Category:Chromosome segregation

Media in category "Chromosome segregation"

The following 200 files are in this category, out of 204 total.

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A-phenanthrene-derived-PARP-inhibitor-is-an-extra-centrosomes-de-clustering-agent-exclusively-1471-2407-11-412-S1.ogv 16 s, 428 × 428; 975 KB
A-phenanthrene-derived-PARP-inhibitor-is-an-extra-centrosomes-de-clustering-agent-exclusively-1471-2407-11-412-S2.ogv 2 min 10 s, 512 × 512; 1.38 MB
Alternative-meiotic-chromatid-segregation-in-the-holocentric-plant-Luzula-elegans-ncomms5979-s2.ogv 7.6 s, 1,796 × 812; 1.6 MB
An-actin-dependent-spindle-position-checkpoint-ensures-the-asymmetric-division-in-mouse-oocytes-ncomms8784-s2.ogv 3.1 s, 320 × 236; 189 KB
An-actin-dependent-spindle-position-checkpoint-ensures-the-asymmetric-division-in-mouse-oocytes-ncomms8784-s3.ogv 18 s, 576 × 594; 697 KB
An-actin-dependent-spindle-position-checkpoint-ensures-the-asymmetric-division-in-mouse-oocytes-ncomms8784-s4.ogv 10 s, 1,024 × 1,024; 1.05 MB
An-actin-dependent-spindle-position-checkpoint-ensures-the-asymmetric-division-in-mouse-oocytes-ncomms8784-s5.ogv 2.0 s, 1,920 × 1,080; 76 KB
An-actin-dependent-spindle-position-checkpoint-ensures-the-asymmetric-division-in-mouse-oocytes-ncomms8784-s6.ogv 10 s, 1,920 × 1,080; 808 KB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s2.ogv 19 s, 768 × 768; 7.3 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s3.ogv 18 s, 512 × 512; 1.97 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s4.ogv 12 s, 788 × 784; 3.35 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s5.ogv 22 s, 1,024 × 512; 2.72 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s6.ogv 29 s, 1,024 × 512; 2.82 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s7.ogv 20 s, 688 × 688; 2.59 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s8.ogv 20 s, 688 × 688; 4.01 MB
Bivalent-separation-into-univalents-precedes-age-related-meiosis-I-errors-in-oocytes-ncomms8550-s9.ogv 20 s, 688 × 688; 4.96 MB
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
Cdc20-Is-Critical-for-Meiosis-I-and-Fertility-of-Female-Mice-pgen.1001147.s004.ogv 22 s, 1,404 × 700; 527 KB
Cdc20-Is-Critical-for-Meiosis-I-and-Fertility-of-Female-Mice-pgen.1001147.s005.ogv 24 s, 1,404 × 700; 616 KB
Cep57-is-a-Mis12-interacting-kinetochore-protein-involved-in-kinetochore-targeting-of-Mad1–Mad2-ncomms10151-s2.ogv 8.2 s, 852 × 532; 102 KB
Cep57-is-a-Mis12-interacting-kinetochore-protein-involved-in-kinetochore-targeting-of-Mad1–Mad2-ncomms10151-s3.ogv 1.8 s, 852 × 532; 93 KB
Chiasmatic-and-achiasmatic-inverted-meiosis-of-plants-with-holocentric-chromosomes-ncomms6070-s2.ogv 5.5 s, 312 × 280; 76 KB
Chiasmatic-and-achiasmatic-inverted-meiosis-of-plants-with-holocentric-chromosomes-ncomms6070-s3.ogv 5.5 s, 280 × 280; 37 KB
Chiasmatic-and-achiasmatic-inverted-meiosis-of-plants-with-holocentric-chromosomes-ncomms6070-s4.ogv 18 s, 350 × 280; 89 KB
Chiasmatic-and-achiasmatic-inverted-meiosis-of-plants-with-holocentric-chromosomes-ncomms6070-s5.ogv 6.0 s, 350 × 400; 66 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s2.ogv 9.0 s, 248 × 248; 25 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s3.ogv 9.0 s, 240 × 240; 67 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s4.ogv 6.0 s, 300 × 300; 10 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s5.ogv 6.0 s, 210 × 210; 47 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s6.ogv 13 s, 278 × 330; 58 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s7.ogv 5.0 s, 330 × 270; 21 KB
Clks-1-2-and-4-prevent-chromatin-breakage-by-regulating-the-Aurora-B-dependent-abscission-checkpoint-ncomms11451-s8.ogv 6.0 s, 300 × 270; 26 KB
