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

3. The molecular interaction pattern of lenvatinib enables inhibition of wild-type or kinase-mutated FGFR2-driven cholangiocarcinoma

8. First-in-class MKK4 inhibitors enhance liver regeneration and prevent liver failure

9. HDAC specificity and kinase off-targeting by purine-benzohydroxamate anti-hematological tumor agents

12. Hemin-induced platelet activation is regulated via ACKR3 chemokine surface receptor - implications for passivation of vulnerable atherosclerotic plaque

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

19. ACKR3 regulates platelet activation and ischemia-reperfusion tissue injury

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

26. Targeting Lewy body dementia with neflamapimod‐rasagiline hybrids

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

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

39. LXRα activation and Raf inhibition trigger lethal lipotoxicity in liver cancer

44. HDAC specificity and kinase off-targeting by purine-benzohydroxamate anti-hematological tumor agents

47. SARS-CoV-2 mutations in Brazil: from genomics to putative clinical conditions

48. Discovery of potent p38α MAPK inhibitors through a funnel like workflow combining in silico screening and in vitro validation

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