Category:Cell polarity

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cell polarity

polar morphology of a cell, a specific orientation of the cell structure

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Instance of

morphology (cell)
concept (cell biology)

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Q189100
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Subcategories

This category has the following 3 subcategories, out of 3 total.

A

Arp2/3-mediated F-actin formation controls regulated exocytosis in vivo‎ (26 F)

P

Planar cell polarity‎ (13 F)

S

Sfrp Controls Apicobasal Polarity and Oriented Cell Division in Developing Gut Epithelium‎ (4 F)

Media in category "Cell polarity"

The following 200 files are in this category, out of 514 total.

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A-Mathematical-Model-for-Neutrophil-Gradient-Sensing-and-Polarization-pcbi.0030036.sv002.ogv 5.6 s, 432 × 336; 1.09 MB
A-Polarised-Population-of-Dynamic-Microtubules-Mediates-Homeostatic-Length-Control-in-Animal-Cells-pbio.1000542.s005.ogv 26 s, 96 × 428; 522 KB
A-Polarised-Population-of-Dynamic-Microtubules-Mediates-Homeostatic-Length-Control-in-Animal-Cells-pbio.1000542.s006.ogv 14 s, 153 × 245; 830 KB
A-Polarised-Population-of-Dynamic-Microtubules-Mediates-Homeostatic-Length-Control-in-Animal-Cells-pbio.1000542.s007.ogv 5.1 s, 223 × 225; 500 KB
A-Rho-Scaffold-Integrates-the-Secretory-System-with-Feedback-Mechanisms-in-Regulation-of-Auxin-pbio.1000282.s019.ogv 3.8 s, 520 × 1,024; 380 KB
Actin-binding-domains-direct-actin-binding-proteins-to-different-cytoskeletal-locations-1471-2121-9-10-S1.ogv 5.6 s, 299 × 113; 114 KB
Actin-binding-domains-direct-actin-binding-proteins-to-different-cytoskeletal-locations-1471-2121-9-10-S2.ogv 3.1 s, 296 × 115; 100 KB
Actin-binding-domains-direct-actin-binding-proteins-to-different-cytoskeletal-locations-1471-2121-9-10-S4.ogv 1.1 s, 390 × 280; 67 KB
Actin-binding-domains-direct-actin-binding-proteins-to-different-cytoskeletal-locations-1471-2121-9-10-S5.ogv 13 s, 512 × 512; 557 KB
Actin-nucleation-at-the-centrosome-controls-lymphocyte-polarity-ncomms10969-s2.ogv 3.3 s, 501 × 250; 128 KB
Actin-nucleation-at-the-centrosome-controls-lymphocyte-polarity-ncomms10969-s3.ogv 4.5 s, 175 × 90; 24 KB
Actin-nucleation-at-the-centrosome-controls-lymphocyte-polarity-ncomms10969-s4.ogv 4.0 s, 240 × 240; 56 KB
Actin-nucleation-at-the-centrosome-controls-lymphocyte-polarity-ncomms10969-s5.ogv 4.0 s, 240 × 240; 54 KB
Afferent-Neurons-of-the-Zebrafish-Lateral-Line-Are-Strict-Selectors-of-Hair-Cell-Orientation-pone.0004477.s002.ogv 3.2 s, 204 × 190; 59 KB
Afferent-Neurons-of-the-Zebrafish-Lateral-Line-Are-Strict-Selectors-of-Hair-Cell-Orientation-pone.0004477.s003.ogv 14 s, 212 × 206; 177 KB
Afferent-Neurons-of-the-Zebrafish-Lateral-Line-Are-Strict-Selectors-of-Hair-Cell-Orientation-pone.0004477.s004.ogv 29 s, 344 × 178; 293 KB
Afferent-Neurons-of-the-Zebrafish-Lateral-Line-Are-Strict-Selectors-of-Hair-Cell-Orientation-pone.0004477.s005.ogv 14 s, 332 × 210; 226 KB
Aging-and-Death-in-an-Organism-That-Reproduces-by-Morphologically-Symmetric-Division-pbio.0030045.sv001.ogv 7.0 s, 232 × 240; 142 KB
Alignment-between-PIN1-Polarity-and-Microtubule-Orientation-in-the-Shoot-Apical-Meristem-Reveals-a-pbio.1000516.s002.ogv 1.5 s, 202 × 202; 66 KB
An-Experimental-and-Computational-Study-of-the-Effect-of-ActA-Polarity-on-the-Speed-of-Listeria-pcbi.1000434.s011.ogv 6.1 s, 640 × 640; 1.46 MB
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Apical-Transport-of-Influenza-A-Virus-Ribonucleoprotein-Requires-Rab11-positive-Recycling-Endosome-pone.0021123.s012.ogv 8.3 s, 752 × 376; 444 KB
