Authors: Hambrock, A Loffler-Walz, C Russ, U Lange, U Quast, U

Citation: A. Hambrock et al., Characterization of a mutant sulfonylurea receptor SUR2B with high affinity for sulfonylureas and openers: Differences in the coupling to Kir6.x subtypes, MOLEC PHARM, 60(1), 2001, pp. 190-199

Authors: Russ, U Lange, U Loffler-Walz, C Hambrock, A Quast, U

Citation: U. Russ et al., Interaction of the sulfonylthiourea HMR 1833 with sulfonylurea receptors and recombinant ATP-sensitive K+ channels: Comparison with glibenclamide, J PHARM EXP, 299(3), 2001, pp. 1049-1055

Authors: Manley, PW Loffler-Walz, C Russ, U Hambrock, A Moenius, T Quast, U

Citation: Pw. Manley et al., Synthesis and characterization of a novel tritiated K-ATP channel opener with a benzopyran structure, BR J PHARM, 133(2), 2001, pp. 275-285

Authors: Russ, U Hambrock, A Artunc, F Loffler-Walz, C Horio, Y Kurachi, Y Quast, U

Citation: U. Russ et al., Coexpression with the inward rectifier K+ channel Kir6.1 increases the affinity of the vascular sulfonylurea receptor SUR2B for glibenclamide, MOLEC PHARM, 56(5), 1999, pp. 955-961

Authors: Hambrock, A Loffler-Walz, C Kloor, D Delabar, U Horio, Y Kurachi, Y Quast, U

Citation: A. Hambrock et al., ATP-sensitive K+ channel modulator binding to sulfonylurea receptors SUR2Aand SUR2B: Opposite effects of MgADP, MOLEC PHARM, 55(5), 1999, pp. 832-840