Category:Videos of medical microbiology

From Wikimedia Commons, the free media repository

Jump to navigation Jump to search

Subcategories

This category has only the following subcategory.

B

Videos of biofilms (1 C, 15 F)

Media in category "Videos of medical microbiology"

The following 200 files are in this category, out of 231 total.

(previous page) (next page)

A-MultiSite-Gateway-Toolkit-for-Rapid-Cloning-of-Vertebrate-Expression-Constructs-with-Diverse-pone.0159277.s001.ogv 6.8 s, 568 × 444; 44 KB
A-New-Method-to-Extract-Dental-Pulp-DNA-Application-to-Universal-Detection-of-Bacteria-pone.0001062.s002.ogv 30 s, 375 × 288; 1.34 MB
A-Novel-Approach-for-Purification-and-Selective-Capture-of-Membrane-Vesicles-of-the-pone.0095137.s004.ogv 6.0 s, 512 × 512; 2.53 MB
A-Novel-Approach-for-Purification-and-Selective-Capture-of-Membrane-Vesicles-of-the-pone.0095137.s005.ogv 6.0 s, 512 × 512; 1.8 MB
A-Precise-Temperature-Responsive-Bistable-Switch-Controlling-Yersinia-Virulence-ppat.1006091.s013.ogv 13 s, 514 × 326; 506 KB
A-Precise-Temperature-Responsive-Bistable-Switch-Controlling-Yersinia-Virulence-ppat.1006091.s014.ogv 6.3 s, 400 × 506; 133 KB
A-Precise-Temperature-Responsive-Bistable-Switch-Controlling-Yersinia-Virulence-ppat.1006091.s015.ogv 7.5 s, 400 × 534; 114 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s007.ogv 12 s, 134 × 154; 91 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s008.ogv 11 s, 124 × 90; 42 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s009.ogv 7.3 s, 192 × 109; 40 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s010.ogv 14 s, 284 × 280; 361 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s011.ogv 17 s, 178 × 122; 104 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s012.ogv 16 s, 178 × 122; 86 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s013.ogv 9.3 s, 144 × 133; 104 KB
A-Tetraploid-Intermediate-Precedes-Aneuploid-Formation-in-Yeasts-Exposed-to-Fluconazole-pbio.1001815.s014.ogv 6.3 s, 144 × 133; 63 KB
A-Translocated-Effector-Required-for-Bartonella-Dissemination-from-Derma-to-Blood-Safeguards-ppat.1004187.s010.ogv 36 s, 1,414 × 714; 4.82 MB
A-Translocated-Effector-Required-for-Bartonella-Dissemination-from-Derma-to-Blood-Safeguards-ppat.1004187.s011.ogv 37 s, 1,728 × 872; 6.05 MB
A-Translocated-Effector-Required-for-Bartonella-Dissemination-from-Derma-to-Blood-Safeguards-ppat.1004187.s012.ogv 35 s, 1,710 × 864; 3.88 MB
A-Translocated-Effector-Required-for-Bartonella-Dissemination-from-Derma-to-Blood-Safeguards-ppat.1004187.s013.ogv 12 s, 1,240 × 1,384; 1.56 MB
A-Translocated-Effector-Required-for-Bartonella-Dissemination-from-Derma-to-Blood-Safeguards-ppat.1004187.s014.ogv 13 s, 840 × 720; 1.75 MB
A-Translocated-Effector-Required-for-Bartonella-Dissemination-from-Derma-to-Blood-Safeguards-ppat.1004187.s015.ogv 49 s, 640 × 480; 4.71 MB
Adherence-of-Staphylococcus-aureus-to-Dyneema-Purity®-Patches-and-to-Clinically-Used-Cardiovascular-pone.0162216.s001.ogv 13 s, 1,392 × 1,040; 6.26 MB
