Category:Cell adhesion
Направо към навигацията
Направо към търсенето
attachment of a cell, to another cell or to an underlying substrate, by cell adhesion molecules | |||||
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Подкатегории
Показани са 7 от общо 7 подкатегории на тази категория.
Файлове в категория „Cell adhesion“
Показани са 200 от общо 1115 файла в тази категория.
(предишна страница) (следваща страница)-
-Adrenergic-Inhibition-of-Contractility-in-L6-Skeletal-Muscle-Cells-pone.0022304.s002.ogv 17 сек, 320 × 240; 877 КБ
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A-Comprehensive-Panel-of-Three-Dimensional-Models-for-Studies-of-Prostate-Cancer-Growth-Invasion-pone.0010431.s013.ogv 1 мин 6 сек, 524 × 384; 8,71 МБ
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A-Gene-Expression-Signature-of-Invasive-Potential-in-Metastatic-Melanoma-Cells-pone.0008461.s008.ogv 15 сек, 640 × 480; 2,11 МБ
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A-Gene-Expression-Signature-of-Invasive-Potential-in-Metastatic-Melanoma-Cells-pone.0008461.s009.ogv 15 сек, 640 × 480; 2,37 МБ
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A-Mathematical-Model-for-EphEphrin-Directed-Segregation-of-Intermingled-Cells-pone.0111803.s003.ogv 1 мин 12 сек, 640 × 480; 19,37 МБ
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A-Mathematical-Model-for-EphEphrin-Directed-Segregation-of-Intermingled-Cells-pone.0111803.s004.ogv 1 мин 36 сек, 640 × 480; 59,23 МБ
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A-Multi-cell-Multi-scale-Model-of-Vertebrate-Segmentation-and-Somite-Formation-pcbi.1002155.s016.ogv 1 мин 3 сек, 640 × 480; 6,71 МБ
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A-Multi-cell-Multi-scale-Model-of-Vertebrate-Segmentation-and-Somite-Formation-pcbi.1002155.s017.ogv 1 мин 2 сек, 640 × 480; 6,06 МБ
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A-Multi-cell-Multi-scale-Model-of-Vertebrate-Segmentation-and-Somite-Formation-pcbi.1002155.s018.ogv 1 мин 2 сек, 640 × 480; 6,04 МБ
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A-Multi-cell-Multi-scale-Model-of-Vertebrate-Segmentation-and-Somite-Formation-pcbi.1002155.s019.ogv 29 сек, 640 × 480; 630 КБ
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A-Multi-cell-Multi-scale-Model-of-Vertebrate-Segmentation-and-Somite-Formation-pcbi.1002155.s020.ogv 2 мин 5 сек, 640 × 480; 5,94 МБ
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A-Novel-CXCL10-Based-GPI-Anchored-Fusion-Protein-as-Adjuvant-in-NK-Based-Tumor-Therapy-pone.0072749.s006.ogv 38 сек, 640 × 480; 2,82 МБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s002.ogv 7,2 сек, 696 × 520; 237 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s003.ogv 7,2 сек, 696 × 520; 226 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s004.ogv 1,8 сек, 696 × 520; 231 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s005.ogv 3,6 сек, 696 × 520; 286 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s006.ogv 5,1 сек, 696 × 520; 208 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s007.ogv 5,1 сек, 696 × 520; 155 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s008.ogv 3,6 сек, 696 × 520; 222 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s009.ogv 9,0 сек, 696 × 520; 263 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s010.ogv 7,0 сек, 696 × 520; 371 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s011.ogv 7,2 сек, 696 × 520; 434 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s012.ogv 3,6 сек, 696 × 520; 252 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s013.ogv 3,6 сек, 696 × 520; 309 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s014.ogv 3,6 сек, 696 × 520; 125 КБ
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A-Role-for-PP1NIPP1-in-Steering-Migration-of-Human-Cancer-Cells-pone.0040769.s015.ogv 3,6 сек, 696 × 520; 225 КБ
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Adhesion diagram.jpg 359 × 252; 84 КБ
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Adhesion-Failures-Determine-the-Pattern-of-Choroidal-Neovascularization-in-the-Eye-A-Computer-pcbi.1002440.s017.ogv 1 мин 1 сек, 637 × 616; 7,11 МБ
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Adhesion-Failures-Determine-the-Pattern-of-Choroidal-Neovascularization-in-the-Eye-A-Computer-pcbi.1002440.s018.ogv 1 мин 1 сек, 588 × 568; 6,38 МБ
