Category:Videos of Caenorhabditis elegans embryos

Media in category "Videos of Caenorhabditis elegans embryos"

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

A-Broad-Requirement-for-TLS-Polymerases-η-and-κ-and-Interacting-Sumoylation-and-Nuclear-Pore-pgen.1002800.s010.ogv 34 s, 407 × 473; 2.51 MB
A-Broad-Requirement-for-TLS-Polymerases-η-and-κ-and-Interacting-Sumoylation-and-Nuclear-Pore-pgen.1002800.s011.ogv 17 s, 400 × 514; 1,017 KB
A-Cell-Cycle-Timer-for-Asymmetric-Spindle-Positioning-pbio.1000088.sv001.ogv 9.2 s, 670 × 332; 154 KB
A-Cell-Cycle-Timer-for-Asymmetric-Spindle-Positioning-pbio.1000088.sv002.ogv 31 s, 330 × 494; 517 KB
A-Cell-Cycle-Timer-for-Asymmetric-Spindle-Positioning-pbio.1000088.sv005.ogv 3.5 s, 456 × 346; 152 KB
A-Cell-Cycle-Timer-for-Asymmetric-Spindle-Positioning-pbio.1000088.sv006.ogv 3.5 s, 340 × 296; 157 KB
A-Genetic-Cascade-of-let-7-ncl-1-fib-1-Modulates-Nucleolar-Size-and-rRNA-Pool-in-Caenorhabditis-pgen.1005580.s006.ogv 4.0 s, 56 × 100; 74 KB
A-Genetic-Cascade-of-let-7-ncl-1-fib-1-Modulates-Nucleolar-Size-and-rRNA-Pool-in-Caenorhabditis-pgen.1005580.s007.ogv 4.0 s, 56 × 100; 9 KB
A-Genetic-Cascade-of-let-7-ncl-1-fib-1-Modulates-Nucleolar-Size-and-rRNA-Pool-in-Caenorhabditis-pgen.1005580.s008.ogv 4.0 s, 56 × 100; 33 KB
A-hybrid-blob-slice-model-for-accurate-and-efficient-detection-of-fluorescence-labeled-nuclei-in-3D-1471-2105-11-580-S10.ogv 13 s, 401 × 402; 1.49 MB
A-hybrid-blob-slice-model-for-accurate-and-efficient-detection-of-fluorescence-labeled-nuclei-in-3D-1471-2105-11-580-S12.ogv 20 s, 512 × 768; 4.88 MB
A-Novel-Sperm-Delivered-Toxin-Causes-Late-Stage-Embryo-Lethality-and-Transmission-Ratio-Distortion-pbio.1001115.s010.ogv 6.4 s, 566 × 502; 2.01 MB
A-Novel-Sperm-Delivered-Toxin-Causes-Late-Stage-Embryo-Lethality-and-Transmission-Ratio-Distortion-pbio.1001115.s011.ogv 6.5 s, 566 × 502; 2.03 MB
Acute-Drug-Treatment-in-the-Early-C.-elegans-Embryo-pone.0024656.s004.ogv 5.6 s, 640 × 208; 21 KB
Acute-Drug-Treatment-in-the-Early-C.-elegans-Embryo-pone.0024656.s005.ogv 2.2 s, 350 × 210; 14 KB
Acute-Drug-Treatment-in-the-Early-C.-elegans-Embryo-pone.0024656.s006.ogv 7.2 s, 350 × 210; 17 KB
Acute-Drug-Treatment-in-the-Early-C.-elegans-Embryo-pone.0024656.s007.ogv 7.6 s, 640 × 202; 50 KB
Acute-Drug-Treatment-in-the-Early-C.-elegans-Embryo-pone.0024656.s008.ogv 0.7 s, 640 × 208; 17 KB
Acute-Drug-Treatment-in-the-Early-C.-elegans-Embryo-pone.0024656.s009.ogv 1.2 s, 640 × 208; 17 KB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s10.ogv 23 s, 319 × 277; 1,014 KB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s11.ogv 19 s, 952 × 404; 805 KB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s12.ogv 11 s, 1,211 × 895; 1.83 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s13.ogv 5.5 s, 1,224 × 649; 1.17 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s2.ogv 3.6 s, 394 × 360; 1.78 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s3.ogv 42 s, 756 × 900; 4.82 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s4.ogv 17 s, 871 × 992; 7.5 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s5.ogv 29 s, 1,344 × 1,024; 51.2 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s6.ogv 1 min 2 s, 658 × 524; 31.81 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s7.ogv 40 s, 2,100 × 1,361; 12.4 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s8.ogv 14 s, 1,406 × 608; 5.38 MB
