移植前后进行淋巴细胞表型分析，监测免疫重建过程。
Phenotype of the peripheral blood lymphocytes was analyzed to observe the immunologic reconstitution after transplantation.
结论免疫表型分析是诊断慢性淋巴细胞系统白血病非常有用的依据。
Conclusion immunophenotypic analysis is an extremely useful adjunct in the diagnosis of chronic lymphoid leukemia.
通过流式细胞仪对细胞表面标记物进行免疫表型分析。
Immunophenotypic analysis of cell surface markers was performed by flow cytometry.
目的分析小儿急性白血病(AL)的免疫表型、异倍体、细胞周期分布状况的临床意义。
Objective To analyse the clinical significance of the immunophenotype, aneuploidy and cell circle distribution in children with acute leukemia (al).
方法采用免疫组化染色和透射电镜方法，对大鼠肠道固有层内淋巴细胞（LPL）表型进行分析，观察其形态特征。
Methods To analyze the surface mark of LPL and observe morphological feathers of them by immunohistochemistry staining and transmission electron microscope(TEM).
目的通过对1例21号环状染色体综合征患者的细胞遗传学分析，探讨21号环状染色体的形成原因，临床表型与染色体区带的关系。
Objective to search the forming cause and the correlation between the clinical phenotype and chromosome band by the cytogenetic analysis on a case of ring chromosome 21 syndrome.
表型检测采用标准的血液学分析技术测量红细胞参数和血红蛋白组分。
Methods Phenotypic analysis was performed using standard hematological tests to measure red blood cell parameters and Hb concentration.
对扩增的细胞进行免疫表型、定向分化、造血祖细胞集落分析及脾集落形成单位的研究。
The expanded cells were further analyzed by phenotype, committed differentiation, progenitor colony assay as well as colony forming unite spleen.
方法采用三色免疫荧光直接标记法及多参数流式细胞术分析13例多发性骨髓瘤的免疫表型。
Methods Three-colour direct immunofluorescence staining and multiparameter flow cytometry were used for analysis of 13 samples of immunophenotyping of multiple myeloma patients.
方法回顾性分析30例HNL患者淋巴活检标本的HE切片，并用免疫组化S- P法检测细胞表型。
Methods HE sections of lymph node biopsies of 30 patients with HNL were analyzed retrospectively and their cell phenotypes were examined by immunohistochemistry S-P method.
结论：CA和RGH患者外周血不同制备方法影响淋巴细胞免疫表型结果分析，裂解全血法优于分离淋巴细胞法。
Conclusion: Peripheral blood cell preparation of patients with CA and RGH influences the levels of the lymphocyte immunophenotyping. The WBL method is better than the F-PBL method.
目的分析CD3-CD4-CD8+胸腺细胞的表型特征，阐明其在胸腺发育中所处地位。
Objective To analyse the phenotype of immature CD3-CD4-CD8+ murine thymocytes and elucidate their stage of differentiation.
方法采用流式细胞仪对53例初治急性白血病进行免疫表型分析。
Methods Immune phenotypes were assayed in 53 patients with acute Leukemia by flow cytometer.
结论胞质抗体具有系列特异性，四色组合流式细胞-免疫表型技术能提供快速多参数的分析数据。
Conclusion Intracellular antibodies possess lineage specificity and four-color combination flow cytometric immunophenotyping can provide fast and multi-parameter data.
目的分析急性早幼粒细胞白血病（APL）免疫表型特点及其临床意义。
Objective To investigate the immunophenoytpe of acute promyelocytic leukemia(APL) and its clinical significance.
流式细胞仪分析细胞表型特征，并应用细胞化学染色法观察细胞体外成骨和成脂肪能力。
Furthermore, cell phenotypic characteristics were analyzed by flow cytometry and the differentiation along adipogenic and osteogenic pathways were assessed by histological staining in vitro.
分析肝脏和其他器官中不同免疫细胞类型的频率和表型。
The frequencies and phenotypes of different immune cell types in the liver and other organs were analyzed.
目的分析急性巨核细胞白血病(amkl)患者的临床特征、免疫表型、分子生物学特征以及预后。
Objective to assess the clinical features, immunophenotypic, and cytogenetic characteristics of acute megakaryocytic leukemia (AMKL).
用免疫细胞化学方法分析诱导前后的细胞表型特点。
The characteristics of treated cells were assayed by immunocytochemistry staining analysis.
体外诱导小鼠树突状细胞(DC)，流式细胞术分析DC表型，评价尿酸钠体外对DC成熟的效应。
Dendritic cells (DC) were induced in vitro, the phenotypes of DC were analyzed by flow cytometry and the effect of UANa on DC maturity was evaluated.
方法采用肿瘤抗原致敏的DC与CIK细胞共培养，分析其免疫表型，并用mtt染色法检测其对肿瘤细胞的杀伤力。
Methods Co-culture tumor antigen-sensitized dendritic cells (DCs) with cytokine induced killer (CIK) cells, analyze the immune epitope and determine the killing effect on tumor cells by MTT method.
对叶片的解剖学分析发现突变体中脉缺少细胞和近轴小维管束，导致披叶表型的产生。
Leaf anatomy results revealed the central vein lacks both clear cells and the adaxial small vascular bundle in dl2 mutant, which seemed to cause the drooping leaf phenotype.
对叶片的解剖学分析发现突变体中脉缺少细胞和近轴小维管束，导致披叶表型的产生。
Leaf anatomy results revealed the central vein lacks both clear cells and the adaxial small vascular bundle in dl2 mutant, which seemed to cause the drooping leaf phenotype.
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