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淋巴细胞

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The recombinant pcDNA3-EBA175/HRPⅡ and pcDNA3-Pfs25 were injected alone or mixedly into mice by intramuscular way respectively. The kinetic changes of IgG antibody value, the splenic lymphocyte proliferation, the ratio of CD4+/CD8+ subgroups and NK cell killing activity in each group were observed.

将恶性疟原虫FCC-1/HN株重组质粒pc DNA3-Pfs25及pcDNA3-EBA175/HRPⅡ经骨骼肌途径分别单独注射或两者混合注射免疫BALB/c小鼠,观察免疫后不同时间点血清中IgG抗体滴度、脾淋巴细胞增殖反应、CD4+/CD8+ T细胞亚群比值和NK细胞杀伤活性的变化。

2B8a was weakly reactive to neutrophils (23.72%) and negative for T cells, NK, DC, RBC and Plt. The antibody reacted to all 3 marrow CD34+ cells with an average positive rate of 39.33% while it was negative for G-CSF-mobilized CD34+ peripheral blood stem/progenitor cells (PBSC, 1.25%). Cell line analysis showed that the antibody notably reacted to three out of 4 cell lines (Raji, SMS-SB, Nalm-6 and Nall-1) with the positive rates of 98.78%, 98.61%, 94.93% respectively and weakly to one of them with 5.68% in B lineage cell lines and monoblastic cell line (U937, 67.78%) while it was only weakly positive or negative for other myeloid leukemia cell lines including Meg01 (33.40%), HL-60 (29.70%),K562 (28.19%), KG1a (16.23 %) and HEL92.1.7 (8.02%). Among 4 T lineage leukemia,5 neuroblastoma and 1 colon cancer cell lines tested, only Molt-3 was found weakly positive (31.40%) for 2B8a, while the remaining 3 T cell lines (Molt4, JM and CCRF-CEM), 5 neuroblastoma cell lines (LA-N1, KCNR, BE, SK-N-SH, SK-N-AS) and the colon cancer cell line (HR8348) tested were negative.

结果表明: 2B8a抗原在外周血B细胞上表达(3/3例,平均阳性细胞数为26.29 %),而在T淋巴细胞和NK细胞上不表达(0/3例);在粒细胞和单核细胞上阳性表达均为2/3例,平均阳性细胞数分别是23.72 %和59.84 %;在DC细胞、红细胞和血小板上均不表达(0/3例)。2B8a抗原在骨髓CD34+细胞上的阳性表达是3/3例,平均阳性细胞数39.33 %,而在G-CSF动员的外周血CD34+细胞上的阳性表达仅1/3例,平均阳性细胞数为1.25 %。2B8a抗原在B系细胞系Raji、SMS-SB、Nalm-6和Nall-1上的平均阳性细胞数分别为98.78 %、98.61 %、94.93 %和5.68 %;在T系细胞系Molt-3上的平均阳性细胞数为31.40 %,而在Molt-4、JM和CCRF-CEM 细胞上不表达;在髓系细胞系U937、Meg-01、HL-60、K562、KG1a和HEL92.1.7上的平均阳性细胞数分别为67.78 %、33.40 %、29.70 %、28.19 %、16.23 %和8.02 %;在神经母细胞瘤细胞系SK-N-SH、KCNR、BE、LAN-1和SK-N-AS细胞以及结肠癌细胞系HR8348细胞上均不表达,而在羊膜细胞系FL细胞上呈一定的阳性表达,平均阳性细胞数为45.03%。

Cell line analysis showed that the antibody notably reacted to three out of 4 cell lines (Raji, SMS-SB, Nalm-6 and Nall-1) with the positive rates of 98.78%, 98.61%, 94.93% respectively and weakly to one of them with 5.68% in B lineage cell lines and monoblastic cell line (U937, 67.78%) while it was only weakly positive or negative for other myeloid leukemia cell lines including Meg01 (33.40%), HL-60 (29.70%),K562 (28.19%), KG1a (16.23 %) and HEL92.1.7 (8.02%). Among 4 T lineage leukemia,5 neuroblastoma and 1 colon cancer cell lines tested, only Molt-3 was found weakly positive (31.40%) for 2B8a, while the remaining 3 T cell lines (Molt4, JM and CCRF-CEM), 5 neuroblastoma cell lines (LA-N1, KCNR, BE, SK-N-SH, SK-N-AS) and the colon cancer cell line (HR8348) tested were negative.

