Resident microglia, and not peripheral macrophages, are the main source of brain tumor mononuclear cells von Müller, Annett, Brandenburg, Susan, Turkowski, Kati, Müller, Susanne, Vajkoczy, Peter

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Structure-Based Design of an in Vivo Active Selective BRD9 Inhibitor von Martin, Laetitia J, Koegl, Manfred, Bader, Gerd, Cockcroft, Xiao-Ling, Fedorov, Oleg, Fiegen, Dennis, Gerstberger, Thomas, Hofmann, Marco H, Hohmann, Anja F, Kessler, Dirk, Knapp, Stefan, Knesl, Petr, Kornigg, Stefan, Müller, Susanne, Nar, Herbert, Rogers, Catherine, Rumpel, Klaus, Schaaf, Otmar, Steurer, Steffen, Tallant, Cynthia, Vakoc, Christopher R, Zeeb, Markus, Zoephel, Andreas, Pearson, Mark, Boehmelt, Guido, McConnell, Darryl

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The ins and outs of selective kinase inhibitor development von Müller, Susanne, Chaikuad, Apirat, Gray, Nathanael S, Knapp, Stefan

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Bromodomains as therapeutic targets von Muller, Susanne, Filippakopoulos, Panagis, Knapp, Stefan

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Discovery and Optimization of Small-Molecule Ligands for the CBP/p300 Bromodomains von Hay, Duncan A, Fedorov, Oleg, Martin, Sarah, Singleton, Dean C, Tallant, Cynthia, Wells, Christopher, Picaud, Sarah, Philpott, Martin, Monteiro, Octovia P, Rogers, Catherine M, Conway, Stuart J, Rooney, Timothy P. C, Tumber, Anthony, Yapp, Clarence, Filippakopoulos, Panagis, Bunnage, Mark E, Müller, Susanne, Knapp, Stefan, Schofield, Christopher J, Brennan, Paul E

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Identification of a Chemical Probe for Family VIII Bromodomains through Optimization of a Fragment Hit von Gerstenberger, Brian S, Trzupek, John D, Tallant, Cynthia, Fedorov, Oleg, Filippakopoulos, Panagis, Brennan, Paul E, Fedele, Vita, Martin, Sarah, Picaud, Sarah, Rogers, Catherine, Parikh, Mihir, Taylor, Alexandria, Samas, Brian, O’Mahony, Alison, Berg, Ellen, Pallares, Gabriel, Torrey, Adam D, Treiber, Daniel K, Samardjiev, Ivan J, Nasipak, Brian T, Padilla-Benavides, Teresita, Wu, Qiong, Imbalzano, Anthony N, Nickerson, Jeffrey A, Bunnage, Mark E, Müller, Susanne, Knapp, Stefan, Owen, Dafydd R

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Discovery of a Chemical Tool Inhibitor Targeting the Bromodomains of TRIM24 and BRPF von Bennett, James, Fedorov, Oleg, Tallant, Cynthia, Monteiro, Octovia, Meier, Julia, Gamble, Vicky, Savitsky, Pavel, Nunez-Alonso, Graciela A, Haendler, Bernard, Rogers, Catherine, Brennan, Paul E, Müller, Susanne, Knapp, Stefan

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LP99: Discovery and Synthesis of the First Selective BRD7/9 Bromodomain Inhibitor von Clark, Peter G. K., Vieira, Lucas C. C., Tallant, Cynthia, Fedorov, Oleg, Singleton, Dean C., Rogers, Catherine M., Monteiro, Octovia P., Bennett, James M., Baronio, Roberta, Müller, Susanne, Daniels, Danette L., Méndez, Jacqui, Knapp, Stefan, Brennan, Paul E., Dixon, Darren J.

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Therapeutic targeting of p300/CBP HAT domain for the treatment of NUT midline carcinoma von Zhang, Xin, Zegar, Tim, Lucas, Anais, Morrison-Smith, Chevaun, Knox, Tatiana, French, Christopher A., Knapp, Stefan, Müller, Susanne, Siveke, Jens T.

