BI 6727, A Polo-like Kinase Inhibitor with Improved Pharmacokinetic Profile and Broad Antitumor Activity by RUDOLPH, Dorothea, STEEGMAIER, Martin, HOFFMANN, Matthias, GRAUERT, Matthias, BAUM, Anke, QUANT, Jens, HASLINGER, Christian, GARIN-CHESA, Pilar, ADOLF, Gunther R

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BI 2536, a Potent and Selective Inhibitor of Polo-like Kinase 1, Inhibits Tumor Growth In Vivo by Steegmaier, Martin, Hoffmann, Matthias, Baum, Anke, Lénárt, Péter, Petronczki, Mark, Krššák, Martin, Gürtler, Ulrich, Garin-Chesa, Pilar, Lieb, Simone, Quant, Jens, Grauert, Matthias, Adolf, Günther R., Kraut, Norbert, Peters, Jan-Michael, Rettig, Wolfgang J.

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Functional interaction of metabotropic glutamate receptor 5 and NMDA-receptor by a metabotropic glutamate receptor 5 positive allosteric modulator by Rosenbrock, Holger, Kramer, Gert, Hobson, Scott, Koros, Eliza, Grundl, Marc, Grauert, Matthias, Reymann, Klaus G., Schröder, Ulrich H.

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BI-D1870 is a specific inhibitor of the p90 RSK (ribosomal S6 kinase) isoforms in vitro and in vivo by Sapkota, Gopal P, Cummings, Lorna, Newell, Felicity S, Armstrong, Christopher, Bain, Jennifer, Frodin, Morten, Grauert, Matthias, Hoffmann, Matthias, Schnapp, Gisela, Steegmaier, Martin, Cohen, Philip, Alessi, Dario R

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Potent Blockade of Sodium Channels and Protection of Brain Tissue from Ischemia by BIII 890 CL by Carter, Adrian J., Grauert, Matthias, Pschorn, Uwe, Bechtel, Wolf Dietrich, Bartmann-Lindholm, Christina, Qu, Yusheng, Scheuer, Todd, Catterall, William A., Weiser, Thomas

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Design, Synthesis, and Evaluation of Indolinones as Inhibitors of the Transforming Growth Factor β Receptor I (TGFβRI) by Roth, Gerald J, Heckel, Armin, Brandl, Trixi, Grauert, Matthias, Hoerer, Stefan, Kley, Joerg T, Schnapp, Gisela, Baum, Patrick, Mennerich, Detlev, Schnapp, Andreas, Park, John E

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N-Methyl-d-aspartate Receptor Channel Block by the Enantiomeric 6,7-Benzomorphans BIII 277 CL and BIII 281 CL by Grauert, Matthias, Rho, Jong M., Subramaniam, Swaminathan, Rogawski, Michael A.

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Functional interaction of metabotropic glutamate receptor 5 and NMDA-receptor by a metabotropic glutamate receptor 5 positive allosteric modulator: Metabotropic Glutamate Receptors... by ROSENBROCK, Holger, KRAMER, Gert, HOBSON, Scott, KOROS, Eliza, GRUNDL, Marc, GRAUERT, Matthias, REYMANN, Klaus G, SCHRÖDER, Ulrich H

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Synthesis and Structure−Activity Relationships of 6,7-Benzomorphan Derivatives as Use-Dependent Sodium Channel Blockers for the Treatment of Stroke by Grauert, Matthias, Bechtel, Wolf D, Weiser, Thomas, Stransky, Werner, Nar, Herbert, Carter, Adrian J

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Synthesis and Structure−Activity Relationships of 6,7-Benzomorphan Derivatives as Antagonists of the NMDA Receptor−Channel Complex by Grauert, Matthias, Bechtel, Wolf Dietrich, Ensinger, Helmut A, Merz, Herbert, Carter, Adrian J

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SYNTHESIS AND IN VITRO AND IN VIVO EVALUATION OF [11C]METHYL-BIII277CL FOR IMAGING THE PCP-BINDING SITE OF THE NMDA RECEPTOR BY PET by Kokic, Marko, Honer, Michael, Kessler, Lea J., Grauert, Matthias, Schubiger, Pius A., Ametamey, Simon M.

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Young Oncologists United (YOU) als interdisziplinäre Nachwuchsarbeitsruppe der DKG gegründet by Mäurer, Matthias, Sulzer, Sabrina, Holzgreve, Adrien, Mäurer, Irina, Fleischmann, Daniel F., Gagelmann, Nico, Krey-Grauert, Ilona, Käsmann, Lukas, Kött, Julian, Oster, Christoph, Meyer, Robert, Nestler, Tim, Rauwolf, Kerstin K., Schlosser-Hupf, Sophie, Staudacher, Jonas J., Weydandt, Laura, Wikert, Julia, Heinrich, Kathrin

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