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