icos
- 网络可诱导共刺激分子;诱导性共刺激分子;诱导性免疫共刺激分子;诱导性协同刺激分子
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The role of ICOS in hematopoietic stem cell transplantation
可诱导共刺激分子在造血干细胞移植中的作用
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New Research on the Relationship Between Exercise and Th Cell and ICOS
运动与Th细胞和ICOS分子研究新进展
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Construction and identification of human ICOS extracellular domain gene recombinant adenovirus
人ICOS胞外区腺病毒载体的构建与鉴定
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And the application of RTOS make ICOS highly portable .
另外,RTOS在ICOS中的应用使得应用程序的移植变得容易,加快了开发的速度。
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As a result the potential applications of ICOS has drawn extensive attention and interesting of people .
其潜在的应用前景引起了人们的广泛关注。
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Establishment of the ICOS Transgenic Mice Model and Its Application to the Study of Schistosomiasis Japonicum
ICOS转基因小鼠模型的建立及其在日本血吸虫病研究中的应用
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B7 and ICOS mRNA expression in human colorectal carcinoma
人结直肠癌组织中B7和ICOS分子mRNA的表达
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Stable expression of ICOS / Fc in CHO cells
ICOS/Fc在CHO细胞中的稳定表达
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Influence of dendritic cells modified with ICOS extracellular region on survival of renal allografts in rats
ICOS胞外区基因修饰的树突状细胞对移植肾存活的影响
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ICOS : a new important costimulatory molecule
ICOS:一种重要的新型诱导共刺激分子
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The serum IgG and IgG1 in ICOS transgenic mice were also significantly higher than those in control .
转基因小鼠血清IgG、IgG1表达水平也均高于对照组。
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Preparation of New Co-stimulatory Molecule ICOS / GL50 and Study on Their Biological Characteristics as Well as Application
新型共刺激分子ICOS/GL50的研制和生物学特征及运用的研究
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Expression of ICOS in the liver of BXSB mice
BXSB小鼠肝脏可诱导共刺激因子的表达
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This research tries to establish the ICOS transgenic mice model and applies it to the study of schistosomiasis Japonicum .
本课题尝试建立ICOS转基因小鼠模型,将其应用于日本血吸虫病的研究。
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The role of ICOS co-stimulatory passageway on corneal transplantation rejection
ICOS共刺激通路参与角膜移植免疫排斥反应的研究
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The establishment of ICOS transgenic mice
诱导性免疫共刺激分子转基因小鼠模型的建立
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Results Three RNA interference retrovirus vectors based on bidirectional promoter were constructed and one of them can suppress ICOS expression effectively .
结果构建了针对ICOS三段序列的逆转录病毒干扰载体MIW-ICOS,并证实其中的一个干扰载体能有效抑制ICOS的表达。
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Function of ICOS / B7RP-1 costimulation in chronic allograft nephropathy of rat
ICOS/B7RP-1共刺激通路在大鼠慢性移植物失功中作用的研究
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CONCLUSIONS : The whole blood gene expression quantities of costimulatory molecules CD154 and ICOS reasonably robustly differentiated rejection patients from control patients .
结论:共刺激分子CD154和ICOS的全血基因表达量能可靠的区分排异患者和对照患者。
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The result of Western blotting showed that the dynamic changes of ICOS protein was identical with the changes of positive-cell number detected by immunohistochemistry .
Western-blotting检测结果显示,ICOS蛋白的动态变化与免疫组织化学显示的阳性细胞数量变化一致。
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Egg Granulomatous Formation of Liver and Molecule Mechanism in Transgenic Mice of Inducible Costimulatory Molecule ( ICOS ) Infected with Schistosoma Japonicum
日本血吸虫感染共刺激分子ICOS转基因小鼠免疫病理及分子机制
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Full-length of ICOS was amplified through RT-PCR from activated human T cells and the cDNA fragment was cloned into T-vector plasmid .
采用RT-PCR法从活化的人T细胞中扩增了ICOS全长基因,装入T-vector克隆载体。
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The percentage of CD28 + ICOS + cells on the peripheral blood CD4 + T cells in untreated primary patients was higher than those with disease relapse ;
初发未治疗SLE病人仅CD4+T细胞中CD28+ICOS+细胞的比例比复发病人明显升高;
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The level of ICOS expression on the peripheral blood CD45RO + cells in the untreated primary patients was higher than those with disease relapse ( P < 0 05 );
初发SLE患者CD45RO+细胞表达ICOS水平明显高于复发患者(P<005);
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Objective To investigate the expression of inducible co-stimulator ( ICOS ) on T lymphocytes in peripheral blood from the patients with systemic lupus erythematosus ( SLE ) .
目的探讨可诱导共刺激分子(ICOS)在系统性红斑狼疮(SLE)患者外周血T淋巴细胞的表达。
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Objective To construct retrovirus vectors expressing siRNA for ICOS by bidirectional promoter RNA interference techno - ( logy ), and study its suppressing effect on ICOS .
目的应用双向启动子技术构建针对共刺激分子ICOS的逆转录病毒干扰载体,观察其对ICOS表达的影响。
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Immunohistochemical staining was performed using polyclonal antibodies to ICOS on the sections of the spleen which were obtained from the rats in immune group at the 7th , 12th , 15th and 21st days after immunisation respectively .
免疫组大鼠分别于免疫后第7、12、15、21天被处死,摘除其脾脏后制作冰冻连续切片并提取组织蛋白。
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It is well-accepted that GL50 / ICOS signal pathway plays a pivotal role in the regulation of inflammatory responses , in the prevention of transplantation rejection and tumor development , as well as in the modulation of autoimmune diseases .
目前的研究业已证明:GL50-ICOS信号途径在机体炎症、自身免疫性疾病、肿瘤和移植排斥等免疫应答过程中发挥着重要的调节作用。
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To investigate the characteristics and biological functions of ICOS expression as well as its inherent relationships to such factors as stress response and T-cell activation at cell level by means of incubation of T-cells of healthy adults peripheral blood cells in vitro . 2 .
研究目的:1、通过普通健康人外周血T细胞的体外实验,研究和探讨ICOS分子的表达特征及生物学功能,从分子水平揭示应激激素、T细胞活化、ICOS分子表达之间的内在联系。
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Conclusions ICOS-2394C / T , - 2119C / T and CD_ 24 E2 + 226C / T polymorphisms are related with MS in Chinese Han people , either ICOS or CD_ 24 or both being one of the genes susceptible to MS or linking with susceptible genes .
结论中国汉族人群ICOS-2394C/T、ICOS-2119C/T及CD24E2+226C/T多态性与MS发病相关,两基因可能均是MS的易患基因或与易患基因相连锁。