Combinatorial-Regulation-of-Meiotic-Holliday-Junction-Resolution-in-C.-elegans-by-HIM-6-(BLM)-pgen.1003591.s011.ogv 3.0 s, 432 × 400; 225 KB
Combinatorial-Regulation-of-Meiotic-Holliday-Junction-Resolution-in-C.-elegans-by-HIM-6-(BLM)-pgen.1003591.s013.ogv 6.7 s, 336 × 352; 249 KB
Contribution-of-Noncentrosomal-Microtubules-to-Spindle-Assembly-in-Drosophila-Spermatocytes-pbio.0020008.v006.ogv 6.5 s, 396 × 308; 396 KB
Defective-sister-chromatid-cohesion-is-synthetically-lethal-with-impaired-APCC-function-ncomms9399-s4.ogv 4.0 s, 181 × 196; 29 KB
Defective-sister-chromatid-cohesion-is-synthetically-lethal-with-impaired-APCC-function-ncomms9399-s5.ogv 4.0 s, 181 × 196; 101 KB
Defective-sister-chromatid-cohesion-is-synthetically-lethal-with-impaired-APCC-function-ncomms9399-s6.ogv 14 s, 221 × 202; 43 KB
Defective-sister-chromatid-cohesion-is-synthetically-lethal-with-impaired-APCC-function-ncomms9399-s7.ogv 14 s, 223 × 204; 154 KB
Defective-sister-chromatid-cohesion-is-synthetically-lethal-with-impaired-APCC-function-ncomms9399-s8.ogv 1 min 32 s, 204 × 205; 1.6 MB
Defective-sister-chromatid-cohesion-is-synthetically-lethal-with-impaired-APCC-function-ncomms9399-s9.ogv 1 min 32 s, 204 × 205; 3.3 MB
Drosophila-Xpd-Regulates-Cdk7-Localization-Mitotic-Kinase-Activity-Spindle-Dynamics-and-Chromosome-pgen.1000876.s003.ogv 19 s, 897 × 897; 11.11 MB
Drosophila-Xpd-Regulates-Cdk7-Localization-Mitotic-Kinase-Activity-Spindle-Dynamics-and-Chromosome-pgen.1000876.s004.ogv 34 s, 897 × 897; 10.35 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S11.ogv 19 s, 320 × 320; 2.31 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S2.ogv 25 s, 384 × 384; 3.44 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S3.ogv 26 s, 340 × 384; 4.65 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S4.ogv 27 s, 680 × 512; 3.05 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S5.ogv 26 s, 448 × 506; 5.45 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S6.ogv 26 s, 448 × 506; 4.15 MB
Drug-induced-cell-cycle-modulation-leading-to-cell-cycle-arrest-nuclear-mis-segregation-or-1471-2121-12-2-S9.ogv 13 s, 280 × 280; 991 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv001.ogv 19 s, 788 × 271; 167 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv002.ogv 14 s, 552 × 277; 469 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv003.ogv 14 s, 608 × 205; 219 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv004.ogv 6.7 s, 1,056 × 312; 119 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv005.ogv 9.7 s, 732 × 258; 191 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv006.ogv 4.0 s, 1,020 × 451; 175 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv007.ogv 5.2 s, 676 × 214; 230 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv008.ogv 7.7 s, 740 × 246; 1.09 MB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv009.ogv 21 s, 696 × 210; 1.48 MB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv010.ogv 17 s, 852 × 249; 611 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv011.ogv 14 s, 752 × 204; 128 KB
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv012.ogv 9.3 s, 596 × 345; 630 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
Genetic-dosage-and-position-effect-of-small-supernumerary-marker-chromosome-(sSMC)-in-human-sperm-srep17408-s2.ogv 8.4 s, 240 × 240; 695 KB
Genetic-dosage-and-position-effect-of-small-supernumerary-marker-chromosome-(sSMC)-in-human-sperm-srep17408-s3.ogv 33 s, 320 × 240; 245 KB
Genetic-Variation-for-Cardiac-Dysfunction-in-Drosophila-pone.0000601.s004.ogv 30 s, 320 × 240; 1.27 MB
