Category:Gastrulation

Subcategories

This category has the following 12 subcategories, out of 12 total.

Media in category "Gastrulation"

The following 199 files are in this category, out of 199 total.

• 
  A conserved developmental mode emerges upon removal of species-specific extraembryonic environments.jpg 1,500 × 815; 216 KB
  
• 
  A putative model of how the organizer induces germ layer specification and patterning.png 3,666 × 2,059; 911 KB
  
• 
  ADMP establishes a self-regulatory network that controls the size of the organizer domain Spemann's organizer.jpg 1,011 × 529; 263 KB
  
• 
  ADMP provides dorsal signal required in Spemann's organizer at the onset of gastrulation.jpg 583 × 1,008; 461 KB
  
• 
  ADMP restricts the size of the organizer domain Spemann's organizer.jpg 818 × 665; 397 KB
  
• 
  Aligning pluripotent cells in culture with the pluripotent lineage in the embryo.png 1,074 × 836; 432 KB
  
• 
  ALK1 is required to restrict the size of the organizer domain Spemann's organizer.jpg 1,374 × 1,026; 1.27 MB
  
• 
  ALK2 is required for the expansion of the organizer domain Spemann's organizer.jpg 607 × 608; 301 KB
  
• 
  AMEs extended from the grafted st. 4 node or isolated st. 5 AME elicits the gathering of surrounding epiblast cells, which develop into secondary brain tissues.jpg 1,170 × 878; 951 KB
  
• 
  Amphibia formation of the neural tube, notochord, mesoderm, and coelom in vertebrates. cross-sections..jpg 1,777 × 712; 592 KB
  
• 
  Antedon rosacea early stages.jpg 801 × 735; 425 KB
  
• 
  Apposition and adhesion of blastocyst to luminal epithelium.jpg 2,017 × 1,363; 597 KB
  
• 
  Arquénteron.jpg 1,066 × 1,061; 73 KB
  
• 
  At E6.5, PGC precursors can still change fate when placed heterotopically.png 1,142 × 1,487; 1.29 MB
  
• 
  Avian development before gastrulation.jpg 2,767 × 3,354; 1.41 MB
  
• 
  Blocking the ALK1 receptor preferentially blocks the anti-organizer activity of ADMP Spemann's organizer.jpg 1,013 × 825; 671 KB
  
• 
  Branchiostoma formation of the neural tube, notochord, mesoderm, and coelom.jpg 1,172 × 857; 562 KB
  
• 
  Caudata process of invagination and mesoderm-formation.jpg 805 × 823; 698 KB
  
• 
  Cell contacts and pericellular matrix in the Xenopus gastrula chordamesoderm Abundance of cell contacts but not relative adhesiveness is reduced in adhesion factor morphants.PNG 1,685 × 2,100; 2.68 MB
  
• 
  Cell contacts and pericellular matrix in the Xenopus gastrula chordamesoderm LSM in FN, Has1 and Syn-4 depleted CM.PNG 1,338 × 2,011; 2.32 MB
  
• 
  Cell contacts and pericellular matrix in the Xenopus gastrula chordamesoderm LSM in gaps..PNG 1,342 × 1,857; 876 KB
  
• 
  Cell contacts and pericellular matrix in the Xenopus gastrula chordamesoderm LSM in normal and C-cad depleted CM..PNG 1,656 × 1,947; 2.9 MB
  
• 
  CENTROLECITHES.png 351 × 540; 12 KB
  
• 
  Characterization of MZfz7ab mutants at the embryo and tissue level.jpg 2,199 × 2,662; 667 KB
  
• 
  Classification of the different types of connective tissues.png 1,448 × 700; 708 KB
  
• 
  Columnar trophoblast-cells from the base of a fcetal villus of the placenta of the cow at the third month of pregnancy, to show phagocytosis.jpg 868 × 830; 208 KB
  
• 
  Comparative embryology of the vertebrates; with 2057 drawings and photos. grouped as 380 illus (1953) (20047812224).jpg 1,878 × 1,822; 927 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s009.ogv 6.2 s, 264 × 264; 701 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s010.ogv 6.2 s, 264 × 264; 388 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s011.ogv 6.2 s, 264 × 264; 454 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s012.ogv 7.6 s, 418 × 416; 1.51 MB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s013.ogv 7.5 s, 419 × 416; 680 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s014.ogv 6.5 s, 512 × 512; 532 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s015.ogv 10 s, 308 × 309; 426 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s016.ogv 11 s, 1,024 × 529; 2.41 MB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s017.ogv 5.7 s, 370 × 383; 589 KB
  