An-automated-microfluidic-platform-for-C.-elegans-embryo-arraying-phenotypingand-long-term-live-srep10192-s9.ogv 11 s, 375 × 319; 685 KB
Asymmetry-of-Early-Endosome-Distribution-in-C.-elegans-Embryos-pone.0000493.s001.ogv 7.0 s, 548 × 198; 3.11 MB
ATX-2-the-C.-elegans-Ortholog-of-Human-Ataxin-2-Regulates-Centrosome-Size-and-Microtubule-Dynamics-pgen.1006370.s007.ogv 8.0 s, 834 × 294; 421 KB
ATX-2-the-C.-elegans-Ortholog-of-Human-Ataxin-2-Regulates-Centrosome-Size-and-Microtubule-Dynamics-pgen.1006370.s008.ogv 12 s, 916 × 298; 744 KB
ATX-2-the-C.-elegans-Ortholog-of-Human-Ataxin-2-Regulates-Centrosome-Size-and-Microtubule-Dynamics-pgen.1006370.s009.ogv 3.0 s, 834 × 294; 184 KB
ATX-2-the-C.-elegans-Ortholog-of-Human-Ataxin-2-Regulates-Centrosome-Size-and-Microtubule-Dynamics-pgen.1006370.s011.ogv 1.0 s, 360 × 260; 36 KB
ATX-2-the-C.-elegans-Ortholog-of-Human-Ataxin-2-Regulates-Centrosome-Size-and-Microtubule-Dynamics-pgen.1006370.s012.ogv 5.0 s, 900 × 311; 620 KB
ATX-2-the-C.-elegans-Ortholog-of-Human-Ataxin-2-Regulates-Centrosome-Size-and-Microtubule-Dynamics-pgen.1006370.s013.ogv 3.0 s, 880 × 299; 276 KB
Bayesian-Inference-of-Forces-Causing-Cytoplasmic-Streaming-in-Caenorhabditis-elegans-Embryos-and-pone.0159917.s006.ogv 21 s, 368 × 196; 712 KB
Bayesian-Inference-of-Forces-Causing-Cytoplasmic-Streaming-in-Caenorhabditis-elegans-Embryos-and-pone.0159917.s007.ogv 14 s, 514 × 504; 3.29 MB
Bayesian-Inference-of-Forces-Causing-Cytoplasmic-Streaming-in-Caenorhabditis-elegans-Embryos-and-pone.0159917.s008.ogv 5.1 s, 350 × 246; 950 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s009.ogv 23 s, 396 × 310; 249 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s010.ogv 31 s, 338 × 360; 430 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s011.ogv 25 s, 444 × 368; 88 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s012.ogv 23 s, 392 × 344; 88 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s013.ogv 14 s, 320 × 268; 66 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s014.ogv 26 s, 300 × 270; 96 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s015.ogv 23 s, 230 × 236; 113 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s016.ogv 36 s, 334 × 196; 124 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s017.ogv 14 s, 562 × 466; 139 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s018.ogv 21 s, 332 × 230; 43 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s019.ogv 30 s, 286 × 266; 99 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s020.ogv 17 s, 230 × 246; 45 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s021.ogv 16 s, 336 × 238; 59 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s022.ogv 9.5 s, 298 × 214; 16 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s023.ogv 9.5 s, 298 × 200; 26 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s024.ogv 8.0 s, 338 × 220; 18 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s025.ogv 8.0 s, 338 × 198; 22 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s026.ogv 9.5 s, 262 × 234; 15 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s027.ogv 9.5 s, 262 × 234; 18 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s028.ogv 11 s, 264 × 270; 58 