Trond Ulven

Trond Ulven

Professor

Member of:


    1. The Pharmacology of TUG-891, a Potent and Selective Agonist of the Free Fatty Acid Receptor 4 (FFA4/GPR120), Demonstrates Both Potential Opportunity and Possible Challenges to Therapeutic Agonism

      Hudson, B. D., Shimpukade, B., Mackenzie, A. E., Butcher, A. J., Pediani, J. D., Ulven, Elisabeth Rexen, Heathcote, H., Tobin, A. B., Ulven, Trond & Milligan, G., 2013, In: Molecular Pharmacology. 84, 5, p. 710-725 16 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    2. The Neutrophil Response Induced by an Agonist for Free Fatty Acid Receptor 2 (GPR43) Is Primed by Tumor Necrosis Factor Alpha and by Receptor Uncoupling from the Cytoskeleton but Attenuated by Tissue Recruitment

      Björkman, L., Mårtensson, J., Winther, M., Gabl, M., Holdfeldt, A., Uhrbom, M., Bylund, J., Højgaard Hansen, A., Pandey, S. K., Ulven, Trond, Forsman, H. & Dahlgren, C., 2016, In: Molecular and Cellular Biology. 36, 20, p. 2583-2595 13 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    3. The GPR120 agonist TUG-891 promotes metabolic health by stimulating mitochondrial respiration in brown fat

      Schilperoort, M., van Dam, A. D., Hoeke, G., Shabalina, I. G., Okolo, A., Hanyaloglu, A. C., Dib, L. H., Mol, I. M., Caengprasath, N., Chan, Y., Damak, S., Miller, A. R., Coskun, T., Shimpukade, B., Ulven, Trond, Kooijman, S., Rensen, P. C. & Christian, M., 17 Jan 2018, In: E M B O Molecular Medicine. 10, 3, 18 p., e8047.

      Research output: Contribution to journalJournal articleResearchpeer-review

    4. Published

      The C-terminal tail of CRTH2 is a key molecular determinant that constrains GalphaI- and downstream-signaling cascade activation

      Schroeder, R., Merten, N., Mathiesen, Jesper M., Martini, L., Letunic, A. K., Krop, F., Blaukat, A., Fang, Y., Tran, E., Ulven, Trond, Drewke, C., Whistler, J., Pardo, L., Gomeza, J. & Kostenis, E., 2009, In: Journal of Biological Chemistry. 284, 2, p. 1324-1336 13 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    5. Published

      Tetrasubstituted phenanthrolines as highly potent, water-soluble, and selective g-quadruplex ligands

      Larsen, A. F., Nielsen, M. C. & Ulven, Trond, 2012, In: Chemistry: A European Journal. 18, 35, p. 10892-10902 11 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    6. Published

      Targeting the prostaglandin D2 receptors DP1 and CRTH2 for treatment of inflammation

      Ulven, Trond & Kostenis, E., 2010, Frontiers in Medicinal Chemistry. Bentham Science Publishers, Vol. 5.

      Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

    7. Published

      Targeting the prostaglandin D2 receptors DP and CRTH2 for treatment of inflammation

      Ulven, Trond & Kostenis, E., 2006, In: Current Topics in Medicinal Chemistry. 6, 13, p. 1427-1444 18 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    8. Published

      Targeting G protein-coupled 7TM receptors in treatment of inflammation

      Ulven, Trond, 2006, In: Current Topics in Medicinal Chemistry. 6, 13, p. 1317-1318 2 p.

      Research output: Contribution to journalJournal articleResearch

    9. Published

      Synthesis of racemic 3,5-O-benzylidene-2-deoxypentoses from 2-phenyl-1,3-dioxan-5-one hydrate

      Ulven, Trond, Sørbye, K. A. & Carlsen, P. H. J., 1997, In: Acta Chemica Scandinavica. 51, 10, p. 1041-1044 4 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    10. Published

      Synthesis of benzylidene-protected dihydroxyacetone

      Carlsen, P. H. J., Sørbye, K. A., Ulven, Trond & Aasbø, K., 1996, In: Acta Chemica Scandinavica. 50, 2, p. 185-187 3 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

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