Adherence-of-Staphylococcus-aureus-to-Dyneema-Purity®-Patches-and-to-Clinically-Used-Cardiovascular-pone.0162216.s002.ogv 13 s, 1,392 × 1,040; 1.09 MB
Agent-Based-Model-of-Human-Alveoli-Predicts-Chemotactic-Signaling-by-Epithelial-Cells-during-Early-pone.0111630.s007.ogv 20 s, 1,280 × 720; 3.96 MB
Agent-Based-Model-of-Human-Alveoli-Predicts-Chemotactic-Signaling-by-Epithelial-Cells-during-Early-pone.0111630.s008.ogv 24 s, 1,280 × 720; 1.33 MB
Agent-Based-Model-of-Human-Alveoli-Predicts-Chemotactic-Signaling-by-Epithelial-Cells-during-Early-pone.0111630.s009.ogv 20 s, 1,280 × 720; 2.57 MB
Agent-Based-Model-of-Human-Alveoli-Predicts-Chemotactic-Signaling-by-Epithelial-Cells-during-Early-pone.0111630.s010.ogv 13 s, 1,280 × 720; 577 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
Anaplasma-phagocytophilum-Ats-1-Is-Imported-into-Host-Cell-Mitochondria-and-Interferes-with-ppat.1000774.s004.ogv 3.6 s, 494 × 480; 296 KB
Antifungal-Activity-and-Action-Mechanism-of-Histatin-5-Halocidin-Hybrid-Peptides-against-Candida-ssp-pone.0150196.s002.ogv 10 s, 595 × 593; 623 KB
Assembly-and-Development-of-the-Pseudomonas-aeruginosa-Biofilm-Matrix-ppat.1000354.s002.ogv 10 s, 512 × 512; 509 KB
Assembly-and-Development-of-the-Pseudomonas-aeruginosa-Biofilm-Matrix-ppat.1000354.s003.ogv 5.0 s, 519 × 512; 191 KB
Assembly-and-Development-of-the-Pseudomonas-aeruginosa-Biofilm-Matrix-ppat.1000354.s004.ogv 8.0 s, 519 × 512; 451 KB
Biofilm-Induced-Tolerance-towards-Antimicrobial-Peptides-pone.0001891.s001.ogv 0.0 s, 512 × 480; 18.13 MB
Bistable-Expression-of-Virulence-Genes-in-Salmonella-Leads-to-the-Formation-of-an-Antibiotic-pbio.1001928.s012.ogv 28 s, 501 × 459; 3.84 MB
Bistable-Expression-of-Virulence-Genes-in-Salmonella-Leads-to-the-Formation-of-an-Antibiotic-pbio.1001928.s013.ogv 43 s, 457 × 453; 4.93 MB
Bistable-Expression-of-Virulence-Genes-in-Salmonella-Leads-to-the-Formation-of-an-Antibiotic-pbio.1001928.s014.ogv 36 s, 514 × 441; 3.99 MB
Bistable-Expression-of-Virulence-Genes-in-Salmonella-Leads-to-the-Formation-of-an-Antibiotic-pbio.1001928.s015.ogv 28 s, 607 × 452; 4.85 MB
Bistable-Expression-of-Virulence-Genes-in-Salmonella-Leads-to-the-Formation-of-an-Antibiotic-pbio.1001928.s016.ogv 38 s, 468 × 410; 1.2 MB
Concerted-Spatio-Temporal-Dynamics-of-Imported-DNA-and-ComE-DNA-Uptake-Protein-during-Gonococcal-ppat.1004043.s009.ogv 15 s, 480 × 240; 301 KB
Concerted-Spatio-Temporal-Dynamics-of-Imported-DNA-and-ComE-DNA-Uptake-Protein-during-Gonococcal-ppat.1004043.s010.ogv 15 s, 60 × 30; 38 KB
Concerted-Spatio-Temporal-Dynamics-of-Imported-DNA-and-ComE-DNA-Uptake-Protein-during-Gonococcal-ppat.1004043.s011.ogv 31 s, 60 × 30; 32 KB
Concerted-Spatio-Temporal-Dynamics-of-Imported-DNA-and-ComE-DNA-Uptake-Protein-during-Gonococcal-ppat.1004043.s012.ogv 20 s, 60 × 30; 32 KB
Concerted-Spatio-Temporal-Dynamics-of-Imported-DNA-and-ComE-DNA-Uptake-Protein-during-Gonococcal-ppat.1004043.s013.ogv 6.7 s, 60 × 30; 12 KB