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s029.ogv 11 s, 264 × 270; 55 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s030.ogv 13 s, 292 × 198; 77 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s031.ogv 13 s, 292 × 198; 93 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s032.ogv 5.5 s, 284 × 234; 55 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s033.ogv 5.5 s, 284 × 234; 57 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s034.ogv 16 s, 280 × 212; 83 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s035.ogv 16 s, 280 × 192; 88 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s036.ogv 17 s, 354 × 262; 72 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s037.ogv 17 s, 354 × 250; 69 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s038.ogv 9.5 s, 360 × 232; 38 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s039.ogv 9.0 s, 408 × 244; 24 KB
Caenorhabditis-elegans-Cyclin-B3-Is-Required-for-Multiple-Mitotic-Processes-Including-Alleviation-pgen.1001218.s040.ogv 7.5 s, 318 × 310; 87 KB
Caenorhabditis-elegans-Myotubularin-MTM-1-Negatively-Regulates-the-Engulfment-of-Apoptotic-Cells-pgen.1000679.s010.ogv 5.0 s, 356 × 252; 41 KB
Caenorhabditis-elegans-Myotubularin-MTM-1-Negatively-Regulates-the-Engulfment-of-Apoptotic-Cells-pgen.1000679.s011.ogv 9.0 s, 348 × 236; 34 KB
Caenorhabditis-elegans-Myotubularin-MTM-1-Negatively-Regulates-the-Engulfment-of-Apoptotic-Cells-pgen.1000679.s012.ogv 18 s, 352 × 220; 81 KB
Caenorhabditis-elegans-Myotubularin-MTM-1-Negatively-Regulates-the-Engulfment-of-Apoptotic-Cells-pgen.1000679.s013.ogv 7.0 s, 360 × 264; 65 KB
Caspase-Dependent-Programmed-Cell-Death-in-Developing-Embryos-A-Potential-Target-for-Therapeutic-pntd.0001306.s004.ogv 30 s, 320 × 240; 5.71 MB
Caspase-Dependent-Programmed-Cell-Death-in-Developing-Embryos-A-Potential-Target-for-Therapeutic-pntd.0001306.s005.ogv 31 s, 320 × 240; 3.17 MB
Caspase-Dependent-Programmed-Cell-Death-in-Developing-Embryos-A-Potential-Target-for-Therapeutic-pntd.0001306.s006.ogv 13 s, 320 × 240; 486 KB
Cell-Interactions-and-Patterned-Intercalations-Shape-and-Link-Epithelial-Tubes-in-C.-elegans-pgen.1003772.s010.ogv 13 s, 364 × 536; 248 KB
Cell-to-Cell-Heterogeneity-in-Cortical-Tension-Specifies-Curvature-of-Contact-Surfaces-in-pone.0030224.s002.ogv 5.0 s, 510 × 306; 1.87 MB
Cell-to-Cell-Heterogeneity-in-Cortical-Tension-Specifies-Curvature-of-Contact-Surfaces-in-pone.0030224.s003.ogv 5.0 s, 488 × 308; 1.28 MB
Characterization-of-sub-nuclear-changes-in-Caenorhabditis-elegans-embryos-exposed-to-brief-1471-2121-6-47-S1.ogv 14 s, 192 × 256; 64 KB
Characterization-of-sub-nuclear-changes-in-Caenorhabditis-elegans-embryos-exposed-to-brief-1471-2121-6-47-S2.ogv 39 s, 352 × 396; 213 KB
Characterization-of-sub-nuclear-changes-in-Caenorhabditis-elegans-embryos-exposed-to-brief-1471-2121-6-47-S3.ogv 19 s, 192 × 192; 25 KB
Confocal microscopy of normal mitosis and anaphase bridging in Caenorhabditis elegans - 1747-1028-3-6-S2.ogv 29 s, 520 × 561; 1.4 MB
Developmental-Characterization-of-the-MicroRNA-Specific-C.-elegans-Argonautes-alg-1-and-alg-2-pone.0033750.s005.ogv 2 min 0 s, 470 × 352; 2.26 MB
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
Dynein-Modifiers-in-C.-elegans-Light-Chains-Suppress-Conditional-Heavy-Chain-Mutants-pgen.0030128.sv001.ogv 11 s, 312 × 168; 401 KB
