Category:Media from StemBook

Media in category "Media from StemBook"

The following 169 files are in this category, out of 169 total.

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  A model for lens repression..jpg 600 × 399; 70 KB
  
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  A model for the behavior of chromatin proteins during embryonic stem cell differentiation..jpg 600 × 271; 53 KB
  
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  A model of endoderm patterning by Wnt and FGF..jpg 432 × 185; 28 KB
  
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  A model of potential epistatic interactions occurring between early-acting transcription factors in the nephrogenic cord at the level of the presumptive metanephros..jpg 500 × 492; 33 KB
  
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  A model of signalling networks regulating myogenic cell-fate..jpg 600 × 378; 61 KB
  
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  A Planarian neoblasts (green) are present throughout the mesenchyme of the animal and express category 1 genes..jpg 584 × 600; 104 KB
  
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  A protein interaction network in mESCs..jpg 600 × 362; 109 KB
  
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  A schematic model of MIS actions at the early stage of Müllerian duct regression..jpg 576 × 406; 59 KB
  
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  A Stages of zebrafish caudal fin regeneration as longitudinal sections..jpg 386 × 600; 120 KB
  
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  A three phase model for Müllerian duct development.jpg 180 × 602; 31 KB
  
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  A What is the differentiation potential of cells in the blastema?.jpg 531 × 600; 93 KB
  
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  A-C..jpg 600 × 546; 126 KB
  
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  A-E..jpg 600 × 176; 58 KB
  
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  An example of hepatoblast delamination..jpg 400 × 189; 54 KB
  
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  Analysis of multiple transcription factor occupancy..jpg 445 × 285; 52 KB
  
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  Anatomy of the skin de.jpg 491 × 625; 162 KB
  
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  Anatomy of the skin.jpg 491 × 625; 152 KB
  
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  Asymmetric cell division in Drosophila larval neuroblasts (NBs; on the left) and mammalian epithelia (on the right)..jpg 600 × 374; 69 KB
  
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  Bile duct formation..jpg 500 × 228; 87 KB
  
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  Bivalent chromatin domains mark the promoters of developmentally important genes in pluripotent ES c.jpg 600 × 349; 83 KB
  
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  BMP, Wnt, and c-Kit signaling are activated in melanocytes in the hair bulb, but not in melanocyte stem cell population at the bulge region..jpg 500 × 335; 94 KB
  
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  Calcium content of titanium (Ti), titanium ECM composites (Ti ECM), and titanium denatured ECM compo.jpg 439 × 600; 30 KB
  
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  Cellular architecture of the liver..jpg 650 × 343; 108 KB
  
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  Characterization of MOVCAR 7 side population cells..jpg 219 × 625; 54 KB
  
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  Chemical burn injury..jpg 300 × 226; 56 KB
  
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  Commonly used cell lineage marking strategies..jpg 400 × 516; 104 KB
  
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  Core transcriptional control of adipogenesis..jpg 600 × 449; 72 KB
  
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  Cultured epithelial autograft in burn treatment..jpg 800 × 202; 63 KB
  
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  Defects in melanocyte development cause white spotting, while the stem cell defect results hair graying..jpg 500 × 385; 80 KB
  
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  Designing PLGA scaffolds that mimicks the architecture of the spinal cord..jpg 600 × 688; 206 KB
  
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  Development of the respiratory system in mice..jpg 600 × 343; 135 KB
  
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  Development of the rodent cornea..jpg 500 × 466; 115 KB
  
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  Diagram representing putative lung epithelial progenitors and their locations in the adult respirato.jpg 600 × 320; 70 KB
  
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  Diagramatic representation of the concept of autologous amniotic mesenchymal stem cell-based fetal tissue engineering for the treatment of congenital anomalies..jpg 446 × 514; 61 KB
  
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  Different incisor phenotypes resulting from the modulation of signal pathways regulating the stem cell niche..jpg 500 × 385; 72 KB
  
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  Direct cell labeling..jpg 360 × 220; 28 KB
  
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  Electrospectroscopic imaging (ESI) in ES cells and ESC-derived neuronal progenitor cells..jpg 550 × 521; 194 KB
  
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  Endoderm derivatives..jpg 351 × 600; 67 KB
  
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  Epigenetics of adipose development..jpg 600 × 565; 65 KB
  
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  ES cell nuclear architecture..jpg 600 × 207; 55 KB
  
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  Examples of reporter gene imaging..jpg 450 × 332; 47 KB
  
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  Extrinsic versus intrinsic aging mechanisms in satellite cells and hematopoietic stem cells..jpg 600 × 454; 112 KB
  
