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Displaying 20 of 197 results for "ESAM"
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  1. ESAM_RAT UniProt:Swiss-Prot

    ID: Q6AYD4

    Description: Endothelial cell-selective adhesion molecule Extracellular Helical Cytopla...

  2. Microarray analyses of ESAM positive cells in the CD34(+) CD38(-) fraction of collagenase-treated bones BioProject

    ID: PRJNA269303

    Keywords: Transcriptome or Gene expression

    Access Type: download

  3. Microarray analyses of ESAM positive cells in the CD34(+) CD38(-) fraction of collagenase-treated bones OmicsDI

    ID: E-GEOD-63877

    Date Released: 01-02-2015

    Description: We previously identified endothelial cell-selective adhesion molecule (ESAM) as ...

  4. Microarray analyses of ESAM positive cells in the CD34(+) CD38(-) fraction of collagenase-treated bones ArrayExpress

    ID: E-GEOD-63877

    Description: We previously identified endothelial cell-selective adhesion molecule (ESAM) as ...

  5. Microarray analysis of WT ESAM+ and ESAM- cDC subsets BioProject

    ID: PRJNA195894

    Keywords: Transcriptome or Gene expression

    Access Type: download

  6. Gene expression analysis of primitive erythroid progenitors from 5-FU-treated WT and ESAM-KO mice. BioProject

    ID: PRJNA297177

    Keywords: Transcriptome or Gene expression

    Access Type: download

  7. Microarray analysis of WT ESAM+ and ESAM- cDC subsets ArrayExpress

    ID: E-GEOD-45679

    Description: echniques to deplete specific classical dendritic cell (cDC) subsets and analyze immunity to the A/E pathogen Citrobacter rodentium. We find that Zbtb46+ cDCs, and specifically Notch2-dependent intestinal CD11b+ cDCs, but not Batf3-dependent CD103+ cDCs, are required for IL-23 production and immunity against C. rodentium. Notch2 controls cDC differentiation at a terminal step mediated by lymphotoxin signaling. Importantly, these results provide the first demonstration of a non-redundant fun...

  8. ESAM_MOUSE UniProt:Swiss-Prot

    ID: Q925F2

    Description: Endothelial cell-selective adhesion molecule Extracellular Helical Cytopla...

  9. The affect of specific ablation of Runx3 from Esam splenic dendritic cells BioProject

    ID: PRJNA210762

    Keywords: Transcriptome or Gene expression

    Access Type: download

  10. Transcription profiling of human ermal lymphatic endothelial cells (LEC) with those isolated from tumours of murine T241/VEGF-C/GFP metastatic fibrosarcoma reveals lymphatic endoth... ArrayExpress

    ID: E-GEOD-6255

    Description: paring the RNA profile of normal dermal lymphatic endothelial cells (LEC) with those isolated from tumours of murine T-241/VEGF-C metastatic fibrosarcoma. Our findings reveal significant changes in the expression of some 792 genes in tumour lymphatics (≥ 2 fold up/downregulation, p ≤ 0.05), involving particularly transcripts associated with junctional adhesion, immunomodulation, extracellular matrix and vessel growth/patterning, several of which we have confirmed by RT-PCR and/or immunohistochemistry. Interestingly, this altered phenotype could not be attributed sol...

  11. Transcription profiling of mouse CD31(+) cells isolated from embryonic stem cells ArrayExpress

    ID: E-TABM-1125

    Description: riment is the identification of genes involved in endothelial differentiation. This is of great interest for the understanding of the cellular and molecular mechanisms involved in the development of new blood vessels. Mouse embryonic stem (mES) cells serve as a potential source of endothelial cells for transcriptomic analysis. We isolated endothelial cells from 8-days old embryoid bodies by immuno-magnetic ...

  12. Microarray analysis of WT ESAM+ and ESAM- cDC subsets OmicsDI

    ID: E-GEOD-45679

    Date Released: 06-17-2013

    Description: echniques to deplete specific classical dendritic cell (cDC) subsets and analyze immunity to the A/E pathogen Citrobacter rodentium. We find that Zbtb46+ cDCs, and specifically Notch2-dependent intestinal CD11b+ cDCs, but not Batf3-dependent CD103+ cDCs, are required for IL-23 production and immunity against C. rodentium. Notch2 controls cDC differentiation at a terminal step mediated by lymphotoxin signaling. Importantly, these results provide the first demonstration of a non-redundant fun...

  13. PECA1_BOVIN UniProt:Swiss-Prot

    ID: P51866

    Description: Platelet endothelial cell adhesion molecule Extracellular Helical Cytoplasmic Ig-li...

  14. The affect of specific ablation of Runx3 from Esam splenic dendritic cells ArrayExpress

    ID: E-GEOD-48590

    Description: Esam/CD4+ dendritic cells are part of the innate immunity essential for priming and activating of CD4+ T cells To identify Runx3 re...

  15. ESAM_MACFA UniProt:Swiss-Prot

    ID: Q95KI3

    Description: Endothelial cell-selective adhesion molecule Extracellular Helical Cytopla...

  16. PECA1_PIG UniProt:Swiss-Prot

    ID: Q95242

    Description: Platelet endothelial cell adhesion molecule Extracellular Helical Cytoplasmic Ig-li...

  17. Notch2 receptor signaling controls functional differentiation of dendritic cells in the spleen and intestine ArrayExpress

    ID: E-GEOD-31551

    Description: distinct population marked by high expression of adhesion molecule Esam. The Notch-dependent Esamhi DC subset also required lymphotoxin beta receptor signaling, proliferated in situ and facilitated efficient CD4+ T cell priming. The Notch-independent Esamlo DCs expressed monocyte-related genes and showed superior cytokine responses. In addition, Notch2 deletion led to the loss of CD11b+ CD103+ DCs in the intestinal lamina propria and to the corresponding decrease of IL-17-producing CD4+ T cells in the intestine. Thus,Notch2 is ...

  18. Lymphatic endothelium of metastatic tumours has a distinct transcription profile. BioProject

    ID: PRJNA99687

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: paring the RNA profile of normal dermal lymphatic endothelial cells (LEC) with those isolated from tumours of murine T-241/VEGF-C metastatic fibrosarcoma. Our findings reveal significant changes in the expression of some 792 genes in tumour lymphatics (≥ 2 fold up/downregulation, p ≤ 0.05), involving particularly transcripts associated with junctional adhesion, immunomodulation, extracellular matrix and vessel growth/patterning, several of which we have confirmed by RT-PCR and/or immunohistochemistry. Interestingly, this altered phenotype could not be attributed sol...
  19. The affect of specific ablation of Runx3 from Esam splenic dendritic cells OmicsDI

    ID: E-GEOD-48590

    Date Released: 06-28-2014

    Description: Esam/CD4+ dendritic cells are part of the innate immunity essential for priming and activating of CD4+ T cells To identify Runx3 re...

  20. Notch2 receptor signaling controls functional differentiation of dendritic cells in the spleen and intestine OmicsDI

    ID: E-GEOD-31551

    Date Released: 12-05-2011

    Description: distinct population marked by high expression of adhesion molecule Esam. The Notch-dependent Esamhi DC subset also required lymphotoxin beta receptor signaling, proliferated in situ and facilitated efficient CD4+ T cell priming. The Notch-independent Esamlo DCs expressed monocyte-related genes and showed superior cytokine responses. In addition, Notch2 deletion led to the loss of CD11b+ CD103+ DCs in the intestinal lamina propria and to the corresponding decrease of IL-17-producing CD4+ T cells in the intestine. Thus,Notch2 is ...


Displaying 20 of 197 results for "ESAM"