Category:Model Protista

Protista as model organisms

Media in category "Model Protista"

The following 115 files are in this category, out of 115 total.

A-Quorum-Sensing-Factor-in-Vegetative-Dictyostelium-Discoideum-Cells-Revealed-by-Quantitative-pone.0026901.s009.ogv 4.8 s, 294 × 67; 106 KB
A-Quorum-Sensing-Factor-in-Vegetative-Dictyostelium-Discoideum-Cells-Revealed-by-Quantitative-pone.0026901.s010.ogv 7.5 s, 1,168 × 354; 4.44 MB
A-Toxoplasma-Palmitoyl-Acyl-Transferase-and-the-Palmitoylated-Armadillo-Repeat-Protein-TgARO-Govern-ppat.1003162.s008.ogv 6.4 s, 1,280 × 720; 545 KB
An-Excitable-Cortex-and-Memory-Model-Successfully-Predicts-New-Pseudopod-Dynamics-pone.0033528.s003.ogv 18 s, 386 × 442; 530 KB
Asymmetric-PTEN-Distribution-Regulated-by-Spatial-Heterogeneity-in-Membrane-Binding-State-pcbi.1002862.s008.ogv 12 s, 372 × 250; 1.81 MB
Asymmetric-PTEN-Distribution-Regulated-by-Spatial-Heterogeneity-in-Membrane-Binding-State-pcbi.1002862.s009.ogv 10 s, 378 × 284; 1.44 MB
Cell-Fate-Regulation-Governed-by-a-Repurposed-Bacterial-Histidine-Kinase-pbio.1001979.s019.ogv 11 s, 640 × 480; 2.3 MB
Cell-Fate-Regulation-Governed-by-a-Repurposed-Bacterial-Histidine-Kinase-pbio.1001979.s020.ogv 5.3 s, 640 × 480; 892 KB
Chemotaxis-of-Dictyostelium-discoideum-Collective-Oscillation-of-Cellular-Contacts-pone.0054172.s008.ogv 20 s, 336 × 256; 6.58 MB
Chemotaxis-of-Dictyostelium-discoideum-Collective-Oscillation-of-Cellular-Contacts-pone.0054172.s009.ogv 20 s, 403 × 307; 425 KB
Chemotaxis-of-Dictyostelium-discoideum-Collective-Oscillation-of-Cellular-Contacts-pone.0054172.s010.ogv 20 s, 403 × 307; 9.4 MB
Chromosome-Segregation-Impacts-on-Cell-Growth-and-Division-Site-Selection-in-Corynebacterium-pone.0055078.s002.ogv 5.9 s, 583 × 976; 1.25 MB
Chromosome-Segregation-Impacts-on-Cell-Growth-and-Division-Site-Selection-in-Corynebacterium-pone.0055078.s003.ogv 12 s, 784 × 736; 556 KB
Chromosome-Segregation-Impacts-on-Cell-Growth-and-Division-Site-Selection-in-Corynebacterium-pone.0055078.s004.ogv 8.5 s, 480 × 555; 527 KB
Chromosome-Segregation-Impacts-on-Cell-Growth-and-Division-Site-Selection-in-Corynebacterium-pone.0055078.s005.ogv 4.5 s, 487 × 829; 433 KB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s007.ogv 8.9 s, 480 × 384; 16.28 MB
Deformation-of-Filamentous-Escherichia-coli-Cells-in-a-Microfluidic-Device-A-New-Technique-to-Study-pone.0083775.s009.ogv 4.2 s, 1,392 × 1,040; 1.98 MB
Deformation-of-Filamentous-Escherichia-coli-Cells-in-a-Microfluidic-Device-A-New-Technique-to-Study-pone.0083775.s010.ogv 1.4 s, 1,392 × 1,040; 127 KB
Deformation-of-Filamentous-Escherichia-coli-Cells-in-a-Microfluidic-Device-A-New-Technique-to-Study-pone.0083775.s011.ogv 1 min 40 s, 508 × 508; 782 KB
