查询词典 blood group

Four rats of either group were sacrificed at the day of 2,4,6,8,10, separately; the level of blood glucose and the contents of adrenocorticotropic hormone,orticosterone and adrenaline were measured as the stress markers,as well as the relative weight of the thymus and spleen.

于第2、4、6、8和10天分批处死大鼠，检测应激指标血糖、促肾上腺皮质激素、皮质类固醇、肾上腺素含量，测量胸腺和脾脏重量与体重的相对比值。

METHODS The experimental diabetic model in rats were induced by tail vein injection of STZ (30 mg/kg), and those in treatment group were given 20 mg of extract of Amomum Xanthoides for 2 weeks, then the blood glucose levels and the morphological changes in pancreatic islet 3-cells were determined to evaluate the effects of extract of Amomum Xanthoides.

方法］利用链脲佐菌素制作大鼠糖尿病动物模型，给糖尿病治疗组大鼠腹腔注射砂仁提取物20mg每日2次，共2周，观察治疗前后血糖的变化及胰岛β细胞超微结构变化。

Get high purity DCs by Cultured plastic-adherent monocytes isolated from healthy human peripheral blood with GM-CSF and IL-4 for 7 days. To observe the morphology of DCs by inverted phase contrast microscope ,electron microscope and laser confocal microscope. Analyse phenotype of DCs with flow cytometry. Investigate the endocytosis ability of DCs as a group by Horseradish peroxidase endocytosis assay. To appraise allogeneic mixed lymphocytes reaction of DCs by MTT reduction assay. Analyse the levels of IL-12 and TNF in liquids of cultured medium by ELISA and MTT reduction assay respectively. Soluble antigens of HCCs was obtained by 3 freeze-and-thaw cycles. Biological characteristics of HC soluble antigens pulsed DCs were monitored by flow cytometry. According to MTT reduction assay estimated the cell proliferation of self lymphocytes activated by HC antigens pulsed DCs. Get high purity BCG HSP 70 protein by SDS-PAGE electrophoresis and determined its biological activity with ELISA. Analyse phenotype of antigen pulsed DCs primed by BCG HSP70 with flow cytometry. By MTT reduction assay estimated the cell proliferation of self lymphocytes and the MLR of DC based vaccine. Analyse expression of HLA-DR molecule on surface of HCC lines. The IFN-γ mRNA in lymphocytes after actived by DC vaccine and the Fas-L expression on DC and DC vaccine primed lymphocytes were detected by in situ hybridization and flow cytometry respectively. Specific cytotoxity lysis of T lymphocytes and nonspecific inhibition of liquids in culture medium against HCC lines were also tested. Detect expression of hAFP on four HCC lines with Cell-ELISA. Induce apoptosis of HCCs with actinomycin-D. Interaction of DCs and apoptotic cells was observed under transmission electron microscope. Growth inhibition test of DC against HCC lines was also performed. Establish the nude mouse model bearing human HC xenografts and indentify the characteristic of tumour by histochemistry and immunohistochemistry techniques. Prevent and treat transplanted human HC on nude mouse with Freezing and anabiotic HC specific lymphocytes.

