原代白血病细胞的再增殖能力低于白血病细胞系。
The regrowth ability of primary leukemia cells was lower than leukemia cell line.
JM是来自人胸腺不成熟t细胞的急性淋巴细胞白血病细胞系。
JM is a acute lymphocytic leukemia cell line derived from immature t lymphocytes in human thymus.
目的探讨异型巨噬细胞集落刺激因子在人白血病细胞系中的表达和性质。
Objective to explore the expression and effects of isoforms of macrophage colony-stimulating factor in human leukemic cell lines.
且和髓细胞白血病细胞系的增殖、凋亡有关，对细胞分化无影响，但作用机制不清楚。
It is related to proliferation and apoptosis in leukemic cells, but the mechanism is unknown.
应用5-杂氮脱氧胞嘧啶处理上述白血病细胞系，观察去甲基化处理对失活基因的影响；
Then it was observed whether the inactived genes in leukemia cell lines were actived after the treatment with 5-aza-deoxycytosin, a kind ofdemethylation agent .
本文以K562人类红白血病细胞系为实验模型，研究了人参皂甙对该细胞系的诱导分化作用。
The effect of Ginsenosides on the induction of differentiation in the human erythroleukemia cell line K562 was investigated.
结论：诱导剂佛波酯和BCR - ABL嵌合基因可以影响EDAG基因在白血病细胞系k562中的表达。
CONCLUSION: PMA and BCR-ABL chimeric gene can influence the expression of EDAG gene in leukemia cell line K562.
目的阐明白细胞介素18 (IL 18)在人白血病细胞系J 61的表达与调控，探讨IL 18在白血病发生中的意义。
Objective To elucidate the expression and regulation of interleukin 18 (IL 18) in human leukemia cell line J6 1, and investigate its possible role in leukemogenesis.
应用图像分析系统对IL2基因转移前后的小鼠肥大细胞瘤细胞系P815细胞及人红白血病细胞系K562细胞进行了形态计量学测定及组间显著性检验。
The morphometric study of P815 mouse mastocytoma cells and human erythroleukemia cell line K562 was performed before and after IL2 gene transduction by means of image analysis system.
方法采用RT P CR技术、硫化pcr结合限制性内切酶技术检测白血病细胞系及正常人外周血单个核细胞WT 1基因的表达及其启动子区DNA甲基化水平。
Method The expression of WT1 gene and its DNA methylation status were assayed in leukemia cell lines and normal peripheral blood mononuclear cells (PBMNC) by RT-PCR and MS-PCR.
前言： 目的：建立人M5型白血病细胞系SHI-1/S CID（重症联合免疫缺陷）小鼠模型，探讨白血病细胞的接种密度与SCID小鼠成瘤率及病理变化的关系。
AIM: To establish a model of human M5 leukemia and investigate the pathomorphological change in severe combined immunodeficient (SCID) mice after being transplanted with SHI-1 cells.
方法：利用体外细胞培养、MTT、NBT染色及吞噬功能测定等方法，观察在不同浓度金龙胶囊作用下人早幼粒白血病细胞系(HL - 60)的细胞形态和功能的变化。
Methods: in vitro cell culture, MTT titration, NBT reduction and phagocytosis determination were employed to study the effects of JLC on HL-60 cells.
目的：检测人白细胞介素-23 (IL - 23)和白细胞介素-12 (IL - 12)亚基在各类白血病细胞系中的表达并探讨佛波二酯对IL - 23和IL - 12亚基表达的调控作用。
Objective: to detect expression of interleukin - 23 (il - 23) and il - 12 subunits in various leukemia cell lines and evaluate the ability of phorbol diester to up - regulate the subunits expression.
目前对于CYP3A5基因参与急性白血病的研究主要限于细胞系的体外研究。
So far the studies on CYP3A5 gene has only been focused on the leukemia cell lines.
目前对于CYP3A5基因参与急性白血病的研究主要限于细胞系的体外研究。
So far the studies on CYP3A5 gene has only been focused on the leukemia cell lines.
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