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- Methods: Human erythroleukemia cell line (HEL) was studied in Prolif eration,Apoptosis,cell proliferous cycle,Cytomorphology with serum-pharmacology methods. 方法:采用血清药理学方法体外培养观察人红白血病细胞系(HEL)的增殖、凋亡、细胞周期、细胞形态等细胞学指标。
- Cancer is caused by mutational damage to genes that otherwise hold a cell's reproductive cycle in check, and thus stop that cell proliferating. 癌症的原因是维持细胞正确再生的基因发生突变，并因此阻止了细胞的增生扩散。
- CyQUANT Cell Proliferation Assay Kit, Molecular Probes, Inc. 细胞增殖检测试剂盒。
- DD3 gene has a certain influence on promoting cell proliferation. DD3基因在促进细胞增值方面起着一定作用。
- MTT assays were carried out to establish cell proliferation. 采用MTT测试法研究多孔磷酸三钙对细胞增殖的影响。
- Proliferating cell nuclear antigen(PCNA)is an objective index to evaluate cell proliferation state. 增殖细胞核抗原(PCNA)是评价细胞增殖状态的客观指标。
- The number of chondrocytes were used as indicators of cell proliferation. 采用软骨细胞计数观察各组细胞增殖情况。
- Detect NK cells proliferating ability by MTT and killing power by51Cr releasing test. MTT珐检测NK细胞增殖能力。 51Cr释放法测定NK细胞杀伤活性。
- Cell proliferation rate and viability were measured by BrdU and MTT. 采用BrdU法和MTT法检测细胞增殖能力和活力;
- Conclusion HMBA can inhibit eryoleukemia cell proliferation and induce differentiation. 结论HMBA能抑制红白血病细胞生长繁殖并可诱导其分化。
- Immunohischemistry stainning, MTT assay and flow cytometry (FACS) were used to detect the expression of proliferating cell nuclear antigen (PCNA), cell proliferation, and cell cycle phase change. 采用免疫组化染色法、MTT法和流式细胞仪检测PCNA表达、细胞增殖和细胞周期变化。
- Conclusion Pine pollen influences on cell proliferation by improving cell growth. 结论:松花粉可通过促进细胞生长而影响细胞增殖。
- Cell count and MTT assay were used to record cell proliferation and cellular activity. MTT法检测细胞增殖活性;
- Cell proliferation was mea-sured by MTT assay and trypan blue excluding experiment. 用MTT和台盼蓝细胞排斥实验检测细胞增殖;
- Like apoptosis, senescence is a stress response, but instead of inducing cell death, it puts a permanent brake on cell proliferation. 与凋亡相似，衰老是一种应激反应，与诱导细胞死亡不同，它是细胞增殖的长期抑制机制。
- Anti-ALR mono-cloned antibody could block the effect of ALR on hepatocyte cell proliferation. 抗ALR单克隆抗体能有效阻断ALR的上述作用。
- Suppression and decrease of MGC 803 cell proliferation was found after treatment by DATS in vitro. DATS处理后 ,培养的MGC 80 3细胞增殖抑制而稀少。
- However, cell proliferation was close to the normal at the dose of EsA 20 mg/kg with LPS as mitogen. 而在LPS刺激的情况下，经20mg/kg EsA处理后，小鼠的淋巴细胞的增殖水平降至正常水平；
- Exogenous SPP treatment, inhibited GS115-edg-1-EGFP cells proliferation. 免疫荧光分析证实表达的重组受体大量定位于酵母细胞膜上。
- Villous edema and trophoblast of cell proliferation without clinical significance. 绒毛水肿和滋养叶细胞增生无临床意义。