Apical-Transport-of-Influenza-A-Virus-Ribonucleoprotein-Requires-Rab11-positive-Recycling-Endosome-pone.0021123.s013.ogv 10 s, 112 × 112; 875 KB
Asymmetry-of-Early-Endosome-Distribution-in-C.-elegans-Embryos-pone.0000493.s001.ogv 7.0 s, 548 × 198; 3.11 MB
Biological-models-pcbi.1002071.s002.ogv 3.2 s, 692 × 678; 211 KB
Biological-models-pcbi.1002071.s003.ogv 3.2 s, 692 × 678; 247 KB
Biological-models-pcbi.1002071.s004.ogv 3.3 s, 692 × 678; 263 KB
Biological-models-pcbi.1002071.s005.ogv 3.7 s, 842 × 828; 348 KB
Biological-models-pcbi.1002071.s006.ogv 2.5 s, 842 × 828; 834 KB
Biological-models-pcbi.1002071.s007.ogv 13 s, 842 × 828; 471 KB
Biological-models-pcbi.1002071.s008.ogv 13 s, 842 × 828; 469 KB
Biological-models-pcbi.1002071.s009.ogv 6.1 s, 1,046 × 1,046; 2.93 MB
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Building-Bridges-toward-Invasion-Tumor-Promoter-Treatment-Induces-a-Novel-Protein-Kinase-C-pone.0090722.s002.ogv 21 s, 300 × 300; 679 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s003.ogv 16 s, 320 × 240; 157 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s004.ogv 26 s, 320 × 240; 459 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s005.ogv 44 s, 320 × 240; 537 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s006.ogv 36 s, 320 × 240; 469 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s007.ogv 47 s, 320 × 240; 269 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s008.ogv 10 s, 1,182 × 390; 231 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s009.ogv 1 min 17 s, 320 × 240; 769 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s010.ogv 1 min 12 s, 320 × 240; 1.01 MB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s011.ogv 1 min 55 s, 324 × 324; 338 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s012.ogv 11 s, 320 × 240; 94 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s013.ogv 8.8 s, 320 × 240; 81 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s014.ogv 21 s, 334 × 334; 92 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s015.ogv 18 s, 240 × 254; 64 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s016.ogv 1 min 8 s, 320 × 240; 166 KB
Cadherin-2-Controls-Directional-Chain-Migration-of-Cerebellar-Granule-Neurons-pbio.1000240.s017.ogv 11 s, 320 × 240; 41 KB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s001.ogv 20 s, 512 × 512; 4.89 MB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s002.ogv 6.5 s, 1,524 × 992; 427 KB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s003.ogv 39 s, 512 × 512; 3.48 MB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s004.ogv 9.0 s, 512 × 512; 2.03 MB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s005.ogv 9.0 s, 512 × 512; 2.21 MB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s006.ogv 3.0 s, 512 × 512; 145 KB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s007.ogv 22 s, 512 × 512; 2.18 MB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s008.ogv 26 s, 512 × 512; 3.45 MB
CCR2-Acts-as-Scavenger-for-CCL2-during-Monocyte-Chemotaxis-pone.0037208.s009.ogv 26 s, 388 × 392; 4.33 MB
Cell-movement-pbio.1001256.s006.ogv 15 s, 375 × 525; 308 KB
Cell-movement-pbio.1001256.s007.ogv 2.7 s, 734 × 512; 356 KB
Cell-movement-pbio.1001256.s008.ogv 4.7 s, 734 × 512; 659 KB
Cell-movement-pbio.1001256.s009.ogv 10 s, 720 × 492; 2.37 MB
Chemotaxis-A-Feedback-Based-Computational-Model-Robustly-Predicts-Multiple-Aspects-of-Real-Cell-pbio.1000618.s003.ogv 33 s, 648 × 648; 1.24 MB
Chemotaxis-A-Feedback-Based-Computational-Model-Robustly-Predicts-Multiple-Aspects-of-Real-Cell-pbio.1000618.s004.ogv 19 s, 648 × 648; 795 KB
