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1. GRA47 is important for the morphology and permeability of the parasitophorous vacuole in Toxoplasma gondii.

2. LC3B labeling of the parasitophorous vacuole membrane of Plasmodium berghei liver stage parasites depends on the V-ATPase and ATG16L1.

3. Contact sites between host organelles and pathogens: boon or bane?

4. VAMP3 and VAMP8 Regulate the Development and Functionality of Parasitophorous Vacuoles Housing Leishmania amazonensis.

5. Proximity-Labeling Reveals Novel Host and Parasite Proteins at the Toxoplasma Parasitophorous Vacuole Membrane.

6. Lessons from Toxoplasma: Host responses that mediate parasite control and the microbial effectors that subvert them.

7. Biotinylation of the Neospora caninum parasitophorous vacuole reveals novel dense granule proteins.

8. Rhoptry kinase protein 39 (ROP39) is a novel factor that recruits host mitochondria to the parasitophorous vacuole of Toxoplasma gondii.

9. A Family of Toxoplasma gondii Genes Related to GRA12 Regulate Cyst Burdens and Cyst Reactivation.

10. Insulinase-like Protease 1 Contributes to Macrogamont Formation in Cryptosporidium parvum.

11. Plasmodium berghei sporozoites in nonreplicative vacuole are eliminated by a PI3P-mediated autophagy-independent pathway.

12. Complement receptor 3 mediates ruffle-like, actin-rich aggregates during phagocytosis of Leishmania infantum metacyclics.

13. Characterization of the erythrocyte GTPase Rac1 in relation to Plasmodium falciparum invasion.

14. During host cell traversal and cell-to-cell passage, Toxoplasma gondii sporozoites inhabit the parasitophorous vacuole and posteriorly release dense granule protein-associated membranous trails.

15. Isolation of intact Leishmania amazonensis large parasitophorous vacuoles from infected macrophages by density gradient fractionation.

16. Phosphorylation of Toxoplasma gondii Secreted Proteins during Acute and Chronic Stages of Infection.

17. Toxoplasma Mechanisms for Delivery of Proteins and Uptake of Nutrients Across the Host-Pathogen Interface.

18. Key role of the macrophage microtubule network in the intracellular lifestyle of Leishmania amazonensis.

19. Naïve CD8 T cell IFNγ responses to a vacuolar antigen are regulated by an inflammasome-independent NLRP3 pathway and Toxoplasma gondii ROP5.

20. Contacting domains segregate a lipid transporter from a solute transporter in the malarial host-parasite interface.

21. The parasitophorous vacuole of the blood-stage malaria parasite.

22. EXP1 is required for organisation of EXP2 in the intraerythrocytic malaria parasite vacuole.

23. Skeleton binding protein 1 (SBP1) of Plasmodium falciparum accumulates in electron-dense material before passing through the parasitophorous vacuole membrane.

24. Coimmunoprecipitation with MYR1 Identifies Three Additional Proteins within the Toxoplasma gondii Parasitophorous Vacuole Required for Translocation of Dense Granule Effectors into Host Cells.

25. Hardly Vacuous: The Parasitophorous Vacuolar Membrane of Malaria Parasites.

26. A malaria parasite subtilisin propeptide-like protein is a potent inhibitor of the egress protease SUB1.

27. Vibrio cholerae residing in food vacuoles expelled by protozoa are more infectious in vivo.

28. A crucial role for the C-terminal domain of exported protein 1 during the mosquito and hepatic stages of the Plasmodium berghei life cycle.

29. The GRA17 Parasitophorous Vacuole Membrane Permeability Pore Contributes to Bradyzoite Viability.

30. Translocation of Dense Granule Effectors across the Parasitophorous Vacuole Membrane in Toxoplasma- Infected Cells Requires the Activity of ROP17, a Rhoptry Protein Kinase.

31. The host cell secretory pathway mediates the export of Leishmania virulence factors out of the parasitophorous vacuole.

32. Delayed death in the malaria parasite Plasmodium falciparum is caused by disruption of prenylation-dependent intracellular trafficking.

33. ATP6V0d2 controls Leishmania parasitophorous vacuole biogenesis via cholesterol homeostasis.

34. Simultaneous Ribosome Profiling of Human Host Cells Infected with Toxoplasma gondii.

35. The dense granule protein 8 (GRA8) is a component of the sub-pellicular cytoskeleton in Toxoplasma gondii.

36. PfVPS45 Is Required for Host Cell Cytosol Uptake by Malaria Blood Stage Parasites.

37. The ESCRT and autophagy machineries cooperate to repair ESX-1-dependent damage at the Mycobacterium-containing vacuole but have opposite impact on containing the infection.

38. Aspartyl Protease 5 Matures Dense Granule Proteins That Reside at the Host-Parasite Interface in Toxoplasma gondii.

39. Toxoplasma Does Not Secrete the GRA16 and GRA24 Effectors Beyond the Parasitophorous Vacuole Membrane of Tissue Cysts.

40. Rounding precedes rupture and breakdown of vacuolar membranes minutes before malaria parasite egress from erythrocytes.

41. An in silico down-scaling approach uncovers novel constituents of the Plasmodium-containing vacuole.

42. The Toxoplasma gondii Active Serine Hydrolase 4 Regulates Parasite Division and Intravacuolar Parasite Architecture.

43. Development of an automated image analysis protocol for quantification of intracellular forms of Leishmania spp.

44. Spatial organization of protein export in malaria parasite blood stages.

45. Toxoplasma Parasite Twisting Motion Mechanically Induces Host Cell Membrane Fission to Complete Invasion within a Protective Vacuole.

46. Toxoplasma gondii reorganizes the host cell architecture during spontaneous cyst formation in vitro.

47. Re-evaluation of the life cycle of Eimeria maxima Tyzzer, 1929 in chickens (Gallus domesticus).

48. Intestinal isosporiasis in patients with acquired immunodeficiency syndrome (AIDS). Pathologic diagnosis in small intestinal mucosal biopsies.

49. Further aspects of Toxoplasma gondii elimination in the presence of metals.

50. Sequence and functional divergence of gametocyte-specific parasitophorous vacuole membrane proteins in Plasmodium parasites.

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