Dynein-Modifiers-in-C.-elegans-Light-Chains-Suppress-Conditional-Heavy-Chain-Mutants-pgen.0030128.sv005.ogv 12 s, 300 × 102; 275 KB
Dynein-Modifiers-in-C.-elegans-Light-Chains-Suppress-Conditional-Heavy-Chain-Mutants-pgen.0030128.sv009.ogv 7.3 s, 312 × 106; 59 KB
Dynein-Modifiers-in-C.-elegans-Light-Chains-Suppress-Conditional-Heavy-Chain-Mutants-pgen.0030128.sv010.ogv 5.7 s, 296 × 103; 46 KB
Dynein-Modifiers-in-C.-elegans-Light-Chains-Suppress-Conditional-Heavy-Chain-Mutants-pgen.0030128.sv013.ogv 5.6 s, 284 × 108; 43 KB
Dynein-Modifiers-in-C.-elegans-Light-Chains-Suppress-Conditional-Heavy-Chain-Mutants-pgen.0030128.sv014.ogv 5.0 s, 300 × 98; 33 KB
Epigenetic-Regulation-of-Histone-H3-Serine-10-Phosphorylation-Status-by-HCF-1-Proteins-in-C.-pone.0001213.s003.ogv 1 min 3 s, 348 × 319; 4.96 MB
Epigenetic-Regulation-of-Histone-H3-Serine-10-Phosphorylation-Status-by-HCF-1-Proteins-in-C.-pone.0001213.s004.ogv 1 min 3 s, 412 × 418; 5.95 MB
Epigenetic-Regulation-of-Histone-H3-Serine-10-Phosphorylation-Status-by-HCF-1-Proteins-in-C.-pone.0001213.s005.ogv 1 min 38 s, 344 × 206; 8.25 MB
Filamin-and-Phospholipase-C--Are-Required-for-Calcium-Signaling-in-the-Caenorhabditis-elegans-pgen.1003510.s007.ogv 50 s, 400 × 200; 750 KB
Filamin-and-Phospholipase-C--Are-Required-for-Calcium-Signaling-in-the-Caenorhabditis-elegans-pgen.1003510.s008.ogv 36 s, 400 × 200; 373 KB
Filamin-and-Phospholipase-C--Are-Required-for-Calcium-Signaling-in-the-Caenorhabditis-elegans-pgen.1003510.s009.ogv 1 min 35 s, 400 × 200; 1.06 MB
Filamin-and-Phospholipase-C--Are-Required-for-Calcium-Signaling-in-the-Caenorhabditis-elegans-pgen.1003510.s012.ogv 1 min 40 s, 400 × 200; 881 KB
Filamin-and-Phospholipase-C--Are-Required-for-Calcium-Signaling-in-the-Caenorhabditis-elegans-pgen.1003510.s015.ogv 54 s, 400 × 200; 3.29 MB
Functional-Dissection-of-Caenorhabditis-elegans-CLK-2TEL2-Cell-Cycle-Defects-during-Embryogenesis-pgen.1000451.s008.ogv 20 s, 320 × 240; 586 KB
Functional-Dissection-of-Caenorhabditis-elegans-CLK-2TEL2-Cell-Cycle-Defects-during-Embryogenesis-pgen.1000451.s009.ogv 20 s, 320 × 240; 541 KB
Functional-Dissection-of-Caenorhabditis-elegans-CLK-2TEL2-Cell-Cycle-Defects-during-Embryogenesis-pgen.1000451.s010.ogv 20 s, 240 × 300; 727 KB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s10.ogv 14 s, 992 × 608; 3.06 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s11.ogv 9.9 s, 1,776 × 800; 6.58 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s12.ogv 6.2 s, 1,776 × 600; 3.26 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s13.ogv 52 s, 1,080 × 720; 19.07 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s2.ogv 7.3 s, 576 × 576; 681 KB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s4.ogv 1 min 20 s, 1,200 × 752; 33.45 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s5.ogv 1 min 20 s, 1,200 × 752; 31.71 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s6.ogv 30 s, 1,344 × 688; 12.54 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s7.ogv 20 s, 1,344 × 688; 6.55 MB
Imaging-multicellular-specimens-with-real-time-optimized-tiling-light-sheet-selective-plane-ncomms11088-s9.ogv 12 s, 1,200 × 800; 9.64 MB
