Löffler-Walz C - Search Results

1

Synthesis and characterization of a novel tritiated KATP channel opener with a benzopyran structure.

Manley PW, Löffler-Walz C, Russ U, Hambrock A, Moenius T, Quast U. Manley PW, et al. Among authors: loffler walz c. Br J Pharmacol. 2001 May;133(2):275-85. doi: 10.1038/sj.bjp.0704071. Br J Pharmacol. 2001. PMID: 11350864 Free PMC article.

2

Glibenclamide binding to sulphonylurea receptor subtypes: dependence on adenine nucleotides.

Hambrock A, Löffler-Walz C, Quast U. Hambrock A, et al. Among authors: loffler walz c. Br J Pharmacol. 2002 Aug;136(7):995-1004. doi: 10.1038/sj.bjp.0704801. Br J Pharmacol. 2002. PMID: 12145099 Free PMC article.

3

Mg2+ sensitizes KATP channels to inhibition by DIDS: dependence on the sulphonylurea receptor subunit.

Gojkovic-Bukarica L, Hambrock A, Löffler-Walz C, Quast U, Russ U. Gojkovic-Bukarica L, et al. Among authors: loffler walz c. Br J Pharmacol. 2002 Oct;137(4):429-40. doi: 10.1038/sj.bjp.0704905. Br J Pharmacol. 2002. PMID: 12359624 Free PMC article.

4

Binding and effect of K ATP channel openers in the absence of Mg2+.

Russ U, Lange U, Löffler-Walz C, Hambrock A, Quast U. Russ U, et al. Among authors: loffler walz c. Br J Pharmacol. 2003 May;139(2):368-80. doi: 10.1038/sj.bjp.0705238. Br J Pharmacol. 2003. PMID: 12770942 Free PMC article.

5

Interaction of a novel dihydropyridine K+ channel opener, A-312110, with recombinant sulphonylurea receptors and KATP channels: comparison with the cyanoguanidine P1075.

Felsch H, Lange U, Hambrock A, Löffler-Walz C, Russ U, Carroll WA, Gopalakrishnan M, Quast U. Felsch H, et al. Among authors: loffler walz c. Br J Pharmacol. 2004 Apr;141(7):1098-105. doi: 10.1038/sj.bjp.0705718. Epub 2004 Mar 15. Br J Pharmacol. 2004. PMID: 15023854 Free PMC article.

6

Binding of K(ATP) channel modulators in rat cardiac membranes.

Löffler-Walz C, Quast U. Löffler-Walz C, et al. Br J Pharmacol. 1998 Apr;123(7):1395-402. doi: 10.1038/sj.bjp.0701756. Br J Pharmacol. 1998. PMID: 9579735 Free PMC article.

7

Mg2+ and ATP dependence of K(ATP) channel modulator binding to the recombinant sulphonylurea receptor, SUR2B.

Hambrock A, Löffler-Walz C, Kurachi Y, Quast U. Hambrock A, et al. Br J Pharmacol. 1998 Oct;125(3):577-83. doi: 10.1038/sj.bjp.0702109. Br J Pharmacol. 1998. PMID: 9806343 Free PMC article.

8

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: loffler walz c. Br J Pharmacol. 2005 Apr;144(8):1078-88. doi: 10.1038/sj.bjp.0706142. Br J Pharmacol. 2005. PMID: 15711591 Free PMC article.

9

Interaction of K(ATP) channel modulators with sulfonylurea receptor SUR2B: implication for tetramer formation and allosteric coupling of subunits.

Löffler-Walz C, Hambrock A, Quast U. Löffler-Walz C, et al. Mol Pharmacol. 2002 Feb;61(2):407-14. doi: 10.1124/mol.61.2.407. Mol Pharmacol. 2002. PMID: 11809866

10

Disruption of the actin cytoskeleton abolishes high affinity 3H-glibenclamide binding in rat aortic rings.

Löffler-Walz C, Quast U. Löffler-Walz C, et al. Naunyn Schmiedebergs Arch Pharmacol. 1998 Feb;357(2):183-5. doi: 10.1007/pl00005153. Naunyn Schmiedebergs Arch Pharmacol. 1998. PMID: 9521492

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