Chemotaxis-A-Feedback-Based-Computational-Model-Robustly-Predicts-Multiple-Aspects-of-Real-Cell-pbio.1000618.s005.ogv 9.1 s, 248 × 222; 548 KB
Chemotaxis-A-Feedback-Based-Computational-Model-Robustly-Predicts-Multiple-Aspects-of-Real-Cell-pbio.1000618.s006.ogv 33 s, 648 × 648; 1.47 MB
Chemotaxis-A-Feedback-Based-Computational-Model-Robustly-Predicts-Multiple-Aspects-of-Real-Cell-pbio.1000618.s007.ogv 33 s, 648 × 648; 2 MB
Coherent-anti-Stokes-Raman-scattering-imaging-of-lipids-in-cancer-metastasis-1471-2407-9-42-S1.ogv 38 s, 776 × 236; 6.37 MB
Collective-Signal-Processing-in-Cluster-Chemotaxis-Roles-of-Adaptation-Amplification-and-Co-pcbi.1005008.s001.ogv 1 min 3 s, 640 × 480; 12.89 MB
Collective-Signal-Processing-in-Cluster-Chemotaxis-Roles-of-Adaptation-Amplification-and-Co-pcbi.1005008.s002.ogv 1 min 3 s, 928 × 306; 11.29 MB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s004.ogv 0.5 s, 736 × 672; 1.57 MB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s005.ogv 1.8 s, 462 × 462; 68 KB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s006.ogv 3.4 s, 640 × 480; 346 KB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s007.ogv 8.5 s, 856 × 792; 1.33 MB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s008.ogv 3.2 s, 640 × 480; 445 KB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s009.ogv 6.1 s, 640 × 480; 1.7 MB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s010.ogv 3.9 s, 462 × 462; 808 KB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s011.ogv 6.6 s, 462 × 462; 1.11 MB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s012.ogv 9.6 s, 462 × 462; 170 KB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s013.ogv 2.0 s, 462 × 462; 40 KB
Comparative-Live-Cell-Imaging-Analyses-of-SPA-2-BUD-6-and-BNI-1-in-Neurospora-crassa-Reveal-Novel-pone.0030372.s014.ogv 6.9 s, 462 × 462; 664 KB
Connexin43-Modulates-Cell-Polarity-and-Directional-Cell-Migration-by-Regulating-Microtubule-Dynamics-pone.0026379.s002.ogv 9.5 s, 220 × 220; 622 KB
Connexin43-Modulates-Cell-Polarity-and-Directional-Cell-Migration-by-Regulating-Microtubule-Dynamics-pone.0026379.s003.ogv 9.5 s, 220 × 220; 600 KB
Connexin43-Modulates-Cell-Polarity-and-Directional-Cell-Migration-by-Regulating-Microtubule-Dynamics-pone.0026379.s004.ogv 11 s, 304 × 464; 899 KB
Connexin43-Modulates-Cell-Polarity-and-Directional-Cell-Migration-by-Regulating-Microtubule-Dynamics-pone.0026379.s005.ogv 21 s, 308 × 433; 2.21 MB
Cyp26-Enzymes-Facilitate-Second-Heart-Field-Progenitor-Addition-and-Maintenance-of-Ventricular-pbio.2000504.s013.ogv 5.2 s, 640 × 360; 303 KB
Cyp26-Enzymes-Facilitate-Second-Heart-Field-Progenitor-Addition-and-Maintenance-of-Ventricular-pbio.2000504.s014.ogv 5.2 s, 640 × 360; 293 KB
DAAM1-Is-a-Formin-Required-for-Centrosome-Re-Orientation-during-Cell-Migration-pone.0013064.s004.ogv 8.0 s, 1,036 × 684; 3.83 MB
DAAM1-Is-a-Formin-Required-for-Centrosome-Re-Orientation-during-Cell-Migration-pone.0013064.s005.ogv 8.0 s, 1,036 × 702; 3.36 MB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S1.ogv 1.6 s, 642 × 236; 66 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S2.ogv 3.1 s, 196 × 112; 23 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S3.ogv 3.1 s, 78 × 224; 24 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S4.ogv 1.6 s, 682 × 285; 29 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S5.ogv 2.0 s, 315 × 189; 221 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S6.ogv 1.6 s, 297 × 186; 6 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S7.ogv 1.6 s, 505 × 409; 70 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S8.ogv 1.6 s, 474 × 548; 84 KB
Dendrites-differ-from-axons-in-patterns-of-microtubule-stability-and-polymerization-during-1749-8104-4-26-S9.ogv 3.1 s, 502 × 619; 148 KB
