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Conclusion The humanized antibody 813-F(ab)2 can strongly bind to the platelets of human,macaque and dog. Thus,it will provide a basis for its pharmacodynamics estimation and toxicological analysis
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结论813-F(ab)2与人、猕猴和毕格犬的血小板均有较强的特异性结合能力,为813-F(ab)2的后续药效学评价、毒理分析等提供了基础。 |
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Conclusion The inactivation of suppressor gene p16 or low expression of protein p16 was associated with the progression,the degree of cell differentiation and neck metastasis in NPC,but it was not associated with the size of primary foci.
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结论抑癌基因p16失活或p16蛋白低表达可能与鼻咽癌的发生、癌细胞的分化程度及颈淋巴结转移有关,而与鼻咽癌原发灶大小无关。 |
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Conclusion The positive rates of S100A2 protein is down-regulated in esophageal squamous cell carcinoma,which is related to the carcinogenesis,differentiation and prognosis of esophageal carcinoma.
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结论S100A2蛋白在食管鳞状细胞癌中阳性表达率下降,与食管癌的发生及分化程度有关。 |
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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.
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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。 |
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Conclusion This convenient high throughput genechip method could detect several BCP and Pre-C mutant codons at the same time.
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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。 |
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Conclusion uPA mRNA and PAI-1 mRNA were over-expressed in ovarian cancer,and negatively correlated with the pathologic differentiation.
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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。 |
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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.
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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。 |
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Conclusion: Chelex-100 assay was simple and conventional in extraction of bacteria DNA.
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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。 |
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Conclusion: Pretreatment with anti-TNF-mAb could up-regulate the expression of protein and mRNA of Bcl-2 gene.
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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: Ser125 IL-2 enhanced the function of cellular immunology and inhibited the growth of tumor.
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结论：Ser125IL－2 有增强细胞免疫和抑制肿瘤生氏的作用。 |
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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.
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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。 |
