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The inward current in OHCs was totally inhibited after the superfusion of 100μmolIL and 200μmo1/L linopirdine respectively. The outward rectifier K(superscript +) current I(subscript K was the dominant K(superscript +) current in the whole cell currents in Deiters' cells. In the presence of 200μmol/L linopirdine, the current was not significantly affected.

在细胞外液中,加入100μmol/L利诺吡啶后,OHCs中的四乙基二乙胺敏感的钾电流峰电流成分被抑制,稳态电流幅值减小,且电流的失活时间常数明显延长;在细胞外液中加入100μmol/L利诺吡吮后,OHCs的内向性钾电流I被完全抑制;而细胞外液中利诺吡啶终浓度为200μmol/L时,Deiters 细胞的外向整流性钾电流幅值无明显变化。

Objective To observe the pathological changes and investigate the hepatocyte apoptosis relating with CYP2E1 in alcoholic liver diseaseof rat. Method the Model of Alcoholic liver Disease: Rats were randomly divided into model group(n=37)and control group(n=33). The dose of 40%ethanol was administerd at 8g/kg body weight by garage twice daily for 8 weeks in model group, and control group was received isovolume saline by gavage. End of 8th week, the activities of serum ALT and AST were detect by autobiochemistry instrument. The pathological changes of liver was observed under light microscope after HE staining, hepatocyte apoptosis was detected by the TUNEL method.

目的: 研究酒精性肝病细胞凋亡程度与细胞色素P4502E1表达的关系方法:用酒精灌胃法制备大鼠酒精性肝病模型,将70只wistar大鼠随机分为正常对照组(33只)和酒精灌胃组(37只),连续灌胃8周后病理切片观察细胞凋亡程度,干化学法测定ALT、AST的含量变化,用PCR法测定细胞色素P450 2E1的表达变化。

But there are few or no visible F-actin ring of blocking proteinase being released in MC of tryptase and chymase immunoreactivity MC(subscript TC and MC of chymase immunoreactivity MC(subscript C. Cell appearance was inflated and intracellular proteinase had been released.

而类胰蛋白酶和类糜蛋白酶免疫反应性的肥大细胞及类糜蛋白酶免疫反应性的肥大细胞内少见或未见明显的阻碍蛋白酶释放的丝状肌动蛋白环;细胞形态膨胀,细胞内蛋白酶已释放。

Based on these previous work, in this research, in order to explore the the molecular mechanism of enhanced tumor cell immunogenicity treated by elemene and mytomycin C compositely, we used murine Hca-F ascitic hepatic carcinoma ( high lymphatic metastasis substrain of H22) as an experimental model to compare the immunoprotective effects on Hca-F cells as well as the mechanism of the effects caused by HSP70-peptide complex purified from untreated tumor cells, EC-TCV and BCG; We studied the mechanism of increased tumor cell membrane HSP expression treated with elemene by the techniques of RT-PCR and immunoelectron microscopy; In order to deeply elucidate the antitumor effects and the molecular mechanism of elemene in increasing tumor cell immunogenicity we analyzed and compared the effects of elemene and heat shock on the gene expressions of tumor cell using gene expression profile chip.

本论文在上述研究成果的基础上,选择小鼠肝癌H22的高淋巴道转移亚系Hca-F为模型,进一步比较了未处理肿瘤细胞来源、榄香烯复合瘤苗来源的和卡介苗来源的HSP70-肽复合物对Hca-F的免疫保护效应、效应机制,探讨榄香烯-丝裂霉素复合处理增强肿瘤细胞免疫原性的分子机制;以Hca-F和人肝癌细胞株HepG〓等为模型研究了榄香烯处理增强肿瘤细胞膜热休克蛋白表达的机制;以HepG〓为模型用表达谱基因芯片研究比较了榄香烯与热休克处理对肿瘤细胞基因表达的影响,从而进一步阐明榄香烯抗肿瘤作用及增强肿瘤细胞免疫原性的分子机制。

The outward rectifier K+ current current was the dominant K+ current in the whole cell currents in Deiters' cells. In the presence of 200μ M linopirdine, the Ik current was not significantly effected. Our findings demonstrated that the KCNQ heteromeric or homomeric potassium channel may be the molecular basis for the peak outward K+ current and testified that the inward IKn current is mediated by KCNQ potassium channel.

