The Symptom Complex of Familial Sinus Node Dysfunction and Myocardial Noncompaction Is Associated With Mutations in the HCN4 Channel von Schweizer, Patrick A., MD, Schröter, Julian, BSc, Greiner, Sebastian, MD, Haas, Jan, PhD, Yampolsky, Pessah, PhD, Mereles, Derliz, MD, Buss, Sebastian J., MD, Seyler, Claudia, PhD, Bruehl, Claus, PhD, Draguhn, Andreas, MD, Koenen, Michael, PhD, Meder, Benjamin, MD, Katus, Hugo A., MD, Thomas, Dierk, MD

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Tiotropium Respimat Inhaler and the Risk of Death in COPD von Wise, Robert A, Anzueto, Antonio, Cotton, Daniel, Dahl, Ronald, Devins, Theresa, Disse, Bernd, Dusser, Daniel, Joseph, Elizabeth, Kattenbeck, Sabine, Koenen-Bergmann, Michael, Pledger, Gordon, Calverley, Peter

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Augmentation of myocardial If dysregulates calcium homeostasis and causes adverse cardiac remodeling von Yampolsky, Pessah, Koenen, Michael, Mosqueira, Matias, Geschwill, Pascal, Nauck, Sebastian, Witzenberger, Monika, Seyler, Claudia, Fink, Thomas, Kruska, Mathieu, Bruehl, Claus, Schwoerer, Alexander P., Ehmke, Heimo, Fink, Rainer H. A., Draguhn, Andreas, Thomas, Dierk, Katus, Hugo A., Schweizer, Patrick A.

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Improved Generation of Human Induced Pluripotent Stem Cell-Derived Cardiac Pacemaker Cells Using Novel Differentiation Protocols von Darche, Fabrice F., Ullrich, Nina D., Huang, Ziqiang, Koenen, Michael, Rivinius, Rasmus, Frey, Norbert, Schweizer, Patrick A.

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Subtype-specific differentiation of cardiac pacemaker cell clusters from human induced pluripotent stem cells von Schweizer, Patrick A, Darche, Fabrice F, Ullrich, Nina D, Geschwill, Pascal, Greber, Boris, Rivinius, Rasmus, Seyler, Claudia, Müller-Decker, Karin, Draguhn, Andreas, Utikal, Jochen, Koenen, Michael, Katus, Hugo A, Thomas, Dierk

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Quantitative Efficacy and Fate of Mesenchymal Stromal Cells Targeted to Cardiac Sites by Radiofrequency Catheter Ablation von Malik, Rizwan, Darche, Fabrice F., Rivinius, Rasmus, Seckinger, Anja, Krause, Ulf, Koenen, Michael, Thomas, Dierk, Katus, Hugo A., Schweizer, Patrick A.

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A Distinct Cardiomyopathy von Schweizer, Patrick A., MD, Koenen, Michael, PhD, Katus, Hugo A., MD, Thomas, Dierk, MD

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Genetic suppression of atrial fibrillation using a dominant-negative ether-a-go-go–related gene mutant von Soucek, Radim, MD, Thomas, Dierk, MD, Kelemen, Kamilla, MD, Bikou, Olympia, MD, Seyler, Claudia, PhD, Voss, Frederik, MD, Becker, Rüdiger, MD, Koenen, Michael, PhD, Katus, Hugo A., MD, Bauer, Alexander, MD

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Decrease in the oral bioavailability of dabigatran etexilate after co‐medication with rifampicin von Härtter, Sebastian, Koenen‐Bergmann, Michael, Sharma, Ashish, Nehmiz, Gerhard, Lemke, Ute, Timmer, Wolfgang, Reilly, Paul A.

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Auswertung von Blockchain-Inhalten zu Strafverfolgungszwecken von Koenen, Dr. Michael

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Acetylcholine receptor channel subtype directs the innervation pattern of skeletal muscle von Koenen, Michael, Peter, Christoph, Villarroel, Alfredo, Witzemann, Veit, Sakmann, Bert

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Novel mouse model reveals distinct activity-dependent and -independent contributions to synapse development von Pacifici, Pier Giorgio, Peter, Christoph, Yampolsky, Pessah, Koenen, Michael, McArdle, Joseph J, Witzemann, Veit

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BS-452757-4 ANTI-ARRHYTHMIC EFFECTS OF ANDROGEN DEPRIVATION THERAPIES IN A SCN5A LOSS-OF-FUNCTION MOUSE MODEL von Schweizer, Patrick A., Kruska, Mathieu, Fink, Thomas, Thomas, Dierk, Frey, Norbert, Koenen, Michael

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Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1 von Thomas, Dierk, Khalil, Markus, Alter, Markus, Schweizer, Patrick A, Karle, Christoph A, Wimmer, Anna-Britt, Licka, Manuela, Katus, Hugo A, Koenen, Michael, Ulmer, Herbert E, Zehelein, Jörg

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Skipping of Exon 1 in the KCNQ1 Gene Causes Jervell and Lange-Nielsen Syndrome von Zehelein, Joerg, Kathoefer, Sven, Khalil, Markus, Alter, Markus, Thomas, Dierk, Brockmeier, Konrad, Ulmer, Herbert E., Katus, Hugo A., Koenen, Michael

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A Distinct Cardiomyopathy: HCN4Syndrome Comprising Myocardial Noncompaction, Bradycardia, Mitral Valve Defects, and Aortic Dilation von Schweizer, Patrick A, Koenen, Michael, Katus, Hugo A, Thomas, Dierk

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GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome von Semino, Francesca, Darche, Fabrice F., Bruehl, Claus, Koenen, Michael, Skladny, Heyko, Katus, Hugo A., Frey, Norbert, Draguhn, Andreas, Schweizer, Patrick A.

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Regulation of fast inactivation of cloned mammalian Ik(A) channels by cysteine oxidation von RUPPERSBERG, J. P, STOCKER, M, PONGS, O, HEINEMANN, S. H, FRANK, R, KOENEN, M

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Pharmacokinetic and Safety Evaluation of BILR 355, a Second-Generation Nonnucleoside Reverse Transcriptase Inhibitor, in Healthy Volunteers von FENGLEI HUANG, KOENEN-BERGMANN, Michael, MACGREGOR, Thomas R, RING, Arne, HATTOX, Susan, ROBINSON, Patrick

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ANK2 functionally interacts with KCNH2 aggravating long QT syndrome in a double mutation carrier von Gessner, Guido, Runge, Sarah, Koenen, Michael, Heinemann, Stefan H., Koenen, Mascha, Haas, Jan, Meder, Benjamin, Thomas, Dierk, Katus, Hugo A., Schweizer, Patrick A.

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