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31.
The present study investigated the effect of As(2)O(3)on malignant lymphoma cells. Cell apoptosis was detected by cell staining and TdT-mediated dUTP Nick-end Labelling (TUNEL). Cellular DNA and protein expression content were determined by immunohistochemistry and flow cytometry. It was found that 0.5-2.0 microm /l As(2)O(3)could inhibit cell growth, including Raji cells and lymphoma cells from patients, and induce apoptosis, such as condensed chromatin and nuclear fragmentation with intact cell membrane, i.e. apoptotic body. It was also found that the cells of the sub-G(1)phase increased significantly and bcl-2 gene expression was greatly downregulated. However, this effect was not observed for Jurkat cells under the same conditions. We concluded that As(2)O(3)at a range of 0.5-2.0 microm /l can inhibit the growth and induce apoptosis in malignant lymphoma cells, which may have therapeutic potential.  相似文献   
32.
SLE患者PBMC凋亡状态及相关基因表达的研究   总被引:5,自引:0,他引:5  
探讨外周血单个核细胞(PBMC)凋亡及其基因调控在系统性红斑狼疮(systemic lupus erythematosus,SLE)发病机制中的作用.用流式细胞仪(FCM)检测PBMC凋亡百分率及T细胞亚群的凋亡状态;用RT-PCR检测PBMC bcl-2和bax的mRNA表达;用FCM检测凋亡相关基因bcl-2,bax,fas,p53和c-myc的蛋白表达.结果显示,SLE患者PBMC凋亡百分率明显高于正常人,且活动期患者高于非活动期患者.SLE活动期患者CD4+,CD8+T细胞数明显低于正常人;非活动期患者CD8+T细胞数明显低于正常人,而CD4+T细胞数与正常人比较无统计学差异;SLE患者PBMC bcl-2和bax mRNA表达与正常人比较无统计学差异;SLE患者PBMC bcl-2,bax和fas蛋白表达明显高于正常人,p53和c-myc蛋白表达在各组之间无统计学差异.SLE患者PBMC凋亡百分率增高、外周血T细胞亚群的异常及bcl-2,bax和fas蛋白表达增高,在SLE发病机制中可能起了一定的作用.  相似文献   
33.
One of the main problems in the culture of Chinese Hamster Ovary (CHO) cells continues to be the inability to maintain the viability of the cultures over an extended period of time. The rapid decline in viability at the end of the culture is exacerbated by the absence of serum. In trying to reduce the extent of death in these cultures, we first tried to determine the mode of death. We found that more than 80% of the cells in a standard serum‐free batch culture of CHO cells in suspension died via apoptosis—as evidenced by condensed chromatin and the appearance of a characteristic DNA ladder. Furthermore, when protein synthesis was inhibited using cycloheximide, the cells underwent rapid apoptosis indicating that death proteins were present in greater abundance than survival proteins in our CHO cells. Cell lysate from CHO cells showed evidence of cysteine protease (caspase) activity. Caspases of the Interleukin‐1‐β‐Converting Enzyme (ICE) family, e.g., CPP32, Mch‐1, etc., have been implicated in the apoptotic process. Surprisingly, a caspase peptide inhibitor, N‐benzyloxycarbonyl‐Val‐Ala‐Asp‐fluoro‐methyl‐ketone (z‐VAD.fmk), was unable to substantially extend the life of a serum‐free batch culture of CHO cells. In addition, z‐VAD.fmk was only marginally able to extend viability in response to withdrawal of growth and survival factors, insulin and transferrin. In both these instances, z‐VAD.fmk was able to prevent cleavage of caspase substrates, but not protect cells from death. However, we found that bcl‐2 expression was able to significantly extend viabilities in CHO batch culture. Bcl‐2 expression also substantially extended the viability of cultures in response to insulin and transferrin withdrawal. These results provide interesting insights into the pathways of death in a CHO cell. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 62: 632–640, 1999.  相似文献   
34.
