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PLOS Genetics

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Es werden 3 von insgesamt 3 Unterkategorien in dieser Kategorie angezeigt:
In Klammern die Anzahl der enthaltenen Kategorien (K), Seiten (S), Dateien (D)

A

A Cholinergic-Regulated Circuit Coordinates the Maintenance and Bi-Stable States of a Sensory-Motor Behavior during Caenorhabditis elegans Male Copulation‎ (11 D)

M

Media from Deyter et al. 2010 - 10.1371/journal.pgen.1001218‎ (32 D)

S

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

Medien in der Kategorie „Media from PLOS Genetics“

Folgende 200 Dateien sind in dieser Kategorie, von 1.273 insgesamt.

(vorherige Seite) (nächste Seite)

A genome alignment of eight Yersinia isolates.png 2.756 × 1.745; 3,14 MB
A-Bow-Tie-Genetic-Architecture-for-Morphogenesis-Suggested-by-a-Genome-Wide-RNAi-Screen-in-pgen.1002010.s010.ogv 2 min 10 s, 1.898 × 1.226; 8,63 MB
A-Bow-Tie-Genetic-Architecture-for-Morphogenesis-Suggested-by-a-Genome-Wide-RNAi-Screen-in-pgen.1002010.s011.ogv 2 min 10 s, 1.898 × 1.226; 10,45 MB
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-Deficiency-of-Ceramide-Biosynthesis-Causes-Cerebellar-Purkinje-Cell-Neurodegeneration-and-pgen.1002063.s008.ogv 33 s, 960 × 540; 4,4 MB
A-Drosophila-Model-for-EGFR-Ras-and-PI3K-Dependent-Human-Glioma-pgen.1000374.s016.ogv 1,3 s, 950 × 930; 1,97 MB
A-Drosophila-Model-for-EGFR-Ras-and-PI3K-Dependent-Human-Glioma-pgen.1000374.s017.ogv 2,4 s, 760 × 970; 1,51 MB
A-Drosophila-Model-for-EGFR-Ras-and-PI3K-Dependent-Human-Glioma-pgen.1000374.s018.ogv 4,7 s, 1.024 × 1.024; 1,58 MB
A-Drosophila-Model-for-EGFR-Ras-and-PI3K-Dependent-Human-Glioma-pgen.1000374.s019.ogv 1,8 s, 526 × 606; 246 KB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s010.ogv 30 s, 320 × 240; 1,66 MB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s011.ogv 30 s, 320 × 240; 1,24 MB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s012.ogv 30 s, 320 × 240; 1,51 MB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s013.ogv 30 s, 320 × 240; 986 KB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s014.ogv 30 s, 320 × 240; 1,23 MB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s015.ogv 30 s, 320 × 240; 742 KB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s016.ogv 30 s, 320 × 240; 2,44 MB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s017.ogv 30 s, 320 × 240; 1,94 MB
A-Drosophila-Model-of-High-Sugar-Diet-Induced-Cardiomyopathy-pgen.1003175.s018.ogv 30 s, 320 × 240; 2,26 MB
A-Dynamic-Response-Regulator-Protein-Modulates-G-Protein–Dependent-Polarity-in-the-Bacterium-pgen.1002872.s011.ogv 8,0 s, 268 × 168; 53 KB
A-Dynamic-Response-Regulator-Protein-Modulates-G-Protein–Dependent-Polarity-in-the-Bacterium-pgen.1002872.s012.ogv 8,0 s, 332 × 320; 93 KB