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Adhesion-Failures-Determine-the-Pattern-of-Choroidal-Neovascularization-in-the-Eye-A-Computer-pcbi.1002440.s020.ogv 1 мин 1 сек, 588 × 568; 6,55 МБ
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Adhesion-Failures-Determine-the-Pattern-of-Choroidal-Neovascularization-in-the-Eye-A-Computer-pcbi.1002440.s021.ogv 1 мин 1 сек, 637 × 616; 7,29 МБ
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Adhesion-Failures-Determine-the-Pattern-of-Choroidal-Neovascularization-in-the-Eye-A-Computer-pcbi.1002440.s022.ogv 1 мин 1 сек, 637 × 616; 7,16 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s001.ogv 17 сек, 1200 × 800; 2,51 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s002.ogv 21 сек, 1200 × 800; 1,71 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s003.ogv 21 сек, 1200 × 800; 1,38 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s004.ogv 21 сек, 1200 × 800; 2,33 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s005.ogv 21 сек, 1200 × 800; 1,75 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s007.ogv 17 сек, 1200 × 800; 1,29 МБ
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Advancing-Edge-Speeds-of-Epithelial-Monolayers-Depend-on-Their-Initial-Confining-Geometry-pone.0153471.s008.ogv 21 сек, 1200 × 800; 1,08 МБ
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Altering-FAK-Paxillin-Interactions-Reduces-Adhesion-Migration-and-Invasion-Processes-pone.0092059.s003.ogv 8,6 сек, 241 × 224; 490 КБ
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Altering-FAK-Paxillin-Interactions-Reduces-Adhesion-Migration-and-Invasion-Processes-pone.0092059.s004.ogv 8,6 сек, 300 × 232; 531 КБ
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Altering-FAK-Paxillin-Interactions-Reduces-Adhesion-Migration-and-Invasion-Processes-pone.0092059.s005.ogv 8,6 сек, 274 × 274; 1,23 МБ
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An-Adhesion-Dependent-Switch-between-Mechanisms-That-Determine-Motile-Cell-Shape-pbio.1001059.s010.ogv 7,0 сек, 256 × 256; 276 КБ
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An-Adhesion-Dependent-Switch-between-Mechanisms-That-Determine-Motile-Cell-Shape-pbio.1001059.s011.ogv 7,0 сек, 256 × 256; 233 КБ
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An-Adhesion-Dependent-Switch-between-Mechanisms-That-Determine-Motile-Cell-Shape-pbio.1001059.s012.ogv 10 сек, 256 × 256; 453 КБ
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An-Adhesion-Dependent-Switch-between-Mechanisms-That-Determine-Motile-Cell-Shape-pbio.1001059.s013.ogv 15 сек, 256 × 256; 164 КБ
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An-Adhesion-Dependent-Switch-between-Mechanisms-That-Determine-Motile-Cell-Shape-pbio.1001059.s014.ogv 25 сек, 256 × 256; 806 КБ
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An-Adhesion-Dependent-Switch-between-Mechanisms-That-Determine-Motile-Cell-Shape-pbio.1001059.s015.ogv 18 сек, 720 × 496; 9,83 МБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 1.ogv 12 сек, 1222 × 866; 536 КБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 2.ogv 12 сек, 1222 × 731; 424 КБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 3.ogv 1 мин 19 сек, 800 × 600; 9,23 МБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 4.ogv 1 мин 20 сек, 800 × 600; 7,37 МБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 5.ogv 1 мин 23 сек, 800 × 600; 8,75 МБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 6.ogv 1 мин 19 сек, 800 × 600; 6,18 МБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 7.ogv 1 мин 20 сек, 800 × 600; 6,51 МБ
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An-Analysis-of-Trafficking-Receptors-Shows-that-CD44-and-P-Selectin-Glycoprotein-Ligand-1-Video 8.ogv 55 сек, 800 × 600; 8,54 МБ
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An-Improved-Chamber-for-Direct-Visualisation-of-Chemotaxis-pone.0015309.s001.ogv 12 сек, 316 × 538; 2,13 МБ
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An-Improved-Chamber-for-Direct-Visualisation-of-Chemotaxis-pone.0015309.s002.ogv 12 сек, 316 × 531; 2,29 МБ
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Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s016.ogv 19 сек, 736 × 608; 9,69 МБ
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Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s017.ogv 33 сек, 592 × 496; 2,42 МБ