• Control-of-Directed-Cell-Migration-In-Vivo-by-Membrane-to-Cortex-Attachment-pbio.1000544.s018.ogv 6.5 s, 370 × 370; 738 KB
  
• 
  Coordination of Cell Polarity during Xenopus Gastrulation A heterogeneous combination of tissues can confer planar cell polarity..png 2,916 × 4,607; 4.35 MB
  
• 
  Coordination of Cell Polarity during Xenopus Gastrulation EB3 shows polarized movement independent of cell morphology in the early phases..png 3,487 × 4,215; 6.24 MB
  
• 
  Coordination of Cell Polarity during Xenopus Gastrulation Notochord-somite boundary andor extra-notochord tissue attracts EB3 movement..png 2,989 × 2,442; 4.15 MB
  
• Cultured ppl explant from MZfz7ab;Tg(gscGFP-CAAX) mutant embryos expressing membrane-RFP and Opto-Fz7 and injected with 9-cis-retinal.ogv 12 s, 986 × 720; 990 KB
  
• Deficient-Induction-Response-in-a-Xenopus-Nucleocytoplasmic-Hybrid-pbio.1001197.s005.ogv 13 s, 434 × 668; 351 KB
  
• 
  DELAMINATION.png 934 × 573; 26 KB
  
• 
  Detection of lymphangiogenesis by whole-mount staining LYVE1 (red) and CD31 (green) at different time points (24 week) after vascular transplantation..png 3,199 × 1,678; 2.5 MB
  
• 
  Development of the notochord in CS9 to CS12 (19–30 days).tiff 1,300 × 1,308; 1.82 MB
  
• 
  Developmental outcome of the node graft labeled with mCherry depended on the graft sites. (A) Development of the node grafts from mCherry-expressing st. 4 Japanese quail embryos.jpg 1,336 × 962; 808 KB
  
• 
  Diagram of cross-sections of vertebrate embryos to show the differentiation of the epimere into dermatome (skin-producer), myotome (muscle-producer), and sclerotome (skeleton-producer).jpg 1,754 × 766; 660 KB
  
• Diaphanous-Related-Formin-2-and-Profilin-I-Are-Required-for-Gastrulation-Cell-Movements-pone.0003439.s006.ogv 8.1 s, 650 × 512; 1.79 MB
  
• 
  Differentiation of the mesoderm in holoblastic and meroblastic types of development.jpg 1,617 × 1,467; 1,022 KB
  
• 
  Diversity of vertebrate gastrulation.jpg 1,073 × 1,021; 415 KB
  
• 
  During gastrulation, the VE is important for the formation of normal number of PGC precursors.jpg 1,200 × 1,263; 990 KB
  
• 
  Early blastocyst adhesion and invasion in primate and mouse.jpg 1,961 × 810; 312 KB
  
• 
  Early ectodermal patterning at the anterior epiblast.jpg 1,168 × 724; 442 KB
  
• 
  Early gastrulation in amphibian embryos.png 3,570 × 1,358; 1,007 KB
  
• 
  Early human embryo (01).jpg 675 × 563; 209 KB
  
• 
  Early human embryo (02).jpg 915 × 432; 257 KB
  
• 
  Early human embryo.jpg 761 × 738; 272 KB
  
• 
  Early pre- and post-implantation mouse embryonic development until the egg cylinder stage.png 1,089 × 1,228; 613 KB
  
• 
  EMBRIO 1 nltxt.jpg 559 × 119; 83 KB
  
• 
  EMBRIO 1.jpg 571 × 116; 14 KB
  
• 
  EMBRIO 2.jpg 943 × 729; 59 KB
  
• 
  EMBRIO 3.jpg 341 × 346; 17 KB
  
• 
  EMBRIO 4.jpg 376 × 193; 10 KB
  
• 
  EMBRIO 5.jpg 398 × 283; 10 KB
  
• 
  Embryonic development in mice versus primates.jpg 1,016 × 1,286; 798 KB
  
• 
  Embryonic origins of skeletal muscles mouse embryo.png 1,573 × 695; 425 KB
  
• 
  Epibolia.jpg 698 × 246; 55 KB
  
• 
  Epibolia.png 1,823 × 791; 468 KB
  
• 
  EPIBOLIE.png 934 × 573; 26 KB
  
• 
  Epiboly Drawing.png 2,550 × 2,073; 5.64 MB
  
• 
  Epiboly svg hariadhi.svg 512 × 512; 17 KB
  
• 
  Example of a Gastruloid.png 673 × 336; 134 KB
  
• 
  Experimental manipulation of the gastrulation mode in different organisms.jpg 1,166 × 1,480; 850 KB
  
• 
  Expression patterns of foxc1a, tbx1 and tbx20 genes resolve into three longitudinal strips in zebrafish head mesoderm (3ss, 11hpf).jpg 1,602 × 799; 843 KB
  
• 
  Extraembryonic tissues during amniote development.jpg 1,456 × 1,398; 1.97 MB
  
• 
  Feto-maternal interface showing uterine milk.jpg 2,994 × 1,475; 458 KB
  
• 
  Fig 3. Proceso de gastrulación en el nemátodo C.elegans..png 1,278 × 427; 121 KB
  
• 
  Figure 2. Types of implantation. Types of implantation strategies employed by mouse, marmoset, rhesus macaque and human.png 1,609 × 730; 647 KB
  
• 
  Formation of the primitive body plan following gastrulation in the mouse.png 1,279 × 1,187; 1,016 KB
  
• 
  Frog egg gray crescent.jpg 1,060 × 816; 133 KB
  
• 
  From mesenchymal stem cells to specific connective tissue cell types.png 1,085 × 877; 337 KB
  
• 
  Gastrulatie.png 1,780 × 1,520; 1.6 MB
  
• LL-Q150 (fra)-WikiLucas00-gastrulation.wav 1.4 s; 131 KB
  
• 
  Gastrulation (01).jpg 1,001 × 980; 289 KB
  
• 
  Gastrulation Animation.gif 1,024 × 768; 33.06 MB
  
• 
  Gastrulation forms in vertebrates.jpeg 1,280 × 1,173; 88 KB
  
• 
  Gastrulation gives rise to the three primary germ layers of the mouse embryo proper..png 1,209 × 806; 202 KB
  
• 
  Gastrulation of Asterina pectinifer.jpg 1,351 × 521; 212 KB
  
• 
  Gastrulation stomodeal invagination, dorsal folds form; elongation of germ band; clear parasegmentation. Aphidoletes aphidimyza.png 850 × 592; 591 KB
  
• 
  Gastrulation.png 801 × 486; 63 KB
  
• 
  Gastrulatsiooni toimumine.jpg 690 × 354; 67 KB
  
• 
  Gastrulação.png 695 × 349; 13 KB
  
• 
  Gray12.png 1,115 × 491; 192 KB
  
• 
  HETEROLECITHES.png 322 × 224; 5 KB
  
• 
  Histological sections of three stage 8 (17–19 days) human embryos.tiff 1,234 × 652; 702 KB
  
• 
  Human embryo Recent findings about tissue-specific lymphatic progenitor cells..jpg 1,380 × 912; 289 KB
  
• 
  Human embryo The molecular pathways involved in LEC differentiation from embryonic progenitors..jpg 2,211 × 1,888; 1.31 MB
  
• 
  Human embryo The molecular pathways responsible for LEC differentiation during adulthood stage.jpg 2,186 × 1,863; 1.2 MB
  
• 
  Human embryo. The origin of lymphatic progenitor cells and physiological lymphagiogenesis process at E12.5.png 3,258 × 1,593; 1.25 MB
  
• 
  Human notochord development textbook concepts compared to our proposed theory..png 1,300 × 504; 118 KB
  
• 
  Implantation depth in primates at lacunar stage.jpg 1,985 × 2,656; 1.13 MB
  
• 
  INGRESSION.png 934 × 573; 26 KB
  
• 
  Initial invasion of luminal epithelium.jpg 1,441 × 622; 281 KB
  
• 
  Koller's Sickle and Avian Gastrulation.jpg 1,967 × 1,968; 863 KB
  
• 
  Koller's sickle and its role in avian gastrulation.jpg 271 × 448; 47 KB
  
• 
  Kudede päritolu gastrulatsioonis.jpg 600 × 700; 74 KB
  
• 
  Lacertilia From medial vertical sections through embryonic disk showing five successive stages in gastrulation.jpg 2,040 × 2,281; 1.58 MB
  
