Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Gudrun Goehring"'
Autor:
Katja Krüger, Martin Wichmann, Razif Gabdoulline, Katharina Götze, Krischan Braitsch, Franziska Modemann, Walter Fiedler, Arne Trummer, Jürgen Krauter, Stephan Kaun, Susanne Rotermund, Andreas Voß, Gudrun Goehring, Yvonne Behrens, Felicitas Thol, Matthias Eder, Gernot Beutel, Michael Stadler, Michael Heuser, Rabia Shahswar
Publikováno v:
HemaSphere, Vol 7, p e19815ef (2023)
Externí odkaz:
https://doaj.org/article/f4ec097299c942ab8ecfc9000edf757a
Autor:
Ulla Wartiovaara-Kautto, Ulrich Germing, Hari Prasanna Subramanian, Tara Cronin, Gudrun Goehring, Elizabeth A. Griffiths, Guimin Gao, Eunice S. Wang, Mary Claire King, Simone Feurstein, Carolyn Owen, Thomas Schroeder, Brigitte Schlegelberger, Outi Kilpivaara, Marja Hakkarainen, Torsten Haferlach, Divij Verma, Felicitas Thol, Stefanie Geyh, Hartmut Döhner, Colin C. Pritchard, Sioban Keel, Juehua Gao, Zejuan Li, Tom Walsh, Daniela S. Krause, Suleyman Gulsuner, Michael Heuser, Lucy A. Godley, Daniela del Gaudio, Ming Lee, Jane E. Churpek, Konstanze Döhner, Soma Das, Christian Pohlkamp
Publikováno v:
Leukemia
Autor:
Kirsten Jahn, Gudrun Goehring, Robert Zweigerdt, Ulrich Martin, Nico Lachmann, Sylvia Merkert, Andre Zeug, Evgeni Ponimaskin, Silke Glage, Andreas Martens, Stephanie Wunderlich, Maximillian Deest, Thomas Moritz, Andreas Kirschning, Wilhelm Korte, Mania Ackermann, Alexandra Haase
Drug-inducible suicide systems may help to minimize risks of cellular therapies due to the tumor forming potential of human induced pluripotent stem cells (hiPSCs). Recent research challenged the usefulness of such systems since rare drug-resistant s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2682b3047991f947448f1b9864d70136
https://doi.org/10.1101/2021.09.19.460940
https://doi.org/10.1101/2021.09.19.460940
Autor:
Wolfram Klapper, Richard Ratei, Gudrun Goehring, Heidi Herbrueggen, Willi Woessmann, Jutta Bradtke, Jonas Rohde, Martin Zimmermann, Stephanie Mueller, Laura Padilla, Andishe Attarbaschi, Anja Moericke, Brigitte Schlegelberger, Reiner Siebert, Monika Brueggemann, Birgit Burkhardt
Publikováno v:
Leukemia. 34:942-946
Autor:
Marcin W. Wlodarski, Christian P. Kratz, Charlotte M. Niemeyer, Kathrin Thomay, Brigitte Schlegelberger, Mwe Mwe Chao, Victor B Pastor, Detlev Schindler, Gudrun Goehring
Publikováno v:
Klinische Pädiatrie. 229:329-334
Individuals with Fanconi anemia (FA) have a high risk of developing myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML), yet the secondary somatic mutations lending to these malignancies remain to be further elucidated. We employed a next
Autor:
Heidi, Herbrueggen, Stephanie, Mueller, Jonas, Rohde, Laura, Arias Padilla, Anja, Moericke, Andishe, Attarbaschi, Martin, Zimmermann, Richard, Ratei, Monika, Brueggemann, Reiner, Siebert, Gudrun, Goehring, Brigitte, Schlegelberger, Jutta, Bradtke, Wolfram, Klapper, Willi, Woessmann, Birgit, Burkhardt
Publikováno v:
Leukemia. 34(3)
Autor:
Gudrun Goehring, Bjoern Petersen, Brigitte Schlegelberger, Andrea Lucas-Hahn, Thomas C. Mettenleiter, Stefanie Kurtz, Heiner Niemann
1AbstractThe sex-determining region on the Y chromosome (SRY) is thought to be the central genetic element of male sex development. Mutations within the SRY gene are associated with a male-to-female sex reversal syndrome in humans and other mammalian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d15883fe5fc0a18267ef5f4307aabec
https://doi.org/10.1101/617589
