Category:Protozoan proteins

Media in category "Protozoan proteins"

The following 188 files are in this category, out of 188 total.

A-Cyclic-GMP-Signalling-Module-That-Regulates-Gliding-Motility-in-a-Malaria-Parasite-ppat.1000599.s006.ogv 10 s, 430 × 240; 367 KB
A-Cyclic-GMP-Signalling-Module-That-Regulates-Gliding-Motility-in-a-Malaria-Parasite-ppat.1000599.s007.ogv 10 s, 430 × 240; 137 KB
A-Cyclic-GMP-Signalling-Module-That-Regulates-Gliding-Motility-in-a-Malaria-Parasite-ppat.1000599.s008.ogv 10 s, 376 × 244; 131 KB
A-Cyclic-GMP-Signalling-Module-That-Regulates-Gliding-Motility-in-a-Malaria-Parasite-ppat.1000599.s009.ogv 10 s, 260 × 152; 89 KB
A-Cyclic-GMP-Signalling-Module-That-Regulates-Gliding-Motility-in-a-Malaria-Parasite-ppat.1000599.s010.ogv 10 s, 196 × 144; 71 KB
A-MAP6-Related-Protein-Is-Present-in-Protozoa-and-Is-Involved-in-Flagellum-Motility-pone.0031344.s007.ogv 37 s, 640 × 480; 1.12 MB
A-MAP6-Related-Protein-Is-Present-in-Protozoa-and-Is-Involved-in-Flagellum-Motility-pone.0031344.s008.ogv 34 s, 320 × 240; 636 KB
A-Novel-Family-of-Toxoplasma-IMC-Proteins-Displays-a-Hierarchical-Organization-and-Functions-in-ppat.1001094.s007.ogv 49 s, 320 × 240; 653 KB
A-Novel-Family-of-Toxoplasma-IMC-Proteins-Displays-a-Hierarchical-Organization-and-Functions-in-ppat.1001094.s008.ogv 43 s, 320 × 240; 456 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s005.ogv 36 s, 900 × 900; 127 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s006.ogv 36 s, 900 × 900; 231 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s007.ogv 21 s, 1,024 × 1,024; 343 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s008.ogv 12 s, 648 × 648; 321 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s009.ogv 36 s, 900 × 900; 245 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s010.ogv 36 s, 900 × 900; 201 KB
A-Proteomic-and-Cellular-Analysis-of-Uropods-in-the-Pathogen-Entamoeba-histolytica-pntd.0001002.s002.ogv 7.3 s, 533 × 232; 490 KB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s10.ogv 15 s, 893 × 271; 673 KB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s11.ogv 7.6 s, 843 × 420; 491 KB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s12.ogv 4.8 s, 678 × 338; 513 KB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s13.ogv 7.6 s, 800 × 316; 1.43 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s14.ogv 7.2 s, 800 × 281; 1.11 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s15.ogv 1.8 s, 725 × 381; 1.38 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s16.ogv 10 s, 968 × 685; 1.11 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s2.ogv 8.3 s, 800 × 286; 1.2 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s3.ogv 9.1 s, 591 × 556; 6.19 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s4.ogv 7.2 s, 1,023 × 356; 5.61 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s5.ogv 18 s, 584 × 290; 5.11 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s6.ogv 15 s, 898 × 296; 18.27 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s7.ogv 6.1 s, 505 × 252; 5.32 MB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s8.ogv 7.6 s, 843 × 420; 401 KB
A-resilient-formin-derived-cortical-actin-meshwork-in-the-rear-drives-actomyosin-based-motility-in-ncomms9496-s9.ogv 10 s, 985 × 490; 1.07 MB