Genetic-Variation-for-Cardiac-Dysfunction-in-Drosophila-pone.0000601.s005.ogv 10 s, 320 × 240; 609 KB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s004.ogv 8.4 s, 1,090 × 812; 5.45 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s005.ogv 13 s, 1,118 × 832; 3.15 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s006.ogv 13 s, 1,118 × 832; 4.3 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s007.ogv 13 s, 1,238 × 922; 15.67 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s008.ogv 5.3 s, 1,126 × 838; 1.39 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s009.ogv 5.3 s, 1,126 × 838; 1.13 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s010.ogv 5.9 s, 1,118 × 832; 5.15 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s011.ogv 2.1 s, 1,090 × 812; 1.58 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s012.ogv 2.1 s, 1,090 × 812; 2.06 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s013.ogv 11 s, 1,226 × 914; 3.24 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s014.ogv 1.6 s, 1,094 × 816; 1.08 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s015.ogv 1.6 s, 1,094 × 816; 1.46 MB
Heterochromatic-Threads-Connect-Oscillating-Chromosomes-during-Prometaphase-I-in-Drosophila-Oocytes-pgen.1000348.s016.ogv 9.3 s, 1,090 × 812; 3.49 MB
Identification-of-a-TPX2-Like-Microtubule-Associated-Protein-in-Drosophila-pone.0028120.s001.ogv 12 s, 842 × 480; 5.5 MB
Identification-of-a-TPX2-Like-Microtubule-Associated-Protein-in-Drosophila-pone.0028120.s002.ogv 13 s, 644 × 750; 1.25 MB
Inter-Cellular-Variation-in-DNA-Content-of-Entamoeba-histolytica-Originates-from-Temporal-and-pntd.0000409.s003.ogv 57 s, 555 × 164; 582 KB
Inter-Cellular-Variation-in-DNA-Content-of-Entamoeba-histolytica-Originates-from-Temporal-and-pntd.0000409.s004.ogv 7.0 s, 280 × 338; 135 KB
Inter-Cellular-Variation-in-DNA-Content-of-Entamoeba-histolytica-Originates-from-Temporal-and-pntd.0000409.s005.ogv 1 min 12 s, 599 × 374; 1.66 MB
Kinetochore-Independent-Chromosome-Poleward-Movement-during-Anaphase-of-Meiosis-II-in-Mouse-Eggs-pone.0005249.s002.ogv 10 s, 512 × 512; 1.1 MB
Kinetochore-Independent-Chromosome-Poleward-Movement-during-Anaphase-of-Meiosis-II-in-Mouse-Eggs-pone.0005249.s003.ogv 19 s, 512 × 512; 484 KB
Loss-of-Function-of-the-Cik1Kar3-Motor-Complex-Results-in-Chromosomes-with-Syntelic-Attachment-That-pgen.1002492.s005.ogv 6.8 s, 518 × 514; 336 KB
Loss-of-Maternal-ATRX-Results-in-Centromere-Instability-and-Aneuploidy-in-the-Mammalian-Oocyte-and-pgen.1001137.s004.ogv 5.3 s, 95 × 107; 14 KB
Loss-of-Maternal-ATRX-Results-in-Centromere-Instability-and-Aneuploidy-in-the-Mammalian-Oocyte-and-pgen.1001137.s005.ogv 5.3 s, 91 × 105; 15 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv001.ogv 4.1 s, 350 × 350; 123 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv002.ogv 4.1 s, 400 × 400; 184 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv003.ogv 4.1 s, 350 × 350; 148 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv004.ogv 4.1 s, 213 × 243; 46 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv005.ogv 24 s, 250 × 250; 502 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv006.ogv 4.1 s, 350 × 350; 113 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv007.ogv 3.1 s, 350 × 350; 65 KB
Meiotic-Pairing-and-Segregation-of-Achiasmate-Sex-Chromosomes-in-Eutherian-Mammals-The-Role-of-pgen.0030198.sv008.ogv 4.1 s, 350 × 350; 84 KB
Mitotic-Spindle-Disruption-by-Alternating-Electric-Fields-Leads-to-Improper-Chromosome-Segregation-srep18046-s2.ogv 23 s, 300 × 300; 409 KB
Mitotic-Spindle-Disruption-by-Alternating-Electric-Fields-Leads-to-Improper-Chromosome-Segregation-srep18046-s3.ogv 36 s, 300 × 300; 517 KB
Molecular-requirements-for-the-inter-subunit-interaction-and-kinetochore-recruitment-of-SKAP-and-ncomms11407-s4.ogv 3.3 s, 246 × 227; 36 KB
Molecular-requirements-for-the-inter-subunit-interaction-and-kinetochore-recruitment-of-SKAP-and-ncomms11407-s5.ogv 3.3 s, 239 × 228; 41 KB
