Researcher Portfolio
Kötting, J.
Department of Membrane Biophysics, MPI for biophysical chemistry, Max Planck Society, Research Group of Phospholipids, MPI for biophysical chemistry, Max Planck Society
Researcher Profile
Position: Research Group of Phospholipids, MPI for biophysical chemistry, Max Planck Society
Position: Department of Membrane Biophysics, MPI for biophysical chemistry, Max Planck Society
Researcher ID: https://pure.mpg.de/cone/persons/resource/persons15354
Publications
: Kaufmann-Kolle, P., Drevs, J., Berger, M. R., Koetting, J., Marschner, N., Unger, C., & Eibl, H. (1994). Pharmacokinetic behavior and antineoplastic activity of liposomal hexadecylphosphocholine. Cancer Chemotherapy and Pharmacology, 34(5), 393-398. [PubMan] : Marschner, N., Koetting, J., Eibl, H., & Unger, C. (1992). Distribution of hexadecylphosphocholine and octadecyl-methyl-glycero-3-phosphocholine in rat tissues during steady-state treatment. Cancer Chemotherapy and Pharmacology, 31(1), 18-22. [PubMan] : Koetting, J., Berger, M. R., Unger, C., & Eibl, H. (1992). Alkylphosphocholines: Influence of structural variation on biodistribution at antineoplastically active concentrations. Cancer Chemotherapy and Pharmacology, 30(2), 105-112. [PubMan] : Koetting, J., Marschner, N., Neumueller, W., Unger, C., & Eibl, H. (1992). Hexadecylphosphocholine and octadecyl-methyl-glycero-3-phosphocholine: a comparison of hemolytic activity, serum binding and tissue distribution. Progress in Experimental Tumor Research, 34, 131-142. [PubMan] : Unger, C., Fleer, E. A. M., Koetting, J., Neumueller, W., & Eibl, H. (1992). Antitumoral activity of alkylphosphocholines and analogues in human leukemia cell lines. Progress in Experimental Tumor Research, 34, 25-32. [PubMan] : Koetting, J., Marschner, N., Unger, C., & Eibl, H. (1992). Determination of alkylphosphocholines and of alkyl-glycero-phosphocholines in biological fluids and tissues. Progress in Experimental Tumor Research, 34, 6-11. [PubMan] : Reitz, R. C., Koetting, J., Unger, C., & Eibl, H. (1992). Comparison of the tissue distribution of hexadecylphosphocholine and erucylphosphocholine. Progress in Experimental Tumor Research, 34, 143-152. [PubMan] : Birk, H.-W., Piberhofer, S., Schütterle, G., Haase, W., Koetting, J., & Koepsell, H. (1991). Analysis of Na+-D-glucose cotransporter and other renal brush border proteins in human urine. Kidney International, 40(5), 823-837. doi:10.1038/ki.1991.282. [PubMan] : Kötting, J., Eibl, H., & Fehrenbach, F. J. (1988). Substrate specificity of Staphylococcus aureus (TEN5) lipases with isomeric oleoyl-sn-glycerol ethers as substrates. Chemistry and Physics of Lipids, 47(2), 117-122. doi:10.1016/0009-3084(88)90080-1. [PubMan] : Kötting, J., Fleer, E., Unger, C., & Eibl, H. J. (1988). Synthetische Alkyllysophospholipide als Antitumormittel - Strukturverwandte des „Platelet Activating Factors”. European Journal of Lipid Science and Technology, 90(9), 345-351. doi:10.1002/lipi.19880900905. [PubMan] : Kötting, J., Unger, C., & Eibl, H. (1987). Substrate specificity of O-alkylglycerol monooxygenase (E.C. 1.14.16.5), solubilized from rat liver microsomes. Lipids, 22(11), 831-835. doi:10.1007/BF02535539. [PubMan] : Kötting, J., Unger, C., & Eibl, H. (1987). A continuous assay for O-alkylglycerol monooxygenase (E.C. 1.14.16.5). Lipids, 2(11), 824-830. doi:10.1007/BF02535538. [PubMan] : Unger, C., Eibl, H., Kim, D. J., Fleer, E., Kötting, J., Bartsch, H. H., Nagel, G. A., & Pfizenmaier, K. (1987). Sensitivity of leukemia cell lines to cytotoxic alkyl-lysophospholipids in relation to O-alkyl cleavage enzyme activities. Journal of the National Cancer Institute, 78(2), 219-222. doi:10.1093/jnci/78.2.219. [PubMan] : Kötting, J., Jürgens, D., Schiller, R., & Fehrenbach, F. J. (1985). Biochemical and biological properties of Staphyococcus aureus lipases (E. C. 3.1.1.3.). Zentralblatt für Bakteriologie, 14, 301-309. [PubMan]