Myoepithelial Carcinoma of Soft Tissue With an EWSR1-KLF15 Gene Fusion in an Infant

por Bodis, Sandor, Kroiss, Sabine, Tchinda, Joëlle, Fritz, Christine, Wagner, Ulrich, Bode, Peter Karl
Publicado 2021

CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions

por Wrona, Dominik, Pastukhov, Oleksandr, Pritchard, Robert S., Raimondi, Federica, Tchinda, Joëlle, Jinek, Martin, Siler, Ulrich, Reichenbach, Janine
Publicado 2020

Identification of oncogenic driver mutations by genome-wide CRISPR-Cas9 dropout screening

por Kiessling, Michael K., Schuierer, Sven, Stertz, Silke, Beibel, Martin, Bergling, Sebastian, Knehr, Judith, Carbone, Walter, de Vallière, Cheryl, Tchinda, Joelle, Bouwmeester, Tewis, Seuwen, Klaus, Rogler, Gerhard, Roma, Guglielmo
Publicado 2016

Ex vivo drug response heterogeneity reveals personalized therapeutic strategies for patients with multiple myeloma

por Kropivsek, Klara, Kachel, Paul, Goetze, Sandra, Wegmann, Rebekka, Festl, Yasmin, Severin, Yannik, Hale, Benjamin D., Mena, Julien, van Drogen, Audrey, Dietliker, Nadja, Tchinda, Joëlle, Wollscheid, Bernd, Manz, Markus G., Snijder, Berend
Publicado 2023

Phenotypic profiling with a living biobank of primary rhabdomyosarcoma unravels disease heterogeneity and AKT sensitivity

por Manzella, Gabriele, Schreck, Leonie D., Breunis, Willemijn B., Molenaar, Jan, Merks, Hans, Barr, Frederic G., Sun, Wenyue, Römmele, Michaela, Zhang, Luduo, Tchinda, Joelle, Ngo, Quy A., Bode, Peter, Delattre, Olivier, Surdez, Didier, Rekhi, Bharat, Niggli, Felix K., Schäfer, Beat W., Wachtel, Marco
Publicado 2020

Alu elements mediate MYB gene tandem duplication in human T-ALL

por O'Neil, Jennifer, Tchinda, Joelle, Gutierrez, Alejandro, Moreau, Lisa, Maser, Richard S., Wong, Kwok-Kin, Li, Wei, McKenna, Keith, Liu, X. Shirley, Feng, Bin, Neuberg, Donna, Silverman, Lewis, DeAngelo, Daniel J., Kutok, Jeffery L., Rothstein, Rodney, DePinho, Ronald A., Chin, Lynda, Lee, Charles, Look, A. Thomas
Publicado 2007

Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options

por Fischer, Ute, Forster, Michael, Rinaldi, Anna, Risch, Thomas, Sungalee, Stéphanie, Warnatz, Hans-Jörg, Bornhauser, Beat, Gombert, Michael, Kratsch, Christina, Stütz, Adrian M., Sultan, Marc, Tchinda, Joelle, Worth, Catherine L., Amstislavskiy, Vyacheslav, Badarinarayan, Nandini, Baruchel, André, Bartram, Thies, Basso, Giuseppe, Canpolat, Cengiz, Cario, Gunnar, Cavé, Hélène, Dakaj, Dardane, Delorenzi, Mauro, Dobay, Maria Pamela, Eckert, Cornelia, Ellinghaus, Eva, Eugster, Sabrina, Frismantas, Viktoras, Ginzel, Sebastian, Haas, Oskar A., Heidenreich, Olaf, Hemmrich-Stanisak, Georg, Hezaveh, Kebria, Höll, Jessica I., Hornhardt, Sabine, Husemann, Peter, Kachroo, Priyadarshini, Kratz, Christian P., te Kronnie, Geertruy, Marovca, Blerim, Niggli, Felix, McHardy, Alice C., Moorman, Anthony V., Panzer-Grümayer, Renate, Petersen, Britt S., Raeder, Benjamin, Ralser, Meryem, Rosenstiel, Philip, Schäfer, Daniel, Schrappe, Martin, Schreiber, Stefan, Schütte, Moritz, Stade, Björn, Thiele, Ralf, von der Weid, Nicolas, Vora, Ajay, Zaliova, Marketa, Zhang, Langhui, Zichner, Thomas, Zimmermann, Martin, Lehrach, Hans, Borkhardt, Arndt, Bourquin, Jean-Pierre, Franke, Andre, Korbel, Jan O., Stanulla, Martin, Yaspo, Marie-Laure
Publicado 2015