Brand Evolution: Moderne Markenfuhrung im digitalen Zeitalter von Alby, Tom, Theobald, Elke, Dragan, Alexander, Haisch, Philipp T, Blahudka, Robert, Bottler, Dietmar, Buddenberg, Danny, Daul, Christian, Dietrich, Anna, Fuchs, Wolfgang, Gaiser, Brigitte, Hauser, Annika, Hammer, Claus, Hassenstein, Katrin, Hau, Sarah-Maria, Henseler, Wolfgang, Hillebrecht, Imke, Hoffmann, Daniel, Lakowski, Boris, Linxweiler, Richard, Marsden, Paul, Martin, Jens Jochen, Meyer, Daniel, Pflaum, Dieter, Pusch, Albert, Reese, Frank, Rota, Franco, Siegle, Alexandra, Schilling, Klaus-Jurgen, Schneider, Holger, Schupferling, Jasmin, Schulze, Sonja, Stolzenburg, Wieland, Teiber, Edwin, Ullsperger, Jana, Vorndran, Elke, Walter, Nadine, Zimmermann, Thomas

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New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing von Keller, Andreas, Graefen, Angela, Ball, Markus, Matzas, Mark, Boisguerin, Valesca, Maixner, Frank, Leidinger, Petra, Backes, Christina, Khairat, Rabab, Forster, Michael, Stade, Björn, Franke, Andre, Mayer, Jens, Spangler, Jessica, McLaughlin, Stephen, Shah, Minita, Lee, Clarence, Harkins, Timothy T., Sartori, Alexander, Moreno-Estrada, Andres, Henn, Brenna, Sikora, Martin, Semino, Ornella, Chiaroni, Jacques, Rootsi, Siiri, Myres, Natalie M., Cabrera, Vicente M., Underhill, Peter A., Bustamante, Carlos D., Vigl, Eduard Egarter, Samadelli, Marco, Cipollini, Giovanna, Haas, Jan, Katus, Hugo, O'Connor, Brian D., Carlson, Marc R.J., Meder, Benjamin, Blin, Nikolaus, Meese, Eckart, Pusch, Carsten M., Zink, Albert

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GlialCAM, a Protein Defective in a Leukodystrophy, Serves as a ClC-2 Cl− Channel Auxiliary Subunit von Jeworutzki, Elena, López-Hernández, Tania, Capdevila-Nortes, Xavier, Sirisi, Sònia, Bengtsson, Luiza, Montolio, Marisol, Zifarelli, Giovanni, Arnedo, Tanit, Müller, Catrin S., Schulte, Uwe, Nunes, Virginia, Martínez, Albert, Jentsch, Thomas J., Gasull, Xavier, Pusch, Michael, Estévez, Raúl

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Strong impact of MammaPrint and BluePrint on treatment decisions in luminal early breast cancer: results of the WSG-PRIMe study von Wuerstlein, R., Kates, R., Gluz, O., Grischke, E. M., Schem, C., Thill, M., Hasmueller, S., Köhler, A., Otremba, B., Griesinger, F., Schindlbeck, C., Trojan, A., Otto, F., Knauer, M., Pusch, R., Harbeck, N.

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Assessing land use and flood management impacts on ecosystem services in a river landscape (Upper Danube, Germany) von Stammel, Barbara, Fischer, Christine, Cyffka, Bernd, Albert, Christian, Damm, Christian, Dehnhardt, Alexandra, Fischer, Helmut, Foeckler, Francis, Gerstner, Lars, Hoffmann, Tim G., Iwanowski, Janette, Kasperidus, Hans D., Linnemann, Kathrin, Mehl, Dietmar, Podschun, Simone A., Rayanov, Marin, Ritz, Stephanie, Rumm, Andrea, Scholz, Mathias, Schulz‐Zunkel, Christiane, Thiele, Julia, Venohr, Markus, Haaren, Christina, Pusch, Martin T., Gelhaus, Marion

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Optically Resonant Bulk Heterojunction PbS Quantum Dot Solar Cell von Tabernig, Stefan W., Yuan, Lin, Cordaro, Andrea, Teh, Zhi Li, Gao, Yijun, Patterson, Robert J., Pusch, Andreas, Huang, Shujuan, Polman, Albert

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A Quantitative Proteomic Analysis of In Vitro Assembled Chromatin von Völker-Albert, Moritz Carl, Pusch, Miriam Caroline, Fedisch, Andreas, Schilcher, Pierre, Schmidt, Andreas, Imhof, Axel

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Avoiding Shading Losses in Concentrator Photovoltaics Using a Soft-Imprinted Cloaking Geometry von Tabernig, Stefan W., Soeriyadi, Anastasia H., Romer, Udo, Pusch, Andreas, Lamers, Dimitry, Juhl, Matthias Klaus, Payne, David N. R., Nielsen, Michael P., Polman, Albert, Ekins-Daukes, Nicholas J.

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Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study von Hawass, Zahi, Ismail, Somaia, Selim, Ashraf, Saleem, Sahar N, Fathalla, Dina, Wasef, Sally, Gad, Ahmed Z, Saad, Rama, Fares, Suzan, Amer, Hany, Gostner, Paul, Gad, Yehia Z, Pusch, Carsten M, Zink, Albert R

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Molecular Identification of Falciparum Malaria and Human Tuberculosis Co-Infections in Mummies from the Fayum Depression (Lower Egypt). e60307 von Lalremruata, Albert, Ball, Markus, Bianucci, Raffaella, Welte, Beatrix, Nerlich, Andreas G, Kun, Juergen FJ, Pusch, Carsten M

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Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina von Wutz, Krisztina, Sauer, Christian, Zrenner, Eberhart, Lorenz, Birgit, Alitalo, Tiina, Broghammer, Martina, Hergersberg, Martin, de la Chapelle, Albert, Weber, Bernhard H F, Wissinger, Bernd, Meindl, Alfons, Pusch, Carsten M

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