Deterministic-Mechanical-Model-of-T-Killer-Cell-Polarization-Reproduces-the-Wandering-of-Aim-pcbi.1000260.s004.ogv 13 s, 320 × 240; 785 KB
Deterministic-Mechanical-Model-of-T-Killer-Cell-Polarization-Reproduces-the-Wandering-of-Aim-pcbi.1000260.s005.ogv 14 s, 320 × 240; 1.46 MB
Deterministic-Mechanical-Model-of-T-Killer-Cell-Polarization-Reproduces-the-Wandering-of-Aim-pcbi.1000260.s006.ogv 9.6 s, 320 × 240; 334 KB
Deterministic-Mechanical-Model-of-T-Killer-Cell-Polarization-Reproduces-the-Wandering-of-Aim-pcbi.1000260.s008.ogv 13 s, 320 × 240; 1.36 MB
Detrimental-Effects-of-Microgravity-on-Mouse-Preimplantation-Development-In-Vitro-pone.0006753.s001.ogv 21 s, 320 × 240; 3.26 MB
Detrimental-Effects-of-Microgravity-on-Mouse-Preimplantation-Development-In-Vitro-pone.0006753.s002.ogv 20 s, 1,052 × 893; 15.37 MB
Detrimental-Effects-of-Microgravity-on-Mouse-Preimplantation-Development-In-Vitro-pone.0006753.s003.ogv 20 s, 1,052 × 893; 12.78 MB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S1.ogv 7.4 s, 450 × 194; 509 KB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S10.ogv 33 s, 720 × 480; 5.32 MB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S11.ogv 20 s, 472 × 146; 2.92 MB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S2.ogv 7.3 s, 720 × 480; 803 KB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S3.ogv 4.9 s, 720 × 480; 576 KB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S4.ogv 23 s, 720 × 480; 3.47 MB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S5.ogv 17 s, 720 × 480; 2.83 MB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S6.ogv 17 s, 720 × 480; 5.02 MB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S7.ogv 19 s, 720 × 480; 712 KB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S8.ogv 6.5 s, 720 × 480; 594 KB
Different-modes-of-state-transitions-determine-pattern-in-the-Phosphatidylinositide-Actin-system-1471-2121-12-42-S9.ogv 6.1 s, 720 × 480; 608 KB
Differential-Effects-of-Tissue-Culture-Coating-Substrates-on-Prostate-Cancer-Cell-Adherence-pone.0112122.s006.ogv 39 s, 1,388 × 1,040; 6.65 MB
Differential-Effects-of-Tissue-Culture-Coating-Substrates-on-Prostate-Cancer-Cell-Adherence-pone.0112122.s007.ogv 39 s, 1,388 × 1,040; 11.03 MB
Differential-Effects-of-Tissue-Culture-Coating-Substrates-on-Prostate-Cancer-Cell-Adherence-pone.0112122.s008.ogv 39 s, 1,388 × 1,040; 6.86 MB
Differential-Effects-of-Tissue-Culture-Coating-Substrates-on-Prostate-Cancer-Cell-Adherence-pone.0112122.s009.ogv 39 s, 1,388 × 1,040; 6.86 MB
Differential-Effects-of-Tissue-Culture-Coating-Substrates-on-Prostate-Cancer-Cell-Adherence-pone.0112122.s010.ogv 39 s, 426 × 240; 2.35 MB
Differential-Effects-of-Tissue-Culture-Coating-Substrates-on-Prostate-Cancer-Cell-Adherence-pone.0112122.s011.ogv 39 s, 1,388 × 1,040; 5.96 MB
Differential-Effects-of-TNF-(TNFSF2)-and-IFN-γ-on-Intestinal-Epithelial-Cell-Morphogenesis-and-pone.0022967.s003.ogv 6.4 s, 836 × 736; 1.25 MB
Differential-Sensitivity-of-Epithelial-Cells-to-Extracellular-Matrix-in-Polarity-Establishment-pone.0112922.s001.ogv 3.0 s, 672 × 512; 138 KB
Differential-Sensitivity-of-Epithelial-Cells-to-Extracellular-Matrix-in-Polarity-Establishment-pone.0112922.s002.ogv 3.0 s, 672 × 512; 150 KB