Concerted-Spatio-Temporal-Dynamics-of-Imported-DNA-and-ComE-DNA-Uptake-Protein-during-Gonococcal-ppat.1004043.s014.ogv 7.0 s, 100 × 50; 24 KB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s002.ogv 4.8 s, 1,344 × 1,024; 8.65 MB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s003.ogv 6.6 s, 320 × 240; 124 KB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s004.ogv 6.5 s, 240 × 320; 331 KB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s005.ogv 12 s, 240 × 320; 548 KB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s006.ogv 7.0 s, 240 × 320; 78 KB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s007.ogv 32 s, 1,525 × 1,140; 10.49 MB
Control-and-Manipulation-of-Pathogens-with-an-Optical-Trap-for-Live-Cell-Imaging-of-Intercellular-pone.0015215.s008.ogv 2.7 s, 240 × 320; 54 KB
Cryo-EM-Structure-of-Isomeric-Molluscan-Hemocyanin-Triggered-by-Viral-Infection-pone.0098766.s008.ogv 29 s, 300 × 300; 11.35 MB
Cryo-EM-Structure-of-Isomeric-Molluscan-Hemocyanin-Triggered-by-Viral-Infection-pone.0098766.s009.ogv 4.1 s, 600 × 600; 678 KB
Discovery-of-a-Natural-Microsporidian-Pathogen-with-a-Broad-Tissue-Tropism-in-Caenorhabditis-elegans-ppat.1005724.s015.ogv 10 s, 640 × 360; 203 KB
Dynamic-Organization-of-SecA-and-SecY-Secretion-Complexes-in-the-B.-subtilis-Membrane-pone.0157899.s011.ogv 44 s, 93 × 18; 172 KB
Efficacy-of-a-Marine-Bacterial-Nuclease-against-Biofilm-Forming-Microorganisms-Isolated-from-pone.0055339.s001.ogv 7.2 s, 1,036 × 1,024; 984 KB
Endothelial-Cells-Use-a-Formin-Dependent-Phagocytosis-Like-Process-to-Internalize-the-Bacterium-ppat.1005603.s008.ogv 3.0 s, 454 × 237; 792 KB
Endothelial-Cells-Use-a-Formin-Dependent-Phagocytosis-Like-Process-to-Internalize-the-Bacterium-ppat.1005603.s009.ogv 3.5 s, 1,024 × 1,024; 5.1 MB
Endothelial-Cells-Use-a-Formin-Dependent-Phagocytosis-Like-Process-to-Internalize-the-Bacterium-ppat.1005603.s010.ogv 6.3 s, 1,024 × 1,024; 20.39 MB
Endothelial-Cells-Use-a-Formin-Dependent-Phagocytosis-Like-Process-to-Internalize-the-Bacterium-ppat.1005603.s011.ogv 3.0 s, 159 × 133; 180 KB
Endothelial-Cells-Use-a-Formin-Dependent-Phagocytosis-Like-Process-to-Internalize-the-Bacterium-ppat.1005603.s012.ogv 20 s, 236 × 179; 696 KB
Evidence-for-Divisome-Localization-Mechanisms-Independent-of-the-Min-System-and-SlmA-in-Escherichia-pgen.1004504.s019.ogv 3.2 s, 103 × 102; 98 KB
Evidence-for-Divisome-Localization-Mechanisms-Independent-of-the-Min-System-and-SlmA-in-Escherichia-pgen.1004504.s020.ogv 3.2 s, 102 × 102; 43 KB
Evidence-for-Divisome-Localization-Mechanisms-Independent-of-the-Min-System-and-SlmA-in-Escherichia-pgen.1004504.s021.ogv 3.6 s, 101 × 101; 168 KB
FleA-Expression-in-Aspergillus-fumigatus-Is-Recognized-by-Fucosylated-Structures-on-Mucins-and-ppat.1005555.s003.ogv 2.4 s, 312 × 312; 31 KB
Francisella-tularensis-IglG-Belongs-to-a-Novel-Family-of-PAAR-Like-T6SS-Proteins-and-Harbors-a-ppat.1005821.s018.ogv 41 s, 669 × 834; 9.71 MB
Genetic-Analysis-of-Collective-Motility-of-Paenibacillus-sp.-NAIST15-1-pgen.1006387.s014.ogv 20 s, 640 × 480; 472 KB
Genetically-Engineered-Alginate-Lyase-PEG-Conjugates-Exhibit-Enhanced-Catalytic-Function-and-pone.0017042.s001.ogv 13 s, 640 × 480; 5.25 MB
