89. Jahrestagung der Deutschen Gesellschaft für Kardiologie

Samstag, 15. April 2023 (Posterbereich 30) 10:00-11:30

Postervorträge

iPSC – Disease modeling

Diskussionsleitung: F. Hohendanner (Berlin), M. Tiburcy (Göttingen)

(P2255) Left ventricular non-compaction cardiomyopathic mutation R634L in RBM20 rewire splicing regulation and guides downstream cellular and functional processes
    S. Rebs, F. Sedaghat-Hamedani, E. Kayvanpour, J. Dudek, A. Wagdi, G. Hasenfuß, C. Maack, B. Meder, K. Streckfuß-Bömeke (Würzburg, Heidelberg, Göttingen)
(P2256) Inflammasome contributes to LPS-induced alteration of phenotypic features of Brugada syndrome
    C. Yan, Z. Meng, M. Li, X. Lei, X. Fan, L. Cyganek, I. El-Battrawy, X. Zhou, I. Akin (Mannheim, Göttingen, Bochum)
(P2257) Chemogenetic inhibition of cardiac contractility in engineered heart tissue results in substantial changes in cardiomyocyte morphology.
    J. Rössinger, K. Bowitz Larsen, T. Stüdemann, M. Nager, T. Myrmel, T. Eschenhagen, F. Weinberger, Å. Birna Birgisdottir (Hamburg; Tromsø, NO)
(P2258) The 1A domain of desmin is a hotspot for putative pathogenic cardiomyopathy associated mutations leading to severe filament assembly defects in iPSC-derived cardiomyocytes
    A. Brodehl, S. Holler, J. Gummert, H. Milting (Bad Oeynhausen)
(P2259) Novel insights in the pathogenic role of fever and inflammation in Brugada syndrome - Study using gene-edited human-induced pluripotent stem cell-derived cardiomyocytes
    Y. Li, L. Rose, T. Prädel, M. Kleinsorge, X. Fan, H. Dinkel, A. Busley, R. Zhong, F. Zhang, Q. Xu, L. Maywald, A. Aweimer, M. Huang, A. Moscu-Gregor, A. Hohn, Z. Yang, L. Qiao, A. Mügge, L. Cyganek, X. Zhou, I. Akin, I. El-Battrawy (Mannheim, Göttingen, Bochum, Martinsried)
(P2260) Physiological maturation medium to enhance metabolic activity, hypertrophic growth and functionality of ventricular iPSC-CMs
    R.-P. Steiner, M. Schubert, W. Li, A. Strano, A. El-Armouche, K. Guan (Dresden)
(P2261) Phenocopying Fabry disease using GLA Knockout hiPSC-derived cardiomyocytes to identify novel treatment options
    M. Juchem, C. Jahn, C. Bär, J. Hoepfner, T. Thum, für die Studiengruppe: IMTTS (Hannover)
(P2262) Modeling the human heart in 3D: Establishing multicellular cardiac organoids as versatile tool to investigate cardiac pathophysiology in vitro
    E. Mohr, H. Hunkler, I. Riedel, T. Thum, C. Bär (Hannover)