Category:Optic vesicle

Media in category "Optic vesicle"

The following 149 files are in this category, out of 149 total.

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  A text-book of embryology for students of medicine (electronic resource) (1907) (20164794550).jpg 2,874 × 1,872; 1.41 MB
  
• Actin dynamics during retinal neuroepithelium (RNE) morphogenesis.ogv 15 s, 300 × 398; 412 KB
  
• Actin dynamics during rim involution video 7.ogv 23 s, 248 × 282; 527 KB
  
• Actin dynamics during rim involution.ogv 17 s, 292 × 340; 867 KB
  
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  All E13.5 mutants have reduced proliferation, but only Rbpj mutants have excess apoptosis.png 2,100 × 1,295; 2.34 MB
  
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  Analysis of the basal surface and actomyosin localisation during Retinal neuroepithelium (RNE) invagination.jpg 1,466 × 1,500; 554 KB
  
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  Anatomy, descriptive and surgical (1897) (14578075268).jpg 1,458 × 2,898; 1.2 MB
  
• Apical domain dynamics during rim involution.ogv 23 s, 290 × 290; 587 KB
  
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  Auge Entwicklung.jpg 3,908 × 2,547; 2.41 MB
  
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  Augenentwicklung-1-nltxt.jpg 1,280 × 720; 170 KB
  
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  Augenentwicklung-2 nltxt.jpg 1,064 × 715; 316 KB
  
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  Aves Transverse section through the fore-brain and optic vesicles of a twenty-five-hour chick.jpg 1,380 × 503; 241 KB
  
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  Canonical Wnt-β-catenin signalling is required for RPE cell commitment.png 1,904 × 2,748; 8.97 MB
  
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  Carpenter's principles of human physiology (1881) (14779392174).jpg 872 × 1,526; 205 KB
  
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  Central and Peripheral Optic Vesicle Domains are Traced to Differentiated Tissues of the Optic Cup.png 2,196 × 2,651; 7.42 MB
  
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  CHD7 Expression in Ocular Morphogenesis and Neural Crest Cell Development.png 1,428 × 881; 547 KB
  
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  Concerted action of basal cell area shrinkage and rim involution shapes the hemispheric retinal neuroepithelium (RNE).jpg 922 × 914; 319 KB
  
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  Congenital eye diseases associated with neural crest defects in the anterior segment.jpg 1,825 × 605; 162 KB
  
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  Cranial neural crest migration into the head.jpg 1,949 × 2,701; 296 KB
  
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  Crucial biomolecules expression in an embryonic mouse at 9.5 days.jpg 797 × 883; 427 KB
  
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  Decreased proliferation and change in physical properties of mutant optic vesicle.png 1,705 × 1,449; 4.23 MB
  
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  Deletion of Smad4 led to changes of retina thickness and degeneration of retinal cells.png 1,738 × 1,338; 3.02 MB
  
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  Development of the Retina.png 262 × 189; 28 KB
  
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  Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease.jpg 936 × 761; 844 KB
  
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  Dorsal shift in expression of retina-specific eye field transcription factors in the mutant optic vesicle.png 926 × 2,797; 5.61 MB
  
• Dorsal view of the optic vesicle (OV) to optic cup (OC) transition visualized in a double Tg(E1-bhlhe40.GFP; rx3.GAL4;UAS.RFP embryo).ogv 9.8 s, 530 × 512; 774 KB
  
• Dorsal view of the optic vesicle (OV) to optic cup (OC) transition visualized in a double Tg(E1-bhlhe40.GFP; rx3.GAL4;UAS.RFP embryo.ogv 9.8 s, 512 × 512; 774 KB
  
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  Down-regulation of the αA, αB, β and γ-crystallins caused by the miak mutation of Pitx3.png 1,588 × 1,680; 2.66 MB
  
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  Dynamic cell-ECM attachment of rim cells is important for retinal neuroepithelium (RNE) orphogenesis.jpg 1,062 × 1,500; 452 KB
  
