Preferred target cells are epithelial cells.
优选的靶细胞为上皮细胞。
The immunoconjugate showed highiy selective cytotoxicity to target cells.
表明此偶合物在体外具有较好的选择性细胞毒作用。
Bacteria and parasites often use special toxins to perforate the membranes of target cells.
细菌和寄生虫经常利用特殊的毒素穿孔于靶细胞的细胞膜。
Results indicated that the immunoconjugate exhibited selective cytotoxicity to target cells.
结果提示，这种免疫结合物对靶细胞具有选择性细胞毒作用。
Moreover, target cells may have some 'correction mechanism' against the introduced foreign genes.
而靶细胞对对外源基因导入可能具有“纠正作用”。
Conclusion: the human fibroblast strain KMB 17 can be used as target cells in BMP 2 gene therapy study.
结论：人成纤维细胞株kmb17可以作为靶细胞用于BMP2基因疗法研究。
The cytotoxicity of effect or cells corresponded positively to the fluorescence released by target cells.
效应细胞的杀伤活性与靶细胞释放的荧光强度呈正相关性。
It is probably due to single exposure of non-target cells to formaldehyde of extremely low concentration.
推测其原因，可能与一次性、极低浓度甲醛、非靶细胞接触有关。
Structurally familiar proteins should evade attack from the immune system while on their way to target cells.
熟悉蛋白质在结构上应回避攻击的免疫系统，而就其方法的靶细胞。
In general, plant hormones are small molecules that probably act on target cells much the way animal hormones do.
通常，植物激素和动物激素相似，是作用与目标细胞的小分子化合物。
Our knowledge about the estrogen target cells and exact signaling pathways in the hair follicle is still very limited.
目前对毛囊中雌激素靶细胞和准确信号通路了解甚少。
The invention also provides compositions and methods for enhancing transduction of target cells by recombinant viruses.
本发明也提供了用于提高重组病毒向靶细胞转导的组合物和方法。
Targeted drug system can selectively be functioned in target organs, target tissues, target cells or intracellular parts.
靶向制剂可以选择性地作用于靶器官、靶组织、靶细胞或细胞内。
Application of hemopoietic stem cells included hemopoietic stem cell transplantation and as target cells for gene therapy.
造血干细胞的应用包括造血干细胞移植和作为基因治疗的靶细胞。
The therapy using BPD can sensitize the target cells or tissue, since these cells can not easily recovery from the radiation.
用苯并卟啉衍生物治疗能敏化靶细胞或组织，因为这些细胞不能轻易地从辐射中复苏。
The aim of gene therapy is to transfect DNA into target cells, in which utilizing antisense oligonucleotides is a main method.
基因治疗是将DNA转染进入目的细胞，修复遗传错误或产生治疗因子。反义寡核苷酸的应用是基因治疗的主要手段之一。
These observations provide evidence that therapy designed to target cells with lytic KSHV replication has activity in KSHV-MCD.
这些观察提供的证据表明，设计针对细胞的KSHV复制裂解疗法对K SHV - MCD有效。
So far the main hurdle has been getting RNA into the target cells, but the eye's accessibility means this is not so much of a problem.
目前为止的主要难题是如何把RNA注入到目标细胞。眼睛的可研究性意味着这不再是个难题了。
ADCC activity is an important function of the human immune system, whereby immune cells can kill target cells, e. g. cancer cells.
免疫细胞之所以能杀死靶细胞比如癌细胞，真是因为，adcc活性是人体免疫系统的一项重要功能。
Stem cells have the potential to self renew and differentiate into many cell types, so they are the ideal target cells in gene therapy.
干细胞由于具有自我更新与多向分化潜能的特性，因此是一种理想的基因治疗靶细胞。
Objective To explore a death mode of astrocytes after permanent local cerebral ischemia by observing morphologic changes of target cells.
目的动态观察大鼠持续性局灶脑缺血后星形胶质细胞的形态学变化，探讨星形胶质细胞的死亡方式。
Depend on the role of proteins, target cells were stimulated differentiation by an autocrine or paracrine manner to promote osteogenesis.
依靠蛋白质的作用，靶细胞被刺激分化，通过自分泌或旁分泌的方式促进成骨。
Structural information about the protein the virus USES to attach itself to its target cells could provide a new strategy to fight infection.
了解麻疹病毒吸附到宿主细胞所借助的蛋白结构信息，可以为抗病毒感染提供一条新的策略。
Chimeric organisms have long been created through breeding and, more recently, through the transfer of native genomes into denucleated target cells.
创造嵌入式生物体，很长时间以来是通过繁殖技术，最近一段时间，通过将自然基因组植入去除细胞核的靶细胞中来完成。
The proliferation of recombinant plasmid in packaging cells (PT67) would be studied further as well as the transducing effect to the target cells.
我们将对此重组质粒在包装细胞（PT67）的扩增以及对靶细胞转导的效应作进一步研究。
Results Artificial synthetic DNA transfer system and modified viral vectors could efficiently transfect target cells and get high level expression.
结果合成的DNA转运系统和经修饰的病毒载体体外转染靶细胞后，可获得显著表达。
The integration sites of provirus, the nature of the target cells and the structure of vectors were closely related to the stability of gene expression.
前病毒整合位点、靶细胞特性和整合后的载体结构与转入基因表达的稳定性紧密相关。
METHODS: Using CHO cells which high express human CD59 as target cells, the phage 12 peptide library was screened for 5 rounds by competitive binding test.
方法：以高表达人CD59的中国仓鼠卵巢细胞（CHO）为靶细胞，采用竞争结合试验，对噬菌体随机12肽库进行5轮亲和筛选。
METHODS: Using CHO cells which high express human CD59 as target cells, the phage 12 peptide library was screened for 5 rounds by competitive binding test.
方法：以高表达人CD59的中国仓鼠卵巢细胞（CHO）为靶细胞，采用竞争结合试验，对噬菌体随机12肽库进行5轮亲和筛选。
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