Category:Videos of nuclear proteins

Subcategories

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

V

Videos of DNA-binding proteins‎ (2 C, 7 F)
Videos of histones‎ (60 F)
Videos of polycomb-group proteins‎ (11 F)

Media in category "Videos of nuclear proteins"

The following 157 files are in this category, out of 157 total.

A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s005.ogv 36 s, 900 × 900; 127 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s006.ogv 36 s, 900 × 900; 231 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s007.ogv 21 s, 1,024 × 1,024; 343 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s008.ogv 12 s, 648 × 648; 321 KB
A-Novel-Toxoplasma-gondii-Nuclear-Factor-TgNF3-Is-a-Dynamic-Chromatin-Associated-Component-ppat.1001328.s010.ogv 36 s, 900 × 900; 201 KB
Amplification-of-neural-stem-cell-proliferation-by-intermediate-progenitor-cells-in-Drosophila-1749-8104-3-5-S1.ogv 16 s, 310 × 210; 694 KB
An-epigenetic-regulator-emerges-as-microtubule-minus-end-binding-and-stabilizing-factor-in-mitosis-ncomms8889-s2.ogv 1.9 s, 150 × 150; 111 KB
An-epigenetic-regulator-emerges-as-microtubule-minus-end-binding-and-stabilizing-factor-in-mitosis-ncomms8889-s3.ogv 13 s, 150 × 150; 603 KB
An-epigenetic-regulator-emerges-as-microtubule-minus-end-binding-and-stabilizing-factor-in-mitosis-ncomms8889-s4.ogv 7.8 s, 150 × 150; 697 KB
An-epigenetic-regulator-emerges-as-microtubule-minus-end-binding-and-stabilizing-factor-in-mitosis-ncomms8889-s5.ogv 12 s, 512 × 512; 1.37 MB
An-epigenetic-regulator-emerges-as-microtubule-minus-end-binding-and-stabilizing-factor-in-mitosis-ncomms8889-s6.ogv 12 s, 512 × 512; 1.59 MB
An-epigenetic-regulator-emerges-as-microtubule-minus-end-binding-and-stabilizing-factor-in-mitosis-ncomms8889-s7.ogv 12 s, 512 × 512; 1.1 MB
An-extended-U2AF65–RNA-binding-domain-recognizes-the-3′-splice-site-signal-ncomms10950-s2.ogv 21 s, 740 × 487; 14.09 MB
BIN1-Localizes-the-L-Type-Calcium-Channel-to-Cardiac-T-Tubules-pbio.1000312.s009.ogv 12 s, 84 × 140; 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
Concerted-Action-of-Two-Formins-in-Gliding-Motility-and-Host-Cell-Invasion-by-Toxoplasma-gondii-ppat.1001132.s002.ogv 14 s, 105 × 110; 363 KB
Concerted-Action-of-Two-Formins-in-Gliding-Motility-and-Host-Cell-Invasion-by-Toxoplasma-gondii-ppat.1001132.s003.ogv 14 s, 103 × 85; 315 KB
Concerted-Action-of-Two-Formins-in-Gliding-Motility-and-Host-Cell-Invasion-by-Toxoplasma-gondii-ppat.1001132.s004.ogv 14 s, 83 × 97; 301 KB
Concerted-Action-of-Two-Formins-in-Gliding-Motility-and-Host-Cell-Invasion-by-Toxoplasma-gondii-ppat.1001132.s005.ogv 14 s, 122 × 121; 357 KB
Concerted-Action-of-Two-Formins-in-Gliding-Motility-and-Host-Cell-Invasion-by-Toxoplasma-gondii-ppat.1001132.s006.ogv 14 s, 112 × 114; 183 KB
Continuous-and-Periodic-Expansion-of-CAG-Repeats-in-Huntington's-Disease-R61-Mice-pgen.1001242.s015.ogv 13 s, 1,198 × 898; 988 KB
