CaV1. 2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism I Splawski, KW Timothy, LM Sharpe, N Decher, P Kumar, R Bloise, ... Cell 119 (1), 19-31, 2004 | 1902 | 2004 |
Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations I Splawski, KW Timothy, N Decher, P Kumar, FB Sachse, AH Beggs, ... Proceedings of the National Academy of Sciences 102 (23), 8089-8096, 2005 | 771 | 2005 |
The pore structure and gating mechanism of K2P channels PL Piechotta, M Rapedius, PJ Stansfeld, MK Bollepalli, G Erhlich, ... The EMBO journal 30 (17), 3607-3619, 2011 | 229 | 2011 |
DCPIB is a novel selective blocker of ICl,swell and prevents swelling‐induced shortening of guinea‐pig atrial action potential duration N Decher, HJ Lang, B Nilius, A Brüggemann, AE Busch, K Steinmeyer British journal of pharmacology 134 (7), 1467-1479, 2001 | 224 | 2001 |
The acid-sensitive potassium channel TASK-1 in rat cardiac muscle C Putzke, K Wemhöner, FB Sachse, S Rinné, G Schlichthörl, XT Li, L Jaé, ... Cardiovascular research 75 (1), 59-68, 2007 | 188 | 2007 |
Characterization of TASK‐4, a novel member of the pH‐sensitive, two‐pore domain potassium channel family N Decher, M Maier, W Dittrich, J Gassenhuber, A Brüggemann, AE Busch, ... FEBS letters 492 (1-2), 84-89, 2001 | 171 | 2001 |
Popeye domain containing proteins are essential for stress-mediated modulation of cardiac pacemaking in mice A Froese, SS Breher, C Waldeyer, RFR Schindler, VO Nikolaev, S Rinné, ... The Journal of clinical investigation 122 (3), 1119-1130, 2012 | 165 | 2012 |
Molecular basis for Kv1. 5 channel block: conservation of drug binding sites among voltage-gated K+ channels N Decher, B Pirard, F Bundis, S Peukert, KH Baringhaus, AE Busch, ... Journal of Biological Chemistry 279 (1), 394-400, 2004 | 159 | 2004 |
Mitochondrial damage by α-synuclein causes cell death in human dopaminergic neurons GK Ganjam, K Bolte, LA Matschke, S Neitemeier, AM Dolga, ... Cell death & disease 10 (11), 865, 2019 | 152 | 2019 |
Tamm-Horsfall glycoprotein interacts with renal outer medullary potassium channel ROMK2 and regulates its function A Renigunta, V Renigunta, T Saritas, N Decher, K Mutig, S Waldegger Journal of Biological Chemistry 286 (3), 2224-2235, 2011 | 150 | 2011 |
Voltage-dependent gating of hyperpolarization-activated, cyclic nucleotide-gated pacemaker channels: molecular coupling between the S4–S5 and C-linkers N Decher, J Chen, MC Sanguinetti Journal of Biological Chemistry 279 (14), 13859-13865, 2004 | 148 | 2004 |
KCNE2 modulates current amplitudes and activation kinetics of HCN4: influence of KCNE family members on HCN4 currents N Decher, F Bundis, R Vajna, K Steinmeyer Pflügers Archiv 446, 633-640, 2003 | 134 | 2003 |
A pharmacological master key mechanism that unlocks the selectivity filter gate in K+ channels M Schewe, H Sun, Ü Mert, A Mackenzie, ACW Pike, F Schulz, ... Science 363 (6429), 875-880, 2019 | 126 | 2019 |
Binding site of a novel Kv1. 5 blocker: a “foot in the door” against atrial fibrillation N Decher, P Kumar, T Gonzalez, B Pirard, MC Sanguinetti Molecular pharmacology 70 (4), 1204-1211, 2006 | 117 | 2006 |
hKChIP2 is a functional modifier of hKv4. 3 potassium channels: cloning and expression of a short hKChIP2 splice variant N Decher, O Uyguner, CR Scherer, B Karaman, M Yüksel-Apak, ... Cardiovascular research 52 (2), 255-264, 2001 | 113 | 2001 |
Mitochondrial small conductance SK2 channels prevent glutamate-induced oxytosis and mitochondrial dysfunction AM Dolga, MF Netter, F Perocchi, N Doti, L Meissner, S Tobaben, ... Journal of Biological Chemistry 288 (15), 10792-10804, 2013 | 108 | 2013 |
A specific two-pore domain potassium channel blocker defines the structure of the TASK-1 open pore AK Streit, MF Netter, F Kempf, M Walecki, S Rinné, MK Bollepalli, ... Journal of biological chemistry 286 (16), 13977-13984, 2011 | 108 | 2011 |
TASK-1 channels may modulate action potential duration of human atrial cardiomyocytes SH Limberg, MF Netter, C Rolfes, S Rinné, G Schlichthörl, M Zuzarte, ... Cellular Physiology and Biochemistry 28 (4), 613-624, 2011 | 106 | 2011 |
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking RFR Schindler, C Scotton, J Zhang, C Passarelli, B Ortiz-Bonnin, ... The Journal of clinical investigation 126 (1), 239-253, 2016 | 102 | 2016 |
Gain-of-function mutations in the calcium channel CACNA1C (Cav1. 2) cause non-syndromic long-QT but not Timothy syndrome K Wemhöner, C Friedrich, B Stallmeyer, AJ Coffey, A Grace, S Zumhagen, ... Journal of molecular and cellular cardiology 80, 186-195, 2015 | 100 | 2015 |