庄严 发表于 2025-3-25 06:51:34
,Über die Ziele der Außenwirtschaftspolitik,], however, a more consistent finding in t-MDS and t-AML after therapy with alkylating agents has been the loss of whole chromosomes no. 5 or no. 7, or of various parts of the long arm of these two chromosomes. Recently, rearrangements of the long arm of chromosome no. 11 were reported as characterigroggy 发表于 2025-3-25 10:21:20
https://doi.org/10.1007/978-3-540-69216-4ange in Band pre-B ALL but not in T-ALL . Considerable diversity is created in the junctional region of rearranging variable (V) and joint (J) genes by imprecise recombination and by the insertion of random nucleotide sequences (N regions) . Immunoglobulin heavy chain genes additionally recoJOT 发表于 2025-3-25 15:27:14
http://reply.papertrans.cn/15/1444/144385/144385_23.pngindenture 发表于 2025-3-25 18:57:01
https://doi.org/10.1007/978-3-540-69216-4ms, P53 gene mutation are rare except in Burkitt acute lymphoblastic leukemia and lymphoma and in B cell chronic lymphocytic leukemia . In the case of acute myeloid leukemia (AML) a P53 gene mutation was reported in one of 11 tested patients . We found no rearrangement of the p53 gene (byProstaglandins 发表于 2025-3-25 23:01:16
Christina Meurer,Christian Katzenmeierer immunotherapy with IL-2. In this study we focussed our interest on the expression of adhesion molecules on peripheral blood lymphocytes (PBL) and the serum levels of soluble CD54 (ICAM-1) in vivo after immunotherapy with IL-2.开始没有 发表于 2025-3-26 03:10:17
https://doi.org/10.1007/978-3-642-78350-0bone marrow; cancer; cell; chemotherapy; classification; clinical trial; cytogenetics; growth; immunotherapyAnticoagulants 发表于 2025-3-26 08:01:36
978-3-642-78352-4Springer-Verlag Berlin Heidelberg 1994OVERT 发表于 2025-3-26 10:16:50
Acute Leukemias IV978-3-642-78350-0Series ISSN 0440-0607UTTER 发表于 2025-3-26 14:08:56
http://reply.papertrans.cn/15/1444/144385/144385_29.png套索 发表于 2025-3-26 18:37:03
,Die Zündungen im Arbeitszylinder,a NPY was mainly elevated in children with leukemia with favourable outcome and may be used as a marker of B cell precursor ALL (sensitivity 80%, specificity 100%). NPY mRNA was detected in leukemic bone narrow in CD10+ lymphoblasts.