Histone-Deacetylase-Inhibitors-Impair-the-Elimination-of-HIV-Infected-Cells-by-Cytotoxic-T-ppat.1004287.s002.ogv 33 s, 112 × 93; 558 KB
Histone-Deacetylase-Inhibitors-Impair-the-Elimination-of-HIV-Infected-Cells-by-Cytotoxic-T-ppat.1004287.s003.ogv 33 s, 167 × 147; 808 KB
Histone-Deacetylase-Inhibitors-Impair-the-Elimination-of-HIV-Infected-Cells-by-Cytotoxic-T-ppat.1004287.s004.ogv 33 s, 140 × 112; 251 KB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s007.ogv 6.1 s, 2,034 × 855; 5.47 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s008.ogv 11 s, 1,914 × 1,053; 1.89 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s009.ogv 30 s, 1,984 × 1,144; 6.79 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s010.ogv 5.0 s, 1,000 × 427; 822 KB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s011.ogv 30 s, 4,602 × 1,434; 24.18 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s012.ogv 6.6 s, 3,820 × 792; 4.19 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s013.ogv 30 s, 1,409 × 619; 14.69 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s014.ogv 2.2 s, 2,271 × 375; 1.21 MB
Host-Gut-Motility-Promotes-Competitive-Exclusion-within-a-Model-Intestinal-Microbiota-pbio.1002517.s015.ogv 30 s, 2,271 × 375; 14.03 MB
Identification-of-a-Novel-Drug-Lead-That-Inhibits-HCV-Infection-and-Cell-to-Cell-Transmission-by-pone.0111333.s002.ogv 15 s, 352 × 288; 1.85 MB
Identification-of-Candida-glabrata-Genes-Involved-in-pH-Modulation-and-Modification-of-the-pone.0096015.s002.ogv 8.5 s, 1,388 × 520; 3.73 MB
Identification-of-SerThr-kinase-and-Forkhead-Associated-Domains-in-Mycobacterium-ulcerans-pntd.0003315.s011.ogv 32 s, 496 × 476; 16.49 MB
Identification-of-SerThr-kinase-and-Forkhead-Associated-Domains-in-Mycobacterium-ulcerans-pntd.0003315.s012.ogv 48 s, 572 × 532; 24.53 MB
Identification-of-SerThr-kinase-and-Forkhead-Associated-Domains-in-Mycobacterium-ulcerans-pntd.0003315.s013.ogv 48 s, 572 × 532; 18.65 MB
IFNs-Modify-the-Proteome-of-Legionella-Containing-Vacuoles-and-Restrict-Infection-Via-IRG1-Derived-ppat.1005408.s013.ogv 16 s, 223 × 237; 264 KB
Image-Restoration-and-Analysis-of-Influenza-Virions-Binding-to-Membrane-Receptors-Reveal-Adhesion-pone.0163437.s004.ogv 30 s, 512 × 512; 60.76 MB
Image-Restoration-and-Analysis-of-Influenza-Virions-Binding-to-Membrane-Receptors-Reveal-Adhesion-pone.0163437.s005.ogv 30 s, 512 × 512; 60.7 MB
Initial-Characterization-of-the-FlgE-Hook-High-Molecular-Weight-Complex-of-Borrelia-burgdorferi-pone.0098338.s001.ogv 40 s, 640 × 480; 3.76 MB
Intravaginal-Chlamydia-trachomatis-Challenge-Infection-Elicits-TH1-and-TH17-Immune-Responses-in-pone.0162445.s007.ogv 11 s, 472 × 500; 387 KB
Intravaginal-Chlamydia-trachomatis-Challenge-Infection-Elicits-TH1-and-TH17-Immune-Responses-in-pone.0162445.s008.ogv 11 s, 472 × 500; 266 KB
Live-Cell-Imaging-Reveals-Novel-Functions-of-Salmonella-enterica-SPI2-T3SS-Effector-Proteins-in-pone.0115423.s004.ogv 4.2 s, 854 × 538; 3.39 MB
Live-Cell-Imaging-Reveals-Novel-Functions-of-Salmonella-enterica-SPI2-T3SS-Effector-Proteins-in-pone.0115423.s028.ogv 6.4 s, 450 × 375; 99 KB
Low-Cost-3D-Printers-Enable-High-Quality-and-Automated-Sample-Preparation-and-Molecular-Detection-pone.0158502.s006.ogv 1 min 35 s, 1,920 × 1,080; 28.95 MB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s008.ogv 9.0 s, 231 × 77; 66 KB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s009.ogv 11 s, 201 × 63; 418 KB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s010.ogv 4.3 s, 552 × 116; 191 KB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s011.ogv 7.3 s, 696 × 235; 554 KB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s012.ogv 7.3 s, 1,086 × 299; 1.41 MB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s013.ogv 40 s, 1,312 × 576; 22.23 MB
Macropinosomes-are-Key-Players-in-Early-Shigella-Invasion-and-Vacuolar-Escape-in-Epithelial-Cells-ppat.1005602.s014.ogv 42 s, 1,104 × 592; 28.56 MB
Mannose-Binding-Lectin-Inhibits-the-Motility-of-Pathogenic-Salmonella-by-Affecting-the-Driving-pone.0154165.s005.ogv 6.0 s, 315 × 210; 551 KB
Mannose-Binding-Lectin-Inhibits-the-Motility-of-Pathogenic-Salmonella-by-Affecting-the-Driving-pone.0154165.s006.ogv 6.0 s, 324 × 224; 402 KB
Mannose-Binding-Lectin-Inhibits-the-Motility-of-Pathogenic-Salmonella-by-Affecting-the-Driving-pone.0154165.s007.ogv 5.9 s, 587 × 396; 488 KB
Mannose-Binding-Lectin-Inhibits-the-Motility-of-Pathogenic-Salmonella-by-Affecting-the-Driving-pone.0154165.s008.ogv 14 s, 50 × 50; 1.31 MB
Mannose-Binding-Lectin-Inhibits-the-Motility-of-Pathogenic-Salmonella-by-Affecting-the-Driving-pone.0154165.s009.ogv 30 s, 50 × 50; 1.31 MB
Mathematical-and-Live-Meningococcal-Models-for-Simple-Sequence-Repeat-Dynamics---Coherent-pone.0101637.s008.ogv 40 s, 812 × 612; 1.42 MB
Mathematical-Modeling-Predicts-that-Increased-HSV-2-Shedding-in-HIV-1-Infected-Persons-Is-Due-to-pone.0155124.s010.ogv 1 min 19 s, 1,920 × 1,080; 4.25 MB
Mechanistic-Insight-into-Bunyavirus-Induced-Membrane-Fusion-from-Structure-Function-Analyses-of-the-ppat.1005813.s010.ogv 16 s, 1,280 × 652; 38.83 MB
Mechanistic-Insight-into-Bunyavirus-Induced-Membrane-Fusion-from-Structure-Function-Analyses-of-the-ppat.1005813.s011.ogv 16 s, 1,280 × 652; 36.26 MB
Mechanistic-Insight-into-Bunyavirus-Induced-Membrane-Fusion-from-Structure-Function-Analyses-of-the-ppat.1005813.s012.ogv 16 s, 1,280 × 652; 19.36 MB
Mechanistic-Insight-into-Bunyavirus-Induced-Membrane-Fusion-from-Structure-Function-Analyses-of-the-ppat.1005813.s013.ogv 21 s, 3,000 × 2,000; 5.04 MB
Modelling-the-Structure-and-Dynamics-of-Biological-Pathways-pbio.1002530.s008.ogv 5 min 48 s, 1,280 × 720; 43.93 MB
Modulation-of-Neutrophil-Function-by-a-Secreted-Mucinase-of-Escherichia-coli-O157∶H7-ppat.1000320.s004.ogv 4.0 s, 429 × 339; 251 KB
Modulation-of-Phagosomal-pH-by-Candida-albicans-Promotes-Hyphal-Morphogenesis-and-Requires-Stp2p-a-ppat.1003995.s006.ogv 1 min 25 s, 672 × 512; 1.3 MB
Modulation-of-Phagosomal-pH-by-Candida-albicans-Promotes-Hyphal-Morphogenesis-and-Requires-Stp2p-a-ppat.1003995.s007.ogv 1 min 25 s, 672 × 512; 1,002 KB
Motility-and-Chemotaxis-Mediate-the-Preferential-Colonization-of-Gastric-Injury-Sites-by-ppat.1004275.s010.ogv 20 s, 749 × 742; 7.01 MB