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  Dynamics of ECM distribution and cell-ECM attachment during retinal neuroepithelium (RNE) morphogenesis.jpg 986 × 1,500; 344 KB
  
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  EB3-GFP dynamics during retinal pigment epithelium (RPE) cell remodelling.jpg 1,366 × 1,500; 615 KB
  
• Eb3GFP dynamics 14, 17, and 23 hpf, when retinal pigment epithelium (RPE) cells have a neuroepithelial, cuboidal or squamous conformation.ogv 1 min 7 s, 352 × 288; 1.62 MB
  
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  Effect of perturbed cell-ECM attachment on the optic cup.jpg 1,277 × 1,500; 493 KB
  
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  Effect of Rockout and HU+Aphi treatment on the retinal neuroepithelium (RNE).jpg 1,500 × 940; 364 KB
  
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  Evaluation of the efficiency of morpholino mediated knockdown of laminin α-1and opo.jpg 1,500 × 998; 311 KB
  
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  Expression analyses of Pitx3 transcripts and PITX3 protein in wild-type and miak mice.png 1,983 × 1,654; 3.37 MB
  
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  Expression of pituitary specific genes in wild type and Rx-deficient mouse embryos.png 1,502 × 1,127; 2.21 MB
  
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  Eye development and degeneration. Right surface fish eye develops with a normal lens.jpg 1,233 × 811; 559 KB
  
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  FGF signalling promotes the one-dimensional budding of the LG.jpg 1,698 × 1,977; 396 KB
  
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  Formation of the posterior pituitary in chimeric mouse embryos.png 1,502 × 1,498; 2.83 MB
  
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  Formation of three anterior cranial placodes during mid-stage mouse embryogenesis.png 4,275 × 2,514; 2.26 MB
  
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  Functions of FGF signalling in the three-dimensional retinal development.jpg 1,627 × 1,008; 167 KB
  
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  Generation of RPE-like and NR-like tissues in vitro using Wntβ-catenin or Fgf stimulation.jpg 2,140 × 1,958; 2.16 MB
  
• GFP-ras expressing opo morphant clone in mCherry-UtrCH expressing control background.ogv 9.6 s, 774 × 462; 677 KB
  
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  Gray977.png 779 × 872; 540 KB
  
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  H1. Optic vesicle (V08a).png 461 × 232; 39 KB
  
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  Hes genes in the embryonic mouse eye.PNG 2,056 × 856; 2.48 MB
  
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  Hes1 and Hes5 expression in Rbpj, dnMAML and Hes triple retinal mutants.png 2,100 × 1,865; 5.66 MB
  
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  Hes1 and HesTKO retina-ONH boundary phenotypes.png 2,100 × 1,405; 4.54 MB
  
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  Histological analysis in the wild-type and miak-miak mice at embryonic stages.png 1,938 × 1,725; 5.83 MB
  
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  Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.jpg 555 × 409; 103 KB
  
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  Identification of Central Optic Cup Fields in the Optic Vesicle.png 2,196 × 2,560; 4.36 MB
  
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  Impairment of actomyosin-driven basal constriction or proliferation does not prevent RNE formation.jpg 1,172 × 1,500; 359 KB
  
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  Impairment of rim involution leads to mispositioning of neuroepithelial cells.jpg 1,457 × 1,500; 567 KB
  
• Integrin dynamics during rim involution.ogv 15 s, 250 × 250; 648 KB
  
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  Journal of morphology (1893) (14780418754).jpg 2,012 × 2,912; 572 KB
  
• Lateral view of optic cup (OC) growth visualized in a Tg(E1-bhlhe40.GFP) embryo.ogv 6.0 s, 512 × 546; 1.88 MB
  
• Lateral view of the optic cup (OC) folding visualized in a Tg(E1-bhlhe40.GFP) embryo injected with H2B-RFP mRNA (magenta).ogv 9.0 s, 512 × 528; 769 KB
  
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  Localization and expression of the MIP proteins during lens development in wild-type and miak mice during embryonic stages.png 1,004 × 1,054; 1.22 MB
  
