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2. 1,3-Diphenylureido hydroxamate as a promising scaffold for generation of potent antimalarial histone deacetylase inhibitors

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

6. Structure-based design of bitopic ligands for the µ-opioid receptor

8. An allosteric inhibitor against the therapy-resistant mutant forms of EGFR in non-small cell lung cancer

9. SR9883 is a novel small-molecule enhancer of α4β2* nicotinic acetylcholine receptor signaling that decreases intravenous nicotine self-administration in rats.

10. Chemical systems biology reveals mechanisms of glucocorticoid receptor signaling

11. Synthesis and Evaluation of Oxyguanidine Analogues of the Cysteine Protease Inhibitor WRR-483 against Cruzain

16. Binding Mode and Potency of N‑Indolyloxopyridinyl-4-aminopropanyl-Based Inhibitors Targeting Trypanosoma cruzi CYP51

18. 4‑Aminopyridyl-Based CYP51 Inhibitors as Anti-Trypanosoma cruzi Drug Leads with Improved Pharmacokinetic Profile and in Vivo Potency

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

21. 1,3-diphenylureido hydroxamate: a promising scaffold for generation of potent antimalarial histone deacetylase inhibitors

23. Basolateral Amygdala Corticotrophin Releasing Factor Receptor 2 Interacts with Nonmuscle Myosin II to Destabilize Memory

24. Table S3 from Single and Dual Targeting of Mutant EGFR with an Allosteric Inhibitor

25. Figure S1 from Single and Dual Targeting of Mutant EGFR with an Allosteric Inhibitor

26. Data from Single and Dual Targeting of Mutant EGFR with an Allosteric Inhibitor

27. Supplemental Methods from Single and Dual Targeting of Mutant EGFR with an Allosteric Inhibitor

28. Data from A Novel HER2-Selective Kinase Inhibitor Is Effective in HER2 Mutant and Amplified Non–Small Cell Lung Cancer

29. Supplementary Data from A Novel HER2-Selective Kinase Inhibitor Is Effective in HER2 Mutant and Amplified Non–Small Cell Lung Cancer

30. Data from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

31. Supplementary Figure 6 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

32. Supplementary Figure 4 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

33. Supplementary Figure 8 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

34. Supplementary Methods, Figure Legend from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

35. Supplementary Figure 3 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

36. Supplementary Figure 2 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

37. Supplementary Figure 7 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

38. Supplementary Figure 5 from Blocking Lactate Export by Inhibiting the Myc Target MCT1 Disables Glycolysis and Glutathione Synthesis

42. Structure-based design of bitopic ligands for the µ-opioid receptor

43. Identification and Characterization of a Novel Indoleamine 2,3-Dioxygenase 1 Protein Degrader for Glioblastoma

44. Dual Inhibitors of Main Protease (MPro) and Cathepsin L as Potent Antivirals against SARS-CoV2

50. A Novel HER2-Selective Kinase Inhibitor Is Effective in HER2 Mutant and Amplified Non–Small Cell Lung Cancer

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