Differential-Sensitivity-of-Epithelial-Cells-to-Extracellular-Matrix-in-Polarity-Establishment-pone.0112922.s003.ogv 3.0 s, 672 × 512; 140 KB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S10.ogv 25 s, 372 × 372; 2 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S11.ogv 25 s, 396 × 272; 1.51 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S12.ogv 22 s, 372 × 284; 1.82 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S13.ogv 23 s, 324 × 412; 2.63 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S14.ogv 15 s, 352 × 244; 591 KB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S15.ogv 31 s, 464 × 352; 1.75 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S16.ogv 29 s, 288 × 364; 2.4 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S17.ogv 5.8 s, 266 × 236; 175 KB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S4.ogv 18 s, 376 × 170; 1.22 MB
Diverse-roles-of-actin-in-C.-elegans-early-embryogenesis-1471-213X-7-142-S9.ogv 23 s, 352 × 364; 1.36 MB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S1.ogv 12 s, 696 × 520; 184 KB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S2.ogv 12 s, 452 × 436; 105 KB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S3.ogv 26 s, 231 × 156; 97 KB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S4.ogv 23 s, 696 × 520; 685 KB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S5.ogv 34 s, 696 × 520; 2.76 MB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S6.ogv 23 s, 696 × 520; 837 KB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S7.ogv 35 s, 696 × 520; 1.75 MB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S8.ogv 26 s, 292 × 116; 115 KB
Dynacortin-facilitates-polarization-of-chemotaxing-cells-1741-7007-5-53-S9.ogv 16 s, 128 × 211; 84 KB
Dynamic-operation-of-optical-fibres-beyond-the-single-mode-regime-facilitates-the-orientation-of-ncomms6481-s2.ogv 7.0 s, 432 × 432; 154 KB
Dynamic-operation-of-optical-fibres-beyond-the-single-mode-regime-facilitates-the-orientation-of-ncomms6481-s3.ogv 3.0 s, 248 × 240; 38 KB
Dynamic-operation-of-optical-fibres-beyond-the-single-mode-regime-facilitates-the-orientation-of-ncomms6481-s4.ogv 8.1 s, 320 × 240; 72 KB
Dynamic-operation-of-optical-fibres-beyond-the-single-mode-regime-facilitates-the-orientation-of-ncomms6481-s5.ogv 24 s, 160 × 120; 147 KB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s008.ogv 22 s, 300 × 300; 1.19 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s009.ogv 26 s, 300 × 300; 2.01 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s010.ogv 22 s, 300 × 300; 1.43 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s011.ogv 13 s, 300 × 300; 838 KB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s012.ogv 20 s, 260 × 260; 1.12 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s013.ogv 45 s, 320 × 402; 15.65 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s014.ogv 45 s, 560 × 408; 24.53 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s015.ogv 23 s, 320 × 402; 10.09 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s016.ogv 45 s, 458 × 418; 14.56 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s017.ogv 40 s, 340 × 340; 14.89 MB
Dynamics-of-Cell-Ensembles-on-Adhesive-Micropatterns-Bridging-the-Gap-between-Single-Cell-Spreading-pcbi.1004863.s018.ogv 40 s, 340 × 340; 13.58 MB
Factors-necessary-to-produce-basoapical-polarity-in-human-glandular-epithelium-formed-in-1741-7007-7-77-S2.ogv 7.0 s, 820 × 791; 977 KB
Factors-necessary-to-produce-basoapical-polarity-in-human-glandular-epithelium-formed-in-1741-7007-7-77-S3.ogv 12 s, 300 × 300; 1.94 MB
Factors-necessary-to-produce-basoapical-polarity-in-human-glandular-epithelium-formed-in-1741-7007-7-77-S4.ogv 7.8 s, 300 × 300; 233 KB
Filopodial-Tension-Model-of-Convergent-Extension-of-Tissues-pcbi.1004952.s005.ogv 10 s, 440 × 490; 1.91 MB
Filopodial-Tension-Model-of-Convergent-Extension-of-Tissues-pcbi.1004952.s006.ogv 13 s, 320 × 650; 2.92 MB
Filopodial-Tension-Model-of-Convergent-Extension-of-Tissues-pcbi.1004952.s007.ogv 9.5 s, 320 × 430; 1.96 MB