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  Localization and expression of the PROX1 (A) and FOXE3 (B) proteins during lens development in wild-type and miak mice at embryonic stages.png 1,588 × 1,693; 2.61 MB
  
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  Loss of Smad4 affected the differentiation of retinal ganglion cells, bipolar cells, and Müller cells.png 1,738 × 1,066; 1.45 MB
  
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  Loss of Smad4 led to excessive proliferation of the retina cells at early development and abundant apoptosis later as assessed by pulse BrDU labeling and staining as well as TUNEL assay.png 1,680 × 1,795; 1.77 MB
  
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  Mapping Central and Peripheral Eye Domains.png 2,093 × 1,044; 268 KB
  
• Membrane dynamics during rim involution.ogv 18 s, 262 × 282; 331 KB
  
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  Microphthalmia phenotype in Texel sheep.png 1,162 × 1,746; 1.39 MB
  
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  Microtubule and myosin dynamics during rim involution.jpg 1,500 × 795; 191 KB
  
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  Microtubule dynamics is required for retinal pigment epithelium (RPE) cell flattening and optic vesicle (OV) folding.jpg 1,500 × 1,437; 424 KB
  
• Myosin dynamics during retinal neuroepithelium (RNE) morphogenesis.ogv 17 s, 300 × 398; 594 KB
  
• Myosin dynamics during rim involution.ogv 19 s, 262 × 282; 199 KB
  
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  New spontaneous microphthalmia and aphakia (miak) mutations in mice.png 1,004 × 2,545; 4.21 MB
  
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  Nocodazole treatment does not alter retinal pigment epithelium (RPE) specification and polarity.jpg 1,500 × 1,109; 387 KB
  
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  Nonradioactive RNA in situ hybridization was used to confirm Gli2, Gli3 and Wnt2b expression changes in the cKO retinas.png 1,765 × 1,290; 2.96 MB
  
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  Notch pathway activities and integration points with other genetic pathways in the embryonic eye.png 1,500 × 1,052; 262 KB
  
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  NSRW Eye.jpg 480 × 296; 65 KB
  
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  Ocular dysplasia in Smad4-cKO mutants compared to the wild type mice.(A-C).tiff 1,070 × 398; 592 KB
  
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  Ocular images from individuals with ARHGAP35 variants.jpg 1,520 × 1,354; 1.41 MB
  
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  Ocular tissue patterning defects among Notch pathway mutants.png 2,100 × 1,319; 3.02 MB
  
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  Optic cup development, gene expression, and schematic diagram of SFEBq culture.jpg 1,615 × 1,928; 1.86 MB
  
• Paxillin dynamics during retinal neuroepithelium (RNE) morphogenesis.ogv 17 s, 300 × 398; 358 KB
  
• Paxillin dynamics during rim involution in opo morphant.ogv 26 s, 474 × 192; 504 KB
  
• Paxillin dynamics during rim involution.ogv 13 s, 250 × 250; 184 KB
  
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  Perturbed basal lamellipodial activity leads to compromised rim involution and impairs retinal neuroepithelium (RNE) morphogenesis.jpg 1,134 × 1,500; 434 KB
  
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  Pharmacological inhibition of apoptosis in the posterior placodal area (PPA) of embryonic mice.jpg 1,443 × 1,483; 1.64 MB
  
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  Phenotypic appearance in patients with sclerocornea, aphakia, and microphthalmia.jpg 544 × 402; 235 KB
  
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  Photograph of an aphakic eye with a proliferative capsular bag.png 2,825 × 993; 3.56 MB
  
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  Photographs of the six patients with MLS syndrome and a heterozygous HCCS mutation or Xp22 monosomy.jpg 1,200 × 664; 619 KB
  
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  Proliferation accounts for retinal pigment epithelium (RPE) surface increase during amniotes optic vesicle (OV) folding.jpg 742 × 1,500; 399 KB
  
• Protrusion dynamics during rim involution in ezrin morphant.ogv 10 s, 344 × 160; 156 KB
  