https://doi.org/10.1101/617589
Autor:
Anja Stölzle, Verena I. Gaidzik, Heinz Kirchen, Sabine Kayser, Marie von Lilienfeld-Toal, Arnold Ganser, Daniela Späth, Wolfram Brugger, Jürgen Krauter, Hans Günter Derigs, Richard F. Schlenk, Michael Girschikofsky, Volker Runde, Richard Greil, Lars Bullinger, Mohammed Wattad, Maria-Veronica Teleanu, Stephan Kremers, Andrea Kuendgen, Aruna Raghavachar, Peter Paschka, Brigitte Schlegelberger, Hartmut Döhner, Andreas L. Petzer, Michael Heuser, Gerhard Heil, Gudrun Goehring, Mark Ringhoffer, Konstanze Döhner, Helmut R. Salih
Publikováno v:
Blood. 121:4769-4777
In this study, we evaluated the frequency and prognostic impact of DNMT3A mutations (DNMT3A(mut)) in 1770 younger adult patients with acute myeloid leukemia (AML) in the context of other genetic alterations and the European LeukemiaNet (ELN) classifi
Autor:
Astrid Gnekow, Claudia Paret, Helmut Hanenberg, Claudia Spix, Dieter Körholz, Roland Kappler, Uwe Kordes, Michaela Kuhlen, Markus Metzler, Kornelius Kerl, Peter Vorwerk, Ines B. Brecht, Martin Stanulla, Mareike Rasche, Thorsten Simon, Gudrun Goehring, Birgit Burkhardt, Martin Schrappe, Ivo Leuschner, Norbert Graf, Reinhard Schneppenheim, Tim Ripperger, Dietmar R. Lohmann, Udo Kontny, Ewa Koscielniak, Stefan S. Bielack, Katja von Hoff, Kristian W. Pajtler, Olaf Rieß, Martin Zenker, Dietrich von Schweinitz, Christian P. Kratz, Willy Wössmann, Kathrin Thomay, Dominik T. Schneider, Christof M. Kramm, Monika Sparber-Sauer, Miriam Erlacher, Julia Hauer, Lüder Hinrich Meyer, Michael C. Frühwald, Uta Dirksen, Peter Kaatsch, Doris Steinemann, Britta Lamottke, Alexandra Russo, Gudrun Fleischhack, Christopher Schroeder, Marcin W. Wlodarski, Olga Moser, Simone Hettmer, Barbara Hero, Dirk Reinhardt, Rainer Nustede, Arndt Borkhardt, Thomas Klingebiel, Andreas E. Kulozik, Olaf Witt, Petra Temming, Stefan M. Pfister, Klaus-Michael Debatin, Juliane Hoyer, Brigitte Schlegelberger, Angelika Eggert, Stefanie Zimmermann, Stefan Rutkowski, Cornelia Eckert, Martin A. Horstmann, Charlotte M. Niemeyer, Hedwig E. Deubzer, Andrea Meinhardt, André O. von Bueren, Brigitte Strahm, Gabriele Calaminus, Thomas Illig, Michaela Nathrath
Publikováno v:
American Journal of Medical Genetics. A, Vol. 173, No 4 (2017) pp. 1017-1037
Heritable predisposition is an important cause of cancer in children and adolescents. Although a large number of cancer predisposition genes and their associated syndromes and malignancies have already been described, it appears likely that there are
Autor:
Frauke Devens, Volker Hovestadt, Jan Loeffen, Manasi Ratnaparkhe, Masatoshi Takagi, Mario Hlevnjak, Jules P.P. Meijerink, Eberhard Maass, Michaela Nathrath, Brigitte Schlegelberger, Takashi Taga, Agata Rode, Christof M. Kramm, Andrey Korshunov, Joachim B. Kunz, Jessica I. Hoell, Andreas E. Kulozik, Peter Lichter, Barbara C. Worst, Stefan Zielen, Krystyna H. Chrzanowska, Jan O. Korbel, Stefan M. Pfister, David T.W. Jones, Agata Pastorczak, Anna Jauch, Eugen Tausch, Till Milde, Shlomi Constantini, Gudrun Goehring, Ute Fischer, Thorsten Kolb, Stephanie Sungalee, Wojciech Młynarski, Aurélie Ernst, Reiner Siebert, Marc Zapatka, Kendra K. Maass
Publikováno v:
Cancer Research. 77:509-509
Recent developments in sequencing technologies lead to the discovery of a novel form of genome instability, termed chromothripsis. This catastrophic genomic event, involved in cancer formation, is characterized by tens to hundreds of locally clustere