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Medical Physics|June 7, 2000
In-phantom response of LiF TLD-100 for dosimetry of 192Ir HDR sourceA S Pradhan, U QuastArzneimittel-Forschung|January 1, 1984
Binding of beta-adrenoceptor antagonists to rat and rabbit lung: special reference to levobunololU Quast, K O VollmerJournal of Medicinal Chemistry|June 12, 1992
Structure-activity studies of potassium channel opening in pinacidil-type cyanoguanidines, nitroethenediamines, thioureas, and ureasP W Manley, U QuastLife Sciences|January 1, 1988
Leiurus quinquestriatus venom inhibits BRL 34915-induced 86Rb+ efflux from the rat portal veinU Quast, N S CookNaunyn-Schmiedeberg'S Archives of Pharmacology|April 1, 1998
Disruption of the actin cytoskeleton abolishes high affinity 3H-glibenclamide binding in rat aortic ringsC Löffler-Walz, U QuastBritish Journal of Pharmacology|May 14, 1998
Binding of K(ATP) channel modulators in rat cardiac membranesC Löffler-Walz, U QuastThe Journal of Biological Chemistry|June 15, 1992
A specific binding site for K+ channel openers in rat aortaK M Bray, U QuastZeitschrift Fur Kardiologie|January 1, 1992
On the role of Ca++ binding proteins as possible targets for Ca++ sensitizing agentsJ W Herzig, U QuastThe Journal of Pharmacology and Experimental Therapeutics|July 1, 1989
In vitro and in vivo comparison of two K+ channel openers, diazoxide and cromakalim, and their inhibition by glibenclamideU Quast, N S CookStrahlentherapie|April 1, 1979
[Fully automatical control of patient positioning--a new technique leading to exact and safe radiation therapy (author's transl)]U Quast, K H SchickPageof 15