Publications by authors named "Ulrich Russ"

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Importance of the Kir6.2 N-terminus for the interaction of glibenclamide and repaglinide with the pancreatic K(ATP) channel.
Petra Kühner, Renate Prager, Damian Stephan, Ulrich Russ, Marcus Winkler

Naunyn Schmiedebergs Arch Pharmacol· March 2012

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Role of the amino-terminal transmembrane domain of sulfonylurea receptor SUR2B for coupling to K(IR)6.2, ligand binding, and oligomerization.
Marcus Winkler, Petra Kühner, Ulrich Russ, David Ortiz, Joseph Bryan

Naunyn Schmiedebergs Arch Pharmacol· March 2012

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Substitution of the Walker A lysine by arginine in the nucleotide-binding domains of sulphonylurea receptor SUR2B: effects on ligand binding and channel activity.
Tobias Amann, Sophie Schell, Petra Kühner, Marcus Winkler, Mathias Schwanstecher, Ulrich Russ

Naunyn Schmiedebergs Arch Pharmacol· June 2010

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Cyclic AMP increases cytoplasmic free calcium in renin-secreting cells from rat kidney.
Julia Laske-Ernst, Marc Chmielnicki, Ulrich Quast, Ulrich Russ

Gen Physiol Biophys· December 2009

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Analysis of two KCNJ11 neonatal diabetes mutations, V59G and V59A, and the analogous KCNJ8 I60G substitution: differences between the channel subtypes formed with SUR1.
Marcus Winkler, Rebekka Lutz, Ulrich Russ, Ulrich Quast, Joseph Bryan

J Biol Chem· March 2009

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Effect of adenosine on membrane potential and Ca2+ in juxtaglomerular cells. Comparison with angiotensin II.
Julia Laske-Ernst, Alexander Stehle, Volker Vallon, Ulrich Quast, Ulrich Russ

Kidney Blood Press Res· June 2008

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The mutation Y1206S increases the affinity of the sulphonylurea receptor SUR2A for glibenclamide and enhances the effects of coexpression with Kir6.2.
Damian Stephan, Eva Stauss, Ulf Lange, Holger Felsch, Cornelia Löffler-Walz, Ulrich Russ

Br J Pharmacol· April 2005

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The impact of ATP-sensitive K+ channel subtype selectivity of insulin secretagogues for the coronary vasculature and the myocardium.
Ulrich Quast, Damian Stephan, Susanne Bieger, Ulrich Russ

Diabetes· December 2004

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Electrophysiological and molecular characterization of the inward rectifier in juxtaglomerular cells from rat kidney.
Anke Leichtle, Ulrich Rauch, Margitta Albinus, Peter Benöhr, Hubert Kalbacher, Ulrich Russ

J Physiol· October 2004

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Interaction of a novel dihydropyridine K+ channel opener, A-312110, with recombinant sulphonylurea receptors and KATP channels: comparison with the cyanoguanidine P1075.
Holger Felsch, Ulf Lange, Annette Hambrock, Cornelia Löffler-Walz, Ulrich Russ

Br J Pharmacol· April 2004

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Binding and effect of K ATP channel openers in the absence of Mg2+.
Ulrich Russ, Ulf Lange, Cornelia Löffler-Walz, Annette Hambrock, Ulrich Quast

Br J Pharmacol· May 2003

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The stereoenantiomers of a pinacidil analog open or close cloned ATP-sensitive K+ channels.
Ulf Lange, Cornelia Löffler-Walz, Heinrich C Englert, Annette Hambrock, Ulrich Russ

J Biol Chem· October 2002

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Mg2+ sensitizes KATP channels to inhibition by DIDS: dependence on the sulphonylurea receptor subunit.
Ljiljana Gojkovic-Bukarica, Annette Hambrock, Cornelia Löffler-Walz, Ulrich Quast, Ulrich Russ

Br J Pharmacol· October 2002

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Four novel splice variants of sulfonylurea receptor 1.
Annette Hambrock, Regina Preisig-Müller, Ulrich Russ, Anke Piehl, Peter J Hanley

Am J Physiol Cell Physiol· August 2002

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KCO912: a potent and selective opener of ATP-dependent potassium (K(ATP)) channels which suppresses airways hyperreactivity at doses devoid of cardiovascular effects.
Karl-Heinz Buchheit, Paul W Manley, Ulrich Quast, Ulrich Russ, Lazzaro Mazzoni

Naunyn Schmiedebergs Arch Pharmacol· March 2002

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