Dictyostelium-Cells-Migrate-Similarly-on-Surfaces-of-Varying-Chemical-Composition-pone.0087981.s002.ogv 6.5 s, 520 × 520; 5.4 MB
Dynamic-Organization-of-SecA-and-SecY-Secretion-Complexes-in-the-B.-subtilis-Membrane-pone.0157899.s010.ogv 1 min 59 s, 120 × 17; 1.08 MB
Dynamic-Organization-of-SecA-and-SecY-Secretion-Complexes-in-the-B.-subtilis-Membrane-pone.0157899.s011.ogv 44 s, 93 × 18; 172 KB
Efficient-Multiple-Object-Tracking-Using-Mutually-Repulsive-Active-Membranes-pone.0065769.s001.ogv 13 min 28 s, 256 × 256; 14.06 MB
Efficient-Multiple-Object-Tracking-Using-Mutually-Repulsive-Active-Membranes-pone.0065769.s002.ogv 3 min 54 s, 400 × 400; 19.06 MB
Efficient-Multiple-Object-Tracking-Using-Mutually-Repulsive-Active-Membranes-pone.0065769.s003.ogv 27 s, 512 × 512; 35.32 MB
Efficient-Multiple-Object-Tracking-Using-Mutually-Repulsive-Active-Membranes-pone.0065769.s004.ogv 27 s, 512 × 512; 2.48 MB
Entamoeba-lysyl-tRNA-Synthetase-Contains-a-Cytokine-Like-Domain-with-Chemokine-Activity-towards-pntd.0001398.s008.ogv 14 s, 514 × 392; 8.15 MB
Entamoeba-lysyl-tRNA-Synthetase-Contains-a-Cytokine-Like-Domain-with-Chemokine-Activity-towards-pntd.0001398.s009.ogv 10 s, 514 × 392; 6.08 MB
Evidence-for-Divisome-Localization-Mechanisms-Independent-of-the-Min-System-and-SlmA-in-Escherichia-pgen.1004504.s019.ogv 3.2 s, 103 × 102; 98 KB
Evidence-for-Divisome-Localization-Mechanisms-Independent-of-the-Min-System-and-SlmA-in-Escherichia-pgen.1004504.s020.ogv 3.2 s, 102 × 102; 43 KB
Evidence-for-Divisome-Localization-Mechanisms-Independent-of-the-Min-System-and-SlmA-in-Escherichia-pgen.1004504.s021.ogv 3.6 s, 101 × 101; 168 KB
Filament-Depolymerization-Can-Explain-Chromosome-Pulling-during-Bacterial-Mitosis-pcbi.1002145.s009.ogv 54 s, 1,036 × 690; 20.84 MB
Filament-Depolymerization-Can-Explain-Chromosome-Pulling-during-Bacterial-Mitosis-pcbi.1002145.s010.ogv 22 s, 1,036 × 690; 10.5 MB
Filament-Depolymerization-Can-Explain-Chromosome-Pulling-during-Bacterial-Mitosis-pcbi.1002145.s011.ogv 32 s, 1,036 × 690; 11.71 MB
FYVE-Dependent-Endosomal-Targeting-of-an-Arrestin-Related-Protein-in-Amoeba-pone.0015249.s007.ogv 12 s, 256 × 256; 112 KB
Genetic-Analysis-of-Collective-Motility-of-Paenibacillus-sp.-NAIST15-1-pgen.1006387.s014.ogv 20 s, 640 × 480; 472 KB
Heritable-Change-Caused-by-Transient-Transcription-Errors-pgen.1003595.s007.ogv 18 s, 960 × 370; 665 KB
High-Speed-Imaging-of-Amoeboid-Movements-Using-Light-Sheet-Microscopy-pone.0050846.s003.ogv 3.0 s, 600 × 400; 346 KB
High-Speed-Imaging-of-Amoeboid-Movements-Using-Light-Sheet-Microscopy-pone.0050846.s004.ogv 6.0 s, 336 × 256; 833 KB
High-Speed-Imaging-of-Amoeboid-Movements-Using-Light-Sheet-Microscopy-pone.0050846.s005.ogv 5.2 s, 384 × 288; 352 KB