Molecular-requirements-for-the-inter-subunit-interaction-and-kinetochore-recruitment-of-SKAP-and-ncomms11407-s6.ogv 3.3 s, 262 × 260; 200 KB
Molecular-requirements-for-the-inter-subunit-interaction-and-kinetochore-recruitment-of-SKAP-and-ncomms11407-s7.ogv 3.3 s, 249 × 236; 151 KB
Molecular-requirements-for-the-inter-subunit-interaction-and-kinetochore-recruitment-of-SKAP-and-ncomms11407-s8.ogv 3.3 s, 243 × 230; 124 KB
Non-SMC-condensin-I-complex-proteins-control-chromosome-segregation-and-survival-of-proliferating-1471-213X-9-40-S3.ogv 7.5 s, 640 × 480; 164 KB
Non-SMC-condensin-I-complex-proteins-control-chromosome-segregation-and-survival-of-proliferating-1471-213X-9-40-S4.ogv 5.1 s, 220 × 256; 256 KB
Non-SMC-condensin-I-complex-proteins-control-chromosome-segregation-and-survival-of-proliferating-1471-213X-9-40-S5.ogv 5.1 s, 220 × 257; 135 KB
Non-SMC-condensin-I-complex-proteins-control-chromosome-segregation-and-survival-of-proliferating-1471-213X-9-40-S6.ogv 7.1 s, 316 × 330; 1.92 MB
PIASγ-Is-Required-for-Faithful-Chromosome-Segregation-in-Human-Cells-pone.0000053.s005.ogv 1 min 17 s, 341 × 401; 1.03 MB
PIASγ-Is-Required-for-Faithful-Chromosome-Segregation-in-Human-Cells-pone.0000053.s006.ogv 1 min 40 s, 694 × 520; 2.97 MB
PIASγ-Is-Required-for-Faithful-Chromosome-Segregation-in-Human-Cells-pone.0000053.s007.ogv 1 min 17 s, 372 × 465; 1.41 MB
PIASγ-Is-Required-for-Faithful-Chromosome-Segregation-in-Human-Cells-pone.0000053.s008.ogv 1 min 39 s, 694 × 520; 5.07 MB
PICH-promotes-sister-chromatid-disjunction-and-co-operates-with-topoisomerase-II-in-mitosis-ncomms9962-s2.ogv 13 s, 300 × 200; 98 KB
PICH-promotes-sister-chromatid-disjunction-and-co-operates-with-topoisomerase-II-in-mitosis-ncomms9962-s3.ogv 4.0 s, 200 × 200; 76 KB
PICH-promotes-sister-chromatid-disjunction-and-co-operates-with-topoisomerase-II-in-mitosis-ncomms9962-s4.ogv 12 s, 512 × 512; 326 KB
Ribonuclease-Activity-of-Dis3-Is-Required-for-Mitotic-Progression-and-Provides-a-Possible-Link-pone.0000317.s002.ogv 41 s, 180 × 100; 350 KB
Ribonuclease-Activity-of-Dis3-Is-Required-for-Mitotic-Progression-and-Provides-a-Possible-Link-pone.0000317.s003.ogv 40 s, 180 × 100; 397 KB
Ribonuclease-Activity-of-Dis3-Is-Required-for-Mitotic-Progression-and-Provides-a-Possible-Link-pone.0000317.s004.ogv 14 s, 180 × 100; 130 KB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s012.ogv 13 s, 1,648 × 880; 8.17 MB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s013.ogv 11 s, 1,648 × 880; 7.24 MB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s014.ogv 5.7 s, 1,648 × 880; 961 KB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s015.ogv 5.7 s, 1,648 × 880; 2.31 MB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s016.ogv 8.9 s, 1,648 × 880; 659 KB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s017.ogv 8.9 s, 1,648 × 880; 1.49 MB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s018.ogv 6.8 s, 1,648 × 880; 2.38 MB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s019.ogv 10 s, 1,648 × 880; 2.39 MB
Separase-Is-Required-for-Homolog-and-Sister-Disjunction-during-Drosophila-melanogaster-Male-Meiosis-pgen.1005996.s020.ogv 6.8 s, 1,648 × 880; 2.36 MB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v001.ogv 11 s, 1,024 × 768; 359 KB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v002.ogv 19 s, 1,024 × 768; 276 KB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v003.ogv 13 s, 1,024 × 768; 710 KB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v004.ogv 13 s, 1,024 × 768; 404 KB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v005.ogv 22 s, 1,024 × 768; 1.12 MB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v006.ogv 22 s, 1,024 × 768; 1,012 KB
