查询词典 conditional expression

But there are no correlations between gene expression and gene expression specificity or gene expression level.

有趣的是，基因的组织特异性和基因的表达量与基因表达的进化则可能没有相关性。

Results VEGF-C and VEGFR-3 are all expressed on both mesenchymal cells and vascular endothelium of the embryos during early period. In middle and latter period, VEGFR-3mRNA is mainly expressed on cell plasm of alimentary canal, but it has no expression on vascular and lymphatic endothelium; The expression of VEGFR-3 is extensive and positive expression is seen on the vascular and lymphatic endothelium.

在胚胎中、后期消化道组织中VEGF-C主要表达于消化管壁组织细胞以及肠系膜内，在血管和淋巴管内皮细胞则无表达；VEGFR-3亦表现为广泛的表达，于血管和淋巴管内皮细胞可见阳性表达，并随着胚胎的发育，其在淋巴管内皮细胞的阳性表达率明显增加。

In the functional mechanism, we should use the technique "use the DNA Microarray to build the gene expression difference chart" to lead to the combination of Traditional Chinese Pharmacy and gene expression difference chart to study. Meanwhile,we can establish a totally new method of screening modern Traditional Chinese Pharmacy based on the gene expression difference chart, it can really make the modernization and internationalization of Traditional Chinese Pharmacy.

在中药作用机制方面，应采用&利用基因芯片建立基因表达差异谱&技术，将中药与基因表达差异谱有机地结合起来进行研究，同时以基因表达差异谱为基础建立一种全新的现代中药筛选方法，使中药真正实现现代化、国际化。

The results of SS investigating indicated that the SS protein expression in leaf at seedling stage was high comparatively, when at jointing and heading stage, SS expression was low in leaves and stems, along with sorghum development, since flowering stage, SS expression increased sharply, decreased at dough stage.

2对SS表达检测结果表明，甜高粱苗期叶片中SS蛋白质表达量较高，拔节、抽穗期叶片和茎中SS蛋白质表达量较低，随着高粱的生长发育，开花以后叶片和茎中SS的表达量普遍升高，腊熟期略有下降。

To better understand the mechanism of sucrose accumulation, the correlation of sucrose content and sucrose phosphate synthetase、sucrose synthase expression was analyzed by monitoring the expression of SPS in leaves and stems.(1) The results of SPS investigating indicated that the sucrose content, the expression of SPS in leaves and stems were increased along with the growth of sorghum, reached the highest level at grain filling stage, and decreased at dough stage.

1对SPS表达检测结果表明，在高粱的生长发育过程中，茎中蔗糖含量、叶片和茎中SPS蛋白质表达量持续上升，灌浆期达到最高，腊熟期略有下降，它们之间的变化趋势基本一致，甜高粱茎蔗糖含量与叶片SPS蛋白质的表达相关系数为0.895，与茎SPS蛋白质的表达相关系数为0.781；甜高粱和普通高粱相比，其叶片中SPS表达量差别不明显，而甜高粱茎中SPS表达量明显高于普通高粱。

Results The activation of NF-κB, proliferation response, and expression of IL-4 and I L-5 mRNA and protein in T lymphocytes stimulated by PMA were significantly hig her than those of their blank control (P.01), while those indexes of T l ymphocytes stimulated by PMA and PDTC simultaneously were significantly lower th an those stimulated by PMA alone (P.01). The apoptotic index of T lympho cytes stimulated with PMA were significantly lower than that of their blank cont rol (P.01), and the apoptotic index of asthmatic guinea pig T lymphocytes stimulated with PMA and PDTC simultaneously were significantly higher than that stimulated by PMA alone (P.01). The significant positive correlations w ere found between the activation of NF-κB and the proliferation (r=0.64, P.001), and the expression of IL-4 and IL-5 mRNA and protein of T lymph ocytes, respectively (r=0.55-0.68, P.001). There was also signific ant negative correlation between the activation of NF-κB and apoptosis of T l ymphocytes (r=0.62, P.001). Conclusions NF-κB may participate in the signal conduction of PKC regulated proliferation, apoptosis and expression of IL-4 and IL-5 of T lymphocytes in asthma.

