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急性淋巴细胞白血病all     
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  “急性淋巴细胞白血病(all)”译为未确定词的双语例句
     cCD79a(100%) ,CD19(92. 1%) were chiefly expressed in B-ALL patients, and in T-ALL patients, cCD3(100%) and CD2(83. 3%) were expressed;
     急性淋巴细胞白血病(ALL)患者 中B-ALL主要表达cCD79a(100%)、CD19(92.1%),T-ALL表达cCD3(100%)、CD2(83.3%);
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     In 35 patients with B-lineage acute lymphoblastic leukemia, the antigens were mainly CD19(100.00%), HLA-DR(100.00%), CD10(74.29%), CD34(60.00%) and CD20(31.40%).
     B细胞系急性淋巴细胞白血病(ALL)35例(17.4%),主要表达CD19(100.00%)、HLA DR(100.00%)、CD10(74.29%)、CD34(60.00%)、CD20(31.40%)。
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     Results The positive rate of expression of CD11b in acute myelocytic leukemia (AML) was 44.7% (42/94) and that in acute lymphocytic leukemia (ALL) was 11.8% (12/102,χ2=26.55,P<0.01).
     结果CD11b在44.7% (42/94)的急性髓细胞白血病(AML)表达 ,高于其在急性淋巴细胞白血病 (ALL)中的阳性率11.8 % (12/102 ,χ2=26.55,P<0.01)。
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     Results The WT1 mRNA positive rates in acute myeloid leukemias and lymphoblastic leukemias were 77.3% (17/22) and 54.5%(6/11) .
     结果急性髓细胞白血病(AML)和急性淋巴细胞白血病(ALL)WT1表达阳性率分别为77.3%(17/22)和54.5%(6/11)。
短句来源
     In 29 patients with acute lymphoblastic leukemia (ALL), the expressed antigens were mainly HLA-DR, CD10, CD19, CD34 and CD7, and 34.5% of these patients were found to be positive for myeloid antigen expression.
     (2)29例急性淋巴细胞白血病(ALL)患者主要表达HLA-DR、CD10、CD19、CD34和CD7,34.5%的ALL患者伴有髓系抗原的表达。
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     Objective:To explore the curative effect of children with acute lymphoblastic leukemia(ALL).
     目的:探讨小儿急性淋巴细胞白血病(ALL)的治疗效果。
短句来源
     Objective To analyse the immunophenotype of childhood acute lymphoblastic leukemia(ALL).
     分析儿童急性淋巴细胞白血病 (ALL)的免疫表型特点。
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     To investigate the clonal diversity in childhood acute lymphoblastic leukemia (ALL).
     目的探讨小儿急性淋巴细胞白血病ALL)的克隆多样性。
短句来源
     No significant Ievels of MPO mRNA was detected in lymphoid celi lines and all typical acute lymphoid leukemias (ALL).
     淋巴细胞系和急性淋巴细胞白血病(ALL)细胞不表达MPOmRNA;
短句来源
     Objective To analyse the immunophenotype of childhood acute lynphoblastic leukemia(ALL).
     目的分析儿童急性淋巴细胞白血病(ALL)的免疫表型特点。
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  acute lymphoblastic leukemia (all)
Invasive procedures, such as the lumbar puncture, can cause anxiety and pain in children undergoing treatment for acute lymphoblastic leukemia (ALL).
      
The aim of this investigation was to evaluate the changes in PAF concentrations in the plasma, PBMC and BMMC of patients with acute lymphoblastic leukemia (ALL) and acute myeloblastic leukemia (AML).
      
In addition, we analyzed a leukemia dataset collected from 38 leukemia patients with 27 samples diagnosed as acute lymphoblastic leukemia (ALL) and 11 samples as acute myeloid leukemia (AML).
      
Nine patients had acute lymphoblastic leukemia (ALL), nine had other hematologic/oncologic diagnoses, and five had cystic fibrosis.
      
In order to assess the significance of BCR/ABC fusion gene in adult acute lymphoblastic Leukemia (ALL), 28 patients who were diagnosed as ALL were enrolled to detect BCR/ABC gene using nested-RT-PCR.
      
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  acute lymphocytic leukemia (all)
One of them was a Ph1 positive acute lymphocytic leukemia (ALL) and the other 2 had gaining or missing in groups C, D or E.
      
Of the 15 patients in our group, 11 with chronic, myelocytic leukemia (CML), 3 with Ph-negative acute lymphocytic leukemia (ALL), one with myelodysplastic syndrome (MDS).
      
Four patients suffered from acute lymphocytic leukemia (ALL) and four from acute non-lymphocytic leukemia (ANLL).
      
Natural killer (NK) activity against cells of the K-562 line was significantly depressed in 12 of 18 children (66%) with untreated acute lymphocytic leukemia (ALL).
      
Twenty-three children with acute lymphocytic leukemia (ALL) were examined with cranial CT at least twice with a minimal interval of 10 months.
      
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  acute lymphoid leukemia (all)
The results showed that the expression of the HSP27 gene was enhanced in 4 cases of acute lymphoid leukemia (ALL), 7 cases of acute nonlymphoid leukemia (ANLL) and 2 cases of myelodysplastic syndrome.
      
The aim of this study was to see whether pleiotropic or myeloid hematopoietic growth factors, which do not stimulate normal lymphoid cells, can induce proliferation of blast cells of the acute lymphoid leukemia (ALL) of childhood.
      
The authors report the case of a mother and her infant who both suffered from acute lymphoid leukemia (ALL).
      
None of acute lymphoid leukemia (ALL) had CD117 expression, except one case of T-ALL.
      
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