• 
  Left-right asymmetry in the sea urchin - journal.pbio.1001404.g001.png 1,459 × 420; 235 KB
  
• Live imaging of Histone H2B–GFP mouse embryo at E6.5.ogv 6.4 s, 804 × 631; 674 KB
  
• Live imaging of mouse embryo at E5.5.ogv 4.3 s, 366 × 375; 145 KB
  
• Live imaging of mouse embryo at E6.ogv 8.6 s, 520 × 491; 497 KB
  
• 
  Live imaging of the whole mouse embryo at E6 (A to D) and E5.5. (E to H).png 1,910 × 2,240; 3.3 MB
  
• 
  Live imaging of the whole mouse embryo at E6.5 using DSLM.png 2,059 × 1,366; 2.24 MB
  
• 
  Mathematical model for the interaction between ALK1, ALK2, and ADMP Spemann's organizer.jpg 1,189 × 766; 293 KB
  
• 
  Mesoderm-ring to -crescent transition.jpg 1,173 × 1,826; 1.01 MB
  
• 
  Meyers b5 s0350 b1.png 570 × 218; 53 KB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s002.ogv 17 s, 648 × 492; 16.95 MB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s003.ogv 9.5 s, 700 × 350; 5.23 MB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s004.ogv 21 s, 700 × 350; 17.02 MB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s005.ogv 22 s, 1,050 × 350; 19.89 MB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s007.ogv 15 s, 700 × 700; 10.8 MB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s008.ogv 30 s, 1,050 × 350; 22.29 MB
  
• Modeling-Gastrulation-in-the-Chick-Embryo-Formation-of-the-Primitive-Streak-pone.0010571.s009.ogv 0.0 s, 1,056 × 352; 22.13 MB
  
• 
  Morphological characterization of END2, PYS2 and XEN cells.png 2,068 × 1,632; 2.77 MB
  
• 
  Morphological differences between human and mouse gastrulation.jpg 2,994 × 3,411; 397 KB
  
• Movement of MZfz7ab mutant and wt donor ppl cells (magenta) transplanted into the ppl of wt Tg(gscGFP-CAAX) host embryos.ogv 10 s, 960 × 720; 1.64 MB
  
• Movement of MZfz7ab mutant donor ppl cells expressing Opto-Fz7, injected with 9-cis-retinal and transplanted into the ppl of a wt Tg(gscGFP-CAAX) host.ogv 10 s, 960 × 720; 817 KB
  
• MZfz7ab donor cells expressing Opto-Fz7 and injected with 9-cis-retinal transplanted into the ppl of a wt Tg(gscGFP-CAAX) host ppl.ogv 9.1 s, 960 × 720; 1.4 MB
  
• MZfz7ab mutant and wt donor ppl cells (magenta) transplanted into the ppl of a Tg(gscGFP-CAAX) host embryo with the same genotype (homotypic transplantations).ogv 17 s, 960 × 720; 1.1 MB
  
• 
  MZfz7ab prechordal plate progenitor migration.jpg 1,747 × 1,802; 438 KB
  
• 
  MZfz7ab prechordal plate progenitor protrusion formation.jpg 2,042 × 2,918; 599 KB
  
• 
  Nematode Variations in gastrulation.jpg 1,800 × 1,909; 1.74 MB
  
• 
  Neurula.png 873 × 317; 21 KB
  
• 
  OLIGOLECITHES.png 324 × 235; 4 KB
  
• 
  Only epiblast cells that contact the posterior part of the embryo become PGCs.png 1,102 × 1,378; 1.06 MB
  
• 
  Organization of endodermal progenitors and extraembryonic endoderm at onset of gastrulation in chick and mouse embryos..jpg 751 × 776; 335 KB
  
• 
  Overview of the developing notochord in relation to the fusion of the dorsal aortae human embryo.png 1,300 × 880; 673 KB
  
• 
  Paracentrotus lividus gastrula.jpg 1,245 × 934; 1.08 MB
  
• PhOTO-Zebrafish-A-Transgenic-Resource-for-In-Vivo-Lineage-Tracing-during-Development-and-pone.0032888.s005.ogv 1.7 s, 1,984 × 1,952; 2.06 MB
  
