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Conclusion: Pretreatment with anti-TNF-mAb could up-regulate the expression of protein and mRNA of Bcl-2 gene.
中文意思:
结论:抗肿瘤坏死因子单克隆抗体预处理能上调Bcl-2基因蛋白及mRNA表达。


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Conclusion There is a close relationship between genome DNA polymorphism and drug resistance in Candida albicans,which will provide theoretical basis for the clinical diagnosis,treatment and epidemiological investigation. 结论白色念珠菌的基因组DNA多态性与耐药性有密切关系,该结果为白色念球菌的临床诊治及流行病学调查提供了理论依据。
Conclusion This convenient high throughput genechip method could detect several BCP and Pre-C mutant codons at the same time. 结论 该基因芯片具有便捷、高通量的特点 ,能同时检测多个BCP、Pre C突变位点。
Conclusion uPA mRNA and PAI-1 mRNA were over-expressed in ovarian cancer,and negatively correlated with the pathologic differentiation. 结论卵巢癌组织中uPA及PAI-1 mRNA呈高表达,且与卵巢癌的病理分化程度相关。
Conclusion: Apoptosis of Hela cell line is the important anticancer mechanism of CEPC and the increase of intracellular Ca2+ level might participate in the process. 结论CEPC对Hela细胞有生长抑制作用,诱导细胞凋亡是这种作用的主要形式,胞内Ca2+浓度升高可能是细胞凋亡的作用机制之一。
Conclusion: Chelex-100 assay was simple and conventional in extraction of bacteria DNA. 结论:Chelex-100法抽提细菌基因组DNA适用于对大样本牙周炎患者作细菌学检测分析。
Conclusion: Pretreatment with anti-TNF-mAb could up-regulate the expression of protein and mRNA of Bcl-2 gene. 结论:抗肿瘤坏死因子单克隆抗体预处理能上调Bcl-2基因蛋白及mRNA表达。
Conclusion: Ser125 IL-2 enhanced the function of cellular immunology and inhibited the growth of tumor. 结论:Ser125IL-2 有增强细胞免疫和抑制肿瘤生氏的作用。
Conclusion: Using recombinant plasmid pET28a(+)-GNLY/BL21(DE3)pLysS expression systems, the GNLY protein with biologic activity could be produced, and the strategy is available to prepare human GNLY in large quantity by gene engineering technique. 结论:用含重组质粒pET28a(+)-GNLY的大肠杆菌BL21(DE3)pLysS表达系统,可得到具有生物活性的重组颗粒溶素,为大批量生产提供了条件。
Conclusion:Acupuncturing pericardium channel points can effectively protect myocardial cell by regulating the contenits of ATP,ADP and AMP. 结论:针刺手厥阴心包经穴可明显改变ATP、ADP和AMP含量,保护心肌的有氧代谢,降低氧自由基的产生,从而有效地保护心肌细胞。
Conclusion:Digestion of rat spinal cord by 0.125% trypsin for 45 and 60 minutes could collect neural stem cells most effectively. 结论:0.125%胰蛋白酶37℃振荡消化45、60min可以最有效的分离大鼠脊髓来源神经干细胞。
Conclusion:Highly mixed DC/Th0 ration induced Th0 differentiation to Th1, low mixed DC/Th0 ration induced Th0 differentiation to Th2, DC regulating immunology response type were plastic which provided the basis for clinic GVHD therapy. 低比例混合时 ,诱导Th0向Th2分化。 显示人外周血DC在调控T淋巴细胞免疫应答类型上具有可塑性 ,为临床移植物抗宿主病 (GVHD)免疫干预治疗奠定基础。
 
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