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1. Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitors

9. Development of Highly Potent and Selective Covalent FGFR4 Inhibitors Based on SNAr Electrophiles

10. Correction to “Cathepsin-Targeting SARS-CoV-2 Inhibitors: Design, Synthesis, and Biological Activity”

19. Cathepsin-Targeting SARS-CoV-2 Inhibitors: Design, Synthesis, and Biological Activity

20. Development of Highly Potent and Selective FGFR4 Inhibitors Based on SNAr Electrophiles

23. Second Opinions and Diagnostic Uncertainty in Expert Markets.

24. The origin of potency and mutant-selective inhibition by bivalent ATP-allosteric EGFR inhibitors

25. Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitors

26. Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitors

30. Examining molecular factors of inactive versus active bivalent EGFR inhibitors: A missing link in fragment-based drug design.

33. Horizontal mergers, cost savings, and network effects

34. Engineered Myeloid Precursors Differentiate into Osteoclasts and Resorb Heterotopic Ossification in Mice

41. Drivers overtaking cyclists on rural roads: How does visibility affect safety?: Results from a naturalistic study

46. Collusion by Algorithm: The Role of Unobserved Actions

47. Combinable products, price discrimination, and collusion

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