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Histone Recognition and Large-Scale Structural Analysis of the Human Bromodomain Family von Filippakopoulos, Panagis, Picaud, Sarah, Mangos, Maria, Keates, Tracy, Lambert, Jean-Philippe, Barsyte-Lovejoy, Dalia, Felletar, Ildiko, Volkmer, Rudolf, Müller, Susanne, Pawson, Tony, Gingras, Anne-Claude, Arrowsmith, Cheryl H., Knapp, Stefan

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RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain von Picaud, Sarah, Wells, Christopher, Felletar, Ildiko, Brotherton, Deborah, Martin, Sarah, Savitsky, Pavel, Diez-Dacal, Beatriz, Philpott, Martin, Bountra, Chas, Lingard, Hannah, Fedorov, Oleg, Müller, Susanne, Brennan, Paul E., Knapp, Stefan, Filippakopoulos, Panagis

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Development of Selective Pyrido[2,3‑d]pyrimidin-7(8H)‑one-Based Mammalian STE20-Like (MST3/4) Kinase Inhibitors von Rak, Marcel, Menge, Amelie, Tesch, Roberta, Berger, Lena M., Balourdas, Dimitrios-Ilias, Shevchenko, Ekaterina, Krämer, Andreas, Elson, Lewis, Berger, Benedict-Tilman, Abdi, Ismahan, Wahl, Laurenz M., Poso, Antti, Kaiser, Astrid, Hanke, Thomas, Kronenberger, Thales, Joerger, Andreas C., Müller, Susanne, Knapp, Stefan

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Targeting the Bromome: are we there yet? von Müller, Susanne

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Development of a potent and selective chemical probe for the pleiotropic kinase CK2 von Wells, Carrow I., Drewry, David H., Pickett, Julie E., Tjaden, Amelie, Krämer, Andreas, Müller, Susanne, Gyenis, Laszlo, Menyhart, Daniel, Litchfield, David W., Knapp, Stefan, Axtman, Alison D.

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Cell adhesion and proliferation on RGD-modified recombinant spider silk proteins von Wohlrab, Stefanie, Müller, Susanne, Schmidt, Andreas, Neubauer, Stefanie, Kessler, Horst, Leal-Egaña, Aldo, Scheibel, Thomas

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Discovery and Characterization of GSK2801, a Selective Chemical Probe for the Bromodomains BAZ2A and BAZ2B von Chen, Peiling, Chaikuad, Apirat, Bamborough, Paul, Bantscheff, Marcus, Bountra, Chas, Chung, Chun-wa, Fedorov, Oleg, Grandi, Paola, Jung, David, Lesniak, Robert, Lindon, Matthew, Müller, Susanne, Philpott, Martin, Prinjha, Rab, Rogers, Catherine, Selenski, Carolyn, Tallant, Cynthia, Werner, Thilo, Willson, Timothy M, Knapp, Stefan, Drewry, David H

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Application of Zero-Bias Quasi-Optical Schottky-Diode Detectors for Monitoring Short-Pulse and Weak Terahertz Radiation von Semenov, Alexei, Cojocari, Oleg, Hübers, Heinz-Wilhelm, Fengbin Song, Klushin, Alexander, Müller, Anke-Susanne

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Development of Selective CBP/P300 Benzoxazepine Bromodomain Inhibitors von Popp, Tobias A, Tallant, Cynthia, Rogers, Catherine, Fedorov, Oleg, Brennan, Paul E, Müller, Susanne, Knapp, Stefan, Bracher, Franz

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The future of chemical probes is diversity von Müller, Susanne, Frye, Stephen, Baell, Jonathan

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Opening the human spirit to sustainability transformation: the potential for individual human–nature resonance and integrative rituals von Müller, Susanne, Artmann, Martina, Surrey, Caroline

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