Motility-and-Chemotaxis-Mediate-the-Preferential-Colonization-of-Gastric-Injury-Sites-by-ppat.1004275.s011.ogv 5.0 s, 2,090 × 1,091; 2.13 MB
MRI-Based-Localisation-and-Quantification-of-Abscesses-following-Experimental-S.-aureus-Intravenous-pone.0154705.s005.ogv 20 s, 512 × 512; 1.81 MB
MRI-Based-Localisation-and-Quantification-of-Abscesses-following-Experimental-S.-aureus-Intravenous-pone.0154705.s006.ogv 15 s, 512 × 512; 1.6 MB
MRI-Based-Localisation-and-Quantification-of-Abscesses-following-Experimental-S.-aureus-Intravenous-pone.0154705.s007.ogv 31 s, 512 × 512; 4.26 MB
MRI-Based-Localisation-and-Quantification-of-Abscesses-following-Experimental-S.-aureus-Intravenous-pone.0154705.s008.ogv 3 min 26 s, 504 × 504; 22.19 MB
Mycobacterium-tuberculosis-Proteins-Involved-in-Mycolic-Acid-Synthesis-and-Transport-Localize-pone.0097148.s013.ogv 20 s, 1,800 × 750; 308 KB
Mycobacterium-tuberculosis-Responds-to-Chloride-and-pH-as-Synergistic-Cues-to-the-Immune-Status-of-ppat.1003282.s002.ogv 3.1 s, 702 × 702; 2.6 MB
Mycobacterium-tuberculosis-Responds-to-Chloride-and-pH-as-Synergistic-Cues-to-the-Immune-Status-of-ppat.1003282.s003.ogv 3.1 s, 702 × 702; 2.7 MB
Mycobacterium-tuberculosis-Responds-to-Chloride-and-pH-as-Synergistic-Cues-to-the-Immune-Status-of-ppat.1003282.s004.ogv 3.1 s, 758 × 670; 2.52 MB
Mycobacterium-tuberculosis-Responds-to-Chloride-and-pH-as-Synergistic-Cues-to-the-Immune-Status-of-ppat.1003282.s005.ogv 3.1 s, 758 × 670; 2.3 MB
Neisseria-meningitidis-Differentially-Controls-Host-Cell-Motility-through-PilC1-and-PilC2-pone.0006834.s003.ogv 22 s, 300 × 225; 2.5 MB
Neisseria-meningitidis-Differentially-Controls-Host-Cell-Motility-through-PilC1-and-PilC2-pone.0006834.s004.ogv 21 s, 300 × 225; 1.93 MB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s009.ogv 2.0 s, 208 × 216; 26 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s010.ogv 2.0 s, 208 × 216; 6 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s011.ogv 9.0 s, 176 × 176; 55 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s012.ogv 9.0 s, 176 × 176; 17 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s013.ogv 8.5 s, 84 × 60; 14 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s014.ogv 8.5 s, 84 × 60; 7 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s015.ogv 8.0 s, 104 × 108; 14 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s016.ogv 8.0 s, 104 × 108; 7 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s017.ogv 0.3 s, 172 × 284; 47 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s018.ogv 13 s, 72 × 60; 31 KB
Neutrophil-Attack-Triggers-Extracellular-Trap-Dependent-Candida-Cell-Wall-Remodeling-and-Altered-ppat.1005644.s019.ogv 13 s, 72 × 60; 11 KB
Oral-and-Fecal-Campylobacter-concisus-Strains-Perturb-Barrier-Function-by-Apoptosis-Induction-in-HT-pone.0023858.s001.ogv 13 s, 768 × 576; 7.79 MB
Osteopontin-Reduces-Biofilm-Formation-in-a-Multi-Species-Model-of-Dental-Biofilm-pone.0041534.s006.ogv 20 s, 640 × 480; 595 KB