A-Toxoplasma-MORN1-Null-Mutant-Undergoes-Repeated-Divisions-but-Is-Defective-in-Basal-Assembly-pone.0012302.s007.ogv 31 s, 518 × 514; 228 KB
Ca2+-regulation-in-the-absence-of-the-iplA-gene-product-in-Dictyostelium-discoideum-1471-2121-6-13-S1.ogv 41 s, 805 × 308; 977 KB
Ca2+-regulation-in-the-absence-of-the-iplA-gene-product-in-Dictyostelium-discoideum-1471-2121-6-13-S2.ogv 41 s, 804 × 308; 953 KB
Ca2+-regulation-in-the-absence-of-the-iplA-gene-product-in-Dictyostelium-discoideum-1471-2121-6-13-S3.ogv 41 s, 804 × 308; 996 KB
Characterization-of-a-Subunit-of-the-Outer-Dynein-Arm-Docking-Complex-Necessary-for-Correct-pntd.0000586.s001.ogv 35 s, 640 × 480; 1.21 MB
Characterization-of-a-Subunit-of-the-Outer-Dynein-Arm-Docking-Complex-Necessary-for-Correct-pntd.0000586.s002.ogv 35 s, 640 × 480; 1.1 MB
Characterization-of-a-Subunit-of-the-Outer-Dynein-Arm-Docking-Complex-Necessary-for-Correct-pntd.0000586.s003.ogv 35 s, 640 × 480; 1.5 MB
Chemical-Rescue-of-Malaria-Parasites-Lacking-an-Apicoplast-Defines-Organelle-Function-in-Blood-pbio.1001138.s008.ogv 8.0 s, 724 × 640; 639 KB
Chemical-Rescue-of-Malaria-Parasites-Lacking-an-Apicoplast-Defines-Organelle-Function-in-Blood-pbio.1001138.s009.ogv 12 s, 672 × 496; 459 KB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s013.ogv 20 s, 512 × 512; 112 KB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s014.ogv 28 s, 512 × 512; 571 KB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s015.ogv 28 s, 512 × 512; 1.39 MB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s016.ogv 10 s, 512 × 512; 1.03 MB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s017.ogv 21 s, 512 × 512; 485 KB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s018.ogv 7.1 s, 512 × 512; 281 KB
Comprehensive-Analysis-Reveals-Dynamic-and-Evolutionary-Plasticity-of-Rab-GTPases-and-Membrane-pgen.1001155.s019.ogv 10 s, 512 × 512; 258 KB
Copine-A-plays-a-role-in-the-differentiation-of-stalk-cells-and-the-initiation-of-culmination-in-1471-213X-10-59-S1.ogv 52 s, 640 × 480; 3.49 MB
Copine-A-plays-a-role-in-the-differentiation-of-stalk-cells-and-the-initiation-of-culmination-in-1471-213X-10-59-S2.ogv 1 min 6 s, 640 × 480; 2.96 MB
Coupling-of-lysosomal-and-mitochondrial-membrane-permeabilization-in-trypanolysis-by-APOL1-ncomms9078-s2.ogv 22 s, 960 × 540; 16.38 MB
Coupling-of-lysosomal-and-mitochondrial-membrane-permeabilization-in-trypanolysis-by-APOL1-ncomms9078-s3.ogv 20 s, 960 × 540; 14.2 MB
Coupling-of-lysosomal-and-mitochondrial-membrane-permeabilization-in-trypanolysis-by-APOL1-ncomms9078-s4.ogv 19 s, 960 × 540; 10.69 MB
Cytoskeletal-Components-of-an-Invasion-Machine—The-Apical-Complex-of-Toxoplasma-gondii-ppat.0020013.sv001.ogv 24 s, 400 × 300; 520 KB
Cytoskeletal-Components-of-an-Invasion-Machine—The-Apical-Complex-of-Toxoplasma-gondii-ppat.0020013.sv002.ogv 17 s, 485 × 388; 2.51 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s005.ogv 8.2 s, 640 × 480; 13.81 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s006.ogv 7.1 s, 640 × 480; 11.61 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s007.ogv 8.9 s, 480 × 384; 16.28 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s008.ogv 9.0 s, 480 × 384; 20.37 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s009.ogv 13 s, 480 × 384; 18.45 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s010.ogv 12 s, 480 × 384; 19.94 MB