• PhOTO-Zebrafish-A-Transgenic-Resource-for-In-Vivo-Lineage-Tracing-during-Development-and-pone.0032888.s006.ogv 1.7 s, 1,984 × 1,476; 1.5 MB
  
• PhOTO-Zebrafish-A-Transgenic-Resource-for-In-Vivo-Lineage-Tracing-during-Development-and-pone.0032888.s007.ogv 2.5 s, 1,972 × 1,972; 5.84 MB
  
• PhOTO-Zebrafish-A-Transgenic-Resource-for-In-Vivo-Lineage-Tracing-during-Development-and-pone.0032888.s008.ogv 2.5 s, 1,972 × 1,476; 3.08 MB
  
• 
  Pluripotency factor expression during early embryonic development. Pluripotency factors are expressed throughout the pluripotency state (2).jpg 1,015 × 642; 186 KB
  
• 
  Pluripotency factor expression during early embryonic development. Pluripotency factors are expressed throughout the pluripotency state (3).jpg 1,298 × 758; 234 KB
  
• 
  Pluripotency factor expression during early embryonic development. Pluripotency factors are expressed throughout the pluripotency state.jpg 1,158 × 791; 489 KB
  
• Ppl and overlying neurectoderm cell movements in MZfz7ab mutant and wt Tg(gscGFP-CAAX) embryos from 7 to 10 hpf.ogv 13 s, 884 × 720; 2.83 MB
  
• Ppl movement in a MZfz7ab; Tg(gscTurbo-RFP) embryo expressing H2B-GFP and Opto-Fz7 and injected with 9-cis-retinal.ogv 13 s, 718 × 720; 3.52 MB
  
• 
  Presumptive primitive streak area of ROCK-inhibited embryos reveals abnormality of orientation of cell divisions as well as of actin distribution.jpg 1,277 × 1,154; 921 KB
  
• 
  Primary axis formation during gastrulation in metazoan embryos and corresponding artificial systems.jpg 1,500 × 1,014; 199 KB
  
• 
  Primary Bovine Extra-Embryonic Cultured Cells. Phenotypes of in vivo micro-dissected cell types at D18.png 1,153 × 1,153; 972 KB
  
• 
  Proximal VE and ExE are sufficient to induce PGCs in distal epiblast.png 1,142 × 2,493; 2.96 MB
  
• 
  Proximal visceral endoderm and extraembryonic ectoderm regulate the formation of primordial germ cell precursors.tiff 1,791 × 827; 678 KB
  
• Reconstructed epiblast nuclei from a lateral view.ogv 6.4 s, 1,031 × 728; 518 KB
  
• Reconstructed epiblast nuclei from distal view.ogv 6.4 s, 924 × 636; 571 KB
  
• Reconstructed trajectories of mesodermal cells.ogv 4.3 s, 637 × 567; 807 KB
  
• Regulation-of-Embryonic-Cell-Adhesion-by-the-Prion-Protein-pbio.1000055.sv001.ogv 8.0 s, 299 × 299; 1.19 MB
  
• Regulation-of-Embryonic-Cell-Adhesion-by-the-Prion-Protein-pbio.1000055.sv002.ogv 8.0 s, 356 × 357; 1.66 MB
  
• Regulation-of-Embryonic-Cell-Adhesion-by-the-Prion-Protein-pbio.1000055.sv003.ogv 12 s, 158 × 155; 88 KB
  
• Regulation-of-Embryonic-Cell-Adhesion-by-the-Prion-Protein-pbio.1000055.sv004.ogv 12 s, 158 × 156; 92 KB
  
• Regulation-of-Embryonic-Cell-Adhesion-by-the-Prion-Protein-pbio.1000055.sv005.ogv 2.1 s, 1,024 × 1,024; 1.68 MB
  
• Regulation-of-Embryonic-Cell-Adhesion-by-the-Prion-Protein-pbio.1000055.sv006.ogv 12 s, 523 × 512; 340 KB
  
• 
  RG347357480 Fig1.png 850 × 377; 60 KB
  
• 
  Rho kinase (ROCK1) is expressed during the mammalian gastrulation.jpg 795 × 563; 466 KB
  