CtIP-Mutations-Cause-Seckel-and-Jawad-Syndromes-pgen.1002310.s006.ogv 2.8 s, 1,024 × 1,024; 6.31 MB
CtIP-Mutations-Cause-Seckel-and-Jawad-Syndromes-pgen.1002310.s007.ogv 2.8 s, 1,024 × 1,024; 5.76 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s005.ogv 8.2 s, 640 × 480; 13.81 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s006.ogv 7.1 s, 640 × 480; 11.61 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s007.ogv 8.9 s, 480 × 384; 16.28 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s008.ogv 9.0 s, 480 × 384; 20.37 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s009.ogv 13 s, 480 × 384; 18.45 MB
Deficiency-of-Huntingtin-Has-Pleiotropic-Effects-in-the-Social-Amoeba-Dictyostelium-discoideum-pgen.1002052.s010.ogv 12 s, 480 × 384; 19.94 MB
Drosophila-type-II-neuroblast-lineages-keep-Prospero-levels-low-to-generate-large-clones-that-1749-8104-5-26-S2.ogv 10 s, 608 × 480; 2.08 MB
Essential-role-of-the-Cdk2-activator-RingoA-in-meiotic-telomere-tethering-to-the-nuclear-envelope-ncomms11084-s2.ogv 3.1 s, 404 × 367; 94 KB
Essential-role-of-the-Cdk2-activator-RingoA-in-meiotic-telomere-tethering-to-the-nuclear-envelope-ncomms11084-s3.ogv 3.1 s, 346 × 303; 55 KB
Expression-of-Constitutively-Active-CDK1-Stabilizes-APC-Cdh1-Substrates-and-Potentiates-Premature-pone.0033835.s006.ogv 26 s, 120 × 120; 102 KB
Expression-of-Constitutively-Active-CDK1-Stabilizes-APC-Cdh1-Substrates-and-Potentiates-Premature-pone.0033835.s007.ogv 26 s, 120 × 120; 48 KB
Expression-of-Constitutively-Active-CDK1-Stabilizes-APC-Cdh1-Substrates-and-Potentiates-Premature-pone.0033835.s008.ogv 14 s, 150 × 150; 1.74 MB
Genetic-and-pharmacological-inhibition-of-calcineurin-corrects-the-BDNF-transport-defect-in-1756-6606-2-33-S1.ogv 4.8 s, 298 × 200; 335 KB
Genetic-and-pharmacological-inhibition-of-calcineurin-corrects-the-BDNF-transport-defect-in-1756-6606-2-33-S2.ogv 4.8 s, 443 × 200; 980 KB
Genome-Wide-Analysis-of-Histidine-Repeats-Reveals-Their-Role-in-the-Localization-of-Human-Proteins-pgen.1000397.s015.ogv 5.8 s, 512 × 512; 49 KB
Genome-Wide-Analysis-of-Histidine-Repeats-Reveals-Their-Role-in-the-Localization-of-Human-Proteins-pgen.1000397.s016.ogv 5.9 s, 512 × 512; 37 KB
Glucocorticoid-affects-dendritic-transport-of-BDNF-containing-vesicles-srep12684-s2.ogv 19 s, 640 × 480; 453 KB
Glucocorticoid-affects-dendritic-transport-of-BDNF-containing-vesicles-srep12684-s3.ogv 9.6 s, 942 × 142; 404 KB
Glucocorticoid-affects-dendritic-transport-of-BDNF-containing-vesicles-srep12684-s4.ogv 10 s, 938 × 146; 304 KB
Golgi-localisation-of-GMAP210-requires-two-distinct-cis-membrane-binding-mechanisms-1741-7007-7-56-S1.ogv 9.0 s, 453 × 212; 261 KB
Golgi-localisation-of-GMAP210-requires-two-distinct-cis-membrane-binding-mechanisms-1741-7007-7-56-S2.ogv 26 s, 256 × 182; 112 KB