In the present study, the prognostic impact of factors involved in the apoptosis pathway were tested on 67 consecutive patients treated with surgical resection. Included in the study were all patients resected for pancreatic adenocarcinoma from 1988 to 2003. Expression analysis for p53, Bax, and Bcl-2 were performed by immunohistochemical staining. Apoptotic cells were identified by the TUNEL method. These data were correlated with survival. Sixty-seven tumor specimens were included in the study. A strong positive correlation was recorded between p53 overexpression and Bax expression levels (P < 0.001). By univariate analysis, overall survival seemed to be improved with Bcl-2 and Bax expression (respectively, P = 0.0379 and 0.0311). The median survival time in patients with low apoptotic index was better versus those with a high index (P = 0.0127). Lymph node involvement was the only clinico-pathologic parameter that significantly correlated with overall survival (P = 0.0202). By a multivariate Cox regression analysis, the only immunohistochemical parameter that influenced overall survival was the apoptotic index (P = 0.040). Tumor's overexpression of both Bax and Bcl-2 resulted the strongest independent prognostic factor (P = 0.013). This is the first study to report a statistically significant association of apoptosis to overall survival for pancreatic cancer patients treated with surgical resection. The contemporary overexpression of Bax and Bcl-2 represents the strongest prognostic factor.  相似文献   
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 以RT PCR法从大鼠脑组织中克隆bcl XL 基因 ,将其定向插入带rep cap基因和neu基因的三功能腺相关病毒 (AAV)载体 ,转染HeLa细胞并以G4 18筛选 ,然后用腺病毒感染筛选后的细胞克隆 ,包装成重组腺相关病毒 .用带rep cap基因的C12细胞筛选和滴定产生重组腺相关病毒的细胞克隆 ,粗制细胞裂解物中病毒滴度最高只有 3× 10 5IU ml.从产病毒量较高的克隆大量制备重组病毒 ,经肝素柱高压液相亲和层析法纯化、浓缩病毒后获得了高达 4× 10 11IU ml的重组病毒 .为研究脑缺血动物模型中BCL XL 的抗脑细胞凋亡作用打下了基础  相似文献   
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38.
Qin XQ  Sun XH  Luo ZQ 《生理学报》1999,51(4):419-424
为探索肺内调节血管活性肠肽(VIP)和表皮生长因子(EGF)抗氧化保护的基因机制,用逆转录聚合酶链式反应(RT-PCR)及Southemblot杂交等方法检测的代培养的兔支气管上皮(BEC)内bcl-2和c-myc基因的表达中加入去甲肾上腺素观察VIP、EGF热应激对这两个基因表达的影响。结果显示:(1)基基础情况下BEC内有bcl-2和c-myc基因的低水平表达;(2)EGF和VIP明显增强bc  相似文献   
39.
采用免疫组织化学与原位杂交方法检测了25例急性髓系或淋巴系白血病骨髓活检组织及6种白血病细胞株中bcl-2蛋白及其mRNA水平。结果21例白血病标本中存在bcl-2蛋白及其mRNA的一致性高表达;5种白血病细胞株(CEM、Raji、HL-60、U937及K562)均能表达一定水平的bcl-2蛋白及其mRNA(Molt-4例外)。提示bcl-2基因的功能状态与淋巴造血系统肿瘤密切相关。  相似文献   
40.
探讨蛋白酶ICH1 与凋亡基因bcl2 的关系及在鼻咽癌发生中的作用。应用免疫组化方法对46例鼻咽癌组织中ICH1 (ICH1L和ICH1S) 和bcl2 的表达进行观察。结果发现11 例良性病变中2 例ICH1L阳性, 1 例ICH1S阳性。46 例鼻咽癌中16 例ICH1L阳性, 22 例ICH1S阳性, 阳性率分别为348% 和478% , 各组织学分型间无明显差异(P> 005)。癌细胞ICH1 表达较良性病变增加, 但ICH1L与良性病变比较无显著性差异 (P> 005)。良性鼻咽上皮bcl2 阴性。46 例鼻咽癌中38 例bcl2 阳性, 阳性率为826% , bcl2 表达与组织分型也无明显关系 (P> 005)。ICH1L与bcl2 呈反向表达关系。提示ICH1 和bcl2 表达异常可能与鼻咽上皮的癌变有关。bcl2 对ICH1L表达可能有影响。  相似文献   
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