用GM-CSF和IL-4从健康人外周血诱导DC；分别用倒置相差显微镜、电子显微镜及激光共聚焦显微镜观察DC形态；流式细胞术检测DC表型；HRP吞噬实验测定DC的群体内吞能力；MTT法检测同种异体混合淋巴细胞反应；ELISA法和MTT法分别测定DC培养上清液中IL-12和TNF水平；冻融法制备肝癌细胞可溶性抗原；流式细胞术检测负载肝癌可溶性抗原后DC的生物学特性；MTT法检测DC负载肝癌抗原后对自身淋巴细胞增殖的影响；SDS-PAGE制备电泳纯化BCG HSP70并鉴定纯度，ELISA测定活性；流式细胞术检测负载抗原DC经BCGHSP 70活化后的表型；MTT法检测肝癌DC疫苗对自身淋巴细胞增殖的影响和混合淋巴细胞反应；流式细胞术检测肝癌细胞表面HLA-DR表达；MTT法检测肝癌DC疫苗对自身淋巴细胞的活化；原位杂交法检测肝癌DC疫苗活化后的淋巴细胞IFN-γmRNA表达；流式细胞术检测DC和肝癌DC疫苗活化后淋巴细胞表面Fas-L；MTT法分别检测肝癌DC疫苗活化的淋巴细胞和其培养上清对肝癌细胞的特异性杀伤和非特异性抑制作用；Cell-ELISA检测人肝癌细胞hAFP表达；MTT法检测负载AFP表位肽和凋亡肝癌细胞DC对自身淋巴细胞增殖的影响；ELISA法和MTT法分别测定活化后淋巴细胞培养上清中TNF和IL-12水平；肝癌细胞凋亡的诱导和检测；DC吞噬凋亡肝癌细胞后的电子显微镜观察；DC对肝癌细胞的生长抑制试验；人肝癌裸鼠皮下移植瘤动物模型的建立及其组织学和免疫组织化学鉴定；DC及肝癌特异性淋巴细胞预防和治疗人肝癌裸鼠皮下移植瘤；冻存和复苏后的肝癌特异性淋巴细胞预防和治疗人肝癌裸鼠皮下移植瘤。

The changes of blood flow on the antebrachium,palm and the back of the handare not significantwith in30min in control group.

不针刺对照组在30min内前臂、手掌和手背血流的自然波动较小。

In the bilateral group, the blood flow on both sides was detectable during antegrade selective cerebral perfusion.

在基底动脉环完整，存在有效侧支循环条件下，单侧灌注操作较为简便，双侧灌注在ASCP期间两侧脑灌注较为均衡，但两种灌注方法对S100蛋白浓度的影响无显著性差异。

The number of the white blood cell , the sum total of lymphocytes and the activity of T lymphocytes ANAE+ in the ataxic chicks were significantly lower than that of the control group.

脑软化雏鸡外周血中WBC数、淋巴细胞总数、ANAE阳性率均显著低于C组（P.05，P.01），说明V〓缺乏致使患雏的细胞免疫功能降低。

Result: In blood culture, Pseudomonas aeruginosa accounted for 23.5％ remained in the first place, while Staphylococcus epidermidis fell to the third place. In group 2, Gram negative bacillus accounted for 58.8％ and Gram positive coccus 29.4％. In wound culture, Pseudomonas aeruginosa ranked the top (19.5％) while Staphylococcus aureous fell to the sixth, Gram negative bacillus accounted for 73.5％, Gram positive coccus 22.2％.

结果：两组比较，血培养显示铜绿假单孢菌继续保持第一位，占23.5％，表皮葡萄球菌退居第三位，其中第二组G－杆菌占58.8％，G＋球菌占29.4％；创面培养，铜绿假单孢菌上升至第一位，占19.5％，金黄色葡萄球菌退至第6位，其中第二组G－杆菌占73.5％，G＋球菌占22.2％。5年内重要菌群G－杆菌居首位，近3年常用抗菌药物如头孢他啶等耐药性较前2年明显增加。

Blood quacks support pylon, automatic group therapy, automa...

热血江湖医生辅助外挂，自动群疗，自动疾风，自动喝红、蓝。

Then CHD group were divided into two subunits that 37 cases with normal blood lipid and 55 cases with abnormal bood lipid.

选取CHD患者92例为CHD组和健康成人40例为对照组，分别测定清晨空腹血脂水平及TNF，根据血脂水平将CHD组分为血脂正常组37例和血脂异常组55例两个亚组，比较各组间TNF和血

Results: we estalished ideal copd models in stort time. there existed the expression of nos in both the normal lung tissue and the lung tissue of copd,mainly orienrared in the cytoplasm of cell.the immunohistochemical result indicated that inos increased significantly ,in comparison with the control group, in bronchiolar mycoderma epithelial and enos remakably decreased in pulmonary blood vessel.

结果：联合应用烟熏和ppe在较短的时间内建立了较理想的copd模型；一氧化氮合酶在正常肺组织与copd的肺组织均有表达，主要定位在细胞浆内；免疫组化结果表明模型组inos在支气管黏膜上皮呈强阳性表达，肺血管enos表达明显减弱，与健康对照组比较有显著性（p.01）。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。