Golgi-localisation-of-GMAP210-requires-two-distinct-cis-membrane-binding-mechanisms-1741-7007-7-56-S3.ogv 22 s, 421 × 262; 551 KB
Golgi-localisation-of-GMAP210-requires-two-distinct-cis-membrane-binding-mechanisms-1741-7007-7-56-S4.ogv 16 s, 429 × 374; 286 KB
HHV-8-encoded-LANA-1-alters-the-higher-organization-of-the-cell-nucleus-1476-4598-6-28-S1.ogv 3.6 s, 699 × 266; 407 KB
HHV-8-encoded-LANA-1-alters-the-higher-organization-of-the-cell-nucleus-1476-4598-6-28-S2.ogv 3.6 s, 452 × 532; 798 KB
High-Content-Chemical-and-RNAi-Screens-for-Suppressors-of-Neurotoxicity-in-a-Huntington's-Disease-pone.0023841.s003.ogv 15 s, 320 × 240; 1.16 MB
Hole-in-One-Mutant-Phenotypes-Link-EGFRERK-Signaling-to-Epithelial-Tissue-Repair-in-Drosophila-pone.0028349.s002.ogv 32 s, 400 × 400; 4.72 MB
Hole-in-One-Mutant-Phenotypes-Link-EGFRERK-Signaling-to-Epithelial-Tissue-Repair-in-Drosophila-pone.0028349.s003.ogv 32 s, 400 × 400; 5.46 MB
Identification-and-functional-analysis-of-NOL7-nuclear-and-nucleolar-localization-signals-1471-2121-11-74-S1.ogv 12 s, 443 × 443; 692 KB
Identification-of-a-TPX2-Like-Microtubule-Associated-Protein-in-Drosophila-pone.0028120.s001.ogv 12 s, 842 × 480; 5.5 MB
Interactions-of-an-Arabidopsis-RanBPM-homologue-with-LisH-CTLH-domain-proteins-revealed-high-1471-2229-12-83-S7.ogv 3.3 s, 1,344 × 1,024; 153 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s014.ogv 12 s, 656 × 106; 355 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s015.ogv 15 s, 150 × 55; 105 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s016.ogv 15 s, 165 × 55; 154 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s017.ogv 15 s, 135 × 45; 130 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s018.ogv 15 s, 90 × 30; 58 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s019.ogv 15 s, 135 × 45; 156 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s020.ogv 15 s, 135 × 45; 110 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s021.ogv 15 s, 135 × 45; 145 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s022.ogv 15 s, 167 × 57; 300 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s023.ogv 15 s, 165 × 55; 80 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s024.ogv 15 s, 165 × 55; 101 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s025.ogv 15 s, 177 × 59; 153 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s026.ogv 15 s, 165 × 55; 241 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s027.ogv 15 s, 166 × 55; 158 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s028.ogv 15 s, 180 × 60; 229 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s029.ogv 15 s, 165 × 55; 90 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s030.ogv 15 s, 165 × 55; 97 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s031.ogv 15 s, 180 × 60; 124 KB
LeptoteneZygotene-Chromosome-Movement-Via-the-SUNKASH-Protein-Bridge-in-Caenorhabditis-elegans-pgen.1001219.s032.ogv 15 s, 180 × 60; 193 KB
