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Category:Gene deletion

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Media in category "Gene deletion"

The following 91 files are in this category, out of 91 total.

A-Deletion-in-the-N-Myc-Downstream-Regulated-Gene-1-(NDRG1)-Gene-in-Greyhounds-with-Polyneuropathy-pone.0011258.s003.ogv 9.9 s, 320 × 240; 2.38 MB
A-Deletion-in-the-N-Myc-Downstream-Regulated-Gene-1-(NDRG1)-Gene-in-Greyhounds-with-Polyneuropathy-pone.0011258.s004.ogv 35 s, 320 × 240; 4.04 MB
A-Toxoplasma-MORN1-Null-Mutant-Undergoes-Repeated-Divisions-but-Is-Defective-in-Basal-Assembly-pone.0012302.s007.ogv 31 s, 518 × 514; 228 KB
Acute-Multiple-Organ-Failure-in-Adult-Mice-Deleted-for-the-Developmental-Regulator-Wt1-pgen.1002404.s012.ogv 29 s, 418 × 480; 1.42 MB
Acute-Multiple-Organ-Failure-in-Adult-Mice-Deleted-for-the-Developmental-Regulator-Wt1-pgen.1002404.s013.ogv 30 s, 416 × 480; 2.06 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
CLRN1-Is-Nonessential-in-the-Mouse-Retina-but-Is-Required-for-Cochlear-Hair-Cell-Development-pgen.1000607.s009.ogv 21 s, 320 × 240; 879 KB
Coronin-Is-a-Component-of-the-Endocytic-Collar-of-Hyphae-of-Neurospora-crassa-and-Is-Necessary-for-pone.0038237.s002.ogv 3.3 s, 519 × 512; 266 KB
Coronin-Is-a-Component-of-the-Endocytic-Collar-of-Hyphae-of-Neurospora-crassa-and-Is-Necessary-for-pone.0038237.s003.ogv 11 s, 847 × 248; 1.27 MB
Coronin-Is-a-Component-of-the-Endocytic-Collar-of-Hyphae-of-Neurospora-crassa-and-Is-Necessary-for-pone.0038237.s004.ogv 11 s, 351 × 587; 881 KB
Coronin-Is-a-Component-of-the-Endocytic-Collar-of-Hyphae-of-Neurospora-crassa-and-Is-Necessary-for-pone.0038237.s005.ogv 7.4 s, 1,111 × 512; 2.33 MB
Coronin-Is-a-Component-of-the-Endocytic-Collar-of-Hyphae-of-Neurospora-crassa-and-Is-Necessary-for-pone.0038237.s006.ogv 12 s, 519 × 512; 724 KB
Coronin-Is-a-Component-of-the-Endocytic-Collar-of-Hyphae-of-Neurospora-crassa-and-Is-Necessary-for-pone.0038237.s007.ogv 5.5 s, 519 × 512; 143 KB
Critical-Endothelial-Regulation-by-LRP5-during-Retinal-Vascular-Development-pone.0152833.s001.ogv 3.0 s, 512 × 512; 765 KB
Critical-Endothelial-Regulation-by-LRP5-during-Retinal-Vascular-Development-pone.0152833.s002.ogv 19 s, 512 × 512; 1.53 MB
Critical-Endothelial-Regulation-by-LRP5-during-Retinal-Vascular-Development-pone.0152833.s003.ogv 5.9 s, 512 × 512; 1.64 MB
Critical-Endothelial-Regulation-by-LRP5-during-Retinal-Vascular-Development-pone.0152833.s004.ogv 13 s, 512 × 512; 588 KB
Critical-Endothelial-Regulation-by-LRP5-during-Retinal-Vascular-Development-pone.0152833.s005.ogv 9.4 s, 512 × 512; 820 KB
Critical-Endothelial-Regulation-by-LRP5-during-Retinal-Vascular-Development-pone.0152833.s006.ogv 6.3 s, 512 × 512; 1,001 KB
CRL4–DCAF1-ubiquitin-E3-ligase-directs-protein-phosphatase-2A-degradation-to-control-oocyte-meiotic-ncomms9017-s2.ogv 38 s, 1,002 × 500; 4.59 MB
CRL4–DCAF1-ubiquitin-E3-ligase-directs-protein-phosphatase-2A-degradation-to-control-oocyte-meiotic-ncomms9017-s3.ogv 38 s, 1,056 × 500; 2.96 MB
Crmp4-deletion-promotes-recovery-from-spinal-cord-injury-by-neuroprotection-and-limited-scar-srep08269-s2.ogv 28 s, 640 × 360; 1.67 MB
Erk1-and-Erk2-Regulate-Endothelial-Cell-Proliferation-and-Migration-during-Mouse-Embryonic-pone.0008283.s011.ogv 12 s, 1,392 × 1,040; 4.79 MB
Erk1-and-Erk2-Regulate-Endothelial-Cell-Proliferation-and-Migration-during-Mouse-Embryonic-pone.0008283.s012.ogv 12 s, 1,392 × 1,040; 1.81 MB
Immunological-Responses-and-Actin-Dynamics-in-Macrophages-Are-Controlled-by-N-Cofilin-but-Are-pone.0036034.s004.ogv 21 s, 696 × 520; 903 KB
Immunological-Responses-and-Actin-Dynamics-in-Macrophages-Are-Controlled-by-N-Cofilin-but-Are-pone.0036034.s005.ogv 9.9 s, 384 × 288; 340 KB