结果加入PMA培养的哮喘组T淋巴细胞NF-κB的活化、细胞增殖反应、IL-4和IL-5的mRNA和蛋白质的表达均显著高于其空白对照(P.01)，而同时加入PMA和PDTC培养的哮喘组T 淋巴细胞以上指标均显著低于只加入PMA培养的哮喘组T淋巴细胞(P.01)；加入PMA 培养的哮喘组T淋巴细胞的凋亡指数显著低于其空白对照(P.01)，而同时加入PMA 和PDTC培养的哮喘组T淋巴细胞凋亡指数显著高于只加入PMA培养的哮喘组T淋巴细胞(P 。01)。T淋巴细胞NF-κB的活化与增殖反应呈显著正相关(r=0.64，P.00 1)，与IL-4和IL-5的mRNA和蛋白质的表达也均呈显著正相关(r=0.55-0.68，P 。001)，而与凋亡指数呈显著负相关(r=-0.62，P.001)。

OBJECTIVE To evaluate the expression of epidermal growth factor receptor as a molecular target for oropharyngeal squamous cell carcinomas measured by automated quantitative analysis and its significance of EGFR expression, especially nuclear EGER expression in the prognosis of cancer.

目的 评价自动定量分析法(automated quantitative analysis， AQUA)测定表皮生长因子受体(epidermal growth factor receptor EGFR)在口咽部鳞状细胞癌组织中的表达水平，了解其在判定预后中的价值。

Expression patterns of genes differentially expressed in starch metabolism and cell cycle during endosperm development7 DAP kernals, 15 DAP endosperms and 25 DAP endosperms of B73, ae/wx and sh1 were used to study the expression patterns of 18 differentially expressed genes in sugar metabolism and 9 differentially expressed genes in cell cycle. We found that the expression patterns of Pul, SBEⅡa, UGPase, SUS3, SSⅡa in sh1 and Sh2-1, SUS3, SSⅡa in ae/wx were altered, revealing that these genes may interact with each other.

碳水化合物代谢基因和细胞周期基因随胚乳发育的变化以B73、ae/wx、sh1授粉后7天种子、15天和25天胚乳为材料，分析18个糖代谢差异基因和9个细胞周期调节相关的差异基因的表达模式，研究发现sh1突变体中Pul、SBEⅡa、UGPase、SUS3和SSⅡa基因表达模式发生改变，ae/wx突变体中Sh2-1、SUS3和SSⅡa基因表达模式发生改变，揭示了突变体对这些基因的巨大影响，反映了它们可能存在相互作用。

In a word, we extracted first cotyledon of buckwheat total RNA, by method of RT-PCR and 3RACE, get the C terminal cDNA sequence of PI from Ukraine buckwheat, and do some bioinformatics analyse on this cDNA sequence of PI from buckwheat, such as gene characteristics, expression mode. All of this will be help for the forward research on functional protein and high performance of procaryon expression or eukaryon expression.

综上所述，我们利用RT-PCR和3′RACE技术首次从吉乌一号甜荞第一对子叶中克隆获得荞麦蛋白酶抑制剂基因并对其基因特性、表达模式进行生物信息学分析，同时构建了该基因序列羧基端原核表达载体，为今后进一步研究荞麦功能性蛋白的分子机制及高效原核、真核表达载体的构建奠定了基础。

Cell lines were co-tranfected with bi-plasmids and cultured at 1% O〓 condition, luciferase assay demonstrated that all of the expression systems with different domains could be hypoxia-activated. GAL-CAD achieved more than 100-fold induction in A549 cell and more than 40-fold in HepG2; expression level of the system markedly increased after addition of glycin arm, almost 10-fold enhancement in HepG2 cell. Because basic expression also increased, the induction fold by hypoxia decreased.

双质粒共转染不同细胞株后，在1％O〓环境下培养24h，荧光素酶活性检测结果提示含不同结构域的表达系统均有受缺氧激活的能力，其中GAL-CAD在A549中获得100倍以上的诱导，在HepG2中获得40倍以上的诱导；加入甘氨酸臂后该表达系统的转录活性大为增强，在HepG2细胞中增强了10倍以上，但是由于基础表达也有所增加，受缺氧诱导的倍数下降。

Don not attempt to do something which you can not to do.

不要企图做那些办不到的事情。

The expression of CTGF and TNF-αweredetected by immunochemistry and the number of Clara Cells was calculated.

光镜下观察肺组织的病理变化，采用免疫组化染色观察肺组织中结缔组织生长因子和肿瘤坏死因子-α的表达和Clara细胞的数量。