Search Results - Arnulf Pekrun

  • Showing 1 - 10 results of 10
Refine Results
  1. 1
    Induction of fetal hemoglobin expression by the histone deacetylase inhibitor apicidin

    Induction of fetal hemoglobin expression by the histone deacetylase inhibitor apicidin by Olaf Witt, Sven Mönkemeyer, Gabi Rönndahl, Bernhard Erdlenbruch, Dirk Reinhardt, Katrin Kanbach, Arnulf Pekrun

    Published 2003
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Evidence for malignant transformation in acute myeloid leukemia at the level of early hematopoietic stem cells by cytogenetic analysis of CD34+ subpopulations

    Evidence for malignant transformation in acute myeloid leukemia at the level of early hematopoietic stem cells by cytogenetic analysis of CD34+ subpopulations by D. Haase, Michaela Feuring‐Buske, Stephanie Könemann, Christa Fonatsch, C. Troff, Walter Verbeek, Arnulf Pekrun, W. Hiddemann, Bernhard Wörmann

    Published 1995
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Treatment and prognostic impact of transient leukemia in neonates with Down syndrome

    Treatment and prognostic impact of transient leukemia in neonates with Down syndrome by Jan‐Henning Klusmann, Ursula Creutzig, Martin Zimmermann, Michael Dworzak, Norbert Jorch, Claudia Langebrake, Arnulf Pekrun, Katarina Macakova-Reinhardt, Dirk Reinhardt

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    Inherited Metabolic Myopathy and Hemolysis Due to a Mutation in Aldolase A

    Inherited Metabolic Myopathy and Hemolysis Due to a Mutation in Aldolase A by Joachim Kreuder, Arndt Borkhardt, Reinald Repp, Arnulf Pekrun, B. Göttsche, U Gottschalk, Heinz Reichmann, W. Schachenmayr, Kurt Schlegel, Fritz Lampert

    Published 1996
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)

    Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5) by Julia Pagel, Karin Beutel, Kai Lehmberg, Florian Koch, Andrea Maul‐Pavicic, Anna‐Katharina Rohlfs, Abdullah Al‐Jefri, Rita Beier, Lilian Bomme Ousager, Karoline Ehlert, U. Gross‐Wieltsch, Norbert Jorch, Bernhard Kremens, Arnulf Pekrun, Monika Sparber‐Sauer, Ester Mejstříková, Angela Wawer, Stephan Ehl, Udo zur Stadt, Gritta Janka

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiency

    Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiency by Anne Rensing‐Ehl, Simon Völkl, Carsten Speckmann, Myriam Ricarda Lorenz, Julia Ritter, Aleš Janda, Mario Abinun, Hanspeter Pircher, Bertram Bengsch, Robert Thimme, Ilka Fuchs, Sandra Ammann, Andrea Allgäuer, Karim Kentouche, Andrew J. Cant, Sophie Hambleton, Claudia Bettoni da Cunha, Sebastian Huetker, Ingrid Kühnle, Arnulf Pekrun, Markus G. Seidel, Michael Hummel, Andréas Mackensen, Klaus Schwarz, Stephan Ehl

    Published 2014
    Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak

    GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak by Yvonne G. Weber, Alexander Storch, Thomas V. Wuttke, Knut Brockmann, Judith Kempfle, Snezana Maljevic, Lucia Margari, Christoph Kamm, Susanne A. Schneider, Stephan M. Huber, Arnulf Pekrun, Robert Roebling, Guiscard Seebohm, Saisudha Koka, Camelia Lang, Eduard Kraft, Dragica Blazevic, Alberto Salvo‐Vargas, Michael Fauler, Felix M. Mottaghy, Alexander Münchau, Mark J. Edwards, Anna Presicci, Francesco Margari, Thomas Gasser, Florian Läng, Kailash P. Bhatia, Frank Lehmann‐Horn, Holger Lerche

    Published 2008
    Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor

    Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor by Jenny Wegert, Silke Appenzeller, Taryn D. Treger, Heike Streitenberger, Barbara Ziegler, Sabrina Bausenwein, Christian Vokuhl, Conor Parks, Eva Jüttner, Susanne Gramlich, Karen Ernestus, Sheena Warman, Jörg Fuchs, Jochen Hubertus, Dietrich von Schweinitz, Birgit Fröhlich, Norbert Jorch, Ralf Knöfler, Carsten Friedrich, Selim Corbacioglu, Michael C. Frühwald, Arnulf Pekrun, Dominik T. Schneider, Jörg Faber, Jana Stursberg, Markus Metzler, Nils Welter, Kathy Pritchard‐Jones, Norbert Graf, Rhoikos Furtwängler, Sam Behjati, Manfred Gessler

    Published 2025
    Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis

    Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis by Abigail K. Suwala, Damian Stichel, Daniel Schrimpf, Matthias Kloor, Annika K. Wefers, Annekathrin Reinhardt, Sybren L. N. Maas, Christian P. Kratz, Leonille Schweizer, Martin Hasselblatt, Matija Snuderl, Malak Abedalthagafi, Zied Abdullaev, Camelia M. Monoranu, Markus Bergmann, Arnulf Pekrun, Christian F. Freyschlag, Eleonora Aronica, Christof M. Kramm, Felix Hinz, Philipp Sievers, Andrey Korshunov, Marcel Kool, Stefan M. Pfister, Dominik Sturm, David Jones, Wolfgang Wick, Andreas Unterberg, Christian Hartmann, Andrew Dodgshun, Uri Tabori, Pieter Wesseling, Felix Sahm, Andreas von Deimling, David Reuß

    Published 2020
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma

    Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma by Dominik Sturm, Hendrik Witt, Volker Hovestadt, Dong-Anh Khuong-Quang, David Jones, Carolin Konermann, Elke Pfaff, Martje Tönjes, Martin Sill, Sebastian Bender, Marcel Kool, Marc Zapatka, Natália Becker, Manuela Zucknick, Thomas Hielscher, Xiao-Yang Liu, Adam M. Fontebasso, Marina Ryzhova, Steffen Albrecht, Karine Jacob, Marietta Wolter, Martin Ebinger, Martin U. Schuhmann, Timothy Van Meter, Michael C. Frühwald, Holger Hauch, Arnulf Pekrun, Bernhard Radlwimmer, Tim Niehues, Gregor von Komorowski, Matthias Dürken, Andreas E. Kulozik, Jenny Madden, Andrew M. Donson, Nicholas K. Foreman, Rachid Drissi, Maryam Fouladi, Wolfram Scheurlen, Andreas von Deimling, Camelia Monoranu, Wolfgang Roggendorf, Christel Herold‐Mende, Andreas Unterberg, Christof M. Kramm, Jörg Felsberg, Christian Hartmann, Benedikt Wiestler, Wolfgang Wick, Till Milde, Olaf Witt, Anders M. Lindroth, Jeremy Schwartzentruber, Damien Faury, Adam Fleming, Magdalena Zakrzewska, Paweł P. Liberski, Krzysztof Zakrzewski, Péter Hauser, Miklós Garami, Álmos Klekner, László Bognár, A. Sorana Morrissy, Florence M.G. Cavalli, Michael D. Taylor, Peter van Sluis, Jan Köster, Rogier Versteeg, Richard Volckmann, Tom Mikkelsen, Kenneth Aldape, Guido Reifenberger, V. Peter Collins, Jacek Majewski, Andrey Korshunov, Peter Lichter, Christoph Plass, Nada Jabado, Stefan M. Pfister

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: