Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ilka Bondzio"'
Autor:
Jan Rohr, Karin Beutel, Andrea Maul-Pavicic, Thomas Vraetz, Jens Thiel, Klaus Warnatz, Ilka Bondzio, Ute Gross-Wieltsch, Michael Schündeln, Barbara Schütz, Wilhelm Woessmann, Andreas H. Groll, Brigitte Strahm, Julia Pagel, Carsten Speckmann, Gritta Janka, Gillian Griffiths, Klaus Schwarz, Udo zur Stadt, Stephan Ehl
Publikováno v:
Haematologica, Vol 95, Iss 12 (2010)
Background Familial hemophagocytic lymphohistiocytosis is a genetic disorder of lymphocyte cytotoxicity that usually presents in the first two years of life and has a poor prognosis unless treated by hematopoietic stem cell transplantation. Atypical
Externí odkaz:
https://doaj.org/article/011b5e64da624c7c934bd9291ccfa495
Antiviral and Regulatory T Cell Immunity in a Patient with Stromal Interaction Molecule 1 Deficiency
Autor:
Klaus Schwarz, Almuth Caliebe, Petra Kaiser, Thomas Vraetz, Regina Fölster-Holst, Sebastian Fuchs, Melina J. Benson, Bertram Bengsch, Carsten Speckmann, Robert Thimme, Stephan Ehl, Annette Schmitt-Graeff, Stefan Feske, Thilo Bass, Brigitte Strahm, Tobias Ankermann, Anne Rensing-Ehl, Andrea Maul-Pavicic, Ilka Bondzio, Wolfgang W. A. Schamel
Publikováno v:
The Journal of Immunology. 188:1523-1533
Stromal interaction molecule 1 (STIM1) deficiency is a rare genetic disorder of store-operated calcium entry, associated with a complex syndrome including immunodeficiency and immune dysregulation. The link from the molecular defect to these clinical
Autor:
G Dueckers, Volker Schuster, Ruth Draeger, Markus G. Seidel, Klaus Warnatz, Ales Janda, Y. Joos, Matti Korhonen, Kathrin Siepermann, Anne Rensing-Ehl, Sophie Hambleton, Stephan Ehl, Sebastian Fuchs, Michael Schlesier, Tim Niehues, Ulrich Salzer, Catherine Waruiru, M. Gomes, Fiona Shackley, Kirsti H. Sirkia, Klaus Schwarz, Ilka Bondzio, Andrew J. Cant, Thomas Wiesel, Karin Beutel, Matthias V. Kopp, Terry Flood, Carsten Speckmann, Milen Minkov, Mario Abinun
Publikováno v:
Clinical Immunology. 137:357-365
Autoimmune lymphoproliferative syndrome (ALPS) is mainly caused by defects in the CD95 pathway. Raised CD3+TCRαβ+CD4-CD8- double negative T cells and impaired T cell apoptosis are hallmarks of the disease. In contrast, the B cell compartment has be
Autor:
Maurizio Aricò, Andrea Maul-Pavicic, Raffaella Meazza, Kai Lehmberg, Daniela Pende, Samuel C. C. Chiang, Jan-Inge Henter, Lorenzo Moretta, Kimberly Gilmour, Yenan T. Bryceson, Gritta Janka, Udo zur Stadt, Thomas Vraetz, Nadine Binder, Karin Beutel, Stephan Ehl, Ilka Bondzio, Stefania Marcenaro, Heike Ufheil, Denise Walshe
Publikováno v:
Blood; Vol 119
Familial hemophagocytic lymphohistiocytosis (FHL) is a life-threatening disorder of immune regulation caused by defects in lymphocyte cytotoxicity. Rapid differentiation of primary, genetic forms from secondary forms of hemophagocytic lymphohistiocyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a796e4b46e5d424e8cfff726527ba461
http://hdl.handle.net/11567/384116
http://hdl.handle.net/11567/384116
Publikováno v:
Blood. 110:3877-3877
Natural Killer (NK) cells show potent anti-leukemic activity in vitro and thus NK cells isolated using the CliniMACS® Cell Separation System are currently under clinical evaluation as part of a treatment for acute myeloid leukemia (AML). (Uharek L e
Publikováno v:
Blood. 110:3878-3878
Killer cell immunoglobulin-like receptors (KIRs) are known to modulate the cytotoxic ability of human Natural Killer (NK) cells, as well as a subset of T cells. To date, only a very small number of publications have discussed the role of KIRs on T ce
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