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1. Discovery of 1,3,4-oxadiazoles with slow-action activity against Plasmodium falciparum malaria parasites

2. Structural reassignment of a dibenz[b,f][1,4]oxazepin-11(10H)-one with potent antigiardial activity

7. The frequency of malaria is similar among women receiving either lopinavir/ritonavir or nevirapine-based antiretroviral treatment.

10. Discovery of 1,3,4-oxadiazoles with slow-action activity againstPlasmodium falciparummalaria parasites

14. Identification of Potent and Selective Inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PfM18AAP) of Human Malaria via High-Throughput Screening

17. Structural Basis for the Inhibition of the Essential Plasmodium falciparum M1 Neutral Aminopeptidase

19. QSAR Classification Models for Prediction of Hydroxamate Histone Deacetylase Inhibitor Activity against Malaria Parasites

25. The Key Glycolytic Enzyme Phosphofructokinase Is Involved in Resistance to Antiplasmodial Glycosides

32. Comparison of Plasmodium falciparum transfection methods

33. Catalyst-Controlled Stereoselective Synthesis Secures the Structure of the Antimalarial Isocyanoterpene Pustulosaisonitrile-1

34. Anti-GiardiaDrug Discovery: Current Status and Gut Feelings

35. A Plasmodium falciparum S33 proline aminopeptidase is associated with changes in erythrocyte deformability

37. Synthesis and antimalarial evaluation of amide and urea derivatives based on the thiaplakortone A natural product scaffold

39. Lysine Acetylation in Sexual Stage Malaria Parasites Is a Target for Antimalarial Small Molecules

42. Total Synthesis of Thiaplakortone A: Derivatives as Metabolically Stable Leads for the Treatment of Malaria

43. Saquinavir Inhibits the malaria parasite's chloroquine resistance transporter

44. Reply to Savarino et al

46. HIV-malaria interactions: Don't forget the drugs [3]

48. The Aminopeptidase Inhibitor CHR-2863 Is an Orally Bioavailable Inhibitor of Murine Malaria

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