High-Speed-Imaging-of-Amoeboid-Movements-Using-Light-Sheet-Microscopy-pone.0050846.s006.ogv 2.9 s, 336 × 256; 591 KB
High-Speed-Imaging-of-Amoeboid-Movements-Using-Light-Sheet-Microscopy-pone.0050846.s007.ogv 4.3 s, 336 × 256; 1.21 MB
High-Speed-Imaging-of-Amoeboid-Movements-Using-Light-Sheet-Microscopy-pone.0050846.s008.ogv 12 s, 800 × 600; 1.19 MB
Impact-of-Microscopic-Motility-on-the-Swimming-Behavior-of-Parasites-Straighter-Trypanosomes-are-pcbi.1002058.s003.ogv 1 min 20 s, 320 × 240; 3.78 MB
Impact-of-Microscopic-Motility-on-the-Swimming-Behavior-of-Parasites-Straighter-Trypanosomes-are-pcbi.1002058.s004.ogv 1 min 40 s, 320 × 240; 2.54 MB
Impact-of-Microscopic-Motility-on-the-Swimming-Behavior-of-Parasites-Straighter-Trypanosomes-are-pcbi.1002058.s005.ogv 1 min 40 s, 160 × 120; 521 KB
Innate-Non-Specific-Cell-Substratum-Adhesion-pone.0042033.s001.ogv 14 s, 550 × 406; 1.44 MB
Innate-Non-Specific-Cell-Substratum-Adhesion-pone.0042033.s002.ogv 12 s, 484 × 356; 1.26 MB
Investigating-the-Effect-of-Emetic-Compounds-on-Chemotaxis-in-Dictyostelium-Identifies-a-Non-pone.0024439.s001.ogv 15 s, 278 × 208; 876 KB
Investigating-the-Effect-of-Emetic-Compounds-on-Chemotaxis-in-Dictyostelium-Identifies-a-Non-pone.0024439.s002.ogv 15 s, 278 × 208; 1.15 MB
Live-Cell-Imaging-of-Germination-and-Outgrowth-of-Individual-Bacillus-subtilis-Spores-the-Effect-of-pone.0058972.s002.ogv 24 s, 696 × 520; 3.36 MB
Live-Cell-Imaging-of-Germination-and-Outgrowth-of-Individual-Bacillus-subtilis-Spores-the-Effect-of-pone.0058972.s003.ogv 22 s, 696 × 520; 4.1 MB
Live-Cell-Imaging-of-Germination-and-Outgrowth-of-Individual-Bacillus-subtilis-Spores-the-Effect-of-pone.0058972.s004.ogv 24 s, 634 × 484; 1.07 MB
Live-Cell-Imaging-of-Germination-and-Outgrowth-of-Individual-Bacillus-subtilis-Spores-the-Effect-of-pone.0058972.s005.ogv 24 s, 682 × 491; 1.61 MB
Live-Cell-Imaging-of-Germination-and-Outgrowth-of-Individual-Bacillus-subtilis-Spores-the-Effect-of-pone.0058972.s006.ogv 24 s, 647 × 497; 3.62 MB
Low-Cost-3D-Printers-Enable-High-Quality-and-Automated-Sample-Preparation-and-Molecular-Detection-pone.0158502.s006.ogv 1 min 35 s, 1,920 × 1,080; 28.95 MB
Modeling-E.-coli-Tumbles-by-Rotational-Diffusion.-Implications-for-Chemotaxis-pone.0035412.s001.ogv 8.8 s, 272 × 236; 738 KB
Myxococcus-xanthus-Gliding-Motors-Are-Elastically-Coupled-to-the-Substrate-as-Predicted-by-the-pcbi.1003619.s009.ogv 5.1 s, 1,000 × 1,000; 617 KB
Myxococcus-xanthus-Gliding-Motors-Are-Elastically-Coupled-to-the-Substrate-as-Predicted-by-the-pcbi.1003619.s010.ogv 5.1 s, 1,000 × 1,000; 318 KB
Myxococcus-xanthus-Gliding-Motors-Are-Elastically-Coupled-to-the-Substrate-as-Predicted-by-the-pcbi.1003619.s011.ogv 2.6 s, 75 × 50; 16 KB