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  Pseudorasbora parva (10.3897-zoologia.35.e22162) Figures 2–39.jpg 1,997 × 1,494; 1.42 MB
  
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  Quain's elements of anatomy (1882) (14779925632).jpg 1,724 × 886; 280 KB
  
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  Retinal formation in chimeric mammalian embryos.png 1,502 × 1,048; 1.89 MB
  
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  Retinal neuroepithelium (RNE) invagination is accompanied by basal cell surface area shrinkage and basal actomyosin accumulation.jpg 1,195 × 1,500; 359 KB
  
• Retinal neuroepithelium (RNE) morphogenesis in ezrin morphant.ogv 15 s, 430 × 464; 1.09 MB
  
• Retinal neuroepithelium (RNE) morphogenesis in laminin morphant.ogv 18 s, 430 × 464; 1.16 MB
  
• Retinal neuroepithelium (RNE) morphogenesis in Opo morphant.ogv 18 s, 430 × 464; 605 KB
  
• Retinal neuroepithelium (RNE) morphogenesis in Rockout treated embryos.ogv 14 s, 1,000 × 510; 2.21 MB
  
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  Retinal pigment epithelium (RPE) region selection from the GFP-positive domain.jpg 1,500 × 1,401; 154 KB
  
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  Retinal pigment epithelium (RPE) volume is conserved during initial tissue morphogenesis.jpg 1,344 × 1,500; 232 KB
  
• Rim cell dynamics in Rockout treated embryos.ogv 16 s, 262 × 282; 208 KB
  
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  Rim involution involves active cell migration of connected epithelial cells.jpg 1,425 × 1,500; 443 KB
  
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  Scenario of the evolution of the cranium of vertebrates.png 907 × 919; 428 KB
  
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  Schematic diagram of regulatory interactions taking place during retinal development.png 1,502 × 795; 175 KB
  
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  Schematic illustration of the groups of key transcription factors whose expression is associated with the main successive stages of eye development.png 2,778 × 1,529; 863 KB
  
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  Schematic of eye morphogenesis in zebrafish.png 3,710 × 2,106; 905 KB
  
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  Schematic representation of the different mechanisms described for optic cup morphogenesis.jpg 686 × 755; 328 KB
  
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  Schematic representation of tissue organization during optic vesicle evagination.jpg 743 × 549; 217 KB
  
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  Schematic representation of vertebrate eye development (01).png 3,230 × 1,577; 1.12 MB
  
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  Schematic representation of vertebrate eye development.png 1,200 × 357; 239 KB
  
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  Sclerocornea, i.e., peripheral scleralization of the cornea, accompanied by the feature of cornea plana (CNA2, OMIM 217300).jpg 819 × 572; 347 KB
  
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  Shifts in RGC and early photoreceptor fates correlate with changes in Otx2, but not Atoh7, expression.png 2,079 × 1,841; 2.88 MB
  
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  Spatial expression of sox4 and sox11 during Xenopus laevis embryogenesis.png 2,083 × 1,651; 3.38 MB
  
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  Spatio-temporal expression of cranial paraxial mesoderm marker genes (foxc1a and fsta) during zebrafish early development.jpg 1,598 × 1,345; 1.02 MB
  
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  Stages in the early development of the human eye.png 771 × 698; 160 KB
  
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  Summary of species-specific modes of retinal pigment epithelium (RPE) differentiation and its contribution to optic vesicle (OV) folding.jpg 1,262 × 1,500; 282 KB
  
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  Temporal and spatial expression of FGF signalling during mouse eye development.jpg 1,958 × 2,626; 680 KB
  
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  The American journal of anatomy (1901) (14597356810).jpg 1,756 × 2,716; 1.25 MB
  
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  The American journal of anatomy (1901) (14597390259).jpg 1,752 × 2,824; 1.11 MB
  
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  The American journal of anatomy (1901) (14597394829).jpg 1,748 × 2,796; 1.09 MB
  
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  The American journal of anatomy (1901) (14597396709).jpg 1,724 × 2,828; 1.01 MB
  
