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1
Characterization of novel, recurrent genomic rearrangements as sensitive MRD targets in childhood B-cell precursor ALL حسب zur Stadt, Udo, Alawi, Malik, Adao, Manuela, Indenbirken, Daniela, Escherich, Gabriele, Horstmann, Martin A.
منشور في 2019نص -
2
Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR) حسب Weber, Axel, Taube, Sylvia, zur Stadt, Udo, Horstmann, Martin, Krohn, Knut, Bradtke, Jutta, Teigler-Schlegel, Andrea, Leiblein, Sabine, Christiansen, Holger
منشور في 2012نص -
3
Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T‐cell activation, differentiation and repertoire حسب Ammann, Sandra, Lehmberg, Kai, zur Stadt, Udo, Janka, Gritta, Rensing‐Ehl, Anne, Klemann, Christian, Heeg, Maximilian, Bode, Sebastian, Fuchs, Ilka, Ehl, Stephan
منشور في 2017نص -
4
Syntaxin 11 is required for NK and CD8(+) T-cell cytotoxicity and neutrophil degranulation حسب D’Orlando, Orietta, Zhao, Fang, Kasper, Brigitte, Orinska, Zane, Müller, Jürgen, Hermans-Borgmeyer, Irm, Griffiths, Gillian M., Zur Stadt, Udo, Bulfone-Paus, Silvia
منشور في 2012نص -
5
Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease حسب Heeg, Maximilian, Ammann, Sandra, Klemann, Christian, Panning, Marcus, Falcone, Valeria, Hengel, Harmut, Lehmberg, Kai, zur Stadt, Udo, Wustrau, Katharina, Janka, Gritta, Ehl, Stephan
منشور في 2018نص -
6
Refinement of IKZF1 recombination hotspots in pediatric BCP-ALL patients حسب Meyer, Claus, zur Stadt, Udo, Escherich, Gabriele, Hofmann, Julia, Binato, Renata, Barbosa, Thayana da Conceição, Emerenciano, Mariana, Pombo-de-Oliveira, Maria S, Horstmann, Martin, Marschalek, Rolf
منشور في 2013نص -
7
Disease-causing mutations in the XIAP BIR2 domain impair NOD2-dependent immune signalling حسب Damgaard, Rune Busk, Fiil, Berthe Katrine, Speckmann, Carsten, Yabal, Monica, zur Stadt, Udo, Bekker-Jensen, Simon, Jost, Philipp J, Ehl, Stephan, Mailand, Niels, Gyrd-Hansen, Mads
منشور في 2013نص -
8
In Vivo Imaging Enables High Resolution Preclinical Trials on Patients’ Leukemia Cells Growing in Mice حسب Terziyska, Nadia, Alves, Catarina Castro, Groiss, Volker, Schneider, Katja, Farkasova, Katarina, Ogris, Manfred, Wagner, Ernst, Ehrhardt, Harald, Brentjens, Renier J., zur Stadt, Udo, Horstmann, Martin, Quintanilla-Martinez, Leticia, Jeremias, Irmela
منشور في 2012نص -
9
Clofarabine increases the eradication of minimal residual disease of primary B-precursor acute lymphoblastic leukemia compared to high-dose cytarabine without improvement of outcom... حسب Escherich, Gabriele, zur Stadt, Udo, Borkhardt, Arndt, Dilloo, Dagmar, Faber, Jörg, Feuchtinger, Tobias, Imschweiler, Thomas, Jorch, Norbert, Pekrun, Arnulf, Schmid, Irene, Schramm, Franziska, Spohn, Michael, Zimmermann, Martin, Horstmann, Martin A
منشور في 2021نص -
10
STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5 حسب Cetica, Valentina, Santoro, Alessandra, Gilmour, Kimberly C, Sieni, Elena, Beutel, Karin, Pende, Daniela, Marcenaro, Stefania, Koch, Florian, Grieve, Samantha, Wheeler, Rachel, Zhao, Fang, zur Stadt, Udo, Griffiths, Gillian M, Aricò, Maurizio
منشور في 2010نص -
11
COBL is a novel hotspot for IKZF1 deletions in childhood acute lymphoblastic leukemia حسب Lopes, Bruno Almeida, Meyer, Claus, Barbosa, Thayana Conceição, zur Stadt, Udo, Horstmann, Martin, Venn, Nicola C., Heatley, Susan, White, Deborah L., Sutton, Rosemary, Pombo-de-Oliveira, Maria S., Marschalek, Rolf, Emerenciano, Mariana
منشور في 2016نص -
12
The role of constitutive activation of FMS-related tyrosine kinase-3 and NRas/KRas mutational status in infants with KMT2A-rearranged acute lymphoblastic leukemia حسب Fedders, Henning, Alsadeq, Ameera, Schmäh, Juliane, Vogiatzi, Fotini, Zimmermann, Martin, Möricke, Anja, Lenk, Lennart, zur Stadt, Udo, Horstmann, Martin A., Pieters, Rob, Schrappe, Martin, Stanulla, Martin, Cario, Gunnar, Schewe, Denis M.