Osteopontin-Reduces-Biofilm-Formation-in-a-Multi-Species-Model-of-Dental-Biofilm-pone.0041534.s007.ogv 20 s, 640 × 480; 811 KB
Penicillin-Induced-Persistence-in-Chlamydia-trachomatis-High-Quality-Time-Lapse-Video-Analysis-of-pone.0007723.s002.ogv 3 min 11 s, 480 × 360; 28.36 MB
Penicillin-Induced-Persistence-in-Chlamydia-trachomatis-High-Quality-Time-Lapse-Video-Analysis-of-pone.0007723.s003.ogv 1 min 31 s, 480 × 360; 36.69 MB
Penicillin-Induced-Persistence-in-Chlamydia-trachomatis-High-Quality-Time-Lapse-Video-Analysis-of-pone.0007723.s004.ogv 2 min 24 s, 480 × 360; 20.12 MB
Phospholipase-C-Related-Catalytically-Inactive-Protein-Participates-in-the-Autophagic-Elimination-pone.0098285.s003.ogv 22 s, 640 × 480; 885 KB
Phospholipase-C-Related-Catalytically-Inactive-Protein-Participates-in-the-Autophagic-Elimination-pone.0098285.s004.ogv 23 s, 640 × 480; 629 KB
Phylogeography-of-Rift-Valley-Fever-Virus-in-Africa-and-the-Arabian-Peninsula-pntd.0005226.s009.ogv 1 min 33 s, 1,920 × 1,080; 35.09 MB
Polarized-Cell-Division-of-Chlamydia-trachomatis-ppat.1005822.s004.ogv 16 s, 1,440 × 1,072; 125 KB
Polarized-Cell-Division-of-Chlamydia-trachomatis-ppat.1005822.s005.ogv 15 s, 1,440 × 1,072; 121 KB
PSGL-1-on-Leukocytes-is-a-Critical-Component-of-the-Host-Immune-Response-against-Invasive-ppat.1005500.s004.ogv 1.7 s, 512 × 512; 889 KB
PSGL-1-on-Leukocytes-is-a-Critical-Component-of-the-Host-Immune-Response-against-Invasive-ppat.1005500.s005.ogv 4.4 s, 512 × 512; 787 KB
Rabies-Virus-Infection-Induces-the-Formation-of-Stress-Granules-Closely-Connected-to-the-Viral-ppat.1005942.s001.ogv 17 s, 1,352 × 694; 2.48 MB
Rabies-Virus-Infection-Induces-the-Formation-of-Stress-Granules-Closely-Connected-to-the-Viral-ppat.1005942.s002.ogv 9.9 s, 1,352 × 694; 1,019 KB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s017.ogv 5.8 s, 976 × 884; 2.49 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s018.ogv 6.7 s, 496 × 488; 2.68 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s019.ogv 5.7 s, 734 × 712; 3.32 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s020.ogv 8.6 s, 510 × 510; 3.67 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s021.ogv 5.1 s, 512 × 512; 2.24 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s022.ogv 9.3 s, 510 × 510; 3.04 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s023.ogv 8.7 s, 704 × 576; 4.33 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s024.ogv 7.9 s, 704 × 576; 4.36 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s025.ogv 5.7 s, 740 × 690; 3.63 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s026.ogv 9.5 s, 704 × 576; 4.85 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s027.ogv 7.0 s, 750 × 712; 4.09 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s028.ogv 29 s, 940 × 912; 7 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s029.ogv 9.3 s, 512 × 510; 4.34 MB
Reorganization-of-the-Endosomal-System-in-Salmonella-Infected-Cells-The-Ultrastructure-of-ppat.1004374.s030.ogv 29 s, 886 × 878; 2.12 MB
Salmonella-Transiently-Reside-in-Luminal-Neutrophils-in-the-Inflamed-Gut-pone.0034812.s003.ogv 6.7 s, 252 × 276; 198 KB