Immunological-Responses-and-Actin-Dynamics-in-Macrophages-Are-Controlled-by-N-Cofilin-but-Are-pone.0036034.s006.ogv 9.9 s, 384 × 288; 129 KB
Iron-Insufficiency-Compromises-Motor-Neurons-and-Their-Mitochondrial-Function-in-Irp2-Null-Mice-pone.0025404.s005.ogv 49 s, 704 × 288; 5.84 MB
Macroautophagy-Mediated-Degradation-of-Whole-Nuclei-in-the-Filamentous-Fungus-Aspergillus-oryzae-pone.0015650.s006.ogv 4.0 s, 232 × 182; 24 KB
Phospholipase-C-ε-Regulates-Epidermal-Morphogenesis-in-Caenorhabditis-elegans-pgen.1000043.s003.ogv 17 s, 568 × 568; 252 KB
PI3Ks-Maintain-the-Structural-Integrity-of-T-Tubules-in-Cardiac-Myocytes-pone.0024404.s004.ogv 5.0 s, 656 × 752; 2.22 MB
PI3Ks-Maintain-the-Structural-Integrity-of-T-Tubules-in-Cardiac-Myocytes-pone.0024404.s005.ogv 5.0 s, 656 × 752; 2.34 MB
Regulation-and-Functions-of-the-lms-Homeobox-Gene-during-Development-of-Embryonic-Lateral-pone.0014323.s001.ogv 22 s, 480 × 360; 959 KB
Regulation-and-Functions-of-the-lms-Homeobox-Gene-during-Development-of-Embryonic-Lateral-pone.0014323.s002.ogv 27 s, 352 × 288; 972 KB
Regulation-and-Functions-of-the-lms-Homeobox-Gene-during-Development-of-Embryonic-Lateral-pone.0014323.s003.ogv 33 s, 352 × 288; 875 KB
Regulation-and-Functions-of-the-lms-Homeobox-Gene-during-Development-of-Embryonic-Lateral-pone.0014323.s004.ogv 33 s, 352 × 288; 911 KB
RhoE-Deficiency-Produces-Postnatal-Lethality-Profound-Motor-Deficits-and-Neurodevelopmental-Delay-pone.0019236.s001.ogv 18 s, 640 × 480; 1.25 MB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S1.ogv 10 s, 458 × 346; 242 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S11.ogv 10 s, 458 × 346; 203 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S12.ogv 6.0 s, 458 × 346; 225 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S14.ogv 20 s, 458 × 346; 486 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S2.ogv 10 s, 458 × 346; 371 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S4.ogv 15 s, 458 × 346; 336 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S7.ogv 8.0 s, 458 × 346; 44 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S8.ogv 13 s, 458 × 346; 883 KB
Single-cell-time-lapse-analysis-of-depletion-of-the-universally-conserved-essential-protein-YgjD-1471-2180-11-118-S9.ogv 10 s, 458 × 346; 406 KB
The-Cerato-Platanin-protein-Epl-1-from-Trichoderma-harzianum-is-involved-in-mycoparasitism-plant-srep17998-s2.ogv 32 s, 640 × 480; 960 KB
The-Cerato-Platanin-protein-Epl-1-from-Trichoderma-harzianum-is-involved-in-mycoparasitism-plant-srep17998-s3.ogv 32 s, 640 × 480; 1.2 MB
Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S1.ogv 3.0 s, 276 × 283; 60 KB
Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S2.ogv 2.1 s, 701 × 701; 47 KB
Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S3.ogv 5.1 s, 236 × 219; 106 KB
Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S4.ogv 3.0 s, 525 × 515; 61 KB
Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S5.ogv 4.0 s, 256 × 255; 949 KB
Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s006.ogv 2.0 s, 432 × 252; 111 KB
Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s007.ogv 1.9 s, 432 × 252; 115 KB
Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s008.ogv 2.0 s, 432 × 252; 149 KB
ΓCOP-Is-Required-for-Apical-Protein-Secretion-and-Epithelial-Morphogenesis-in-Drosophila-pone.0003241.s003.ogv 14 s, 584 × 251; 3.17 MB
ΓCOP-Is-Required-for-Apical-Protein-Secretion-and-Epithelial-Morphogenesis-in-Drosophila-pone.0003241.s004.ogv 14 s, 584 × 251; 2.88 MB
ΓCOP-Is-Required-for-Apical-Protein-Secretion-and-Epithelial-Morphogenesis-in-Drosophila-pone.0003241.s005.ogv 14 s, 584 × 251; 3.39 MB
ΓCOP-Is-Required-for-Apical-Protein-Secretion-and-Epithelial-Morphogenesis-in-Drosophila-pone.0003241.s006.ogv 14 s, 584 × 251; 1.92 MB

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