Loss-of-Drosophila-pseudouridine-synthase-triggers-apoptosis-induced-proliferation-and-promotes-cddis201568x7.ogv 10 s, 640 × 468; 333 KB
Loss-of-Drosophila-pseudouridine-synthase-triggers-apoptosis-induced-proliferation-and-promotes-cddis201568x8.ogv 23 s, 384 × 288; 479 KB
Loss-of-Drosophila-pseudouridine-synthase-triggers-apoptosis-induced-proliferation-and-promotes-cddis201568x9.ogv 21 s, 384 × 288; 540 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
Mammalian-Sperm-Head-Formation-Involves-Different-Polarization-of-Two-Novel-LINC-Complexes-pone.0012072.s005.ogv 6.7 s, 784 × 544; 536 KB
Masked-mRNA-is-stored-with-aggregated-nuclear-speckles-and-its-asymmetric-redistribution-requires-a-1471-2121-12-45-S3.ogv 23 s, 512 × 512; 79 KB
Masked-mRNA-is-stored-with-aggregated-nuclear-speckles-and-its-asymmetric-redistribution-requires-a-1471-2121-12-45-S4.ogv 23 s, 512 × 512; 107 KB
Masked-mRNA-is-stored-with-aggregated-nuclear-speckles-and-its-asymmetric-redistribution-requires-a-1471-2121-12-45-S5.ogv 26 s, 512 × 512; 148 KB
Masked-mRNA-is-stored-with-aggregated-nuclear-speckles-and-its-asymmetric-redistribution-requires-a-1471-2121-12-45-S7.ogv 23 s, 512 × 512; 319 KB
Masked-mRNA-is-stored-with-aggregated-nuclear-speckles-and-its-asymmetric-redistribution-requires-a-1471-2121-12-45-S8.ogv 18 s, 512 × 512; 145 KB
Masked-mRNA-is-stored-with-aggregated-nuclear-speckles-and-its-asymmetric-redistribution-requires-a-1471-2121-12-45-S9.ogv 15 s, 512 × 512; 407 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
Mitotic-Spindle-Assembly-around-RCC1-Coated-Beads-in-Xenopus-Egg-Extracts-pbio.1001225.s004.ogv 2.9 s, 640 × 480; 160 KB
Mitotic-Spindle-Assembly-around-RCC1-Coated-Beads-in-Xenopus-Egg-Extracts-pbio.1001225.s005.ogv 5.0 s, 2,688 × 1,024; 1.04 MB
Mitotic-Spindle-Assembly-around-RCC1-Coated-Beads-in-Xenopus-Egg-Extracts-pbio.1001225.s007.ogv 5.4 s, 944 × 720; 399 KB
Nuclear-envelope-associated-endosomes-deliver-surface-proteins-to-the-nucleus-ncomms9218-s2.ogv 26 s, 768 × 576; 4.38 MB
Nuclear-envelope-associated-endosomes-deliver-surface-proteins-to-the-nucleus-ncomms9218-s3.ogv 36 s, 768 × 576; 2.56 MB
Nuclear-envelope-associated-endosomes-deliver-surface-proteins-to-the-nucleus-ncomms9218-s4.ogv 19 s, 640 × 480; 6.58 MB
Nuclear-envelope-associated-endosomes-deliver-surface-proteins-to-the-nucleus-ncomms9218-s5.ogv 13 s, 768 × 576; 4.99 MB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s006.ogv 9.0 s, 2,048 × 2,048; 92 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s007.ogv 9.0 s, 2,048 × 2,048; 163 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s008.ogv 11 s, 2,048 × 2,048; 104 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s009.ogv 11 s, 1,003 × 808; 67 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s010.ogv 5.1 s, 126 × 165; 694 KB