Determinants-of-GBP-Recruitment-to-Toxoplasma-gondii-Vacuoles-and-the-Parasitic-Factors-That-pone.0024434.s009.ogv 10 s, 720 × 480; 67 KB
Determinants-of-GBP-Recruitment-to-Toxoplasma-gondii-Vacuoles-and-the-Parasitic-Factors-That-pone.0024434.s010.ogv 18 s, 720 × 480; 53 KB
Determinants-of-GBP-Recruitment-to-Toxoplasma-gondii-Vacuoles-and-the-Parasitic-Factors-That-pone.0024434.s011.ogv 17 s, 720 × 480; 257 KB
Distinct-External-Signals-Trigger-Sequential-Release-of-Apical-Organelles-during-Erythrocyte-ppat.1000746.s014.ogv 12 s, 99 × 99; 670 KB
Distinct-External-Signals-Trigger-Sequential-Release-of-Apical-Organelles-during-Erythrocyte-ppat.1000746.s015.ogv 12 s, 99 × 99; 93 KB
Distinct-External-Signals-Trigger-Sequential-Release-of-Apical-Organelles-during-Erythrocyte-ppat.1000746.s016.ogv 12 s, 99 × 99; 1.14 MB
Entamoeba-histolytica-Cysteine-Proteinase-5-Evokes-Mucin-Exocytosis-from-Colonic-Goblet-Cells-via-ppat.1005579.s004.ogv 4.9 s, 1,104 × 1,104; 6.74 MB
Entamoeba-histolytica-Cysteine-Proteinase-5-Evokes-Mucin-Exocytosis-from-Colonic-Goblet-Cells-via-ppat.1005579.s005.ogv 4.5 s, 1,236 × 1,236; 4.43 MB
Entamoeba-histolytica-Cysteine-Proteinase-5-Evokes-Mucin-Exocytosis-from-Colonic-Goblet-Cells-via-ppat.1005579.s006.ogv 6.9 s, 1,024 × 1,024; 4.3 MB
Entamoeba-histolytica-Cysteine-Proteinase-5-Evokes-Mucin-Exocytosis-from-Colonic-Goblet-Cells-via-ppat.1005579.s007.ogv 5.5 s, 1,024 × 1,024; 2.5 MB
Evolutionarily-Divergent-Unstable-Filamentous-Actin-Is-Essential-for-Gliding-Motility-in-ppat.1002280.s008.ogv 6.1 s, 74 × 62; 39 KB
Evolutionarily-Divergent-Unstable-Filamentous-Actin-Is-Essential-for-Gliding-Motility-in-ppat.1002280.s009.ogv 6.1 s, 72 × 65; 21 KB
Evolutionarily-Divergent-Unstable-Filamentous-Actin-Is-Essential-for-Gliding-Motility-in-ppat.1002280.s010.ogv 6.1 s, 74 × 63; 17 KB
Evolutionarily-Divergent-Unstable-Filamentous-Actin-Is-Essential-for-Gliding-Motility-in-ppat.1002280.s011.ogv 6.1 s, 72 × 64; 20 KB
Evolutionarily-Divergent-Unstable-Filamentous-Actin-Is-Essential-for-Gliding-Motility-in-ppat.1002280.s012.ogv 6.1 s, 72 × 63; 30 KB
Evolutionarily-Divergent-Unstable-Filamentous-Actin-Is-Essential-for-Gliding-Motility-in-ppat.1002280.s013.ogv 6.1 s, 72 × 65; 18 KB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s002.ogv 1 min 36 s, 400 × 400; 1.49 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s003.ogv 31 s, 640 × 320; 2.11 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s004.ogv 35 s, 460 × 460; 1.12 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s005.ogv 4 min 42 s, 200 × 200; 2.06 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s006.ogv 25 s, 700 × 350; 6.79 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s007.ogv 44 s, 700 × 700; 7.36 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s008.ogv 50 s, 700 × 700; 6.63 MB
Exploitation-of-Other-Social-Amoebae-by-Dictyostelium-caveatum-pone.0000212.s009.ogv 45 s, 700 × 700; 9.36 MB
