S. Kathöfer

发表

Inhibition of cardiac HERG potassium channels by the atypical antidepressant trazodone

H. Katus, Dierk Thomas, E. Zitron, 2004, Naunyn-Schmiedeberg's Archives of Pharmacology.

Inhibition of cardiac hERG potassium channels by tetracyclic antidepressant mianserin

H. Katus, Dierk Thomas, A. Bauer, 2008, Naunyn-Schmiedeberg's Archives of Pharmacology.

Anticholinergic antiparkinson drug orphenadrine inhibits HERG channels: block attenuation by mutations of the pore residues Y652 or F656

G. Seemann, H. Katus, F. Konrad, 2007, Naunyn-Schmiedeberg's Archives of Pharmacology.

Atypical tetracyclic antidepressant maprotiline is an antagonist at cardiac hERG potassium channels

H. Katus, Dierk Thomas, A. Bauer, 2006, Naunyn-Schmiedeberg's Archives of Pharmacology.

Inhibition of cardiac HERG channels by grapefruit flavonoid naringenin: implications for the influence of dietary compounds on cardiac repolarisation

H. Katus, Dierk Thomas, E. Zitron, 2005, Naunyn-Schmiedeberg's Archives of Pharmacology.

Class Ia anti-arrhythmic drug ajmaline blocks HERG potassium channels: mode of action

Hugo A. Katus, Eberhard P. Scholz, Edgar Zitron, 2004, Naunyn-Schmiedeberg's Archives of Pharmacology.

Drug binding to aromatic residues in the HERG channel pore cavity as possible explanation for acquired Long QT syndrome by antiparkinsonian drug budipine

H. Katus, Dierk Thomas, E. Zitron, 2003, Naunyn-Schmiedeberg's Archives of Pharmacology.

Regulation of two‐pore‐domain (K2P) potassium leak channels by the tyrosine kinase inhibitor genistein

E. Ficker, A. Bauer, J. Gierten, 2008, British journal of pharmacology.

Deletion of Protein Kinase A Phosphorylation Sites in the HERG Potassium Channel Inhibits Activation Shift by Protein Kinase A*

W. Kübler, Dierk Thomas, W. Schöls, 1999, The Journal of Biological Chemistry.

Regulation of HERG potassium channel activation by protein kinase C independent of direct phosphorylation of the channel protein.

H. Katus, Dierk Thomas, S. Kathöfer, 2003, Cardiovascular research.

Human Cardiac Inwardly-Rectifying K+ Channel Kir2.1b Is Inhibited by Direct Protein Kinase C-Dependent Regulation in Human Isolated Cardiomyocytes and in an Expression System

C. Vahl, H. Katus, Dierk Thomas, 2002, Circulation.

Activation of inwardly rectifying Kir2.x potassium channels by β3-adrenoceptors is mediated via different signaling pathways with a predominant role of PKC for Kir2.1 and of PKA for Kir2.2

H. Katus, Dierk Thomas, A. Bauer, 2007, Naunyn-Schmiedeberg's Archives of Pharmacology.

Regulation of cardiac inwardly rectifying potassium current IK1 and Kir2.x channels by endothelin-1

H. Katus, Dierk Thomas, E. Zitron, 2005, Journal of Molecular Medicine.

Human cardiac inwardly rectifying current IKir2.2 is upregulated by activation of protein kinase A.

H. Katus, Dierk Thomas, E. Zitron, 2004, Cardiovascular research.

Inhibition of hK2P3.1 (TASK-1) Potassium Channels by the Tyrosine Kinase Inhibitor Genistein

H. Katus, Dierk Thomas, E. Ficker, 2009 .

Antiarrhythmic drug carvedilol inhibits HERG potassium channels.

S. Kathöfer, J. Kiehn, V. Kreye, 2001, Cardiovascular research.

QTc Prolongation by Grapefruit Juice and Its Potential Pharmacological Basis: HERG Channel Blockade by Flavonoids

R. Owen, H. Katus, F. Niroomand, 2005, Circulation.

Bertosamil blocks HERG potassium channels in their open and inactivated states

Dierk Thomas, E. Zitron, S. Kathöfer, 2002, British journal of pharmacology.

Acute effects of dronedarone on both components of the cardiac delayed rectifier K+ current, HERG and KvLQT1/minK potassium channels

H. Katus, Dierk Thomas, E. Zitron, 2003, British journal of pharmacology.

In vitro modulation of HERG channels by organochlorine solvent trichlormethane as potential explanation for proarrhythmic effects of chloroform.

H. Katus, J. Greten, Dierk Thomas, 2006, Toxicology letters.

[Molecular basis of primary electrical heart diseases].

E. Zitron, C. Kiesecker, E. Scholz, 2005, Herzschrittmachertherapie & Elektrophysiologie.

Rapid component I(Kr) of the guinea-pig cardiac delayed rectifier K(+) current is inhibited by beta(1)-adrenoreceptor activation, via cAMP/protein kinase A-dependent pathways.

E. Zitron, S. Kathöfer, J. Kiehn, 2002, Cardiovascular research.

Human β3-adrenoreceptors couple to KvLQT1/MinK potassium channels in Xenopus oocytes via protein kinase C phosphorylation of the KvLQT1 protein

H. Katus, Dierk Thomas, S. Kathöfer, 2003, Naunyn-Schmiedeberg's Archives of Pharmacology.

Doxazosin induces apoptosis of cells expressing hERG K+ channels.

H. Katus, Dierk Thomas, E. Ficker, 2008, European journal of pharmacology.

Functional coupling of human beta 3-adrenoreceptors to the KvLQT1/MinK potassium channel.

S. Kathöfer, J. Kiehn, W. Schoels, 2000, The Journal of biological chemistry.

Activation of cardiac human ether-a-go-go related gene potassium currents is regulated by α1A-adrenoceptors

H. Katus, Dierk Thomas, E. Zitron, 2004, Journal of Molecular Medicine.

Inhibition of cloned HERG potassium channels by the antiestrogen tamoxifen

H. Katus, Dierk Thomas, S. Kathöfer, 2003, Naunyn-Schmiedeberg's Archives of Pharmacology.

Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.

H. Katus, Dierk Thomas, S. Kathöfer, 2005, Cardiovascular research.

The antipsychotic drug chlorpromazine inhibits HERG potassium channels

Hugo A Katus, H. Katus, Dierk Thomas, 2003, British journal of pharmacology.

Inhibition of cardiac HERG currents by the DNA topoisomerase II inhibitor amsacrine: mode of action

B. Wible, H. Katus, Dierk Thomas, 2004, British Journal of Pharmacology.

Kir2.x inward rectifier potassium channels are differentially regulated by adrenergic alpha1A receptors.

H. Katus, Dierk Thomas, A. Bauer, 2008, Journal of molecular and cellular cardiology.

Biophysical properties of zebrafish ether-à-go-go related gene potassium channels.

Daniel Scherer, Hugo A Katus, Edgar Zitron, 2009, Biochemical and biophysical research communications.

Myocarditis with quetiapine.

M. Weisbrod, M. Schwaninger, S. Kathöfer, 2002, The American journal of psychiatry.

Orange flavonoid hesperetin modulates cardiac hERG potassium channel via binding to amino acid F656.

A. Remppis, H. Katus, J. Greten, 2007, Nutrition, metabolism, and cardiovascular diseases : NMCD.