NUP-1-Is-a-Large-Coiled-Coil-Nucleoskeletal-Protein-in-Trypanosomes-with-Lamin-Like-Functions-pbio.1001287.s011.ogv 15 s, 1,024 × 1,024; 37 KB
P53-Target-Gene-SMAR1-Is-Dysregulated-in-Breast-Cancer-Its-Role-in-Cancer-Cell-Migration-and-pone.0000660.s007.ogv 14 s, 480 × 360; 4.48 MB
P53-Target-Gene-SMAR1-Is-Dysregulated-in-Breast-Cancer-Its-Role-in-Cancer-Cell-Migration-and-pone.0000660.s008.ogv 14 s, 480 × 360; 3.17 MB
P53-Target-Gene-SMAR1-Is-Dysregulated-in-Breast-Cancer-Its-Role-in-Cancer-Cell-Migration-and-pone.0000660.s009.ogv 14 s, 480 × 360; 3.53 MB
PKA-antagonizes-CLASP-dependent-microtubule-stabilization-to-re-localize-Pom1-and-buffer-cell-size-ncomms9445-s2.ogv 5.9 s, 172 × 172; 49 KB
PKA-antagonizes-CLASP-dependent-microtubule-stabilization-to-re-localize-Pom1-and-buffer-cell-size-ncomms9445-s3.ogv 5.9 s, 172 × 172; 72 KB
Polyglutamine-Expansion-Accelerates-the-Dynamics-of-Ataxin-1-and-Does-Not-Result-in-Aggregate-pone.0001503.s001.ogv 27 s, 212 × 187; 779 KB
Resistance-to-Inhibitors-of-Cholinesterase-(Ric)-8A-and-Gαi-Contribute-to-Cytokinesis-Abscission-by-pone.0086680.s002.ogv 8.0 s, 720 × 480; 582 KB
Resistance-to-Inhibitors-of-Cholinesterase-(Ric)-8A-and-Gαi-Contribute-to-Cytokinesis-Abscission-by-pone.0086680.s003.ogv 5.2 s, 720 × 480; 292 KB
Resistance-to-Inhibitors-of-Cholinesterase-(Ric)-8A-and-Gαi-Contribute-to-Cytokinesis-Abscission-by-pone.0086680.s004.ogv 5.4 s, 720 × 480; 248 KB
Resistance-to-Inhibitors-of-Cholinesterase-(Ric)-8A-and-Gαi-Contribute-to-Cytokinesis-Abscission-by-pone.0086680.s005.ogv 2.6 s, 720 × 480; 187 KB
Resistance-to-Inhibitors-of-Cholinesterase-(Ric)-8A-and-Gαi-Contribute-to-Cytokinesis-Abscission-by-pone.0086680.s006.ogv 2.9 s, 720 × 480; 371 KB
Sequential-Loading-of-Cohesin-Subunits-during-the-First-Meiotic-Prophase-of-Grasshoppers-pgen.0030028.sv009.ogv 8.4 s, 372 × 371; 490 KB
Single-Cell-Analysis-of-Transcriptional-Activation-Dynamics-pone.0010272.s005.ogv 4.4 s, 196 × 187; 45 KB
Single-Cell-Analysis-of-Transcriptional-Activation-Dynamics-pone.0010272.s006.ogv 3.6 s, 660 × 155; 129 KB
Single-Cell-Analysis-of-Transcriptional-Activation-Dynamics-pone.0010272.s007.ogv 3.6 s, 645 × 215; 472 KB
Single-Cell-Analysis-of-Transcriptional-Activation-Dynamics-pone.0010272.s008.ogv 3.6 s, 600 × 200; 167 KB
Single-Cell-Analysis-of-Transcriptional-Activation-Dynamics-pone.0010272.s009.ogv 4.0 s, 654 × 212; 209 KB
Single-Cell-Analysis-of-Transcriptional-Activation-Dynamics-pone.0010272.s010.ogv 3.6 s, 555 × 165; 258 KB
Spire-and-Formin-2-Synergize-and-Antagonize-in-Regulating-Actin-Assembly-in-Meiosis-by-a-Ping-Pong-pbio.1001795.s009.ogv 13 s, 136 × 112; 138 KB
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
STK35L1-Associates-with-Nuclear-Actin-and-Regulates-Cell-Cycle-and-Migration-of-Endothelial-Cells-pone.0016249.s005.ogv 4.4 s, 584 × 596; 251 KB
STK35L1-Associates-with-Nuclear-Actin-and-Regulates-Cell-Cycle-and-Migration-of-Endothelial-Cells-pone.0016249.s006.ogv 16 s, 720 × 540; 4.38 MB
