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Communications Psychology|September 6, 2024
Contextual cueing of visual search reflects the acquisition of an optimal, one-for-all oculomotor scanning strategyWerner Seitz, Artyom Zinchenko, Hermann J Müller, et al.
Frontiers in Psychology|March 18, 2021
Why Are Acquired Search-Guiding Context Memories Resistant to Updating?Thomas Geyer, Werner Seitz, Artyom Zinchenko, et al.
Psychonomic Bulletin & Review|July 11, 2023
Mission impossible? Spatial context relearning following a target relocation event depends on cue predictivenessThomas Geyer, Artyom Zinchenko, Werner Seitz, et al.
Bioorganic & Medicinal Chemistry Letters|June 5, 2003
D-Phe-Pro-Arg type thrombin inhibitors: unexpected selectivity by modification of the P1 moietyUdo E W Lange, Dorit Baucke, Wilfried Hornberger, et al.
Bioorganic & Medicinal Chemistry Letters|March 7, 2006
Orally active thrombin inhibitors. Part 1: optimization of the P1-moietyHelmut Mack, Dorit Baucke, Wilfried Hornberger, et al.
Bioorganic & Medicinal Chemistry Letters|February 8, 2006
Orally active thrombin inhibitors. Part 2: optimization of the P2-moietyUdo E W Lange, Dorit Baucke, Wilfried Hornberger, et al.
Bioorganic & Medicinal Chemistry Letters|December 11, 2007
Design and synthesis of novel potent and selective integrin alphanubeta3 antagonists--novel synthetic routes to isoquinolinone, benzoxazinone, and quinazolinone acetatesWerner Seitz, Hervé Geneste, Gisela Backfisch, et al.
Bioorganic & Medicinal Chemistry|March 12, 2003
Design and synthesis of 1,5- and 2,5-substituted tetrahydrobenzazepinones as novel potent and selective integrin alphaVbeta3 antagonistsAndreas Kling, Gisela Backfisch, Jürgen Delzer, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2002
Highly potent and selective alphaVbeta3-receptor antagonists: solid-phase synthesis and SAR of 1-substituted 4-amino-1H-pyrimidin-2-onesChristian Zechel, Gisela Backfisch, Jürgen Delzer, et al.
Bioorganic & Medicinal Chemistry Letters|January 30, 2002
Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective alpha(V)beta(3) antagonistsAndreas Kling, Gisela Backfisch, Jürgen Delzer, et al.
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