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  The American journal of anatomy (1901) (14597405888).jpg 1,716 × 2,748; 1.03 MB
  
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  The American journal of anatomy (1901) (14780865891).jpg 1,684 × 2,768; 860 KB
  
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  The American journal of anatomy (1901) (14783665222).jpg 1,712 × 2,732; 997 KB
  
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  The American journal of anatomy (1901) (14783708912).jpg 1,772 × 2,812; 1.2 MB
  
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  The Biological bulletin (20383507011).jpg 2,080 × 2,600; 1.42 MB
  
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  The Expression of Eye Field Transcription Factors subdivides the Optic Vesicle.png 1,009 × 2,688; 2.11 MB
  
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  The few RPE cells that develop in the mutant embryos are derived from eye committed progenitor cells in the anterior neural plate that escape β-catenin inactivation.png 1,494 × 1,919; 4.79 MB
  
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  The genetics of early optic vesicle development.png 3,220 × 1,808; 875 KB
  
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  The genetics of optic cup and lens formation.png 3,049 × 1,878; 802 KB
  
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  The Peripheral not Central Optic Cup Originates in the Distal Optic Vesicle.png 2,093 × 1,931; 3.61 MB
  
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  The phases of the embryological development of the eye.png 3,402 × 4,739; 3.32 MB
  
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  The retinal pigment epithelium (RPE) converts from a pseudostratified to a squamous epithelium during optic vesicle (OV) folding by increasing individual cell surface.jpg 1,500 × 1,279; 434 KB
  
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  The Tg(E1-bhlhe40GFP) line is a suitable tool to study early retinal pigment epithelium (RPE) generation.jpg 2,362 × 2,142; 987 KB
  
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  The timing and intensity of FGF signalling controls the two-dimensional patterning of the lens.jpg 2,008 × 1,470; 295 KB
  
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  The-individual-CT1-11-showing-complete-congenital-primary-aphakia.jpg 569 × 387; 141 KB
  
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  Transverse section through the fore-brain of a thirty-eight-hour chick embryo.png 873 × 571; 253 KB
  
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  Trpm3-miR-204 expression is dependent on Pax6 activity during eye development.png 2,729 × 2,292; 7.28 MB
  
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  Two stages in the early development of the internal ear.png 911 × 507; 235 KB
  
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  Unique role for Rbpj in regulation photoreceptor versus amacrine fates.png 2,072 × 1,522; 1.35 MB
  
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  Varying degrees of microphthalmia or aphakia in Smad4-cKO mutants compared to the wild type mice.png 1,742 × 1,154; 1.76 MB
  
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  Varying degrees of microphthalmia were observed in Smad4-cKO mutants. (A-C, E-G).tiff 1,772 × 1,042; 2.23 MB
  
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  Vertebrate eye development (human eye).jpg 2,166 × 2,642; 334 KB
  
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  Vertebrate Ocular Development. Schematic representation of ocular development stages from eye field specification to bi-layered optic cup formation.png 1,631 × 408; 373 KB
  
• Vsx2 FP expression during RNE morphogenesis.ogv 13 s, 480 × 536; 1.43 MB
  
• Vsx2 GFP expression during retinal neuroepithelium (RNE) morphogenesis in ezrin morphant.ogv 15 s, 480 × 536; 2.08 MB
  
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  Zebrafish retinal pigment epithelium (RPE) flattening is associated with an abrupt decrease of cell proliferation.jpg 908 × 1,500; 234 KB
  
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  Β-catenin is important for maintenance of dorsoventral patterning of the retina.png 1,196 × 2,644; 5.57 MB
  
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  Β-catenin mutant embryos are anophthalmic.png 1,367 × 2,522; 4.74 MB
  
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  Β-catenin mutant optic vesicles do not form an optic cup.png 1,009 × 2,569; 5.49 MB
  
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  Β-catenin remains associated with N-cadherin and F-actin at the apical side of the cells in the mutant optic vesicle.png 1,009 × 2,068; 2.39 MB