A-Dynamic-Response-Regulator-Protein-Modulates-G-Protein–Dependent-Polarity-in-the-Bacterium-pgen.1002872.s013.ogv 8,0 s, 312 × 328; 87 KB
A-Dynamic-Response-Regulator-Protein-Modulates-G-Protein–Dependent-Polarity-in-the-Bacterium-pgen.1002872.s014.ogv 5,2 s, 284 × 306; 50 KB
A-Follicle-Rupture-Assay-Reveals-an-Essential-Role-for-Follicular-Adrenergic-Signaling-in-pgen.1005604.s009.ogv 20 s, 600 × 471; 2,26 MB
A-Follicle-Rupture-Assay-Reveals-an-Essential-Role-for-Follicular-Adrenergic-Signaling-in-pgen.1005604.s010.ogv 8,9 s, 804 × 756; 1,18 MB
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-Genetic-Cascade-of-let-7-ncl-1-fib-1-Modulates-Nucleolar-Size-and-rRNA-Pool-in-Caenorhabditis-pgen.1005580.s009.ogv 2,2 s, 1.844 × 1.036; 314 KB
A-Genetic-Cascade-of-let-7-ncl-1-fib-1-Modulates-Nucleolar-Size-and-rRNA-Pool-in-Caenorhabditis-pgen.1005580.s010.ogv 0,8 s, 1.844 × 1.036; 489 KB
A-Genetic-RNAi-Screen-for-IP3Ca2+-Coupled-GPCRs-in-Drosophila-Identifies-the-PdfR-as-a-Regulator-of-pgen.1003849.s005.ogv 50 s, 760 × 480; 5,99 MB
A-Genetic-RNAi-Screen-for-IP3Ca2+-Coupled-GPCRs-in-Drosophila-Identifies-the-PdfR-as-a-Regulator-of-pgen.1003849.s006.ogv 52 s, 760 × 480; 5,63 MB
A-Hereditary-Spastic-Paraplegia-Mouse-Model-Supports-a-Role-of-ZFYVE26SPASTIZIN-for-the-pgen.1003988.s009.ogv 3,7 s, 704 × 576; 585 KB
A-Hereditary-Spastic-Paraplegia-Mouse-Model-Supports-a-Role-of-ZFYVE26SPASTIZIN-for-the-pgen.1003988.s010.ogv 2,7 s, 704 × 576; 546 KB
A-High-Incidence-of-Meiotic-Silencing-of-Unsynapsed-Chromatin-Is-Not-Associated-with-Substantial-pgen.1000625.s004.ogv 5,2 s, 948 × 700; 1,07 MB
A-High-Incidence-of-Meiotic-Silencing-of-Unsynapsed-Chromatin-Is-Not-Associated-with-Substantial-pgen.1000625.s005.ogv 11 s, 800 × 400; 254 KB
A-Missense-Change-in-the-ATG4D-Gene-Links-Aberrant-Autophagy-to-a-Neurodegenerative-Vacuolar-pgen.1005169.s010.ogv 1 min 15 s, 640 × 360; 16,52 MB
A-Missense-Mutation-in-a-Highly-Conserved-Alternate-Exon-of-Dynamin-1-Causes-Epilepsy-in-Fitful-Mice-pgen.1001046.s004.ogv 22 s, 320 × 240; 5,49 MB
A-Missense-Mutation-in-the-SERPINH1-Gene-in-Dachshunds-with-Osteogenesis-Imperfecta-pgen.1000579.s007.ogv 29 s, 320 × 240; 2,84 MB
A-Motor-Function-for-the-DEAD-Box-RNA-Helicase-Gemin3-in-Drosophila-pgen.1000265.s002.ogv 20 s, 800 × 400; 967 KB
A-Motor-Function-for-the-DEAD-Box-RNA-Helicase-Gemin3-in-Drosophila-pgen.1000265.s003.ogv 8,9 s, 800 × 400; 397 KB
A-Novel-Mutant-Allele-of-Pw1Peg3-Does-Not-Affect-Maternal-Behavior-or-Nursing-Behavior-pgen.1006053.s001.ogv 2 min 19 s, 649 × 364; 15,26 MB
A-Novel-Role-for-MAPKAPK2-in-Morphogenesis-during-Zebrafish-Development-pgen.1000413.s001.ogv 7,3 s, 900 × 470; 1,97 MB
A-Novel-Role-for-MAPKAPK2-in-Morphogenesis-during-Zebrafish-Development-pgen.1000413.s002.ogv 3,7 s, 432 × 208; 74 KB