Filopodial-Tension-Model-of-Convergent-Extension-of-Tissues-pcbi.1004952.s008.ogv 12 s, 320 × 500; 2.86 MB
Filopodial-Tension-Model-of-Convergent-Extension-of-Tissues-pcbi.1004952.s009.ogv 14 s, 854 × 480; 3.5 MB
Flotillins-Are-Involved-in-the-Polarization-of-Primitive-and-Mature-Hematopoietic-Cells-pone.0008290.s001.ogv 4.7 s, 74 × 107; 10 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s002.ogv 10 s, 800 × 600; 168 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s003.ogv 10 s, 800 × 596; 198 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s004.ogv 6.0 s, 1,200 × 964; 1.24 MB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s005.ogv 24 s, 1,200 × 964; 3.52 MB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s006.ogv 10 s, 960 × 754; 894 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s007.ogv 10 s, 990 × 754; 853 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s008.ogv 10 s, 990 × 754; 863 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s009.ogv 5.0 s, 960 × 754; 843 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s013.ogv 15 s, 900 × 866; 1.13 MB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s014.ogv 6.0 s, 900 × 900; 861 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s015.ogv 38 s, 1,200 × 964; 35.32 MB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s016.ogv 35 s, 1,200 × 964; 32.6 MB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s017.ogv 11 s, 1,200 × 972; 908 KB
Flux-Based-Transport-Enhancement-as-a-Plausible-Unifying-Mechanism-for-Auxin-Transport-in-Meristem-pcbi.1000207.s018.ogv 17 s, 1,650 × 550; 3.19 MB
Functional-Characterization-and-Cellular-Dynamics-of-the-CDC-42-–-RAC-–-CDC-24-Module-in-Neurospora-pone.0027148.s003.ogv 13 s, 640 × 348; 417 KB
Functional-Characterization-and-Cellular-Dynamics-of-the-CDC-42-–-RAC-–-CDC-24-Module-in-Neurospora-pone.0027148.s004.ogv 4.0 s, 640 × 348; 104 KB
Functional-Characterization-and-Cellular-Dynamics-of-the-CDC-42-–-RAC-–-CDC-24-Module-in-Neurospora-pone.0027148.s005.ogv 27 s, 640 × 348; 430 KB
Functional-Characterization-and-Cellular-Dynamics-of-the-CDC-42-–-RAC-–-CDC-24-Module-in-Neurospora-pone.0027148.s006.ogv 7.0 s, 640 × 348; 288 KB
Functional-Characterization-and-Cellular-Dynamics-of-the-CDC-42-–-RAC-–-CDC-24-Module-in-Neurospora-pone.0027148.s007.ogv 4.5 s, 640 × 348; 103 KB
Functional-Characterization-and-Cellular-Dynamics-of-the-CDC-42-–-RAC-–-CDC-24-Module-in-Neurospora-pone.0027148.s008.ogv 12 s, 640 × 348; 272 KB
Gene-Expression-Noise-Enhances-Robust-Organization-of-the-Early-Mammalian-Blastocyst-pcbi.1005320.s002.ogv 8.0 s, 560 × 420; 1.38 MB
Gene-Expression-Noise-Enhances-Robust-Organization-of-the-Early-Mammalian-Blastocyst-pcbi.1005320.s003.ogv 8.0 s, 560 × 420; 1.53 MB
Gene-Expression-Noise-Enhances-Robust-Organization-of-the-Early-Mammalian-Blastocyst-pcbi.1005320.s004.ogv 14 s, 233 × 221; 76 KB
Gene-Expression-Noise-Enhances-Robust-Organization-of-the-Early-Mammalian-Blastocyst-pcbi.1005320.s005.ogv 7.1 s, 512 × 512; 1.09 MB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s017.ogv 32 s, 358 × 260; 326 KB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s018.ogv 35 s, 308 × 224; 477 KB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s019.ogv 33 s, 308 × 224; 598 KB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s020.ogv 32 s, 256 × 186; 850 KB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s021.ogv 34 s, 256 × 186; 556 KB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s022.ogv 13 s, 692 × 678; 1.55 MB
Genetic-Control-of-Organ-Shape-and-Tissue-Polarity-pbio.1000537.s023.ogv 13 s, 792 × 778; 1.34 MB

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