Zobrazeno 1 - 10
of 26
pro vyhledávání: '"E R Panzer-Grümayer"'
Autor:
J. J. M. Van Dongen, V H J van der Velden, Alexander M. Dohnal, Helmut Gadner, Martin Schrappe, Georg Mann, E R Panzer-Grümayer, A Schrauder, Andrea Biondi, Thomas Flohr, Maddalena Paganin, Eva Csinady, Giovanni Cazzaniga
Publikováno v:
Leukemia, 21(4), 642-646. Nature Publishing Group
The t(4;11)-positive acute lymphoblastic leukemia (ALL) is a rare disease in children above the age of 1 year. We studied the clinical and biological characteristics in 32 consecutively diagnosed childhood cases (median age 10.0 years, range 1.0-17.1
Autor:
E R Panzer-Grümayer, André Schrauder, M Konrad, V H J van der Velden, C. R. Bartram, Andrea Biondi, Giovanni Cazzaniga, Thomas Flohr, Martin Schrappe, Giuseppe Basso, Rosemary Sutton, Giuseppe Masera, J. J. M. Van Dongen, J M Wijkhuijs
Publikováno v:
Leukemia, 21(4), 706-713. Nature Publishing Group
Minimal residual disease (MRD) diagnostics is used for treatment stratification in childhood acute lymphoblastic leukemia. We aimed to identify and solve potential problems in multicenter MRD studies to achieve and maintain consistent results between
Publikováno v:
Leukemia & Lymphoma. 38:295-308
The present review summarizes our efforts in developing a novel immunologic approach ("Comparative Phenotype Mapping") targeted at assessing minimal residual disease (MRD) in B-cell precursor (BCP) acute lymphoblastic leukemia (ALL) patients. The met
Autor:
Daniel W. Ghali, Oskar A. Haas, Susanna Lang, Ingrid Simonitsch, Andreas Zoubek, Georg Mann, E. R. Panzer-Grümayer, Thaddaeus Radaszkiewicz, Heinrich Kovar, Christa Pfleiderer, Helmut Gadner
Publikováno v:
Cancer Genetics and Cytogenetics. 83:5-11
We report on a 20-year-old woman who developed a pelvic small round cell tumor with lung metastases 8 years after diagnosis and successful treatment for Ki-1-positive anaplastic large cell lymphoma (Ki-1 + ALCL) with histiocytic differentiation. Mole
Publikováno v:
The Journal of Immunology. 151:92-99
The early stages of lymphoid differentiation preceding T and B lineage commitment remain poorly defined. We hypothesized that early lymphoid precursor cells are possibly common progenitors and would express a very early T cell-associated Ag (CD7) and
Autor:
G Mann, G Fuka, U Kaindl, Anna Kilbey, Oskar A. Haas, James C. Neil, G Krapf, R Joas, A Inthal, E R Panzer-Grümayer
Publikováno v:
Oncogene. 29(22)
Approximately 25% of childhood B-cell precursor acute lymphoblastic leukemia have an ETV6/RUNX1 (E/R) gene fusion that results from a t(12;21). This genetic subgroup of leukemia is associated with near-triploidy, near-tetraploidy, and trisomy 21 as r
Autor:
Susanna Fischer, Eva Csinady, Ruth Joas, J. J. M. Van Dongen, E R Panzer-Grümayer, Ulrike Pötschger, Margit König, J F de Vries, Oskar A. Haas, H B Beverloo, Georg Mann, V H J van der Velden
Publikováno v:
Leukemia, 23(5), 870-876. Nature Publishing Group
Childhood B-cell precursor acute lymphoblastic leukemia (BCP ALL) is generally a clonal disease in which the number of IGH rearrangements per cell does not exceed the number of the IGH alleles on chromosome 14. Consequently, monoclonal high hyperdipl
Autor:
Thorsten Langer, Manuela Krumbholz, Jochen Harbott, E R Panzer-Grümayer, Thomas Keller, U Jacobs, S Semper, V H J van der Velden, Martin Schrappe, Markus Metzler, Wolfgang Rascher, H von Goessel, André Schrauder, J. J. M. Van Dongen
Publikováno v:
Leukemia Research, 33(8), 1082-1088. Elsevier Ltd.
Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL The genomic fusion site, unique to individual patients and specific for the malignant clone, represents an ideal molecular marker for quantification of minimal residu
Autor:
Jan Trka, Thorsten Raff, Peter Bader, Letizia Foroni, J M Cayuela, Kheira Beldjord, André Schrauder, E R Panzer-Grümayer, U zur Stadt, Hélène Cavé, Jeremy Hancock, Cornelia Eckert, Hans O. Madsen, Thomas Flohr, Rosemary Sutton, J. J. M. Van Dongen, Giovanni Cazzaniga, V H J van der Velden, C. E. Van Der Schoot
Publikováno v:
Leukemia, 21(4), 604-611. Nature Publishing Group
Most modern treatment protocols for acute lymphoblastic leukaemia (ALL) include the analysis of minimal residual disease (MRD). To ensure comparable MRD results between different MRD-polymerase chain reaction (PCR) laboratories, standardization and q
Autor:
V H J van der Velden, E R Panzer-Grümayer, M Konrad, Martin Schrappe, Ulrike Pötschger, Thomas Flohr, C. R. Bartram, Giovanni Cazzaniga, Giuseppe Basso, S Hübner, J. J. M. Van Dongen, Andrea Biondi
Publikováno v:
Leukemia, 18, 84-91. Nature Publishing Group
The t(12;21) translocation resulting in the TEL-AML1 gene fusion is found in 25% of childhood B-cell precursor (BCP) acute lymphoblastic leukemias (ALL). Since TEL-AML1 has been reported to induce cell cycle retardation and thus may influence somatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ac4f8c061ae27558ca5c43dd43f72b
https://pure.eur.nl/en/publications/3acb8f7a-9f90-4208-b843-a7dd5a947b84
https://pure.eur.nl/en/publications/3acb8f7a-9f90-4208-b843-a7dd5a947b84