A-Novel-Role-for-MAPKAPK2-in-Morphogenesis-during-Zebrafish-Development-pgen.1000413.s003.ogv 2,8 s, 432 × 208; 44 KB
A-Novel-Role-for-MAPKAPK2-in-Morphogenesis-during-Zebrafish-Development-pgen.1000413.s004.ogv 10 s, 658 × 517; 3,91 MB
A-Novel-Role-for-MAPKAPK2-in-Morphogenesis-during-Zebrafish-Development-pgen.1000413.s005.ogv 8,5 s, 600 × 300; 7,4 MB
A-Novel-Role-for-MAPKAPK2-in-Morphogenesis-during-Zebrafish-Development-pgen.1000413.s006.ogv 19 s, 400 × 300; 135 KB
A-Novel-Zebrafish-ret-Heterozygous-Model-of-Hirschsprung-Disease-Identifies-a-Functional-Role-for-pgen.1006439.s006.ogv 16 s, 1.128 × 512; 5,24 MB
A-Novel-Zebrafish-ret-Heterozygous-Model-of-Hirschsprung-Disease-Identifies-a-Functional-Role-for-pgen.1006439.s007.ogv 16 s, 1.128 × 512; 5,29 MB
A-Novel-Zebrafish-ret-Heterozygous-Model-of-Hirschsprung-Disease-Identifies-a-Functional-Role-for-pgen.1006439.s008.ogv 20 s, 616 × 246; 1,54 MB
A-Novel-Zebrafish-ret-Heterozygous-Model-of-Hirschsprung-Disease-Identifies-a-Functional-Role-for-pgen.1006439.s009.ogv 20 s, 616 × 246; 1,19 MB
A-Novel-Zebrafish-ret-Heterozygous-Model-of-Hirschsprung-Disease-Identifies-a-Functional-Role-for-pgen.1006439.s010.ogv 20 s, 616 × 246; 1,39 MB
A-Ploidy-Sensitive-Mechanism-Regulates-Aperture-Formation-on-the-Arabidopsis-Pollen-Surface-and-pgen.1006060.s007.ogv 15 s, 1.666 × 1.130; 2,69 MB
A-Ploidy-Sensitive-Mechanism-Regulates-Aperture-Formation-on-the-Arabidopsis-Pollen-Surface-and-pgen.1006060.s008.ogv 30 s, 1.320 × 848; 1,51 MB
A-Role-for-Phosphatidic-Acid-in-the-Formation-of-“Supersized”-Lipid-Droplets-pgen.1002201.s005.ogv 5,4 s, 640 × 480; 40 KB
A-Role-for-Phosphatidic-Acid-in-the-Formation-of-“Supersized”-Lipid-Droplets-pgen.1002201.s006.ogv 5,4 s, 640 × 480; 42 KB
A-Role-for-Phosphatidic-Acid-in-the-Formation-of-“Supersized”-Lipid-Droplets-pgen.1002201.s007.ogv 32 s, 640 × 480; 243 KB
A-Role-for-Phosphatidic-Acid-in-the-Formation-of-“Supersized”-Lipid-Droplets-pgen.1002201.s008.ogv 24 s, 640 × 480; 360 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s007.ogv 3,0 s, 556 × 636; 274 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s008.ogv 8,3 s, 680 × 680; 768 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s009.ogv 4,1 s, 660 × 660; 230 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s010.ogv 4,7 s, 596 × 596; 230 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s011.ogv 5,4 s, 704 × 704; 713 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s012.ogv 5,7 s, 650 × 650; 273 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s013.ogv 4,0 s, 668 × 668; 209 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s014.ogv 5,4 s, 750 × 750; 437 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s015.ogv 3,0 s, 686 × 686; 186 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s016.ogv 5,9 s, 670 × 670; 217 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s017.ogv 5,9 s, 726 × 726; 223 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s018.ogv 3,3 s, 790 × 790; 451 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s019.ogv 5,0 s, 656 × 656; 322 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s020.ogv 3,1 s, 608 × 608; 273 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s021.ogv 4,4 s, 720 × 720; 313 KB
