Titlebook: Experimental Hematology Today—1989; Selected Papers from Norbert C. Gorin,Luc Douay Conference proceedings 1990 Springer-Verlag New York In

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Rwanda, the United States, and Genocide (DFS) in acute myelogenous leukemia (AML) to 40% in acute lymphocytic leukemia (ALL). For this reason, we would like to discuss the role of autologous bone marrow transplantation (ABMT) separately for each disease modality.

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Coping Strategies and Genocide Preventionible to visible light by staining them with a photosensitizing dye. Photosensitizers that bind preferentially to neoplastic cells offer interesting opportunities for new approaches to cancer therapy. The preferential retention of intravenously administered hematoporphyrin derivative (HPD) by tumor t

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https://doi.org/10.1057/9781137415110treatment approach has become very widely utilized. However, autologous bone marrow transplantation was used primarily to treat patients with non-Hodgkin lymphoma until the mid 1980’s. Table 1 illustrates that the use of ABMT in the treatment of patients with Hodgkin disease has markedly increased r

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Rat der Europ?ischen Gemeinschaft of false negative results caused by currently used donor tests. 2) There is concern about the transmission of viruses for which donor tests have not yet been developed. 3) There is concern about the mounting costs of donor screening. 4) In certain geographical areas, the pool of seronegative donors

Mast-Cell

K. P. Gopinathan,Omana Joy,Amit Singhcalled T cell growth factor or inteiieukin 2 (IL2) [1]. One of the classical markers of activated T cells is the subseqent expression of specific membrane receptors for interleukin 2 (IL2R) [2]. The expression of these receptors on T cells was shown to be a transient event [3] and restimulation with

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Nicole A. J. Krentz,Francis C. Lynnne (ST-2). IL-3-induced blast colonies, shown to be capable of differentiation into a variety of hematopoietic cells, were used as a source of enriched hematopoietic progenitor cells. These cells were Thy-1. and B220.. In 7 of 211 wells receiving each blast colony, lymphoid cell and myeloid cell gro

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