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Steen Dissing

Researcher at University of Copenhagen

Publications -  73
Citations -  3912

Steen Dissing is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Inositol & Inositol phosphate. The author has an hindex of 34, co-authored 72 publications receiving 3580 citations.

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PDGF-BB induces intratumoral lymphangiogenesis and promotes lymphatic metastasis

TL;DR: In this article, the authors report that members of the PDGF family act as lymphangiogenic factors, and that PDGF-BB stimulated MAP kinase activity and cell motility of isolated lymphatic endothelial cells.
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Placenta Growth Factor-1 antagonizes VEGF-induced angiogenesis and tumor growth by the formation of functionally inactive PlGF-1/VEGF heterodimers

TL;DR: It is demonstrated that PlGF-1, an alternatively spliced isoform of the PlGF gene, antagonizes VEGF-induced angiogenesis when both factors are coexpressed in murine fibrosarcoma cells, and acts as a natural antagonist of V EGF when both Factors are synthesized in the same population of cells.
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Vitamin D is positively associated with sperm motility and increases intracellular calcium in human spermatozoa

TL;DR: 1,25(OH)(2)D(3) increased intracellular calcium concentration, sperm motility and induced the acrosome reaction in mature spermatozoa, and VD serum levels were positively associated with sperm motilities, suggesting a role for VD in human sperm function.
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Collaborative interplay between FGF-2 and VEGF-C promotes lymphangiogenesis and metastasis

TL;DR: It is shown that FGF-2 and VEGF-C collaboratively promote angiogenesis and lymphangiogenesis in the tumor microenvironment, leading to widespread pulmonary and lymph-node metastases and intervention and targeting of the F GF-2– and VGF-C–induced angiogenic andymphangiogenic synergism could be potentially important approaches for cancer therapy and prevention of metastasis.
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CXCR3 Expression and Activation of Eosinophils: Role of IFN-γ-Inducible Protein-10 and Monokine Induced by IFN-γ

TL;DR: The results indicate that CXCR3-γ IP-10 and -Mig receptor-ligand pairs as well as the effects of IL-2 and IL-10 on them may be especially important in the cytokine/chemokine environment for the pathophysiologic events of allergic inflammation, including initiation, progression, and termination in the processes.