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Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s018.ogv 12 сек, 277 × 224; 2,06 МБ
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Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s019.ogv 12 сек, 304 × 304; 1,96 МБ
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Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s020.ogv 9,0 сек, 749 × 706; 2,83 МБ
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Arp23-complex-activity-in-filopodia-of-spreading-cells-1471-2121-9-65-S1.ogv 1 мин 5 сек, 434 × 440; 1,65 МБ
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Arp23-complex-activity-in-filopodia-of-spreading-cells-1471-2121-9-65-S4.ogv 3,8 сек, 210 × 288; 152 КБ
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Arp23-complex-activity-in-filopodia-of-spreading-cells-1471-2121-9-65-S5.ogv 20 сек, 750 × 666; 418 КБ
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Arp23-complex-activity-in-filopodia-of-spreading-cells-1471-2121-9-65-S6.ogv 21 сек, 614 × 394; 2,49 МБ
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Arp23-Inhibition-Induces-Amoeboid-Like-Protrusions-in-MCF10A-Epithelial-Cells-by-Reduced-pone.0100943.s006.ogv 14 сек, 1000 × 200; 1,63 МБ
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Arp23-Inhibition-Induces-Amoeboid-Like-Protrusions-in-MCF10A-Epithelial-Cells-by-Reduced-pone.0100943.s008.ogv 6,9 сек, 970 × 500; 9,07 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s007.ogv 6,9 сек, 156 × 185; 339 КБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s008.ogv 10 сек, 428 × 235; 1,27 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s009.ogv 40 сек, 1024 × 512; 3,32 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s010.ogv 16 сек, 1024 × 512; 4,15 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s011.ogv 11 сек, 1024 × 512; 6,81 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s012.ogv 5,6 сек, 1024 × 512; 2,06 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s013.ogv 16 сек, 1024 × 512; 2,32 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s014.ogv 30 сек, 970 × 512; 8,82 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s015.ogv 9,9 сек, 1024 × 512; 3,1 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s016.ogv 8,8 сек, 1024 × 512; 1,91 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s017.ogv 45 сек, 359 × 404; 16,37 МБ
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Assembly-of-the-Murine-Leukemia-Virus-Is-Directed-towards-Sites-of-Cell–Cell-Contact-pbio.1000163.s018.ogv 45 сек, 1077 × 404; 18,19 МБ
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Bim-and-Bmf-Synergize-To-Induce-Apoptosis-in-Neisseria-Gonorrhoeae-Infection-ppat.1000348.s011.ogv 1,1 сек, 328 × 306; 51 КБ
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Bim-and-Bmf-Synergize-To-Induce-Apoptosis-in-Neisseria-Gonorrhoeae-Infection-ppat.1000348.s012.ogv 11 сек, 300 × 294; 936 КБ
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Biological-soliton-in-multicellular-movement-srep02272-s1.ogv 28 сек, 1365 × 1024; 5,68 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s10.ogv 15 сек, 1280 × 720; 1,1 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s11.ogv 15 сек, 1280 × 720; 6,04 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s12.ogv 6,0 сек, 1280 × 720; 5,65 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s13.ogv 6,0 сек, 1280 × 720; 802 КБ
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Biological-soliton-in-multicellular-movement-srep02272-s14.ogv 1 мин 12 сек, 640 × 480; 6,14 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s2.ogv 36 сек, 640 × 480; 3,84 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s3.ogv 36 сек, 640 × 480; 5,77 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s4.ogv 18 сек, 1365 × 1024; 5,4 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s5.ogv 36 сек, 1365 × 1024; 6,13 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s6.ogv 36 сек, 1365 × 1024; 4,29 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s7.ogv 24 сек, 1365 × 1024; 8,79 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s8.ogv 1 мин 12 сек, 640 × 480; 15,54 МБ
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Biological-soliton-in-multicellular-movement-srep02272-s9.ogv 15 сек, 1280 × 720; 10,4 МБ
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