Pharmacol. 2016. PMID: 27076034 Free PMC article.
The Effect of a Novel Highly Selective Inhibitor of the Sodium/Calcium Exchanger (NCX) on Cardiac Arrhythmias in In Vitro and In Vivo Experiments.
Kohajda Z, Farkas-Morvay N, Jost N, Nagy N, Geramipour A, Horváth A, Varga RS, Hornyik T, Corici C, Acsai K, Horváth B, Prorok J, Ördög B, Déri S, Tóth D, Levijoki J, Pollesello P, Koskelainen T, Otsomaa L, Tóth A, Baczkó I, Leprán I, Nánási PP, Papp JG, Varró A, Virág L. Kohajda Z, et al. Among authors: ordog b. PLoS One. 2016 Nov 10;11(11):e0166041. doi: 10.1371/journal.pone.0166041. eCollection 2016. PLoS One. 2016. PMID: 27832106 Free PMC article.
A novel 'splice site' HCN4 Gene mutation, c.1737+1 G>T, causes familial bradycardia, reduced heart rate response, impaired chronotropic competence and increased short-term heart rate variability.
Hategan L, Csányi B, Ördög B, Kákonyi K, Tringer A, Kiss O, Orosz A, Sághy L, Nagy I, Hegedűs Z, Rudas L, Széll M, Varró A, Forster T, Sepp R. Hategan L, et al. Among authors: ordog b. Int J Cardiol. 2017 Aug 15;241:364-372. doi: 10.1016/j.ijcard.2017.04.058. Epub 2017 Apr 20. Int J Cardiol. 2017. PMID: 28465117
30 results