Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death

Fischer B, Dittmann S, Brodehl A, Unger A, Stallmeyer B, Paul M, Seebohm G, Kayser A, Peischard S, Linke WA, Milting H, Schulze-Bahr E. (2021)

In: International Journal of Cardiology, 329.

Research article (journal)

A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations

Hartung B, Tank A, Dittmann S, Ritz-Timme S, Schulze-Bahr E. (2021)

In: ((Bitte Journal prüfen)), 21.

Research article (journal)

Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia

Decher N, Ortiz-Bonnin B, Friedrich C, Schewe M, Kiper AK, Rinne S, Seemann G, Peyronnet R, Zumhagen S, Bustos D, Kockskamper J, Kohl P, Just S, Gonzalez W, Baukrowitz T, Stallmeyer B, Schulze-Bahr E (2017)

In: ((Bitte Journal prüfen)), 9(4).

Research article (journal)

Design, Synthesis, Pharmacological Evaluation and Docking Studies of GluN2B-Selective NMDA Receptor Antagonists with a Benzo[7]annulen-7-amine Scaffold

Gawaskar S, Temme L, Schreiber JA, Schepmann D, Bonifazi A, Robaa D, Sippl W, Strutz-Seebohm N, Seebohm G, Wunsch B (2017)

In: ChemMedChem, 12(15).

Research article (journal)

Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation

Marczenke M, Fell J, Piccini I, Ropke A, Seebohm G, Greber B (2017)

In: ((Bitte Journal prüfen)), 21.

Research article (journal)

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Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death Fischer B, Dittmann S, Brodehl A, Unger A, Stallmeyer B, Paul M, Seebohm G, Kayser A, Peischard S, Linke WA, Milting H, Schulze-Bahr E. (2021) In: International Journal of Cardiology, 329. Research article (journal)
Long, longer, long QT syndrome: what makes the difference? Dittmann S, Kayser A, Schulze-Bahr E. (2021) In: ((Bitte Journal prüfen)), 117. Research article (journal)
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations Hartung B, Tank A, Dittmann S, Ritz-Timme S, Schulze-Bahr E. (2021) In: ((Bitte Journal prüfen)), 21. Research article (journal)
Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography Zumhagen S, Vrachimis A, Stegger L, Kies P, Wenning C, Ernsting M, Muller J, Seebohm G, Paul M, Schafers K, Stallmeyer B, Schafers M, Schulze-Bahr E (2018) In: Heart, 104(4). Research article (journal)
Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia Decher N, Ortiz-Bonnin B, Friedrich C, Schewe M, Kiper AK, Rinne S, Seemann G, Peyronnet R, Zumhagen S, Bustos D, Kockskamper J, Kohl P, Just S, Gonzalez W, Baukrowitz T, Stallmeyer B, Schulze-Bahr E (2017) In: ((Bitte Journal prüfen)), 9(4). Research article (journal)
Deconstruction - reconstruction approach to analyze the essential structural elements of tetrahydro-3-benzazepine-based antagonists of GluN2B subunit containing NMDA receptors Dey S, Temme L, Schreiber JA, Schepmann D, Frehland B, Lehmkuhl K, Strutz-Seebohm N, Seebohm G, Wunsch B (2017) In: ((Bitte Journal prüfen)), 138. Research article (journal)
Design, Synthesis, Pharmacological Evaluation and Docking Studies of GluN2B-Selective NMDA Receptor Antagonists with a Benzo[7]annulen-7-amine Scaffold Gawaskar S, Temme L, Schreiber JA, Schepmann D, Bonifazi A, Robaa D, Sippl W, Strutz-Seebohm N, Seebohm G, Wunsch B (2017) In: ChemMedChem, 12(15). Research article (journal)
Through modulation of cardiac Ca(2+) handling, UCP2 affects cardiac electrophysiology and influences the susceptibility for Ca(2+) -mediated arrhythmias Larbig R, Reda S, Paar V, Trost A, Leitner J, Weichselbaumer S, Motloch KA, Wernly B, Arrer A, Strauss B, Lichtenauer M, Reitsamer HA, Eckardt L, Seebohm G, Hoppe UC, Motloch LJ (2017) In: ((Bitte Journal prüfen)), 102(6). Research article (journal)
Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation Marczenke M, Fell J, Piccini I, Ropke A, Seebohm G, Greber B (2017) In: ((Bitte Journal prüfen)), 21. Research article (journal)
Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells Marczenke M, Piccini I, Mengarelli I, Fell J, Ropke A, Seebohm G, Verkerk AO, Greber B (2017) In: ((Bitte Journal prüfen)), 8. Research article (journal)