Expression-of-P.-falciparum-var-Genes-Involves-Exchange-of-the-Histone-Variant-H2A.Z-at-the-Promoter-ppat.1001292.s011.ogv 6.2 s, 320 × 240; 23 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s008.ogv 15 s, 720 × 576; 452 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s009.ogv 38 s, 720 × 576; 2 MB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s010.ogv 6.3 s, 720 × 576; 201 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s011.ogv 1 min 14 s, 720 × 576; 3.91 MB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s012.ogv 26 s, 720 × 576; 1.48 MB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s013.ogv 12 s, 720 × 576; 391 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s014.ogv 38 s, 720 × 576; 2.17 MB
Giardia-Flagellar-Motility-Is-Not-Directly-Required-to-Maintain-Attachment-to-Surfaces-ppat.1002167.s002.ogv 36 s, 352 × 288; 572 KB
Giardia-Flagellar-Motility-Is-Not-Directly-Required-to-Maintain-Attachment-to-Surfaces-ppat.1002167.s003.ogv 35 s, 352 × 288; 524 KB
Giardia-Flagellar-Motility-Is-Not-Directly-Required-to-Maintain-Attachment-to-Surfaces-ppat.1002167.s004.ogv 35 s, 352 × 288; 451 KB
Giardia-Flagellar-Motility-Is-Not-Directly-Required-to-Maintain-Attachment-to-Surfaces-ppat.1002167.s005.ogv 42 s, 352 × 288; 493 KB
Giardia-Flagellar-Motility-Is-Not-Directly-Required-to-Maintain-Attachment-to-Surfaces-ppat.1002167.s006.ogv 1 min 1 s, 352 × 288; 1.99 MB
Identification-of-Contractile-Vacuole-Proteins-in-Trypanosoma-cruzi-pone.0018013.s011.ogv 10 s, 518 × 548; 24 KB
Identification-of-Contractile-Vacuole-Proteins-in-Trypanosoma-cruzi-pone.0018013.s012.ogv 10 s, 297 × 299; 14 KB
IFT-Proteins-Accumulate-during-Cell-Division-and-Localize-to-the-Cleavage-Furrow-in-Chlamydomonas-pone.0030729.s005.ogv 7.8 s, 400 × 400; 41 KB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv001.ogv 1 min 48 s, 432 × 360; 1.96 MB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv002.ogv 3 min 17 s, 432 × 360; 1.88 MB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv003.ogv 2 min 39 s, 432 × 360; 1.44 MB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv004.ogv 6 min 26 s, 432 × 360; 3.62 MB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv005.ogv 8 min 42 s, 288 × 240; 3.93 MB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv006.ogv 4 min 17 s, 288 × 240; 3.36 MB
Key-Role-of-Local-Regulation-in-Chemosensing-Revealed-by-a-New-Molecular-Interaction-Based-Modeling-pcbi.0020082.sv007.ogv 5 min 19 s, 432 × 360; 4.2 MB
Large-Scale-Conformational-Changes-of-Trypanosoma-cruzi-Proline-Racemase-Predicted-by-Accelerated-pcbi.1002178.s004.ogv 21 s, 948 × 566; 961 KB
Live-Imaging-of-Mitosomes-and-Hydrogenosomes-by-HaloTag-Technology-pone.0036314.s001.ogv 30 s, 1,000 × 760; 192 KB
Live-Imaging-of-Mitosomes-and-Hydrogenosomes-by-HaloTag-Technology-pone.0036314.s002.ogv 30 s, 800 × 608; 6.75 MB
Live-Imaging-of-Mitosomes-and-Hydrogenosomes-by-HaloTag-Technology-pone.0036314.s003.ogv 30 s, 800 × 608; 54 KB
Live-Imaging-of-Mitosomes-and-Hydrogenosomes-by-HaloTag-Technology-pone.0036314.s004.ogv 30 s, 800 × 610; 378 KB
Loss-of-Dictyostelium-HSPC300-causes-a-scar-like-phenotype-and-loss-of-SCAR-protein-1471-2121-10-13-S3.ogv 4.0 s, 544 × 414; 362 KB
Loss-of-Dictyostelium-HSPC300-causes-a-scar-like-phenotype-and-loss-of-SCAR-protein-1471-2121-10-13-S4.ogv 4.0 s, 544 × 414; 109 KB