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  Feedback loops of secreted factors induce endoderm..jpg 542 × 600; 82 KB
  
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  Future avenues in research of pluripotent cells..jpg 500 × 467; 52 KB
  
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  Gene expression profiling techniques used in studies of pluripotent cells..jpg 600 × 768; 141 KB
  
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  Genetic links between Notch signaling and c-Kit signaling..jpg 500 × 297; 86 KB
  
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  Genome-wide transcription factor location analysis..jpg 416 × 576; 77 KB
  
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  Gross (on the left) and radiographic (on the right) analysis of a subcutaneous transplant of MSCs isolated by flushing the murine adult bone marrow..jpg 500 × 182; 25 KB
  
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  Hair follicle and inter-follicular epidermis morphogenesis..jpg 500 × 261; 95 KB
  
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  Hair follicle StemBook.jpg 226 × 261; 23 KB
  
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  Hepatic induction..jpg 400 × 297; 37 KB
  
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  Hepatocyte and Biliary epithelium lineage segregation..jpg 500 × 410; 91 KB
  
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  Heterochromatin structure in ES cells..jpg 600 × 319; 68 KB
  
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  Hhex expression in the ventral foregut endoderm..jpg 300 × 364; 93 KB
  
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  Histological structure of seminiferous tubules in the adult mouse testes..jpg 310 × 233; 69 KB
  
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  Histology of important stages of tooth development..jpg 500 × 371; 105 KB
  
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  Histology of normal and defective intrahepatic bile ducts..jpg 600 × 245; 151 KB
  
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  Histone methyltransferases and demethylases function antagonistically to control gene expression pat.jpg 600 × 597; 97 KB
  
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  HSC migration from embryonic to fetal hematopoiesis..jpg 600 × 424; 89 KB
  
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  Human stem cell imaging..jpg 576 × 262; 64 KB
  
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  Identification and functional characterization of label retaining cells in the ovarian surface epithelium..jpg 439 × 600; 66 KB
  
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  Illustration of stem cell control by the niche..jpg 550 × 369; 78 KB
  
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  Imaging after direct cell labeling..jpg 459 × 229; 45 KB
  
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  Immunoregulation by regulatory T cells (Treg)..jpg 432 × 311; 46 KB
  
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  In vitro hepatic differentiation from ES cells..jpg 500 × 189; 44 KB
  
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  Instructive growth factors regulating fate decisions in embryonic NCSCs..jpg 500 × 468; 72 KB
  
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  Intraovarian transplantation of the thecal stem cells..jpg 420 × 600; 114 KB
  
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  Isolation and characterization of candidate human ovarian tumor cancer initiating cells form self-renewing, anchorage-independent spheroids under stem cell–selective conditions..jpg 319 × 625; 87 KB
  
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  Key genes for stem progenitor cell control which are frequently, and often concordantly, aberrantly silenced, in association with promoter CpG island DNA hypermethylation in pre-invasive colon lesions..jpg 500 × 378; 73 KB
  
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  Key molecular pathways involved in early metanephric kidney development..jpg 600 × 449; 98 KB
  
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  Light photomicrograph of the connected differentiating spermatogonia..jpg 166 × 86; 13 KB
  
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  Liver bud growth..jpg 500 × 408; 111 KB
  
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  Liver bud morphogenesis..jpg 600 × 268; 93 KB
  
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  Liver cell lineage..jpg 350 × 339; 29 KB
  
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  Localization of melanocyte stem cells in the hair follicle..jpg 600 × 340; 54 KB
  
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  Location of multipotent stem cells with neurogenic potential in facial and trunk skin..jpg 550 × 506; 78 KB
  
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  Location of placode precursors at different developmental stages..jpg 594 × 381; 97 KB
  
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  Location of the intermediate mesoderm nephrogenic cord..jpg 600 × 227; 58 KB
  
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  Longitudinal monitoring of stem cell survival using reporter gene imaging..jpg 432 × 349; 50 KB
  
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  LT-HSCs are in the quiescent state..jpg 600 × 580; 87 KB
  
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  Metanephric nephron formation..jpg 600 × 155; 49 KB
  
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  Methods of nuclear reprogramming, their advantages and limitations..jpg 600 × 536; 156 KB
  
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  Micro- and nanofiber composite PCL scaffolds fabricated by electrospinning.jpg 500 × 182; 83 KB
  
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  Micromechanical substrates enable micrometer-resolution cell positioning..jpg 425 × 236; 51 KB
  
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  MicroRNAs are integral to transcription networks in ESCs..jpg 415 × 287; 50 KB
  