Late embryonic development in Caenorhabditis elegans - pbio.1001115.s012.ogv 6.3 s, 516 × 486; 1.19 MB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s001.ogv 8.1 s, 253 × 175; 456 KB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s002.ogv 21 s, 244 × 185; 2.5 MB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s003.ogv 14 s, 250 × 175; 1.76 MB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s004.ogv 17 s, 231 × 178; 1.27 MB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s005.ogv 7.0 s, 242 × 172; 425 KB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s006.ogv 9.1 s, 238 × 174; 157 KB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s007.ogv 11 s, 284 × 202; 1.84 MB
Long-Astral-Microtubules-and-RACK-1-Stabilize-Polarity-Domains-during-Maintenance-Phase-in-pone.0019020.s008.ogv 17 s, 284 × 202; 3.38 MB
Membrane-Invaginations-Reveal-Cortical-Sites-that-Pull-on-Mitotic-Spindles-in-One-Cell-C.-elegans-pone.0012301.s008.ogv 3.7 s, 336 × 258; 80 KB
Membrane-Invaginations-Reveal-Cortical-Sites-that-Pull-on-Mitotic-Spindles-in-One-Cell-C.-elegans-pone.0012301.s009.ogv 12 s, 254 × 210; 455 KB
Membrane-Invaginations-Reveal-Cortical-Sites-that-Pull-on-Mitotic-Spindles-in-One-Cell-C.-elegans-pone.0012301.s010.ogv 8.4 s, 300 × 200; 340 KB
Morphogenesis-of-the-C.-elegans-Intestine-Involves-Axon-Guidance-Genes-pgen.1005950.s005.ogv 36 s, 432 × 618; 812 KB
Morphogenesis-of-the-C.-elegans-Intestine-Involves-Axon-Guidance-Genes-pgen.1005950.s008.ogv 9.5 s, 480 × 351; 114 KB
Multi-Environment-Model-Estimation-for-Motility-Analysis-of-Caenorhabditis-elegans-pone.0011631.s009.ogv 1 min 20 s, 1,080 × 640; 3.77 MB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s017.ogv 9.8 s, 512 × 512; 2.21 MB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s019.ogv 9.0 s, 448 × 326; 66 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s020.ogv 9.0 s, 448 × 326; 632 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s022.ogv 8.3 s, 448 × 326; 47 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s024.ogv 8.3 s, 448 × 326; 864 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s025.ogv 9.3 s, 448 × 326; 101 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s026.ogv 9.3 s, 448 × 326; 459 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s027.ogv 9.3 s, 448 × 326; 1.14 MB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s028.ogv 5.0 s, 448 × 326; 79 KB
Multisite-Phosphorylation-of-NuMA-Related-LIN-5-Controls-Mitotic-Spindle-Positioning-in-C.-elegans-pgen.1006291.s029.ogv 5.0 s, 448 × 326; 302 KB
Phagocytic-Receptor-CED-1-Initiates-a-Signaling-Pathway-for-Degrading-Engulfed-Apoptotic-Cells-pbio.0060061.sv002.ogv 29 s, 528 × 340; 1.51 MB
Phagocytic-Receptor-CED-1-Initiates-a-Signaling-Pathway-for-Degrading-Engulfed-Apoptotic-Cells-pbio.0060061.sv005.ogv 15 s, 303 × 451; 374 KB
Phagocytic-Receptor-CED-1-Initiates-a-Signaling-Pathway-for-Degrading-Engulfed-Apoptotic-Cells-pbio.0060061.sv006.ogv 14 s, 255 × 403; 330 KB
Phagocytic-Receptor-CED-1-Initiates-a-Signaling-Pathway-for-Degrading-Engulfed-Apoptotic-Cells-pbio.0060061.sv007.ogv 16 s, 302 × 450; 376 KB