Loss-of-Dictyostelium-HSPC300-causes-a-scar-like-phenotype-and-loss-of-SCAR-protein-1471-2121-10-13-S5.ogv 4.0 s, 544 × 414; 259 KB
Loss-of-Dictyostelium-HSPC300-causes-a-scar-like-phenotype-and-loss-of-SCAR-protein-1471-2121-10-13-S7.ogv 6.0 s, 472 × 360; 296 KB
Loss-of-Dictyostelium-HSPC300-causes-a-scar-like-phenotype-and-loss-of-SCAR-protein-1471-2121-10-13-S8.ogv 6.0 s, 472 × 360; 81 KB
Loss-of-the-Histidine-Kinase-DhkD-Results-in-Mobile-Mounds-during-Development-of-Dictyostelium-pone.0075618.s001.ogv 17 s, 685 × 511; 685 KB
Loss-of-the-Histidine-Kinase-DhkD-Results-in-Mobile-Mounds-during-Development-of-Dictyostelium-pone.0075618.s002.ogv 17 s, 685 × 510; 547 KB
Novel-Structural-Components-of-the-Ventral-Disc-and-Lateral-Crest-in-Giardia-intestinalis-pntd.0001442.s006.ogv 3.5 s, 113 × 146; 15 KB
Novel-Structural-Components-of-the-Ventral-Disc-and-Lateral-Crest-in-Giardia-intestinalis-pntd.0001442.s007.ogv 6.0 s, 216 × 133; 14 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s006.ogv 9.0 s, 2,048 × 2,048; 92 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s007.ogv 9.0 s, 2,048 × 2,048; 163 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s008.ogv 11 s, 2,048 × 2,048; 104 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s009.ogv 11 s, 1,003 × 808; 67 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s010.ogv 5.1 s, 126 × 165; 694 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s011.ogv 15 s, 1,024 × 1,024; 37 KB
Organizational-Changes-of-the-Daughter-Basal-Complex-during-the-Parasite-Replication-of-Toxoplasma-ppat.0040010.sv001.ogv 9.0 s, 544 × 206; 132 KB
Organizational-Changes-of-the-Daughter-Basal-Complex-during-the-Parasite-Replication-of-Toxoplasma-ppat.0040010.sv002.ogv 9.5 s, 469 × 220; 100 KB
Organizational-Changes-of-the-Daughter-Basal-Complex-during-the-Parasite-Replication-of-Toxoplasma-ppat.0040010.sv003.ogv 3.7 s, 294 × 199; 47 KB
Phosphoproteomics-reveals-malaria-parasite-Protein-Kinase-G-as-a-signalling-hub-regulating-egress-ncomms8285-s10.ogv 0.3 s, 112 × 112; 23 KB
Phosphoproteomics-reveals-malaria-parasite-Protein-Kinase-G-as-a-signalling-hub-regulating-egress-ncomms8285-s11.ogv 0.4 s, 96 × 100; 6 KB
Phosphoproteomics-reveals-malaria-parasite-Protein-Kinase-G-as-a-signalling-hub-regulating-egress-ncomms8285-s6.ogv 0.6 s, 104 × 100; 18 KB
Phosphoproteomics-reveals-malaria-parasite-Protein-Kinase-G-as-a-signalling-hub-regulating-egress-ncomms8285-s7.ogv 0.1 s, 96 × 96; 5 KB
Phosphoproteomics-reveals-malaria-parasite-Protein-Kinase-G-as-a-signalling-hub-regulating-egress-ncomms8285-s8.ogv 0.5 s, 108 × 112; 26 KB
Phosphoproteomics-reveals-malaria-parasite-Protein-Kinase-G-as-a-signalling-hub-regulating-egress-ncomms8285-s9.ogv 0.3 s, 52 × 48; 6 KB
Plasmodium-falciparum-Heterochromatin-Protein-1-Marks-Genomic-Loci-Linked-to-Phenotypic-Variation-ppat.1000569.s014.ogv 3.0 s, 1,205 × 860; 242 KB
Protein-Kinase-A-Dependent-Phosphorylation-of-Apical-Membrane-Antigen-1-Plays-an-Important-Role-in-ppat.1000941.s005.ogv 5.9 s, 304 × 304; 1.35 MB
Pyrazoleamide-compounds-are-potent-antimalarials-that-target-Na+-homeostasis-in-intraerythrocytic-ncomms6521-s2.ogv 34 s, 392 × 352; 741 KB
Pyrazoleamide-compounds-are-potent-antimalarials-that-target-Na+-homeostasis-in-intraerythrocytic-ncomms6521-s3.ogv 23 s, 452 × 452; 1.3 MB