A-Role-for-the-Chaperone-Complex-BAG3-HSPB8-in-Actin-Dynamics-Spindle-Orientation-and-Proper-pgen.1005582.s022.ogv 5,0 s, 744 × 744; 331 KB
A-SEL1L-Mutation-Links-a-Canine-Progressive-Early-Onset-Cerebellar-Ataxia-to-the-Endoplasmic-pgen.1002759.s007.ogv 1 min 37 s, 640 × 480; 19,73 MB
A-SEL1L-Mutation-Links-a-Canine-Progressive-Early-Onset-Cerebellar-Ataxia-to-the-Endoplasmic-pgen.1002759.s008.ogv 1 min 56 s, 640 × 480; 23,41 MB
A-SEL1L-Mutation-Links-a-Canine-Progressive-Early-Onset-Cerebellar-Ataxia-to-the-Endoplasmic-pgen.1002759.s009.ogv 1 min 48 s, 640 × 480; 18,26 MB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s007.ogv 2,5 s, 746 × 415; 133 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s008.ogv 2,5 s, 746 × 415; 114 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s009.ogv 2,5 s, 745 × 414; 107 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s010.ogv 2,5 s, 745 × 414; 118 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s011.ogv 3,9 s, 456 × 352; 190 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s012.ogv 4,1 s, 456 × 352; 151 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s013.ogv 3,6 s, 456 × 352; 157 KB
A-Sensitized-Screen-for-Genes-Promoting-Invadopodia-Function-In-Vivo-CDC-42-and-Rab-GDI-1-Direct-pgen.1005786.s014.ogv 3,9 s, 456 × 352; 227 KB
A-Simple-Screen-to-Identify-Promoters-Conferring-High-Levels-of-Phenotypic-Noise-pgen.1000307.s006.ogv 6,9 s, 320 × 240; 46 KB
A-Simple-Screen-to-Identify-Promoters-Conferring-High-Levels-of-Phenotypic-Noise-pgen.1000307.s007.ogv 9,5 s, 320 × 240; 114 KB
A-Single-Sex-Pheromone-Receptor-Determines-Chemical-Response-Specificity-of-Sexual-Behavior-in-the-pgen.1002115.s006.ogv 43 s, 480 × 360; 2,65 MB
A-Single-Sex-Pheromone-Receptor-Determines-Chemical-Response-Specificity-of-Sexual-Behavior-in-the-pgen.1002115.s007.ogv 43 s, 480 × 360; 1,66 MB
A-Single-Sex-Pheromone-Receptor-Determines-Chemical-Response-Specificity-of-Sexual-Behavior-in-the-pgen.1002115.s008.ogv 41 s, 480 × 360; 1,99 MB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s009.ogv 11 s, 430 × 270; 524 KB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s010.ogv 11 s, 430 × 270; 525 KB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s011.ogv 9,7 s, 445 × 290; 387 KB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s012.ogv 9,7 s, 445 × 290; 426 KB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s013.ogv 6,0 s, 259 × 602; 966 KB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s014.ogv 6,0 s, 279 × 602; 1,18 MB
