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Journal Article
Fluemann, Ruth, Rehkaemper, Tim, Nieper, Pascal, Pfeiffer, Pauline, Holzem, Alessandra, Klein, Sebastian ORCID: 0000-0002-2188-9377, Bhatia, Sanil
ORCID: 0000-0001-6494-7744, Kochanek, Moritz, Kisis, Ilmars
ORCID: 0000-0001-6207-3991, Pelzer, Benedikt W., Ahlert, Heinz, Hauer, Julia, Guerreiro, Alexandra da Palma, Ryan, Jeremy A., Reimann, Maurice, Riabinska, Arina, Wiederstein, Janica, Krueger, Marcus, Deckert, Martina, Altmueller, Janine, Klatt, Andreas R., Frenzel, Lukas P., Pasqualucci, Laura, Beguelin, Wendy, Melnick, Ari M., Sander, Sandrine, Montesinos-Rongen, Manuel
ORCID: 0000-0003-4724-5526, Brunn, Anna, Lohneis, Philipp, Buettner, Reinhard, Kashkar, Hamid, Borkhardt, Arndt, Letai, Anthony, Persigehl, Thorsten, Peifer, Martin, Schmitt, Clemens A.
ORCID: 0000-0002-4731-2226, Reinhardt, Hans Christian and Knittel, Gero
ORCID: 0000-0001-8395-3701
(2021).
An Autochthonous Mouse Model of Myd88- and BCL2-Driven Diffuse Large B-cell Lymphoma Reveals Actionable Molecular Vulnerabilities.
Blood Cancer Discov., 2 (1).
S. 70 - 92.
PHILADELPHIA:
AMER ASSOC CANCER RESEARCH.
ISSN 2643-3249
Holzem, Alessandra, Nogova, Lucia, Ihle, Michaela, Woempner, Claudia, Bitter, Elisabeth, Michels, Sebastian, Lamanna, Alessandra, Christensen, Britt-Marie, Fischer, Rieke, Kaminsky, Britta, Kern, Jens, Graeven, Ullrich, Kostenko, Anna, Merkelbach-Bruse, Sabine, Buettner, Reinhard, Scheffler, Matthias and Wolf, Jurgen (2017). MAP2K1 Mutations in NSCLC: Clinical Presentation and Co-Occurrence of Additional Genetic Aberrations. J. Thorac. Oncol., 12 (1). S. S982 - 1. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1556-1380
Scheffler, Matthias, Holzem, Alessandra, Kron, Anna, Nogova, Lucia, Ihle, Michaela A., von Levetzow, Cornelia, Fassunke, Jana, Woempner, Claudia, Bitter, Elisabeth, Koleczko, Sophia, Abdulla, Diana S. Y., Michels, Sebastian, Fischer, Rieke, Riedel, Richard, Weber, Jan-Philipp, Westphal, Theresa, Gerigk, Ulrich, Kern, Jens, Kaminsky, Britta, Randerath, Winfried, Kambartel, Karl-Otto, Merkelbach-Bruse, Sabine, Buttner, Reinhard and Wolf, Juergen (2020). Co-occurrence of targetable mutations in Non-small cell lung cancer (NSCLC) patients harboring MAP2K1 mutations. Lung Cancer, 144. S. 40 - 49. CLARE: ELSEVIER IRELAND LTD. ISSN 1872-8332
Scheffler, Matthias, Ihle, Michaela A., Hein, Rebecca, Merkelbach-Bruse, Sabine, Scheel, Andreas H., Siemanowski, Janna, Braegelmann, Johannes, Kron, Anna, Abedpour, Nima, Ueckeroth, Frank, Schueller, Merle, Koleczko, Sophia, Michels, Sebastian, Fassunke, Jana, Pasternack, Helen, Heydt, Carina, Serke, Monika, Fischer, Rieke, Schulte, Wolfgang, Gerigk, Ulrich, Nogova, Lucia, Ko, Yon-Dschun, Abdulla, Diana S. Y., Riedel, Richard, Kambartel, Karl-Otto, Lorenz, Joachim, Sauerland, Imke, Randerath, Winfried, Kaminsky, Britta, Hagmeyer, Lars, Grohe, Christian, Eisert, Anna, Frank, Rieke, Gogl, Leonie, Schaepers, Carsten, Holzem, Alessandra, Hellmich, Martin, Thomas, Roman K., Peifer, Martin, Sos, Martin L., Buettner, Reinhard and Wolf, Juergen (2019). K-ras Mutation Subtypes in NSCLC and Associated Co-occuring Mutations in Other Oncogenic Pathways. J. Thorac. Oncol., 14 (4). S. 606 - 617. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1556-1380