Osteopontin-Reduces-Biofilm-Formation-in-a-Multi-Species-Model-of-Dental-Biofilm-pone.0041534.s006.ogv 20 s, 640 × 480; 595 KB
Osteopontin-Reduces-Biofilm-Formation-in-a-Multi-Species-Model-of-Dental-Biofilm-pone.0041534.s007.ogv 20 s, 640 × 480; 811 KB
Pre-Disposition-and-Epigenetics-Govern-Variation-in-Bacterial-Survival-upon-Stress-pgen.1003148.s021.ogv 11 s, 832 × 514; 188 KB
Pre-Disposition-and-Epigenetics-Govern-Variation-in-Bacterial-Survival-upon-Stress-pgen.1003148.s022.ogv 12 s, 924 × 565; 1.05 MB
Pre-Disposition-and-Epigenetics-Govern-Variation-in-Bacterial-Survival-upon-Stress-pgen.1003148.s023.ogv 10 s, 605 × 601; 533 KB
Prey-Capture-and-Phagocytosis-in-the-Choanoflagellate-Salpingoeca-rosetta-pone.0095577.s003.ogv 46 s, 320 × 608; 7.47 MB
Prey-Capture-and-Phagocytosis-in-the-Choanoflagellate-Salpingoeca-rosetta-pone.0095577.s004.ogv 10 s, 192 × 288; 107 KB
Prey-Capture-and-Phagocytosis-in-the-Choanoflagellate-Salpingoeca-rosetta-pone.0095577.s005.ogv 7.2 s, 800 × 352; 2.45 MB
PROKARYOTIC INITIATION AND ELONGATIONM.jpg 526 × 696; 44 KB
Recruitment-Assembly-and-Molecular-Architecture-of-the-SpoIIIE-DNA-Pump-Revealed-by-Superresolution-pbio.1001557.s015.ogv 5.9 s, 440 × 364; 451 KB
Recruitment-Assembly-and-Molecular-Architecture-of-the-SpoIIIE-DNA-Pump-Revealed-by-Superresolution-pbio.1001557.s016.ogv 6.0 s, 1,190 × 577; 1.14 MB
Recruitment-Assembly-and-Molecular-Architecture-of-the-SpoIIIE-DNA-Pump-Revealed-by-Superresolution-pbio.1001557.s017.ogv 6.0 s, 556 × 277; 437 KB
Regulation-of-Sister-Chromosome-Cohesion-by-the-Replication-Fork-Tracking-Protein-SeqA-pgen.1003673.s012.ogv 11 s, 195 × 193; 1.35 MB
Regulation-of-Sister-Chromosome-Cohesion-by-the-Replication-Fork-Tracking-Protein-SeqA-pgen.1003673.s013.ogv 4.9 s, 158 × 157; 429 KB
Role-of-PKD2-in-Rheotaxis-in-Dictyostelium-pone.0088682.s003.ogv 5.0 s, 248 × 148; 163 KB
Role-of-PKD2-in-Rheotaxis-in-Dictyostelium-pone.0088682.s004.ogv 5.0 s, 248 × 148; 204 KB
Role-of-PKD2-in-Rheotaxis-in-Dictyostelium-pone.0088682.s005.ogv 5.0 s, 248 × 148; 73 KB
Role-of-PKD2-in-Rheotaxis-in-Dictyostelium-pone.0088682.s006.ogv 5.0 s, 248 × 148; 87 KB
Self-Generated-Chemoattractant-Gradients-Attractant-Depletion-Extends-the-Range-and-Robustness-of-pbio.1002404.s002.ogv 37 s, 1,264 × 900; 22.64 MB
Self-Generated-Chemoattractant-Gradients-Attractant-Depletion-Extends-the-Range-and-Robustness-of-pbio.1002404.s003.ogv 47 s, 786 × 300; 32.79 MB
Self-Generated-Chemoattractant-Gradients-Attractant-Depletion-Extends-the-Range-and-Robustness-of-pbio.1002404.s004.ogv 11 s, 1,200 × 1,300; 3.28 MB
Self-Generated-Chemoattractant-Gradients-Attractant-Depletion-Extends-the-Range-and-Robustness-of-pbio.1002404.s005.ogv 18 s, 1,792 × 961; 16.93 MB