A-Taz1--and-Microtubule-Dependent-Regulatory-Relationship-between-Telomere-and-Centromere-Positions-pgen.1006304.s015.ogv 6,0 s, 307 × 540; 971 KB
Abscission-Is-Regulated-by-the-ESCRT-III-Protein-Shrub-in-Drosophila-Germline-Stem-Cells-pgen.1004653.s004.ogv 5,0 s, 1.024 × 1.024; 1,41 MB
Abscission-Is-Regulated-by-the-ESCRT-III-Protein-Shrub-in-Drosophila-Germline-Stem-Cells-pgen.1004653.s005.ogv 5,0 s, 1.024 × 1.024; 716 KB
Abscission-Is-Regulated-by-the-ESCRT-III-Protein-Shrub-in-Drosophila-Germline-Stem-Cells-pgen.1004653.s006.ogv 5,0 s, 1.024 × 1.024; 929 KB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s008.ogv 3,7 s, 200 × 106; 9 KB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s009.ogv 27 s, 960 × 720; 2,27 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s010.ogv 18 s, 960 × 720; 2,06 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s011.ogv 17 s, 960 × 720; 1,64 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s012.ogv 17 s, 960 × 720; 1,71 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s013.ogv 16 s, 960 × 720; 1,68 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s014.ogv 17 s, 960 × 720; 1,72 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s015.ogv 17 s, 960 × 720; 2,57 MB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s016.ogv 4,0 s, 765 × 158; 62 KB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s017.ogv 4,0 s, 756 × 163; 77 KB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s018.ogv 4,0 s, 540 × 163; 52 KB
Active-Transport-and-Diffusion-Barriers-Restrict-Joubert-Syndrome-Associated-ARL13BARL-13-to-an-Inv-pgen.1003977.s019.ogv 9,2 s, 960 × 720; 267 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
Acute-Versus-Chronic-Loss-of-Mammalian-Azi1Cep131-Results-in-Distinct-Ciliary-Phenotypes-pgen.1003928.s009.ogv 36 s, 190 × 166; 254 KB
Acute-Versus-Chronic-Loss-of-Mammalian-Azi1Cep131-Results-in-Distinct-Ciliary-Phenotypes-pgen.1003928.s010.ogv 25 s, 678 × 518; 2,36 MB
Acute-Versus-Chronic-Loss-of-Mammalian-Azi1Cep131-Results-in-Distinct-Ciliary-Phenotypes-pgen.1003928.s011.ogv 17 s, 678 × 518; 3,84 MB
Adaptive-Stress-Response-in-Segmental-Progeria-Resembles-Long-Lived-Dwarfism-and-Calorie-pgen.0020192.sv001.ogv 1 min 54 s, 240 × 180; 4,9 MB
Alec Jeffreys.png 1.534 × 2.017; 3,43 MB
Allatostatin-A-Signalling-in-Drosophila-Regulates-Feeding-and-Sleep-and-Is-Modulated-by-PDF-pgen.1006346.s021.ogv 5,1 s, 530 × 480; 623 KB
Allatostatin-A-Signalling-in-Drosophila-Regulates-Feeding-and-Sleep-and-Is-Modulated-by-PDF-pgen.1006346.s022.ogv 5,1 s, 530 × 480; 920 KB
Allatostatin-A-Signalling-in-Drosophila-Regulates-Feeding-and-Sleep-and-Is-Modulated-by-PDF-pgen.1006346.s023.ogv 3 min 40 s, 854 × 480; 6,47 MB
