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The neural cell adhesion molecule N-CAM simultaneously combines with another N-CAM and a fibroblast growth factor receptor to stimulate the tyrosine kinase activity of that receptor to induce the growth of neurites.
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An example of a pathogenic protozoan is the malarial parasite (Plasmodium falciparum), which uses one adhesion molecule called the circumsporozoite protein to bind to liver cells, and another adhesion molecule called the merozoite surface protein to bind red blood cells.
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Tasonermin affects the morphology and reduces proliferation of endothelial cells and modifies expression of specific cell surface and secretory proteins (including adhesion molecules and proteins modulating coagulation, interleukins and haematopoietic growth factors
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HSCs express the cell surface glycoprotein CD34, a cell-cell adhesion molecule that is lost from mature blood cells.
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The integrins belong to the 4 families of the Cell Adhesion Molecules (CAM): integrin, cadherin, selectin, and the large family of the immunoglobulins.
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Janssen: "The most important conclusion is that Teneurin looks very different from all the traditional cell adhesion molecules, which are the proteins involved in connecting cells together.
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Cell adhesion molecules (CAMs) are proteins located on the cell surface[1] involved in binding with other cells or with the extracellular matrix (ECM) in the process called cell adhesion.
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The new endothelial cells use adhesion molecules like integrins that help them bind to each other to form chains.
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The agent mediates formation of a synapse between the T cell and the tumor cell, upregulation of cell adhesion molecules, production of cytolytic proteins, release of inflammatory cytokines, and proliferation of T cells, resulting in redirected lysis of CD19-positive cells.
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Blinatumomab mediates the formation of a synapse between the T cell and the tumor cell, upregulation of cell-adhesion molecules, production of cytolytic proteins, release of inflammatory cytokines, and proliferation of T cells, resulting in redirected lysis of CD19-positive cells.
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As a matter of fact, the polyphenols in the olive oil promote the reduction of the presence of cell adhesion molecules, increase the availability of nitric oxide, suppress platelet aggregation, protect LDL against oxidation to delay atherosclerosis and reduce in minatory reactions.
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Can master genes be identified that are also relevant to tumors in other hormone-regulated target tissues? 2. What are the underlying mechanisms, and what is the impact of dysregulated expression of cell adhesion molecules and more particularly of the cadherin-catenin system on tumor cell signaling, cell interactions and motility?
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An example of a pathogenic protozoan is the malarial parasite (Plasmodium falciparum), which uses one adhesion molecule called the circumsporozoite protein to bind to liver cells, and another adhesion molecule called the merozoite surface protein to bind red blood cells.
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At the interface between blood and the brain, endothelial cells are stitched together by these tight junctions, which are composed of smaller subunits, frequently biochemical dimers, that are transmembrane proteins such as occludin, claudins, junctional adhesion molecule (JAM), or ESAM, for example.
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Viruses also have adhesion molecules required for viral binding to host cells.
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These include inhibiting the release of proinflammatory cytokines such as IL-4, IL-6, IL-8, and IL-13 from human mast cells/basophils, as well as inhibition of the expression of the adhesion molecule P-selectin on endothelial cells.
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At the interface between blood and the brain, endothelial cells are stitched together by these tight junctions, which are composed of smaller subunits, frequently biochemical dimers, that are transmembrane proteins such as occludin, claudins, junctional adhesion molecule (JAM), or ESAM, for example. Each of these transmembrane proteins is anchored into the endothelial cells by another protein complex that includes zo-1 and associated proteins.
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This "barrier" results from the selectivity of the tight junctions between endothelial cells in CNS vessels that restricts the passage of solutes.[5] At the interface between blood and the brain, endothelial cells are stitched together by these tight junctions, which are composed of smaller subunits, frequently biochemical dimers, that are transmembrane proteins such as occludin, claudins, junctional adhesion molecule (JAM), or ESAM, for example.[3] Each of these transmembrane proteins is anchored into the endothelial cells by another protein complex that includes zo-1 and associated proteins.[3]
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The blood–brain barrier results from the selectivity of the tight junctions between endothelial cells in CNS vessels, which restricts the passage of solutes.[1] At the interface between blood and the brain, endothelial cells are stitched together by these tight junctions, which are composed of smaller subunits, frequently biochemical dimers, that are transmembrane proteins such as occludin, claudins, junctional adhesion molecule (JAM), or ESAM, for example.[5] Each of these transmembrane proteins is anchored into the endothelial cells by another protein complex that includes ZO-1 and associated proteins.[5]
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19 sinne gevind in 13 ms. Hulle kom uit baie bronne en word nie nagegaan nie.