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  Model of epigenetic and genetic abnormalities leading to early abnormal activation of the canonical Wnt pathway in the progression of colon, and other, human cancers..jpg 348 × 500; 72 KB
  
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  Models for the nature of sustained tumor growth.jpg 675 × 438; 126 KB
  
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  MSC osteogenic differentiation on ordered and disordered nanotopographies.jpg 650 × 393; 136 KB
  
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  Myometrial stem cells analyses..jpg 500 × 594; 123 KB
  
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  Notch signaling plays a crucial role in melanocyte development..jpg 500 × 210; 58 KB
  
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  Organization of endodermal progenitors and extraembryonic endoderm at onset of gastrulation in chick and mouse embryos..jpg 751 × 776; 335 KB
  
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  Origin of endoderm cells eventually populating different gut areas in chick and mouse..jpg 550 × 422; 99 KB
  
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  Overview of kidney development..jpg 491 × 600; 65 KB
  
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  Pancreatic lineages in the mouse..jpg 500 × 471; 58 KB
  
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  Photobleaching methods used to study chromatin-protein dynamics in living cells..jpg 600 × 384; 82 KB
  
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  PiRNA pathway is required for germ-cell maintenance in Zebrafish..jpg 500 × 415; 148 KB
  
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  PiRNA pathway is required for spermatogenesis in mouse..jpg 597 × 599; 292 KB
  
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  PiRNA pathway mutants show germline defects in Drosophila..jpg 450 × 380; 103 KB
  
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  Postmigratory NCSCs.jpg 500 × 500; 84 KB
  
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  Progress towards the elimination of ES nucleus following fusion, as described by Matsumura et al. (Matsumura et al., 2007)..jpg 550 × 353; 60 KB
  
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  Proposed pathways of interaction between transplanted hESC derivatives and the immune system continued..jpg 600 × 531; 120 KB
  
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  Proposed pathways of interaction between transplanted hESC derivatives and the immune system..jpg 600 × 567; 113 KB
  
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  Relationship between developing islet and duct cells..jpg 206 × 600; 104 KB
  
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  Representation of chromatin marks in critical genes during specification.jpg 600 × 426; 123 KB
  
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  Representative studies providing evidence that malignant progenitor cells are targeted by GvL responses..jpg 539 × 600; 126 KB
  
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  Repressors modulate transcription output..jpg 552 × 346; 51 KB
  
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  Reprogramming capacity in NT depends on cell-cycle status, as demonstrated by Egli et al. (Egli et al., 2007)..jpg 368 × 701; 117 KB
  
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  Reprogramming the immune system using ES cells..jpg 360 × 492; 61 KB
  
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  Role of the osteoblastic niche in the regulation of HSC quiescence..jpg 600 × 409; 82 KB
  
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  Schematic cross-section during rodent uterine development..jpg 600 × 555; 123 KB
  
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  Schematic depiction of LC-MS MS procedure..jpg 661 × 600; 76 KB
  
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  Schematic depiction of two affinity purification approaches..jpg 563 × 600; 93 KB
  
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  Schematic drawing of melanocyte development in the mouse..jpg 600 × 507; 88 KB
  
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  Schematic overview view of niche components..jpg 350 × 139; 24 KB
  
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  Schematic representation of a flow perfusion bioreactor system, which forces the flow of culture med.jpg 550 × 301; 46 KB
  
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  Schematic representation of current (A and B) and promising future strategies (C and D) to stimulate anti tumor immune responses (in orange)..jpg 428 × 500; 82 KB
  
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  Schematic representation of ovarian embryonic development..jpg 400 × 313; 43 KB
  
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  Schematic representation of selective migration of MSCs to areas of tissue injury and tumours where they contribute to tissue repair and tumour-associated stroma formation..jpg 600 × 322; 70 KB
  
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  Schematic representation of the use of BMSCs as vectors..jpg 700 × 550; 77 KB
  
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  Schematic summary of current evidence for ovarian somatic stem cells..jpg 550 × 425; 82 KB
  
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  Scheme of spermatogonial self-renewal and differentiation in the mouse, showing the subsequent spermatogonial cell types..jpg 450 × 715; 88 KB
  
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  Self assembling peptide scaffolds for neural tissue engineering applications..jpg 600 × 337; 148 KB
  
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  SEM images of scaffold surfaces after culture for 16 days in static culture (A), flow perfusion of 0.jpg 450 × 466; 144 KB
  
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  Sensory placodes and their derivatives..jpg 600 × 383; 84 KB
  
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  Sequential soluble factors specify differentiation programs..jpg 381 × 143; 15 KB
  
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  Sequential subdivision of the placode territory..jpg 600 × 372; 55 KB
  