Shrink-Induced-Superhydrophobic-and-Antibacterial-Surfaces-in-Consumer-Plastics-pone.0040987.s002.ogv 17 s, 640 × 480; 512 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s006.ogv 11 s, 384 × 288; 416 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s007.ogv 11 s, 384 × 288; 416 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s008.ogv 12 s, 384 × 288; 333 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s009.ogv 13 s, 352 × 240; 1.34 MB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s010.ogv 3.3 s, 334 × 897; 675 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s011.ogv 6.3 s, 231 × 264; 440 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s012.ogv 4.8 s, 384 × 288; 69 KB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s001.ogv 3.1 s, 620 × 558; 9.73 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s002.ogv 3.3 s, 546 × 480; 1.11 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s003.ogv 4.2 s, 600 × 212; 1.86 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s004.ogv 3.3 s, 378 × 516; 2.02 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s005.ogv 3.3 s, 538 × 310; 2.06 MB
Thaxter-Myxobacteria-1.jpg 1,921 × 3,161; 1.31 MB
Thaxter-Myxobacteria-2.jpg 1,921 × 3,161; 1.51 MB
Thaxter-Myxobacteria-3.jpg 1,921 × 3,161; 1.55 MB
Thaxter-Myxobacteria-4.jpg 1,921 × 3,161; 1.73 MB
The-C-Terminal-SynMuvDdDUF926-Domain-Regulates-the-Function-of-the-N-Terminal-Domain-of-DdNKAP-pone.0168617.s011.ogv 15 s, 1,360 × 1,024; 14.63 MB
The-C-Terminal-SynMuvDdDUF926-Domain-Regulates-the-Function-of-the-N-Terminal-Domain-of-DdNKAP-pone.0168617.s012.ogv 13 s, 1,360 × 1,024; 10.08 MB
The-C-Terminal-SynMuvDdDUF926-Domain-Regulates-the-Function-of-the-N-Terminal-Domain-of-DdNKAP-pone.0168617.s013.ogv 16 s, 1,360 × 1,024; 25.22 MB
The-Green-Tea-Catechin-Epigallocatechin-Gallate-(EGCG)-Blocks-Cell-Motility-Chemotaxis-and-pone.0059275.s001.ogv 30 s, 568 × 380; 20.43 MB
The-Green-Tea-Catechin-Epigallocatechin-Gallate-(EGCG)-Blocks-Cell-Motility-Chemotaxis-and-pone.0059275.s002.ogv 52 s, 600 × 400; 53.41 MB
The-Green-Tea-Catechin-Epigallocatechin-Gallate-(EGCG)-Blocks-Cell-Motility-Chemotaxis-and-pone.0059275.s003.ogv 14 s, 256 × 256; 7.68 MB
The-Green-Tea-Catechin-Epigallocatechin-Gallate-(EGCG)-Blocks-Cell-Motility-Chemotaxis-and-pone.0059275.s004.ogv 36 s, 256 × 256; 29.02 MB
The-p21-Activated-Kinase-(PAK)-Family-Member-PakD-Is-Required-for-Chemorepulsion-and-Proliferation-pone.0096633.s001.ogv 3.6 s, 484 × 514; 541 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
When-Phase-Contrast-Fails-ChainTracer-and-NucTracer-Two-ImageJ-Methods-for-Semi-Automated-Single-pone.0151267.s003.ogv 5 min 4 s, 922 × 576; 11.47 MB

Category:Model Protista

Media in category "Model Protista"

Navigation menu

Search