Rhomboid-4-(ROM4)-Affects-the-Processing-of-Surface-Adhesins-and-Facilitates-Host-Cell-Invasion-by-ppat.1000858.s002.ogv 11 s, 320 × 264; 184 KB
Rhomboid-4-(ROM4)-Affects-the-Processing-of-Surface-Adhesins-and-Facilitates-Host-Cell-Invasion-by-ppat.1000858.s003.ogv 11 s, 320 × 283; 162 KB
Rhomboid-4-(ROM4)-Affects-the-Processing-of-Surface-Adhesins-and-Facilitates-Host-Cell-Invasion-by-ppat.1000858.s004.ogv 11 s, 320 × 296; 116 KB
Rhomboid-4-(ROM4)-Affects-the-Processing-of-Surface-Adhesins-and-Facilitates-Host-Cell-Invasion-by-ppat.1000858.s005.ogv 11 s, 320 × 214; 146 KB
Spatial-Localisation-of-Actin-Filaments-across-Developmental-Stages-of-the-Malaria-Parasite-pone.0032188.s005.ogv 13 s, 628 × 428; 210 KB
Spatial-Localisation-of-Actin-Filaments-across-Developmental-Stages-of-the-Malaria-Parasite-pone.0032188.s006.ogv 13 s, 628 × 430; 137 KB
Spatial-Localisation-of-Actin-Filaments-across-Developmental-Stages-of-the-Malaria-Parasite-pone.0032188.s007.ogv 6.7 s, 1,524 × 879; 759 KB
Spatial-Localisation-of-Actin-Filaments-across-Developmental-Stages-of-the-Malaria-Parasite-pone.0032188.s008.ogv 6.7 s, 1,524 × 879; 853 KB
Spatial-Localisation-of-Actin-Filaments-across-Developmental-Stages-of-the-Malaria-Parasite-pone.0032188.s009.ogv 13 s, 618 × 714; 986 KB
Spatial-Localisation-of-Actin-Filaments-across-Developmental-Stages-of-the-Malaria-Parasite-pone.0032188.s010.ogv 6.7 s, 582 × 446; 648 KB
Stable-transformation-of-an-episomal-protein-tagging-shuttle-vector-in-the-piscine-diplomonad-1471-2180-8-71-S1.ogv 2.6 s, 734 × 600; 427 KB
Stable-transformation-of-an-episomal-protein-tagging-shuttle-vector-in-the-piscine-diplomonad-1471-2180-8-71-S2.ogv 1.7 s, 734 × 600; 51 KB
Surface-Co-Expression-of-Two-Different-PfEMP1-Antigens-on-Single-Plasmodium-falciparum-Infected-ppat.1001083.s009.ogv 24 s, 720 × 576; 1.16 MB
T.-gondii-RP-Promoters-&-Knockdown-Reveal-Molecular-Pathways-Associated-with-Proliferation-and-Cell-pone.0014057.s007.ogv 15 s, 1,024 × 848; 9.52 MB
Temporal-regulation-of-kin-recognition-maintains-recognition-cue-diversity-and-suppresses-cheating-ncomms8144-s2.ogv 18 s, 1,440 × 1,080; 5.91 MB
The-Armadillo-Repeat-Protein-PF16-Is-Essential-for-Flagellar-Structure-and-Function-in-Plasmodium-pone.0012901.s004.ogv 11 s, 938 × 598; 104 KB
The-Armadillo-Repeat-Protein-PF16-Is-Essential-for-Flagellar-Structure-and-Function-in-Plasmodium-pone.0012901.s005.ogv 8.4 s, 1,182 × 772; 121 KB
The-Aurora-Kinase-in-Trypanosoma-brucei-Plays-Distinctive-Roles-in-Metaphase-Anaphase-Transition-ppat.1000575.s009.ogv 53 s, 700 × 214; 828 KB
The-Aurora-Kinase-in-Trypanosoma-brucei-Plays-Distinctive-Roles-in-Metaphase-Anaphase-Transition-ppat.1000575.s010.ogv 36 s, 868 × 160; 1.5 MB
The-Aurora-Kinase-in-Trypanosoma-brucei-Plays-Distinctive-Roles-in-Metaphase-Anaphase-Transition-ppat.1000575.s011.ogv 36 s, 868 × 152; 1.21 MB
The-Malaria-Secretome-From-Algorithms-to-Essential-Function-in-Blood-Stage-Infection-ppat.1000084.s011.ogv 5.0 s, 512 × 512; 27 KB
The-Plasmodium-berghei-translocon-of-exported-proteins-reveals-spatiotemporal-dynamics-of-tubular-srep12532-s2.ogv 20 s, 640 × 480; 391 KB
