Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tamina Rückert"'
Autor:
Tamina Rückert, Geoffroy Andrieux, Melanie Boerries, Kathrin Hanke-Müller, Nadine M. Woessner, Stephanie Doetsch, Christoph Schell, Konrad Aumann, Julia Kolter, Annette Schmitt-Graeff, Marcel Schiff, Lukas M. Braun, Eileen Haring, Sandra Kissel, Benjamin A. Siranosian, Ami S. Bhatt, Peter Nordkild, Jan Wehkamp, Benjamin A. H. Jensen, Susana Minguet, Justus Duyster, Robert Zeiser, Natalie Köhler
Publikováno v:
Science translational medicine. 14(676)
Acute graft-versus-host disease (aGVHD), which is driven by allogeneic T cells, has a high mortality rate and limited treatment options. Human β-defensin 2 (hBD-2) is an endogenous epithelial cell–derived host-defense peptide. In addition to its a
Autor:
Jenny N. H. G. Ho, Dominik Schmidt, Theresa Lowinus, Jeongmin Ryoo, Elaine-Pashupati Dopfer, Nicolás Gonzalo Núñez, Sara Costa-Pereira, Cristina Toffalori, Marco Punta, Viktor Fetsch, Tobias Wertheimer, Marie-Claire Rittmann, Lukas M. Braun, Marie Follo, Christelle Briere, Janaki Manoja Vinnakota, Marlene Langenbach, Felicitas Koppers, Khalid Shoumariyeh, Helena Engel, Tamina Rückert, Melanie Märklin, Samuel Holzmayer, Anna L. Illert, Federica Magon, Geoffroy Andrieux, Sandra Duquesne, Dietmar Pfeifer, Julian Staniek, Marta Rizzi, Cornelius Miething, Natalie Köhler, Justus Duyster, Hans D. Menssen, Melanie Boerries, Joerg M. Buescher, Nina Cabezas-Wallscheid, Bruce R. Blazar, Petya Apostolova, Luca Vago, Erika L. Pearce, Burkhard Becher, Robert Zeiser
Publikováno v:
Blood
Patients with acute myeloid leukemia (AML) often achieve remission after allogeneic hematopoietic cell transplantation (allo-HCT) but subsequently die of relapse driven by leukemia cells resistant to elimination by allogeneic T cells based on decreas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51581479c9bd27c5d6ac9b2c96107d23
https://hdl.handle.net/21.11116/0000-000D-1481-A
https://hdl.handle.net/21.11116/0000-000D-1481-A
Autor:
Michal Kulinski, Annette Schmitt-Graeff, Tony A. Mueller, Christian Peschel, Melanie Boerries, Christine Dierks, Teresa Poggio, Irith Baumann, Justus Duyster, Milena Pantic, Michael L. Cleary, Nina Cabezas-Wallscheid, Khalid Shoumariyeh, Alina Mueller-Rudorf, Bernhard Kuster, Marie Follo, Hiroyuki Kawaguchi, Simone Lemeer, Miriam Erlacher, Detlev Schindler, Martina Rudelius, Anna Lena Illert, Tamina Rückert, Cathrin Klingeberg, Robert A.J. Oostendorp, Rouzanna Istvanffy, Jesus Duque-Afonso, Stefanie Kreutmair, Marcin W. Wlodarski, Charlotte M. Niemeyer, Dietmar Pfeifer, Geoffroy Andrieux, Robert Zeiser, Melissa Zwick
Publikováno v:
The Journal of Clinical Investigation
J Clin Invest
J Clin Invest
Inherited bone marrow failure syndromes (IBMFSs) are a heterogeneous group of disorders characterized by defective hematopoiesis, impaired stem cell function, and cancer susceptibility. Diagnosis of IBMFS presents a major challenge due to the large v
Autor:
Jacqueline E. Mermoud, Tamina Rückert, Mike R. Dekker, Parysatis Sachs, Marius Klangwart, Raymond A. Poot, Dong Ding, Philipp Bergmaier, Nora Bartels, Jeroen Demmers
Publikováno v:
Journal of Biological Chemistry, 293(8), 2711-2724. American Society for Biochemistry and Molecular Biology Inc.
Chromatin in embryonic stem cells (ESCs) differs markedly from that in somatic cells, with ESCs exhibiting a more open chromatin configuration. Accordingly, ATP-dependent chromatin remodeling complexes are important regulators of ESC homeostasis. Dep
Autor:
Anna Lena Illert, Claudia D. Baldus, Teresa Poggio, Cathrin Klingeberg, Peter Paschka, Allan Bradley, George S. Vassiliou, Alina Rudorf, Stefanie Kreutmair, Robert Zeiser, Tamina Rückert, Sivahari P. Gorantla, Justus Duyster, Anina Gengenbacher, Annette Schmitt-Graeff, Tony Andreas Müller
Publikováno v:
Blood
Activating mutations in FMS-like tyrosine kinase receptor-3 (FLT3) and Nucleophosmin-1 (NPM1) are most frequent alterations in acute myeloid leukemia (AML), and are often coincidental. The mutational status of NPM1 has strong prognostic relevance to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5efddf9ea07046c4e5a4ab4bae2b447
https://europepmc.org/articles/PMC6659255/
https://europepmc.org/articles/PMC6659255/
Autor:
Marie Follo, Melanie Boerries, Melissa Zwick, Justus Duyster, Stefanie Kreutmair, Annette Schmitt-Graeff, Anna Lena Illert, Milena Pantic, Cathrin Klingeberg, Irith Baumann, Bernhard Kuster, Hiroyuki Kawaguchi, Detlev Schindler, Khalid Shoumariyeh, Michal Kulinski, Geoffroy Andrieux, Nina Cabezas-Wallscheid, Dietmar Pfeifer, Rouzanna Istvanffy, Robert Zeiser, Martina Rudelius, Alina Rudorf, Miriam Erlacher, Christian Peschel, Michael D. Cleary, Tony Andreas Müller, Christine Dierks, Robert A.J. Oostendorp, Jesus Duque-Afonso, Teresa Poggio, Simone Lemeer, Charlotte M. Niemeyer, Marcin W. Wlodarski, Tamina Rückert
Publikováno v:
Blood. 134:3741-3741
Inherited bone marrow failure syndromes (IBMFS) are a heterogeneous group of disorders characterized by impaired stem cell function resulting in pancytopenia. Diagnosis of IBMFS presents a major challenge due to limited diagnostic tests and overlappi