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- The cell cycle analysis showed that 90% of MSCs was in G0/G1 phase . 细胞周期显示有 92%25细胞处于G0 /G1期 ;
- Cell cycle analysis indicated that CUR blocked cells in G2/M phase. 流式细胞仪分析表明姜黄素将hfRPE细胞阻滞在G2/M期。
- Apoptosis was detected by morphological observation, DNA electrophoresis, percentage of DNA fragmentation test and flow cytometric cell cycle analysis. 结果：乳香提取物能诱导急性非淋巴性白血病细胞凋亡。
- MSCs showed active proliferative ability in primary and passage cultere before the 14 th . Cell cycle analysis showed that 82% of MSCs was in G 0/G 1 phase. 原代及传代培养显示 ;14代以前的MSCs具有活跃的增殖能力 ;细胞周期分析显示有 82%25的MSCs处于G0 /G1期 .
- Methods:Apoptosis was detected by morphological observation,DNA electrophoresis.Percentage of DNA fragmentation test and flow cyto metric cell cycle analysis. 方法：应用形态学观察，DNA凝胶电泳、DNA片段百分率，流式细胞仪分析检测白血病细胞凋亡及细胞周期。
- Identification of aquatic microbiota, analysis of aquatic abundance and biomass, cell cycle analysis, ecology and physiology research of aquatic microbiota were covered. 包括微型生物的识别、记数和生物量研究，微型生物的细胞周期分析以及生态与生理学研究。
- Cell cycle analysis indicated that about 50% of HL-60 cells stagnated at G0/G1 stage in the presence of rh-LIF or low dosage Ara-c. 细胞周期分析结果表明：rh-LIF、小剂量Ara-c可致50%25左右HL-60细胞停滞于G0/G1期。
- Cell cycle analysis suggested that SW1990-R, ASPC-R, MIA-R, PAN-R and P3-R had lower G_2/M and greater SF_2 (survival fraction after 2 Gy irradiation) compared with the parental cell lines. 耐放射株SW1990-R、ASPC-R、MIA-R、PAN-R及P3-R的G2/M均明显降低,而放射敏感性指标SF2升高9%25~45%25。
- The cell viability was evaluated with MTT chromatometry and cell growth curve was generated. Flow cytometry was performed for cell cycle analysis, and acridine orange staining was utilized for cell aging evaluation. MTT比色法测细胞活性并绘制细胞生长曲线,流式细胞仪测定细胞周期,丫啶橙染色检测细胞的衰老;
- Cell cycle analysis indicated that AraC blocked HL 60 cells in G 1, inhibited cells in S, while EGCG had no effect on cell cycle at the current concentration, but could enhance the cell arrest by AraC. 细胞周期研究结果表明AraC可使HL 6 0细胞阻滞于G1期 ,S期细胞减少 ,低浓度的EGCG对细胞周期几无影响 ,但增强了AraC的细胞周期阻滞作用及细胞凋亡。
- Cell cycle analysis showed a significant decrease in S phase and a remarkable increase in G1/G0 fraction after exposure to antisense EGFR ODN in comparison with missense oligonucleotide-treated cells at the corresponding time. 细胞周期分析EGFR反义ODN作用于细胞后,细胞G0/G1期细胞数明显增多,S期细胞数相应减少,而G2+M期细胞数亦明显减少。
- More than 90% of subcultured MSCs were adhesive in 12 h. The cell cycle analysis showed that 80% of MSCs was in G0/G1 phase. The ultrastructures of MSCs demonstrated the features of infantile cells. MSCs倍增时间约为 3 8h ,传代后 1 2h贴壁达 90%25以上 ,细胞周期显示有 80%25细胞处于G0 G1 期 ,并用电镜照片显示其超微结构。
- Doubling time of these cells were estimated about 30 hours and cell cycle analysis revealed that the majority of cells (over 80 percents) stood in G0-G1 phase while a small population of cells was in (S+G2+M) phase. 细胞周期分析表明80%25以上的细胞都处于G0~G1期。 流式细胞检测表明这些细胞表达CD13、CD29、CD44、CD90、CD105和CD166等MSCs标志物。
- Flow Cytometry applyed to analysis cell cycle. 采用流式细胞仪分析细胞周期。
- And cell cycle was arrested of G0/ G1 phase. 并且将细胞周期阻滞于G0/G1期。
- B, Stem( S)/ progenitor( P) cell inersion through the cell cycle. 干细胞/祖细胞(/)化模型.;大量目前的研究对传统的模型提出了质疑。
- The cell cycle of BFF treated by different methods was examined. 探讨不同的处理方法和处理时间对水牛胎儿成纤维细胞周期的影响。
- cell cycle analysis 细胞周期分析
- Cyclin-cdk compound is composed of Cyclin and cdk different cell cycle. 多种肿瘤存在着Cyclin的异常表达，cdk的激活及其抑制因子的丢失。
- Distribution of cell cycle and apoptosis were analysed using flow cytometry. 流式细胞仪分析细胞周期的分布及凋亡；