Phospholipase-C-ε-Regulates-Epidermal-Morphogenesis-in-Caenorhabditis-elegans-pgen.1000043.s003.ogv 17 s, 568 × 568; 252 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s001.ogv 26 s, 383 × 331; 1.39 MB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s002.ogv 32 s, 347 × 331; 900 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s004.ogv 13 s, 344 × 259; 401 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s005.ogv 17 s, 369 × 273; 295 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s006.ogv 19 s, 356 × 270; 344 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s007.ogv 23 s, 394 × 315; 428 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s008.ogv 18 s, 376 × 265; 735 KB
Profiling-of-the-Mammalian-Mitotic-Spindle-Proteome-Reveals-an-ER-Protein-OSTD-1-as-Being-Necessary-pone.0077051.s009.ogv 21 s, 433 × 316; 733 KB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s005.ogv 20 s, 284 × 176; 702 KB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s006.ogv 20 s, 252 × 168; 676 KB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s007.ogv 5.0 s, 219 × 116; 601 KB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s008.ogv 20 s, 268 × 172; 489 KB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s009.ogv 23 s, 268 × 188; 622 KB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s010.ogv 43 s, 248 × 140; 1.16 MB
RAB-5-Controls-the-Cortical-Organization-and-Dynamics-of-PAR-Proteins-to-Maintain-C.-elegans-Early-pone.0035286.s011.ogv 30 s, 280 × 172; 1.51 MB
RHGF-2-Is-an-Essential-Rho-1-Specific-RhoGEF-that-binds-to-the-Multi-PDZ-Domain-Scaffold-Protein-pone.0031499.s002.ogv 13 s, 320 × 240; 471 KB
Small-Molecule-Injection-into-Single-Cell-C.-elegans-Embryos-via-Carbon-Reinforced-Nanopipettes-pone.0075712.s002.ogv 33 s, 400 × 236; 256 KB
The-AP-2-Transcription-Factor-APTF-2-Is-Required-for-Neuroblast-and-Epidermal-Morphogenesis-in-pgen.1006048.s025.ogv 45 s, 462 × 233; 6.41 MB
The-AP-2-Transcription-Factor-APTF-2-Is-Required-for-Neuroblast-and-Epidermal-Morphogenesis-in-pgen.1006048.s026.ogv 9.7 s, 400 × 135; 1,021 KB
The-AP-2-Transcription-Factor-APTF-2-Is-Required-for-Neuroblast-and-Epidermal-Morphogenesis-in-pgen.1006048.s028.ogv 9.7 s, 205 × 139; 303 KB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s003.ogv 9.0 s, 320 × 240; 462 KB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s004.ogv 2.5 s, 208 × 320; 33 KB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s005.ogv 2.5 s, 213 × 320; 59 KB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s006.ogv 3.0 s, 350 × 216; 151 KB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s007.ogv 15 s, 320 × 192; 1.16 MB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s008.ogv 17 s, 320 × 201; 1.54 MB
The-EFF-1A-Cytoplasmic-Domain-Influences-Hypodermal-Cell-Fusions-in-C.-elegans-But-Is-Not-Dependent-pone.0146874.s009.ogv 32 s, 320 × 305; 3.19 MB
The-Role-of-γ-Tubulin-in-Centrosomal-Microtubule-Organization-pone.0029795.s003.ogv 12 s, 475 × 449; 8.31 MB
The-Role-of-γ-Tubulin-in-Centrosomal-Microtubule-Organization-pone.0029795.s004.ogv 12 s, 455 × 439; 8.86 MB
The-Role-of-γ-Tubulin-in-Centrosomal-Microtubule-Organization-pone.0029795.s005.ogv 8.7 s, 728 × 268; 4.74 MB
The-Role-of-γ-Tubulin-in-Centrosomal-Microtubule-Organization-pone.0029795.s006.ogv 12 s, 924 × 280; 4.83 MB
The-Role-of-γ-Tubulin-in-Centrosomal-Microtubule-Organization-pone.0029795.s007.ogv 12 s, 439 × 448; 5.97 MB
Virtual-finger-boosts-three-dimensional-imaging-and-microsurgery-as-well-as-terabyte-volume-image-ncomms5342-s3.ogv 1 min 4 s, 654 × 660; 3.07 MB