结果表明: 2B8a抗原在外周血B细胞上表达(3/3例,平均阳性细胞数为26.29 %),而在T淋巴细胞和NK细胞上不表达(0/3例);在粒细胞和单核细胞上阳性表达均为2/3例,平均阳性细胞数分别是23.72 %和59.84 %;在DC细胞、红细胞和血小板上均不表达(0/3例)。2B8a抗原在骨髓CD34+细胞上的阳性表达是3/3例,平均阳性细胞数39.33 %,而在G-CSF动员的外周血CD34 细胞上的阳性表达仅1/3例,平均阳性细胞数为1.25 %。2B8a抗原在B系细胞系Raji、SMS-SB、Nalm-6和Nall-1上的平均阳性细胞数分别为98.78 %、98.61 %、94.93 %和5.68 %;在T系细胞系Molt-3上的平均阳性细胞数为31.40 %,而在Molt-4、JM和CCRF-CEM 细胞上不表达;在髓系细胞系U937、Meg-01、HL-60、K562、KG1a和HEL92.1.7上的平均阳性细胞数分别为67.78 %、33.40 %、29.70 %、28.19 %、16.23 %和8.02 %;在神经母细胞瘤细胞系SK-N-SH、KCNR、BE、LAN-1和SK-N-AS细胞以及结肠癌细胞系HR8348细胞上均不表达,而在羊膜细胞系FL细胞上呈一定的阳性表达,平均阳性细胞数为45.03%。

Detecting the expressions of LOX-1 protein in the peripheral blood monocytic macrophages would be a useful method of predicting the occurrence of CHD.

检测外周血淋巴细胞和单核细胞LOX-1表达水平有可能作为临床上预测冠心病的方法之一。

Biological activities were assayed with human peripheral blood mononuclear cells.

以人的外周血单核淋巴细胞测定两重组蛋白的生物活性。

The content of IL-6,leukocyte,monoplast,lymphoidocyte were measurged in blood and CSS score were observed on the first day,third day,seventh day,tenth day,fourteenth day.

测定术后第1、3、7、10、14天清晨空腹外周静脉血清IL-6、白细胞总数、单核细胞、淋巴细胞和CSS 评分变化。

Although atypical lymphocytes are often present in cases of either CMV or EBV infection, the appearance of atypical lymphocytes in CMV infection may be delayed for several weeks, as appeared to happen in this case, and may persist for months.2 During the course of CMV infection in many patients, a rash develops that has been described variably as macular, papular, morbilliform, and scarlatiniform.

虽然非典型淋巴细胞的出现在两种疾病中都常见,但是在CMV 感染中可能会延迟几周出现,就如本例患者,而且可能持续数月[2]。很多病人在CMV感染病程中,皮疹形态各异,如有斑点样、丘疹样、麻疹样和猩红热样。

Results When the culture medium was supplemented with 0 .05μg/ml sodium selenite,the proliferation of transformed cells was significant ly promoted and the transformation did not change remarkably,when supplemented w ith 0.25μg/ml,the proliferation was promoted but the transformation was inh ibited,and when with 0.75μg/ml and 1.50μg/ml,the proliferation was not pro moted and the transformation was strongly inhibited.Big dose of (1.50μg/ml) sodium selenite m ade the nuclei of the untransformed lymphocytes gather together like a few grape s doing,and even caused them to fuse.

结果 在培养物中添加0.05μg/ml亚硒酸钠能显著促进转化细胞增殖;添加0.25μg/ml可促进转化细胞增殖,但显著抑制细胞转化;添加0.75μg/ml和1.50μg/ml,不仅不能促进细胞增殖,而且强烈抑制细胞转化。1.50μg/ml剂量的亚硒酸钠使非转化淋巴细胞发生葡萄状聚集甚至核融合。

Methods HPRT gene mutation frequency was examined by the technique of multinuclear cell assay.

应用多核细胞法检测外周血淋巴细胞HPRT基因突变率。

Methods Multinuclear cell assay was used to investigate the frequency of hprt locus mutation both in normal healthy people and malignant tumor patients prior to and after radiotherapy with a cumulative dose of 54~72Gy.

采用多核细胞法研究肿瘤患者及其接受放疗后外周血淋巴细胞HPRT基因位点的突变频率,并与正常人群进行对比。

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