Results 101 to 110 of about 5,276 (155)
[PINK1 suppresses colorectal cancer cell growth through epigenetic regulation of histone modifications]. [PDF]
Zhejiang Da Xue Xue Bao Yi Xue BanWang M, Luan S, Fan X, Han D, Zhu Y.
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[High-throughput sequencing in identifying somatic hypermutation in immunoglobulin heavy chain variable regions with complex clonal backgrounds]. [PDF]
Zhonghua Xue Ye Xue Za ZhiGao MG +5 more
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[Advances in targeted therapies for chronic spontaneous urticaria]. [PDF]
Zhejiang Da Xue Xue Bao Yi Xue BanZhou L, Hu C, Wang S, Zhang R.
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重组腺病毒载体Ad-LMP-1的构建及其转染 MSC后成骨活性
Zhongshan Daxue xuebao. Yixue kexue ban, 2010 【目的】 快速构建大鼠LIM矿化蛋白-1基因重组腺病毒载体,转染MSC,探讨LMP-1基因对MSC成骨分化和成骨活性的影响65377; 【方法】 从大鼠成骨细胞内提取总RNA,并设计LMP-1特异性引物进行RT-PCR,获取LMP-1基因后利用Invitrogen公司的TOPO定向克隆技术创建入门克隆pENTR/D-LMP-165377;转化TOP10细菌后,挑取阳性克隆摇菌提取质粒,入门克隆再与表达载体pAD/CMV/V5-DEST进行同源重组反应得到病毒载体pAD/CMV/V5-LMP-1 ...
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[Construction of a highly efficient HBV infection cell model based on HBV co-receptor neuropilin-1]. [PDF]
Zhonghua Gan Zang Bing Za ZhiLiu ZH, He XM, Xu KX, Yu HB, Chen J.
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Zhongshan Daxue xuebao. Yixue kexue ban, 2004 ［目的 l 构建人肝豆状核变性病ATP7B基因野生型及常见突变型的小鼠肝脏特异性表达载体 ALB-ATP7B, 为制备转基因小鼠及相关基因治疗作准备。【方法】定点突变法获取人群中常见的Arg778Leu及 Hisl069Gln两种ATP7B基因突变体，定向克隆将小鼠白蛋白启动子ALB序列及野生和突变的ATP7B基因亚克 隆至真核表达载体kbpala上， 得到可在小鼠肝脏特异性表达的人ATP7B基因正常及突变型真核表达载体 ALB-ATP7B。【结果】经测序及酶切鉴定证实， 真核表达载体ALB ...
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[The role and molecular mechanism of transcription factor EB and its target genes in multiple myeloma treatment with bortezomib]. [PDF]
Zhonghua Xue Ye Xue Za ZhiZhang RJ +8 more
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单纯疱疹病毒胸苷激酶与绿色荧光蛋白基因 真核共表达质粒的构建
Zhongshan Daxue xuebao. Yixue kexue ban, 2009 【目的】 构建含有人巨细胞病毒(CMV)调控表达的单纯疱疹病毒胸苷激酶(HSV-tk)与增强型绿色荧光蛋白(EGFP)基因真核表达质粒pCMV-TK-IRES-EGFP。【方法】 设计HSV-tk cDNA的特异引物,PCR扩增获得HSV-tk基因序列, 将PCR产物进行T载体克隆获得重组质粒pMD18T-TK,测序分析选定序列正确的克隆提取质粒,用限制性内切酶SalⅠ和BamHⅠ分别酶切pMD18T-TK和pCMV-IRES-EGFP质粒,将HSV-tk基因定向亚克隆至pCMV-IRES-EGFP载体,
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[Retrospect and Prospect of Immune Caries Prevention Research in China]. [PDF]
Sichuan Da Xue Xue Bao Yi Xue BanXu Q, Fan M.
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Zhongshan Daxue xuebao. Yixue kexue ban, 1999 目的: 构建携带人神经生长因子( hNGF)基因的真核细胞表达载体, 为应用 NGF 进行老年性痴呆(AD)等疾病基 因治疗打基础。方法: 应用基因重组技术将 hNGF cDNA 克隆到逆转录病毒载体 pLXSN 中 ,用限制性内切酶酶切分析重组质粒 pLNGFSN 中 hNGF 基因的插入方向,用 PCR、斑点杂交和 Southern 杂交对重组质粒 pLNGFSN 作进一步鉴定。结果: hNGF cDNA 已正确地克隆到逆转录病毒载体 pLXSN 中,而构建成重组逆转录病毒载体 pLNGFSN ...
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