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  Sex differentiation in mouse and man and subsequent development of the female reproductive organs.jpg 432 × 282; 38 KB
  
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  Signalling pathways in placode formation..jpg 600 × 486; 66 KB
  
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  Simplified schematic showing of key molecules and signaling pathways implicated in melanocyte-keratinocyte interactions..jpg 600 × 416; 96 KB
  
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  Sources of new adult β-cells..jpg 600 × 329; 86 KB
  
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  Specificity of immune responses against the malignant cancer-initiating cell depends on where antigen targets are expressed in the cell differentiation hierarchy..jpg 556 × 600; 117 KB
  
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  Strategies for mapping protein-protein and protein-DNA interactions in mESCs..jpg 600 × 484; 101 KB
  
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  Strategy for affinity purification of Nanog associated protein complexes in mESCs..jpg 600 × 402; 77 KB
  
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  Structure and signaling mechanisms of the C. elegans GSC niche..jpg 650 × 297; 77 KB
  
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  Structure and signaling mechanisms of the Drosophila ovarian GSC niche..jpg 650 × 303; 104 KB
  
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  Structure and signaling mechanisms of the Drosophila testicular GSC niche..jpg 700 × 330; 125 KB
  
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  Structure and signaling mechanisms of the putative mouse testicular GSC niche..jpg 700 × 348; 113 KB
  
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  Structure of the mammalian kidney..jpg 600 × 268; 70 KB
  
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  Summary of proteomic approaches utilized in the study of stem cells..jpg 600 × 439; 117 KB
  
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  Summary of the different imaging strategies that can be used to assess the delivery, short- and long-term monitoring of stem cell viability and biology..jpg 600 × 374; 84 KB
  
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  Summary of the signalling pathways in the neural stem cell microenvironment.jpg 500 × 486; 96 KB
  
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  Summation of results for genome tiling arrays performed in colon cancer cells..jpg 500 × 388; 74 KB
  
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  Temporal changes of gene expression reflect segregation of cell fates..jpg 600 × 425; 70 KB
  
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  Tethered growth factor ligands allow sustained signaling without receptor mediated internalization..jpg 396 × 405; 80 KB
  
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  The adult neural stem cell microenvironment in the subependymal zone (SEZ) and the subgranular zone.jpg 500 × 712; 156 KB
  
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  The basic unit of chromatin organization is the nucleosome, which comprises 147 bp of DNA wrapped ar.jpg 600 × 529; 126 KB
  
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  The Cononical miRNA biogenesis pathway.jpg 600 × 383; 36 KB
  
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  The embryonic neural stem cell microenvironment.jpg 500 × 708; 139 KB
  
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  The endo-siRNA biogenesis pathway.jpg 600 × 402; 54 KB
  
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  The epigenetic landscape and its implications for direct reprogramming..jpg 700 × 324; 83 KB
  
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  The human cornea in cross-section..jpg 400 × 349; 95 KB
  
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  The human limbus..jpg 550 × 394; 109 KB
  
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  The Non-canonical miRNA biogenesis pathway.jpg 600 × 447; 43 KB
  
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  The primary dental lamina.jpg 600 × 210; 44 KB
  
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  The sequential and reciprocal regulatory signaling between epithelium (red) and mesenchyme (blue).jpg 650 × 165; 51 KB
  
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  The spectrum of target antigens associated with tumor immunity and allo-immunity after allogeneic HSCT..jpg 600 × 421; 131 KB
  
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  The steps of regenerative medicine..jpg 432 × 430; 55 KB
  
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  The transcriptome of pluripotent cells..jpg 444 × 295; 43 KB
  
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  The uterus differentiates from the fetal Müllerian ducts..jpg 494 × 477; 76 KB
  
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  Three different types of reporter gene reporter probe strategies..jpg 800 × 246; 70 KB
  
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  Three phases of GVHD immuno-biology.jpg 450 × 303; 77 KB
  
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  Time line of mouse liver development emphazing it.jpg 537 × 187; 60 KB
  
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  Time line of mouse liver development..jpg 700 × 319; 96 KB
  
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  Transcription factor network in endoderm induction..jpg 424 × 500; 59 KB
  
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  Transcription programs in stem cells..jpg 487 × 176; 28 KB
  
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  Treatment of the epidermolysis bullosa by transplantation of laminin5 modified stem cells..jpg 507 × 444; 106 KB
  
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  Typical gross appearance of a tubular cartilaginous construct engineered from amniotic mesenchymal stem cells..jpg 360 × 285; 38 KB
  
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  Uterine anatomy..jpg 800 × 320; 82 KB
  
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  White adipose distribution in the body..jpg 600 × 604; 72 KB