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Titlebook: Acute Leukemias IV; Prognostic Factors a T. Büchner,W. Hiddemann,J. Ritter Conference proceedings 1994 Springer-Verlag Berlin Heidelberg 19

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https://doi.org/10.1007/978-3-540-69216-4. In this chapter we describe a rapid and simple clonal assay for the quantification of blast cells using a recently detected gene rearrangement associated with T-cell lymphoblastic leukemia, named tal-l deletion [1,2].
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,Instrumente der Außenwirtschaftspolitik,nsitivity of the leukemic cells to different cytostatics. Therefore the detection of minimal residual disease (MRD) remains an important goal, not only to predict relapse and, therefore, continue to treat the patient, but also to monitor the effectiveness of therapy and conceivably reduce treatment needs in patients who may already be cured [3].
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https://doi.org/10.1007/978-3-658-27596-9a consequence of their abnormal differentiation programme and the latter assumes that these leukemias arise from the transformation of immature progenitor cells which may normally – in a transient phase of promiscuity – express characteristics of two or more cell lineages.
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Kölner Schriften zum Medizinrechtles like ICAM-1, LFA-1 VCAM-1 and VLA-4 might therefore play an essential role for the regulation and development ofleukemic progenitor cells [6]. We therefore investigated the expression and regulation of ICAM-1 by different cytokines which might play a role for the stroma dependent phase of precursor B-cell development.
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Die internationale Währungsordnungcould be protected from otherwise lethal irradiation by shielding the spleen, an observation that eventually led to the recognition of the potential role of marrow transplantation in the treatment of leukemia.
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Christina Meurer,Christian Katzenmeierte numerical anomalies particularly in neoplasms, for example acute lymphoblastic leukemias (ALL), in which conventional cytogenetic analysis is hampered by a small number of metaphases and poor chromosome quality.
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https://doi.org/10.1007/978-3-540-69216-4udy leukemic cells were examined for aberrant transcripts of two differentiation-associated genes, the protooncogene ETS 1 and the gene for the enzyme marker terminal deoxynucleotidyl transferase (TdT).
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