Resultats de la cerca - zur Stadt, Udo

Characterization of novel, recurrent genomic rearrangements as sensitive MRD targets in childhood B-cell precursor ALL per zur Stadt, Udo, Alawi, Malik, Adao, Manuela, Indenbirken, Daniela, Escherich, Gabriele, Horstmann, Martin A.

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Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR) per Weber, Axel, Taube, Sylvia, zur Stadt, Udo, Horstmann, Martin, Krohn, Knut, Bradtke, Jutta, Teigler-Schlegel, Andrea, Leiblein, Sabine, Christiansen, Holger

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Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T‐cell activation, differentiation and repertoire per Ammann, Sandra, Lehmberg, Kai, zur Stadt, Udo, Janka, Gritta, Rensing‐Ehl, Anne, Klemann, Christian, Heeg, Maximilian, Bode, Sebastian, Fuchs, Ilka, Ehl, Stephan

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Syntaxin 11 is required for NK and CD8(+) T-cell cytotoxicity and neutrophil degranulation per D’Orlando, Orietta, Zhao, Fang, Kasper, Brigitte, Orinska, Zane, Müller, Jürgen, Hermans-Borgmeyer, Irm, Griffiths, Gillian M., Zur Stadt, Udo, Bulfone-Paus, Silvia

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Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease per Heeg, Maximilian, Ammann, Sandra, Klemann, Christian, Panning, Marcus, Falcone, Valeria, Hengel, Harmut, Lehmberg, Kai, zur Stadt, Udo, Wustrau, Katharina, Janka, Gritta, Ehl, Stephan

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Refinement of IKZF1 recombination hotspots in pediatric BCP-ALL patients per 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

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Disease-causing mutations in the XIAP BIR2 domain impair NOD2-dependent immune signalling per 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

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In Vivo Imaging Enables High Resolution Preclinical Trials on Patients’ Leukemia Cells Growing in Mice per 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

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Clofarabine increases the eradication of minimal residual disease of primary B-precursor acute lymphoblastic leukemia compared to high-dose cytarabine without improvement of outcom... per 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

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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5 per 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

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COBL is a novel hotspot for IKZF1 deletions in childhood acute lymphoblastic leukemia per 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

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The role of constitutive activation of FMS-related tyrosine kinase-3 and NRas/KRas mutational status in infants with KMT2A-rearranged acute lymphoblastic leukemia per 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.

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The long-term impact of in vitro drug sensitivity on risk stratification and treatment outcome in acute lymphoblastic leukemia of childhood (CoALL 06-97) per 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.

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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3 per 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

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Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11 per 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

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Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation per 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

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Results of CoALL 07-03 study childhood ALL based on combined risk assessment by in vivo and in vitro pharmacosensitivity per 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

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Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases per 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

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Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome per 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

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Profiling of histone H3 lysine 9 trimethylation levels predicts transcription factor activity and survival in acute myeloid leukemia per 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

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