The-Drosophila-Gene-RanBPM-Functions-in-the-Mushroom-Body-to-Regulate-Larval-Behavior-pone.0010652.s009.ogv 9 min 23 s, 320 × 240; 543 KB
The-Drosophila-Gene-RanBPM-Functions-in-the-Mushroom-Body-to-Regulate-Larval-Behavior-pone.0010652.s010.ogv 1 min 51 s, 640 × 480; 643 KB
The-Glial-Regenerative-Response-to-Central-Nervous-System-Injury-Is-Enabled-by-Pros-Notch-and-Pros-pbio.1001133.s020.ogv 2.7 s, 1,092 × 530; 1.73 MB
The-Glial-Regenerative-Response-to-Central-Nervous-System-Injury-Is-Enabled-by-Pros-Notch-and-Pros-pbio.1001133.s021.ogv 4.0 s, 1,008 × 550; 2.43 MB
The-Golgin-GMAP210TRIP11-Anchors-IFT20-to-the-Golgi-Complex-pgen.1000315.s004.ogv 25 s, 768 × 440; 3.66 MB
The-Golgin-GMAP210TRIP11-Anchors-IFT20-to-the-Golgi-Complex-pgen.1000315.s005.ogv 21 s, 768 × 440; 1.82 MB
The-Golgin-GMAP210TRIP11-Anchors-IFT20-to-the-Golgi-Complex-pgen.1000315.s006.ogv 24 s, 768 × 440; 4.51 MB
The-Structure-of-the-Mitotic-Spindle-and-Nucleolus-during-Mitosis-in-the-Amebo-Flagellate-Naegleria-pone.0034763.s001.ogv 12 s, 166 × 153; 305 KB
The-Structure-of-the-Mitotic-Spindle-and-Nucleolus-during-Mitosis-in-the-Amebo-Flagellate-Naegleria-pone.0034763.s002.ogv 12 s, 166 × 178; 223 KB
The-Structure-of-the-Mitotic-Spindle-and-Nucleolus-during-Mitosis-in-the-Amebo-Flagellate-Naegleria-pone.0034763.s003.ogv 12 s, 170 × 226; 328 KB
The-Structure-of-the-Mitotic-Spindle-and-Nucleolus-during-Mitosis-in-the-Amebo-Flagellate-Naegleria-pone.0034763.s004.ogv 12 s, 310 × 232; 382 KB
The-SUN-Protein-Mps3-Is-Required-for-Spindle-Pole-Body-Insertion-into-the-Nuclear-Membrane-and-pgen.1002365.s009.ogv 22 s, 256 × 256; 247 KB
The-SUN-Protein-Mps3-Is-Required-for-Spindle-Pole-Body-Insertion-into-the-Nuclear-Membrane-and-pgen.1002365.s010.ogv 21 s, 256 × 256; 338 KB
The-SUN-Protein-Mps3-Is-Required-for-Spindle-Pole-Body-Insertion-into-the-Nuclear-Membrane-and-pgen.1002365.s011.ogv 23 s, 256 × 256; 387 KB
The-SUN-Protein-Mps3-Is-Required-for-Spindle-Pole-Body-Insertion-into-the-Nuclear-Membrane-and-pgen.1002365.s012.ogv 27 s, 256 × 256; 492 KB
The-SUN-Protein-Mps3-Is-Required-for-Spindle-Pole-Body-Insertion-into-the-Nuclear-Membrane-and-pgen.1002365.s013.ogv 23 s, 256 × 256; 336 KB
Transcriptional-Activation-of-the-Adenoviral-Genome-Is-Mediated-byCapsid-Protein-VI-ppat.1002549.s009.ogv 5.0 s, 612 × 204; 779 KB
Two-TPX2-Dependent-Switches-Control-the-Activity-of-Aurora-A-pone.0016757.s003.ogv 38 s, 768 × 576; 5.85 MB
Virion-Assembly-Factories-in-the-Nucleus-of-Polyomavirus-Infected-Cells-ppat.1002630.s002.ogv 54 s, 640 × 480; 24.06 MB
Virion-Assembly-Factories-in-the-Nucleus-of-Polyomavirus-Infected-Cells-ppat.1002630.s003.ogv 34 s, 960 × 720; 25.45 MB
Zwint-1-is-required-for-spindle-assembly-checkpoint-function-and-kinetochore-microtubule-attachment-srep15431-s2.ogv 4.2 s, 1,154 × 609; 321 KB