在细胞外液中,加入100 μmol/L利诺吡啶后,OHCs中的四乙基二乙胺敏感的钾电流峰电流成分被抑制,稳态电流幅值减小,且电流的失活时间常数明显延长;在细胞外液中加入100 μmol/L和200 μmol/L利诺吡啶后,OHCs的内向性钾电流IKn被完全抑制;而细胞外液中利诺吡啶终浓度为200 μmol/L 时,Deiters细胞的外向整流性钾电流幅值无明显变化。

At histopathologic analysis, neuronal tumors are usually classified as pure neuronal cell tumors (gangliocytoma, Lhermitte-Duclos disease , central neurocytoma) and mixed neuronal-glial tumors (ganglioglioma, desmoplastic infantile ganglioglioma, dysembryoplastic neuroepithelial tumor, ganglioneuroma).

根据组织病理学的分析,神经元肿瘤通常被分为:单纯的神经元细胞肿瘤(神经节细胞瘤,Lhermitte-Duclos 病〔发育不良性小脑神经节细胞〕瘤),中枢神经细胞瘤)和混合性的神经元-胶质肿瘤(神经节神经胶质瘤,成结缔组织性婴儿节细胞胶质瘤,胚胎发育不良性神经上皮瘤,神经节瘤)。

This review focuses on the current research progress of the liver cell differentiation source, and it also discusses the advantages and disadvantages of various hepatic stem cells and nonhepatic stem cells, expecting to provide a reference for liver cell source selection during tissue engineering, an adequate and suitable source for bioartificial liver and hepatocyte transplantation and to help to treat liver diseases.

本文着重论述了目前肝脏细胞的分化来源研究进展情况,并对各种肝源性和非肝源性干细胞的优缺点进行了讨论,以期为肝组织工程选择细胞来源提供参考,为生物人工肝、肝细胞移植提供充足、合适的细胞来源,协助治疗肝脏疾病。

Results: Human stem cells were successfully transplanted into 6 fetal sheep and 5 lambs were born and lived. PCR analysis showed that there was human derived cell engraftment in the liver of the 5 lambs. Immunohistochemical staining and ISH with Alu probe showed human derived hepatocytes in the lobes or around periportal area, expressing albumin and CR18. Alu ISH also showed there were positive cells in the epithelia of bile duets.

结果:在移植的 6 只胎羊中,5 只顺利生产;PCR 检测显示 5 只实验羊肝脏组织中均有人源性细胞的嵌合:免疫组化及 Alu 探针原位杂交显示人源性细胞分布於门管区周围和肝小叶中,表达白蛋白、CK18 等肝细胞分化标志;Alu 探针阳胜细胞也分布於胆管上皮中。

He experiment results indicate that (1) The extract of Rubia Cordifolia L has the effects of anti-proliferation and inducing APO;(2) Whenadministrating with 5-fu, the extract of Rubia Cordifolia L obviously enhanced the effects of anti-proliferation and inducing APO of 5-fu;(3) The basement of molecular biology of the extract of Rubia Cordifolia L for inducing APO of MGC-803 cells is correlated with inhibiting the expression of bcl-2 of anti-apoptosis gene.

UNEL法与PCNA的免疫细胞化学法的结果:0.2、0.4、0.8、1.0mg/ml浓度的茜草提取物与2、4、8、16μg/ml浓度的5-Fu,分别诱导细胞凋亡和抑制细胞增殖,表现出浓度、时间依赖性关系,除个别浓度与个别时间之间无显著性差异(P>0.05)外,不同浓度与不同作用时间之间均有显著性差异(P<0.05或P<0.01),并且两种药物联合使用时,MGC-803细胞的APO%显著提高,降低PCNA的阳性表达率(P<0.05或P<0.01)。

Result: Schwann-like cells disperse in the hole of nerve graft at oneweek under Scanning Electronic Microscope, the processes of thesatellite-like cells adhere to the wall of graft.There was no statisticaldifference of activity of cells in both group(P>0.05) using MTT. At 12weeks,the result of appearance, histology and TEM were similar, therewere no statistical difference in SFI%, NEP and quantitative analysis ofrecovery rate of myelinated fiber populations, diameter of myelinatedfiber and thickness of myelin sheat.

结果:1w后扫描电镜下可见接种的类Schwann细胞分散在材料表面的孔隙内,细胞形态为星状,细胞突起与支架管壁粘附;MTT法测定细胞活性示神经支架组在各时间点与对照组无显著性差异P>0.05;12w时两组动物坐骨神经外观、组织学光镜观察、透射电镜观察结果相似、两组坐骨神经功能指数恢复率、神经电生理、再生有髓神经纤维计数恢复率、神经纤维直径恢复率、髓鞘厚度恢复率等指标相比无显著性差异(P>0.05)。

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