The-Plasmodium-berghei-translocon-of-exported-proteins-reveals-spatiotemporal-dynamics-of-tubular-srep12532-s3.ogv 15 s, 640 × 480; 1.33 MB
The-Plasmodium-berghei-translocon-of-exported-proteins-reveals-spatiotemporal-dynamics-of-tubular-srep12532-s4.ogv 14 s, 640 × 480; 1.05 MB
The-Plasmodium-berghei-translocon-of-exported-proteins-reveals-spatiotemporal-dynamics-of-tubular-srep12532-s5.ogv 31 s, 640 × 480; 1.31 MB
The-Plasmodium-berghei-translocon-of-exported-proteins-reveals-spatiotemporal-dynamics-of-tubular-srep12532-s6.ogv 23 s, 640 × 480; 1.24 MB
The-Plasmodium-berghei-translocon-of-exported-proteins-reveals-spatiotemporal-dynamics-of-tubular-srep12532-s7.ogv 11 s, 640 × 480; 214 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s004.ogv 20 s, 96 × 106; 94 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s005.ogv 1 min 22 s, 80 × 80; 229 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s006.ogv 14 s, 100 × 100; 146 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s007.ogv 10 s, 100 × 100; 59 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s008.ogv 2 min 3 s, 100 × 103; 856 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s009.ogv 12 s, 59 × 45; 66 KB
The-Toxoplasma-Acto-MyoA-Motor-Complex-Is-Important-but-Not-Essential-for-Gliding-Motility-and-Host-pone.0091819.s010.ogv 39 s, 102 × 98; 403 KB
Three-Dimensional-Structure-of-the-Trypanosome-Flagellum-Suggests-that-the-Paraflagellar-Rod-pone.0025700.s007.ogv 6.7 s, 300 × 300; 2.34 MB
Three-Dimensional-Structure-of-the-Trypanosome-Flagellum-Suggests-that-the-Paraflagellar-Rod-pone.0025700.s008.ogv 23 s, 150 × 269; 6.06 MB
Three-Dimensional-Structure-of-the-Trypanosome-Flagellum-Suggests-that-the-Paraflagellar-Rod-pone.0025700.s009.ogv 13 s, 190 × 191; 2.99 MB
Three-Dimensional-Structure-of-the-Trypanosome-Flagellum-Suggests-that-the-Paraflagellar-Rod-pone.0025700.s010.ogv 17 s, 300 × 300; 2.06 MB
Three-Dimensional-Structure-of-the-Trypanosome-Flagellum-Suggests-that-the-Paraflagellar-Rod-pone.0025700.s011.ogv 39 s, 400 × 349; 4.91 MB
Three-Dimensional-Structure-of-the-Trypanosome-Flagellum-Suggests-that-the-Paraflagellar-Rod-pone.0025700.s012.ogv 6.0 s, 320 × 240; 231 KB
Toxoplasma-gondii-Chromodomain-Protein-1-Binds-to-Heterochromatin-and-Colocalises-with-Centromeres-pone.0032671.s007.ogv 26 s, 512 × 492; 680 KB
Toxoplasma-MIC2-Is-a-Major-Determinant-of-Invasion-and-Virulence-ppat.0020084.sv001.ogv 7.1 s, 203 × 187; 239 KB
Toxoplasma-MIC2-Is-a-Major-Determinant-of-Invasion-and-Virulence-ppat.0020084.sv002.ogv 5.1 s, 202 × 264; 262 KB
Toxoplasma-MIC2-Is-a-Major-Determinant-of-Invasion-and-Virulence-ppat.0020084.sv003.ogv 6.2 s, 342 × 297; 46 KB
Toxoplasma-MIC2-Is-a-Major-Determinant-of-Invasion-and-Virulence-ppat.0020084.sv004.ogv 6.0 s, 361 × 344; 93 KB
Transition-of-Plasmodium-Sporozoites-into-Liver-Stage-Like-Forms-Is-Regulated-by-the-RNA-Binding-ppat.1002046.s019.ogv 6.7 s, 1,516 × 912; 4.95 MB
Transition-of-Plasmodium-Sporozoites-into-Liver-Stage-Like-Forms-Is-Regulated-by-the-RNA-Binding-ppat.1002046.s020.ogv 6.7 s, 1,516 × 912; 4.07 MB
Transition-of-Plasmodium-Sporozoites-into-Liver-Stage-Like-Forms-Is-Regulated-by-the-RNA-Binding-ppat.1002046.s021.ogv 7.1 s, 2,124 × 1,288; 4.57 MB

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