• 
  Schematic dorsal overview of the developing notochord and the fusion of the paired dorsal aortae in humans.tiff 1,300 × 619; 146 KB
  
• 
  Sea Urchin Gastrulation.png 752 × 300; 187 KB
  
• 
  Single-cell RNA-sequencing (scRNAseq) analysis of the posterior tissue precursors during posterior axis formation chicken embryo.jpg 1,888 × 2,855; 1,001 KB
  
• 
  Spatio-temporal expression of anterior lateral plate mesoderm (ALPM) marker tbx20 during zebrafish early development.jpg 1,598 × 695; 531 KB
  
• 
  Spatio-temporal expression of cranial lateral mesoderm marker genes (tbx1, cyp26c1 and alx1) during zebrafish early development.jpg 1,595 × 1,988; 2.31 MB
  
• 
  Spatio-temporal expression of cranial paraxial mesoderm marker genes (foxc1a and fsta) during zebrafish early development.jpg 1,598 × 1,345; 1.02 MB
  
• 
  Spatio-temporal expression of prechordal plate marker genes (gsc, pitx2 and isl1) during zebrafish early development.jpg 1,595 × 1,354; 1.42 MB
  
• 
  Spectrum of pluripotency in the human embryo.jpg 1,950 × 1,006; 324 KB
  
• 
  Spectrum of pluripotency in the mouse embryo.jpg 1,959 × 838; 904 KB
  
• 
  Stages of mammals embryos.jpg 976 × 1,102; 849 KB
  
• 
  Staging Human Gastrulation.jpg 3,493 × 3,010; 538 KB
  
• 
  TELOLECITHES.png 487 × 384; 5 KB
  
• 
  The ALK2 receptor positively regulates the expression of organizer genes Spemann's organizer.jpg 1,156 × 845; 961 KB
  
• 
  The Biological bulletin (19758011533).jpg 2,004 × 1,310; 608 KB
  
• 
  The changing morphology and tissue composition of the mouse conceptus.jpg 1,881 × 1,891; 651 KB
  
• 
  The evolution of man (1920) plate III.jpg 753 × 1,173; 1.21 MB
  
• 
  The evolution of man- a popular exposition of the principal points of human ontogeny and phylogeny (1920) (14760848311).jpg 909 × 1,445; 1.87 MB
  
• 
  The process during the embryo implantation.jpg 1,944 × 567; 217 KB
  
• Time-lapse changes of triangles connected neighboring nuclei at the first time point (2).ogv 5.5 s, 638 × 541; 1.77 MB
  
• Time-lapse migrations of mesodermal cells.ogv 9.1 s, 635 × 569; 2.26 MB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s003.ogv 32 s, 450 × 500; 9.66 MB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s004.ogv 28 s, 450 × 500; 7.62 MB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s005.ogv 4.4 s, 481 × 509; 1.93 MB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s006.ogv 20 s, 256 × 246; 952 KB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s007.ogv 11 s, 200 × 237; 205 KB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s008.ogv 3.1 s, 430 × 428; 664 KB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s009.ogv 1.8 s, 430 × 428; 388 KB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s010.ogv 6.9 s, 508 × 511; 4.04 MB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s011.ogv 12 s, 500 × 355; 6.95 MB
  
• Tissue-Tissue-Interaction-Triggered-Calcium-Elevation-Is-Required-for-Cell-Polarization-during-pone.0008897.s012.ogv 33 s, 508 × 510; 13.02 MB
  
• 
  Tracking of EB3-GFP movement shows microtubule growth in Xenopus explants.png 2,243 × 2,960; 1.42 MB
  
• 
  Transversal sections of the notochord in a 24 hour stage chicken embryo.tiff 348 × 621; 283 KB
  
• 
  VE and ExE are both important for the formation of PGC precursors.jpg 1,200 × 800; 554 KB
  
• 
  Vertebrates Transverse sections through the germshield of a higher Vertebrate, showing the origin of the tubular from the bent germ-layerrudimentary.jpg 1,515 × 689; 663 KB
  
• Xenopus-Nucleocytoplasmic-Hybrid.ogv 15 s, 292 × 782; 557 KB
  
• Α5β1-Integrin-Mediated-Adhesion-to-Fibronectin-Is-Required-for-Axis-Elongation-and-Somitogenesis-in-pone.0022002.s007.ogv 13 s, 554 × 445; 1.08 MB