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1.CONCLUSIONS: The abnormal expression of costimulatory molecule CD134 was well evidenced in LN.
结论 :LN患者存在CD134共刺激分子的异常表达 ;收藏指正
2.Relationship between costimulatory molecule CD80/CD86 expressing on antigen presenting cells and spontaneous abortion.
抗原递呈细胞表面共刺激分子CD80/CD86表达与自然流产的关系收藏指正
3.Major histocompatibility complex classⅡantigen and costimulatory molecule exp ression on the surface of breast cancer cells
乳腺癌细胞表面MHCⅡ类抗原和共刺激分子表达的研究收藏指正
4.The Basic and Clinical Study of Local Immune Status in Gastric Cancer and Costimulatory Molecules 4-1BBL
胃癌局部免疫状态及共刺激分子4-1BBL的基础与临床研究收藏指正
5.CONCLUSION: 4-1BB molecule could provide a costimulatory signal for activation and proliferation of CD4 + T cells and CD8 + T cells.
结论 :4 1BB分子可在CD4 + T细胞和CD8+ T细胞的活化、增殖中提供协同刺激信号。收藏指正
6.Mechanisms of Cyclosporine A and Tacrolimus Inhibiting the Expression of Costimulatory Molecule 4-1BB in Alloimmune Response after Heart Transplantation in Mice
环孢霉素A和他克莫司抑制小鼠心脏移植免疫反应中4-1BB分子的表达及其机制研究收藏指正
7.Objective To investigate the relationship between the gene polymorphism of the inducible costimulatory molecules (ICOS),CD_(28),CD_(24) and susceptibility to multiple sclerosis(MS).
目的探讨可诱导协同刺激分子(ICOS)、CD28、CD24基因多态性与多发性硬化(multiple sclerosis,MS)遗传易患性的相关性。收藏指正
8.Preparation of the agonist/antagonist monoclonal antibodies against B7 and CD28 molecules and analysis of their effects on costimulatory signals transduction
B7:CD28激发/拮抗型单抗的研制及其在共刺激信号传导中的调节作用研究收藏指正
9.B7 transfected CHO cells were used as artificial antigen presentation cells (APCs) in MLR to exclude the effects of other costimulatory molecules.
为了排除其它粘附分子的作用 ,应用联合转染DR7或 (和 )B7分子基因的CHO细胞系作为人工抗原递呈细胞 (APC)介导混合淋巴细胞反应 (MLR)。收藏指正
10.The cDNA encoding the extracellular domain of human costimulatory molecule B7 1/CD80 was cloned from human peripheral blood monocytes by using RT PCR method and sequenced by Sanger chain termination method.
用RT PCR法从人外周血单核细胞克隆了编码共刺激分子B7 1 /CD80胞外区的cDNA ,并用Sanger链终止法进行测序 .收藏指正
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