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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. Among authors: dittmann s. 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
Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation.
Veerman CC, Mengarelli I, Lodder EM, Kosmidis G, Bellin M, Zhang M, Dittmann S, Guan K, Wilde AAM, Schulze-Bahr E, Greber B, Bezzina CR, Verkerk AO. Veerman CC, et al. Among authors: dittmann s. J Am Heart Assoc. 2017 Jul 24;6(7):e005135. doi: 10.1161/JAHA.116.005135. J Am Heart Assoc. 2017. PMID: 28739862 Free PMC article.
[Genetic testing to prevent sudden cardiac death].
Stallmeyer B, Dittmann S, Schulze-Bahr E. Stallmeyer B, et al. Among authors: dittmann s. Internist (Berl). 2018 Aug;59(8):776-789. doi: 10.1007/s00108-018-0462-x. Internist (Berl). 2018. PMID: 29943240 Review. German.
Data on the role of cardiac α-actin (ACTC1) gene mutations on SRF-signaling.
Rangrez AY, Kilian L, Stiebeling K, Dittmann S, Yadav P, Schulze-Bahr E, Frey N, Frank D. Rangrez AY, et al. Among authors: dittmann s. Data Brief. 2020 Jan 2;28:105071. doi: 10.1016/j.dib.2019.105071. eCollection 2020 Feb. Data Brief. 2020. PMID: 31921954 Free PMC article.
POPDC2 a novel susceptibility gene for conduction disorders.
Rinné S, Ortiz-Bonnin B, Stallmeyer B, Kiper AK, Fortmüller L, Schindler RFR, Herbort-Brand U, Kabir NS, Dittmann S, Friedrich C, Zumhagen S, Gualandi F, Selvatici R, Rapezzi C, Arbustini E, Ferlini A, Fabritz L, Schulze-Bahr E, Brand T, Decher N. Rinné S, et al. Among authors: dittmann s. J Mol Cell Cardiol. 2020 Aug;145:74-83. doi: 10.1016/j.yjmcc.2020.06.005. Epub 2020 Jun 11. J Mol Cell Cardiol. 2020. PMID: 32535041
151 results