Structure-Guided-Mutations-in-the-Terminal-Organelle-Protein-MG491-Cause-Major-Motility-and-ppat.1005533.s009.ogv 31 s, 600 × 600; 538 KB
Structure-Guided-Mutations-in-the-Terminal-Organelle-Protein-MG491-Cause-Major-Motility-and-ppat.1005533.s010.ogv 31 s, 600 × 600; 1.82 MB
Structure-Guided-Mutations-in-the-Terminal-Organelle-Protein-MG491-Cause-Major-Motility-and-ppat.1005533.s011.ogv 15 s, 600 × 600; 70 KB
Structure-Guided-Mutations-in-the-Terminal-Organelle-Protein-MG491-Cause-Major-Motility-and-ppat.1005533.s012.ogv 31 s, 600 × 600; 277 KB
Structure-Guided-Mutations-in-the-Terminal-Organelle-Protein-MG491-Cause-Major-Motility-and-ppat.1005533.s013.ogv 31 s, 600 × 600; 846 KB
Structure-Guided-Mutations-in-the-Terminal-Organelle-Protein-MG491-Cause-Major-Motility-and-ppat.1005533.s014.ogv 31 s, 600 × 600; 140 KB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s001.ogv 3.1 s, 620 × 558; 9.73 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s002.ogv 3.3 s, 546 × 480; 1.11 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s003.ogv 4.2 s, 600 × 212; 1.86 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s004.ogv 3.3 s, 378 × 516; 2.02 MB
Super-Resolution-Fluorescence-Microscopy-and-Tracking-of-Bacterial-Flotillin-(Reggie)-Paralogs-pgen.1006116.s005.ogv 3.3 s, 538 × 310; 2.06 MB
The-Antimicrobial-Peptide-Histatin-5-Causes-a-Spatially-Restricted-Disruption-on-the-Candida-ppat.1000190.s002.ogv 5.0 s, 216 × 198; 42 KB
The-Antimicrobial-Peptide-Histatin-5-Causes-a-Spatially-Restricted-Disruption-on-the-Candida-ppat.1000190.s003.ogv 12 s, 586 × 588; 143 KB
The-Antimicrobial-Peptide-Histatin-5-Causes-a-Spatially-Restricted-Disruption-on-the-Candida-ppat.1000190.s004.ogv 5.0 s, 216 × 198; 20 KB
The-Antimicrobial-Peptide-Histatin-5-Causes-a-Spatially-Restricted-Disruption-on-the-Candida-ppat.1000190.s005.ogv 10 s, 782 × 664; 594 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s001.ogv 10 s, 1,024 × 512; 425 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s002.ogv 10 s, 1,024 × 512; 465 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s003.ogv 45 s, 760 × 380; 980 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s004.ogv 50 s, 760 × 380; 882 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s005.ogv 15 s, 760 × 380; 364 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s006.ogv 50 s, 760 × 380; 758 KB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s007.ogv 6.7 s, 3,097 × 1,884; 12.04 MB
The-Bimodal-Lifestyle-of-Intracellular-Salmonella-in-Epithelial-Cells-Replication-in-the-Cytosol-pone.0038732.s008.ogv 6.7 s, 3,097 × 1,873; 14.14 MB
The-Effects-of-Acute-Neutrophil-Depletion-on-Resolution-of-Acute-Influenza-Infection-Establishment-pone.0164247.s007.ogv 10 s, 1,066 × 714; 1.65 MB
The-Invertebrate-Lysozyme-Effector-ILYS-3-Is-Systemically-Activated-in-Response-to-Danger-Signals-ppat.1005826.s025.ogv 6.7 s, 514 × 512; 86 KB

(previous page) (next page)

Retrieved from "https://commons.wikimedia.org/w/index.php?title=Category:Videos_of_medical_microbiology&oldid=298806941"