AlpEnigma-Family-Proteins-Cooperate-in-Z-Disc-Formation-and-Myofibril-Assembly-pgen.1003342.s007.ogv 1 min 0 s, 360 × 360; 5,06 MB
Altered-Behavioral-Performance-and-Live-Imaging-of-Circuit-Specific-Neural-Deficiencies-in-a-pgen.1004615.s005.ogv 3,3 s, 512 × 512; 107 KB
An-Alpha-Catulin-Homologue-Controls-Neuromuscular-Function-through-Localization-of-the-Dystrophin-pgen.1001077.s004.ogv 30 s, 696 × 520; 580 KB
An-ALS-Linked-Mutant-SOD1-Produces-a-Locomotor-Defect-Associated-with-Aggregation-and-Synaptic-pgen.1000350.s013.ogv 29 s, 640 × 480; 1,04 MB
An-ALS-Linked-Mutant-SOD1-Produces-a-Locomotor-Defect-Associated-with-Aggregation-and-Synaptic-pgen.1000350.s014.ogv 30 s, 480 × 360; 425 KB
An-ALS-Linked-Mutant-SOD1-Produces-a-Locomotor-Defect-Associated-with-Aggregation-and-Synaptic-pgen.1000350.s015.ogv 30 s, 480 × 360; 366 KB
An-EMT–Driven-Alternative-Splicing-Program-Occurs-in-Human-Breast-Cancer-and-Modulates-Cellular-pgen.1002218.s018.ogv 9,7 s, 1.208 × 892; 1,95 MB
An-EMT–Driven-Alternative-Splicing-Program-Occurs-in-Human-Breast-Cancer-and-Modulates-Cellular-pgen.1002218.s019.ogv 10 s, 1.208 × 892; 3,33 MB
An-EMT–Driven-Alternative-Splicing-Program-Occurs-in-Human-Breast-Cancer-and-Modulates-Cellular-pgen.1002218.s020.ogv 17 s, 1.176 × 960; 1,57 MB
An-Engineering-Approach-to-Extending-Lifespan-in-C.-elegans-pgen.1002780.s010.ogv 30 s, 640 × 480; 981 KB
An-Engineering-Approach-to-Extending-Lifespan-in-C.-elegans-pgen.1002780.s011.ogv 30 s, 640 × 480; 1,01 MB
An-Engineering-Approach-to-Extending-Lifespan-in-C.-elegans-pgen.1002780.s012.ogv 30 s, 640 × 480; 901 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s017.ogv 11 s, 750 × 500; 417 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s018.ogv 16 s, 500 × 500; 293 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s019.ogv 10 s, 1.050 × 350; 177 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s020.ogv 17 s, 300 × 300; 88 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s021.ogv 16 s, 300 × 300; 63 KB
An-Essential-Role-for-DYF-11MIP-T3-in-Assembling-Functional-Intraflagellar-Transport-Complexes-pgen.1000044.s001.ogv 22 s, 131 × 149; 64 KB
An-Essential-Role-for-Katanin-p80-and-Microtubule-Severing-in-Male-Gamete-Production-pgen.1002698.s006.ogv 6,5 s, 1.024 × 1.024; 3,56 MB
An-Essential-Role-for-Katanin-p80-and-Microtubule-Severing-in-Male-Gamete-Production-pgen.1002698.s007.ogv 4,5 s, 1.024 × 1.024; 1,52 MB
An-Essential-Role-for-Katanin-p80-and-Microtubule-Severing-in-Male-Gamete-Production-pgen.1002698.s008.ogv 5,0 s, 1.024 × 1.024; 106 KB
An-Essential-Role-for-Katanin-p80-and-Microtubule-Severing-in-Male-Gamete-Production-pgen.1002698.s009.ogv 5,0 s, 1.024 × 1.024; 54 KB
An-Essential-Role-of-the-Arginine-Vasotocin-System-in-Mate-Guarding-Behaviors-in-Triadic-pgen.1005009.s021.ogv 10 s, 480 × 360; 344 KB
