core DNA
- 网络核心DNA
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Effect of HCV envelope gene on core DNA vaccine in mice
丙型肝炎病毒包膜基因对核心基因DNA疫苗免疫应答强度的影响
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Enhancement of Immune Responses of Hepatitis B Virus Core DNA Vaccine by a Signal Peptide and a Universal Helper T Lymphocyte Epitope
信号肽和辅助性T细胞表位增强HBV核心抗原DNA疫苗诱导的免疫应答
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Construction of hepatitis B virus core antigen DNA vaccine and its immunogenic analysis
乙肝核心抗原DNA疫苗的构建及其免疫原性分析
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Construction of duck hepatitis B virus core antigen DNA vaccine and induced humoral immune response
鸭乙型肝炎病毒核心抗原DNA疫苗的构建及其诱导的体液免疫应答
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Impact to immune responses by interleukin 12 on optimized hepatitis B core antigen DNA vaccine in mice
IL-12对结构优化的HBV核心抗原DNA疫苗诱导免疫应答的影响
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Direct ex vivo kinetic and distribution analysis of CD8 ~ + T cells responses induced by hepatitis B virus core gene DNA vaccine
乙肝病毒核心抗原DNA疫苗诱导小鼠抗原特异性CD8~+T细胞动态变化和动态分布
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COM component is the technology core of Windows DNA system .
COM组件是WindowSDNA体系的技术核心。
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Furthermore , experimental data revealed that three regions of strong interactions between core histones and DNA sequences in a nucleosome .
还有实验数据揭示在一个核小体中,组蛋白和DNA相互作用有三个作用很强烈的区域。
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At 100 ~ 2 000 μ g / ml , it can remarkably decrease the level of viral core associated HBV DNA in the cytoplasm .
浓度为100~2000μg/ml时,能明显降低2.2.15细胞胞浆核心颗粒HBVdna水平;
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Anderson core facilities for DNA sequencing , peptide synthesis , nucleic acid extraction , and histopathology are supported by a grant from the US National Cancer Institute ( NCI CA-16672 ) .
安德森癌症中心的DNA测序,多肽合成,核酸提取,与病理等设施由美国国立癌症研究所(NCICA-16672)资助。
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Conclusion HCV core protein could promote DNA synthesize , cell cycle , and involves in carcinogenesis .
结论HCV核心蛋白可能通过调节某些基因的转录与表达,增加细胞DNA合成,扰乱细胞周期,进而参与致癌过程。
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This paper mainly explains the core technology of Windows DNA , MTS ( Microsoft Transaction Server ) .
本文重点讲述WindowSDNA中的核心技术MTS(微软的事务服务器)。
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Core histone around which DNA is wound plays a key role as a terminal protein of inflammatory signal transduction on gene transcription .
染色体核心组蛋白分子作为各种炎症因子和炎症信号转导的关键性终端蛋白质分子,具有基因转录开关分子的功能,其活性受组蛋白转乙酰酶/脱乙酰酶(HAT/HDAC)的调节。
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This paper is stated on the core of the Windows DNA and COM + , and for the purpose of studying C / S and B / S tight coupling . It explores the applicative systematic structure of developing N storeyes .
该文以WindowSDNA和COM+技术为核心,研究C/S与B/S紧偶合为目的,探索建设N层应用体系架构。