Russ U - Search Results

1

Selectivity of repaglinide and glibenclamide for the pancreatic over the cardiovascular K(ATP) channels.

Stephan D, Winkler M, Kühner P, Russ U, Quast U. Stephan D, et al. Among authors: russ u. Diabetologia. 2006 Sep;49(9):2039-48. doi: 10.1007/s00125-006-0307-3. Epub 2006 Jul 25. Diabetologia. 2006. PMID: 16865362

2

The impact of ATP-sensitive K+ channel subtype selectivity of insulin secretagogues for the coronary vasculature and the myocardium.

Quast U, Stephan D, Bieger S, Russ U. Quast U, et al. Among authors: russ u. Diabetes. 2004 Dec;53 Suppl 3:S156-64. doi: 10.2337/diabetes.53.suppl_3.s156. Diabetes. 2004. PMID: 15561904 Review.

3

The mutation Y1206S increases the affinity of the sulphonylurea receptor SUR2A for glibenclamide and enhances the effects of coexpression with Kir6.2.

Stephan D, Stauss E, Lange U, Felsch H, Löffler-Walz C, Hambrock A, Russ U, Quast U. Stephan D, et al. Among authors: russ u. Br J Pharmacol. 2005 Apr;144(8):1078-88. doi: 10.1038/sj.bjp.0706142. Br J Pharmacol. 2005. PMID: 15711591 Free PMC article.

4

Analysis of two KCNJ11 neonatal diabetes mutations, V59G and V59A, and the analogous KCNJ8 I60G substitution: differences between the channel subtypes formed with SUR1.

Winkler M, Lutz R, Russ U, Quast U, Bryan J. Winkler M, et al. Among authors: russ u. J Biol Chem. 2009 Mar 13;284(11):6752-62. doi: 10.1074/jbc.M805435200. Epub 2009 Jan 12. J Biol Chem. 2009. PMID: 19139106 Free PMC article.

5

Substitution of the Walker A lysine by arginine in the nucleotide-binding domains of sulphonylurea receptor SUR2B: effects on ligand binding and channel activity.

Amann T, Schell S, Kühner P, Winkler M, Schwanstecher M, Russ U, Quast U. Amann T, et al. Among authors: russ u. Naunyn Schmiedebergs Arch Pharmacol. 2010 Jun;381(6):507-16. doi: 10.1007/s00210-010-0510-0. Epub 2010 Mar 30. Naunyn Schmiedebergs Arch Pharmacol. 2010. PMID: 20352196

6

Importance of the Kir6.2 N-terminus for the interaction of glibenclamide and repaglinide with the pancreatic K(ATP) channel.

Kühner P, Prager R, Stephan D, Russ U, Winkler M, Ortiz D, Bryan J, Quast U. Kühner P, et al. Among authors: russ u. Naunyn Schmiedebergs Arch Pharmacol. 2012 Mar;385(3):299-311. doi: 10.1007/s00210-011-0709-8. Epub 2011 Nov 15. Naunyn Schmiedebergs Arch Pharmacol. 2012. PMID: 22083559

7

Role of the amino-terminal transmembrane domain of sulfonylurea receptor SUR2B for coupling to K(IR)6.2, ligand binding, and oligomerization.

Winkler M, Kühner P, Russ U, Ortiz D, Bryan J, Quast U. Winkler M, et al. Among authors: russ u. Naunyn Schmiedebergs Arch Pharmacol. 2012 Mar;385(3):287-98. doi: 10.1007/s00210-011-0708-9. Epub 2011 Nov 17. Naunyn Schmiedebergs Arch Pharmacol. 2012. PMID: 22089636

8

Interaction of the sulfonylthiourea HMR 1833 with sulfonylurea receptors and recombinant ATP-sensitive K(+) channels: comparison with glibenclamide.

Russ U, Lange U, Löffler-Walz C, Hambrock A, Quast U. Russ U, et al. J Pharmacol Exp Ther. 2001 Dec;299(3):1049-55. J Pharmacol Exp Ther. 2001. PMID: 11714894

9

Incomplete dissociation of glibenclamide from wild-type and mutant pancreatic K ATP channels limits their recovery from inhibition.

Russ U, Kühner P, Prager R, Stephan D, Bryan J, Quast U. Russ U, et al. Br J Pharmacol. 2009 Jan;156(2):354-61. doi: 10.1111/j.1476-5381.2008.00005.x. Epub 2009 Jan 13. Br J Pharmacol. 2009. PMID: 19154434 Free PMC article.

10

Four novel splice variants of sulfonylurea receptor 1.

Hambrock A, Preisig-Müller R, Russ U, Piehl A, Hanley PJ, Ray J, Daut J, Quast U, Derst C. Hambrock A, et al. Among authors: russ u. Am J Physiol Cell Physiol. 2002 Aug;283(2):C587-98. doi: 10.1152/ajpcell.00083.2002. Am J Physiol Cell Physiol. 2002. PMID: 12107069 Free article.

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