An-Essential-Role-of-the-Arginine-Vasotocin-System-in-Mate-Guarding-Behaviors-in-Triadic-pgen.1005009.s022.ogv 14 s, 480 × 360; 531 KB
An-Essential-Role-of-the-Arginine-Vasotocin-System-in-Mate-Guarding-Behaviors-in-Triadic-pgen.1005009.s023.ogv 9,5 s, 1.280 × 720; 837 KB
An-Essential-Role-of-the-Arginine-Vasotocin-System-in-Mate-Guarding-Behaviors-in-Triadic-pgen.1005009.s024.ogv 9,2 s, 1.280 × 720; 797 KB
An-Essential-Role-of-the-Arginine-Vasotocin-System-in-Mate-Guarding-Behaviors-in-Triadic-pgen.1005009.s025.ogv 11 s, 480 × 360; 280 KB
An-Integrated-Strategy-for-Analyzing-the-Unique-Developmental-Programs-of-Different-Myoblast-pgen.0020016.sv001.ogv 12 s, 435 × 435; 674 KB
Analysis-of-Meiosis-in-SUN1-Deficient-Mice-Reveals-a-Distinct-Role-of-SUN2-in-Mammalian-Meiotic-pgen.1004099.s002.ogv 5,1 s, 550 × 500; 537 KB
Anillin-Phosphorylation-Controls-Timely-Membrane-Association-and-Successful-Cytokinesis-pgen.1006511.s009.ogv 17 s, 400 × 400; 1,69 MB
Anillin-Phosphorylation-Controls-Timely-Membrane-Association-and-Successful-Cytokinesis-pgen.1006511.s010.ogv 43 s, 500 × 500; 8,92 MB
Anillin-Phosphorylation-Controls-Timely-Membrane-Association-and-Successful-Cytokinesis-pgen.1006511.s011.ogv 39 s, 800 × 800; 6,51 MB
Anillin-Phosphorylation-Controls-Timely-Membrane-Association-and-Successful-Cytokinesis-pgen.1006511.s012.ogv 23 s, 500 × 500; 2,18 MB
Anillin-Phosphorylation-Controls-Timely-Membrane-Association-and-Successful-Cytokinesis-pgen.1006511.s013.ogv 29 s, 700 × 500; 5,63 MB
Arabidopsis-AtMORC4-and-AtMORC7-Form-Nuclear-Bodies-and-Repress-a-Large-Number-of-Protein-Coding-pgen.1005998.s011.ogv 14 s, 252 × 218; 47 KB
Arabidopsis-AtMORC4-and-AtMORC7-Form-Nuclear-Bodies-and-Repress-a-Large-Number-of-Protein-Coding-pgen.1005998.s012.ogv 1,6 s, 204 × 210; 19 KB
Arabidopsis-COG-Complex-Subunits-COG3-and-COG8-Modulate-Golgi-Morphology-Vesicle-Trafficking-pgen.1006140.s013.ogv 5,3 s, 1.022 × 1.018; 392 KB
Arabidopsis-COG-Complex-Subunits-COG3-and-COG8-Modulate-Golgi-Morphology-Vesicle-Trafficking-pgen.1006140.s014.ogv 8,5 s, 1.002 × 972; 862 KB
Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s016.ogv 19 s, 736 × 608; 9,69 MB
Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s017.ogv 33 s, 592 × 496; 2,42 MB
Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s018.ogv 12 s, 277 × 224; 2,06 MB
Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s019.ogv 12 s, 304 × 304; 1,96 MB
Arginylation-Dependent-Neural-Crest-Cell-Migration-Is-Essential-for-Mouse-Development-pgen.1000878.s020.ogv 9,0 s, 749 × 706; 2,83 MB
Asymmetry-of-Chromosome-Replichores-Renders-the-DNA-Translocase-Activity-of-FtsK-Essential-for-Cell-pgen.1000288.s007.ogv 21 s, 350 × 316; 531 KB
Asymmetry-of-Chromosome-Replichores-Renders-the-DNA-Translocase-Activity-of-FtsK-Essential-for-Cell-pgen.1000288.s008.ogv 21 s, 308 × 272; 402 KB