Sgol2-provides-a-regulatory-platform-that-coordinates-essential-cell-cycle-processes-during-meiosis-elife01133v007.ogv 6.6 s, 1,024 × 768; 684 KB
Spindle-assembly-checkpoint-inactivation-fails-to-suppress-neuroblast-tumour-formation-in-aurA-ncomms9879-s2.ogv 1.9 s, 420 × 139; 770 KB
Spindle-assembly-checkpoint-inactivation-fails-to-suppress-neuroblast-tumour-formation-in-aurA-ncomms9879-s3.ogv 3.4 s, 420 × 140; 1.35 MB
Spindle-assembly-checkpoint-inactivation-fails-to-suppress-neuroblast-tumour-formation-in-aurA-ncomms9879-s4.ogv 1.6 s, 279 × 93; 301 KB
Spindle-assembly-checkpoint-inactivation-fails-to-suppress-neuroblast-tumour-formation-in-aurA-ncomms9879-s5.ogv 4.1 s, 279 × 93; 637 KB
Spindle-assembly-checkpoint-inactivation-fails-to-suppress-neuroblast-tumour-formation-in-aurA-ncomms9879-s6.ogv 5.0 s, 279 × 93; 884 KB
Spindle-assembly-checkpoint-inactivation-fails-to-suppress-neuroblast-tumour-formation-in-aurA-ncomms9879-s7.ogv 10 s, 279 × 93; 1.75 MB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s10.ogv 1.9 s, 706 × 633; 698 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s11.ogv 4.4 s, 518 × 514; 293 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s12.ogv 2.8 s, 518 × 514; 162 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s2.ogv 5.0 s, 518 × 514; 366 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s3.ogv 7.4 s, 518 × 514; 243 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s4.ogv 4.9 s, 518 × 514; 329 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s5.ogv 5.3 s, 758 × 743; 595 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s6.ogv 5.7 s, 518 × 514; 642 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s7.ogv 2.4 s, 518 × 514; 264 KB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s8.ogv 9.3 s, 780 × 718; 2.01 MB
Stable-kinetochore–microtubule-attachment-is-sufficient-to-silence-the-spindle-assembly-checkpoint-ncomms10036-s9.ogv 6.5 s, 762 × 643; 1.34 MB
Stretching-the-Rules-Monocentric-Chromosomes-with-Multiple-Centromere-Domains-pgen.1002777.s005.ogv 18 s, 921 × 494; 5.33 MB
Stretching-the-Rules-Monocentric-Chromosomes-with-Multiple-Centromere-Domains-pgen.1002777.s006.ogv 6.7 s, 1,152 × 912; 6.93 MB
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-Cellular-Phenotype-of-Roberts-Syndrome-Fibroblasts-as-Revealed-by-Ectopic-Expression-of-ESCO2-pone.0006936.s001.ogv 12 s, 1,392 × 1,040; 4.42 MB
The-Cellular-Phenotype-of-Roberts-Syndrome-Fibroblasts-as-Revealed-by-Ectopic-Expression-of-ESCO2-pone.0006936.s002.ogv 21 s, 720 × 480; 660 KB
The-Chromosomal-Passenger-Complex-and-a-Mitotic-Kinesin-Interact-with-the-Tousled-Like-Kinase-in-pone.0003814.s001.ogv 45 s, 904 × 381; 601 KB
The-Inhibition-of-Polo-Kinase-by-Matrimony-Maintains-G2-Arrest-in-the-Meiotic-Cell-Cycle-pbio.0050323.sv001.ogv 37 s, 512 × 512; 841 KB
The-Inhibition-of-Polo-Kinase-by-Matrimony-Maintains-G2-Arrest-in-the-Meiotic-Cell-Cycle-pbio.0050323.sv002.ogv 47 s, 512 × 512; 887 KB
The-Inhibition-of-Polo-Kinase-by-Matrimony-Maintains-G2-Arrest-in-the-Meiotic-Cell-Cycle-pbio.0050323.sv003.ogv 48 s, 512 × 512; 247 KB
The-Metabolic-Enzyme-ManA-Reveals-a-Link-between-Cell-Wall-Integrity-and-Chromosome-Morphology-pgen.1001119.s011.ogv 3.8 s, 640 × 480; 305 KB
The-Metabolic-Enzyme-ManA-Reveals-a-Link-between-Cell-Wall-Integrity-and-Chromosome-Morphology-pgen.1001119.s012.ogv 3.8 s, 640 × 480; 124 KB
When-the-Genome-Plays-Dice-Circumvention-of-the-Spindle-Assembly-Checkpoint-and-Near-Random-pone.0001871.s001.ogv 33 s, 519 × 512; 686 KB
When-the-Genome-Plays-Dice-Circumvention-of-the-Spindle-Assembly-Checkpoint-and-Near-Random-pone.0001871.s002.ogv 15 s, 519 × 512; 644 KB

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