منشور في 2017نص -
13
The long-term impact of in vitro drug sensitivity on risk stratification and treatment outcome in acute lymphoblastic leukemia of childhood (CoALL 06-97) حسب Escherich, Gabriele, Tröger, Anja, Göbel, Ulrich, Graubner, Ulrike, Pekrun, Arnulf, Jorch, Norbert, Kaspers, Gjl, Zimmermann, Martin, zur Stadt, Udo, Kazemier, Karin, Pieters, Rob, Den Boer, Monique L., Horstmann, Martin, Janka, Gritta E.
منشور في 2011نص -
14
Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3 حسب Sieni, Elena, Cetica, Valentina, Santoro, Alessandra, Beutel, Karin, Mastrodicasa, Elena, Meeths, Marie, Ciambotti, Benedetta, Brugnolo, Francesca, zur Stadt, Udo, Pende, Daniela, Moretta, Lorenzo, Griffiths, Gillian M, Henter, Jan-Inge, Janka, Gritta, Aricò, Maurizio
منشور في 2011نص -
15
Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11 حسب zur Stadt, Udo, Rohr, Jan, Seifert, Wenke, Koch, Florian, Grieve, Samantha, Pagel, Julia, Strauß, Julia, Kasper, Brigitte, Nürnberg, Gudrun, Becker, Christian, Maul-Pavicic, Andrea, Beutel, Karin, Janka, Gritta, Griffiths, Gillian, Ehl, Stephan, Hennies, Hans Christian
منشور في 2009نص -
16
Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation حسب Klemann, Christian, Ammann, Sandra, Heizmann, Miriam, Fuchs, Sebastian, Bode, Sebastian F, Heeg, Maximilian, Fuchs, Hans, Lehmberg, Kai, zur Stadt, Udo, Roll, Claudia, Vraetz, Thomas, Speckmann, Carsten, Ricarda Lorenz, Myriam, Schwarz, Klaus, Rohr, Jan, Feske, Stefan, Ehl, Stephan
منشور في 2017نص -
17
Results of CoALL 07-03 study childhood ALL based on combined risk assessment by in vivo and in vitro pharmacosensitivity حسب Schramm, Franziska, zur Stadt, Udo, Zimmermann, Martin, Jorch, Norbert, Pekrun, Arnulf, Borkhardt, Arndt, Imschweiler, Thomas, Christiansen, Holger, Faber, Jörg, Schmid, Irene, Feuchtinger, Tobias, Beron, Gerhard, den Boer, Monique L., Pieters, Rob, Horstmann, Martin A., Janka-Schaub, Gritta E., Escherich, Gabriele
منشور في 2019نص -
18
Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases حسب Rohr, Jan, Beutel, Karin, Maul-Pavicic, Andrea, Vraetz, Thomas, Thiel, Jens, Warnatz, Klaus, Bondzio, Ilka, Gross-Wieltsch, Ute, Schündeln, Michael, Schütz, Barbara, Woessmann, Wilhelm, Groll, Andreas H., Strahm, Brigitte, Pagel, Julia, Speckmann, Carsten, Janka, Gritta, Griffiths, Gillian, Schwarz, Klaus, zur Stadt, Udo, Ehl, Stephan
منشور في 2010نص -
19
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome حسب Ammann, Sandra, Schulz, Ansgar, Krägeloh-Mann, Ingeborg, Dieckmann, Nele M.G., Niethammer, Klaus, Fuchs, Sebastian, Eckl, Katja Martina, Plank, Roswitha, Werner, Roland, Altmüller, Janine, Thiele, Holger, Nürnberg, Peter, Bank, Julia, Strauß, Anne, von Bernuth, Horst, zur Stadt, Udo, Grieve, Samantha, Griffiths, Gillian M., Lehmberg, Kai, Hennies, Hans Christian, Ehl, Stephan
منشور في 2016نص -
20
Profiling of histone H3 lysine 9 trimethylation levels predicts transcription factor activity and survival in acute myeloid leukemia حسب Müller-Tidow, Carsten, Klein, Hans-Ulrich, Hascher, Antje, Isken, Fabienne, Tickenbrock, Lara, Thoennissen, Nils, Agrawal-Singh, Shuchi, Tschanter, Petra, Disselhoff, Christine, Wang, Yipeng, Becker, Anke, Thiede, Christian, Ehninger, Gerhard, zur Stadt, Udo, Koschmieder, Steffen, Seidl, Matthias, Müller, Frank U., Schmitz, Wilhelm, Schlenke, Peter, McClelland, Michael, Berdel, Wolfgang E., Dugas, Martin, Serve, Hubert
منشور في 2010نص