Attenuation-of-Notch-and-Hedgehog-Signaling-Is-Required-for-Fate-Specification-in-the-Spinal-Cord-pgen.1002762.s004.ogv 1 min 1 s, 942 × 570; 2,77 MB
Attenuation-of-Notch-and-Hedgehog-Signaling-Is-Required-for-Fate-Specification-in-the-Spinal-Cord-pgen.1002762.s005.ogv 19 s, 799 × 440; 1,87 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.s010.ogv 7,0 s, 870 × 300; 1,18 MB
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
Aurora-A-Dependent-Control-of-TACC3-Influences-the-Rate-of-Mitotic-Spindle-Assembly-pgen.1005345.s011.ogv 14 s, 850 × 850; 204 KB
Aurora-A-Dependent-Control-of-TACC3-Influences-the-Rate-of-Mitotic-Spindle-Assembly-pgen.1005345.s012.ogv 5,8 s, 850 × 850; 248 KB
Aurora-A-Dependent-Control-of-TACC3-Influences-the-Rate-of-Mitotic-Spindle-Assembly-pgen.1005345.s013.ogv 11 s, 850 × 850; 949 KB
Aurora-A-Dependent-Control-of-TACC3-Influences-the-Rate-of-Mitotic-Spindle-Assembly-pgen.1005345.s014.ogv 6,6 s, 850 × 850; 741 KB
Autophosphorylation-of-the-Bacterial-Tyrosine-Kinase-CpsD-Connects-Capsule-Synthesis-with-the-Cell-pgen.1005518.s010.ogv 4,5 s, 854 × 480; 113 KB
Auxin-Influx-Carriers-Control-Vascular-Patterning-and-Xylem-Differentiation-in-Arabidopsis-thaliana-pgen.1005183.s019.ogv 7,0 s, 1.200 × 600; 297 KB
Basolateral-Mg2+-Extrusion-via-CNNM4-Mediates-Transcellular-Mg2+-Transport-across-Epithelia-A-Mouse-pgen.1003983.s006.ogv 10 s, 123 × 107; 19 KB
Beclin-1-Is-Required-for-Neuron-Viability-and-Regulates-Endosome-Pathways-via-the-UVRAG-VPS34-pgen.1004626.s006.ogv 23 s, 640 × 480; 9,37 MB
Beclin-1-Is-Required-for-Neuron-Viability-and-Regulates-Endosome-Pathways-via-the-UVRAG-VPS34-pgen.1004626.s007.ogv 13 s, 640 × 480; 8,81 MB
Bilaterian-Giant-Ankyrins-Have-a-Common-Evolutionary-Origin-and-Play-a-Conserved-Role-in-Patterning-pgen.1006457.s006.ogv 19 s, 330 × 352; 782 KB
Bmp-and-Nodal-Independently-Regulate-lefty1-Expression-to-Maintain-Unilateral-Nodal-Activity-during-pgen.1002289.s008.ogv 17 s, 616 × 400; 3,59 MB
Bmp-and-Nodal-Independently-Regulate-lefty1-Expression-to-Maintain-Unilateral-Nodal-Activity-during-pgen.1002289.s009.ogv 17 s, 616 × 400; 3,11 MB
Bmp-and-Nodal-Independently-Regulate-lefty1-Expression-to-Maintain-Unilateral-Nodal-Activity-during-pgen.1002289.s010.ogv 17 s, 640 × 480; 2,27 MB
Bruce Alberts.png 1.335 × 1.849; 3,2 MB
C.-elegans-Dopaminergic-D2-Like-Receptors-Delimit-Recurrent-Cholinergic-Mediated-Motor-Programs-pgen.1003015.s014.ogv 11 s, 640 × 480; 4,48 MB
C.-elegans-Dopaminergic-D2-Like-Receptors-Delimit-Recurrent-Cholinergic-Mediated-Motor-Programs-pgen.1003015.s015.ogv 13 s, 640 × 480; 3,48 MB
CA8-Mutations-Cause-a-Novel-Syndrome-Characterized-by-Ataxia-and-Mild-Mental-Retardation-with-pgen.1000487.s001.ogv 1 min 2 s, 320 × 240; 3,69 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

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