Objective To construct a recombinant adenoviral vector carrying the human BMP-2 gene which may be applicable in gene therapy. 目的构建人骨形成蛋白-2(BMP-2)基因的重组腺病毒表达载体,为应用BMP-2基因治疗的研究奠定基础。
Construction and identification of recombinant human bone morphogenetic protein-2 gene adenoviral vector 重组人骨形态发生蛋白2腺病毒载体的构建与鉴定
Experimental study of the targeting recombinant adenoviral vector in reversing the mdr hepatocarcinoma cells 靶向重组腺病毒载体逆转肝癌细胞多药耐药的实验研究
The purpose of this study is to covalently modify adenoviral capsid with chitosan, a cationic and natural polymer. 本篇研究,我们利用一个正电性的天然高分子几丁聚醣来对腺病毒外壳进行共价性的修饰。
Adenoviral Mediated HSV-TK/ GCV Suicide Gene Transfer in Treatment of Prostate Cancer Cells in Vitro 腺病毒介导的HSV-TK/GCV自杀基因治疗前列腺癌的体外实验
Construction of conditionally replication-competent adenoviral vectors targeting hepatocarcinoma and their in vitro anti-tumor effect 携带XAF1的复制型溶瘤腺病毒治疗恶性肿瘤的研究肝癌选择性溶瘤腺病毒的构建及其体外抑瘤作用
Construction and identification of the recombinant adenoviral expressing system with hepatitis B virus reverse polymerase gene 乙型肝炎病毒聚合酶基因重组腺病毒表达系统的构建和初步鉴定
Adenoviral vector systems were utilized for a variety of animal virus vaccine, and considered to be effective. 腺病毒载体是一种目前被广泛用于表现外来基因的系统。
Adenoviral Gene Transfer of Rat Insulin-like Growth Factor 1 to Rat Islet β-Cell Prevents Cell Impairment in Vitro 携有鼠胰岛素样生长因子1重组腺病毒对胰岛β细胞的保护性研究
Construction of a More Effective Conditional Replication-Competent Adenoviral Vectors Targeting Liver Cancer and Its Cancerostatic Effect in Vitro 一种更有效的肝癌靶向性条件复制型腺病毒的构建及体外抑瘤作用
This review focused on the progress in the biotherapy of HBV infection using adenoviral vector. 本文就腺病毒载体在乙型肝炎生物治疗研究中的应用作一综述。
Construction of adenoviral vector encoding Calponin-1 siRNA and its effect on human myometrium cells in vitro 调宁蛋白基因siRNA重组腺病毒载体构建及其对体外子宫平滑肌细胞的作用
Study of the Different Immune Responses between the First-generation Adenoviral Vectors and the Third-generation Adenoviral Vectors 第一代腺病毒载体和第三代腺病毒载体免疫反应差异的研究
Purification and application of adenoviral vectors in tumor gene therapy 腺病毒载体纯化及在肿瘤基因治疗中的应用
Advances in helper-dependent adenoviral vector-A review 辅助病毒依赖型腺病毒载体研究进展
Comparison of Immune Responses Induced by the First-generation and the Third-generation Adenoviral Vector by Intrathecal Injection 鞘内注射一代和三代腺病毒载体免疫反应的比较
Experimental Study of Intralipid Effects on Transgene Expression with an Recombinant Adenoviral Vector Expressing Interleukin 12 in Vivo Intralipid对重组鼠IL-12腺病毒转基因表达影响的体内实验研究
An adenoviral vector with a report gene Lac Z transferred to brain from nasal cavity of adult rats 将含有报告基因LACZ的重组腺病毒载体从大鼠鼻腔转移至脑的实验研究
Package of HBsAg-Expressing Recombinant Adenoviral Vector and It's Expression HBsAg重组腺病毒载体的包装和表达
Objective To construct recombinant human Bcl-2 adenoviral vector. 目的构建人bcl-2重组腺病毒载体。
Conclusions Adenoviral vector may successfully transduct HSV tk gene ( suicide gene) into calf lens epithelial cells. 结论腺病毒载体可将HSVtK基因转导入牛晶状体上皮细胞中;
Adenoviral vector has some properties which make it an attractive gene vector in gene therapy of HBV infection. 腺病毒载体由于其特有的一些优点在抗HBV的基因治疗中受到重视。文中就腺病毒载体在抗HBV基因治疗中的应用作了综述。
Results: The recombinant adenoviral vectors were harvested with high titer and purity. 结果:获得了高纯度、高滴度的重组腺病毒载体。
Both adenoviral vector and foreign gene are related to the liver damage. 腺病毒载体和转基因均与肝损害有关。
Objective To investigate an effective method for extraction, purification and titration of recombinant adenoviral vector. 目的探讨提取、纯化和滴定重组腺病毒表达载体的有效方法。
Objective: To clone the human and murine origin RANTES genes and construct the adenoviral expression vectors. 目的:克隆人和小鼠的活化T细胞表达与分泌调节基因(RANTES基因)并分别构建腺病毒表达载体。
Conclusion Oncolytic adenoviral vector carrying human TRAIL gene holds great promising in cancer therapy. 结论携带人TRAIL基因的肿瘤特异性增殖型腺病毒在肿瘤治疗方面有着非常广阔的应用前景。