sometimes uses market index futures to hedge out systematic (market) risk.

hepatocyte growth factor gene therapy attenuates liver fibrosis induced by bile duct ligation

肝细胞生长因子基因治疗减轻胆管结扎肝纤维化的实验研究

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the discovery of cpps sheds bright light on the use of biomacromolecules in treating diseases. it has a very good applicable prospect in such research fields as cytobiology, gene-therapy, drug transduction in vivo, evaluation of clinical medicine and medical immunology.

CPPs的发现为生物大分子用于疾病治疗带来了曙光，在细胞生物学、基因治疗、药物体内转运、临床药效评价及细胞免疫学等研究领域均具有良好的应用前景。

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results: hgf gene therapy markedly attenuated collagen deposition, as showed by masson-trichrome staining and immunofluorescence staining of collagen ⅰ,ⅲ in the peri-biliary region.

结果：肝细胞生长因子基因治疗能显著减少胆管周围胶原的沉积，表现在：肝胶原染色（Masson-Trichrome染色）减少；胆管周围Ⅰ型和Ⅲ型胶原的免疫荧光染色减少。

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in recent investigations, cell transplantation and gene therapy have been the most prospective way, but it is important to be resolved to explore the sources of ideal transplantation cells.

近年开展的细胞移植及基因治疗提供了最可能根治PD的方法，是PD治疗的研究热点。而选择理想的移植替代来源至关重要。

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cell-transplanting and gene therapy are new therapies to cure pd and prove effective, their short-time effect is definitely but long-time effect is not significant.

细胞移植和基因治疗是治疗PD的新方法，已显示一定的治疗效果，短期疗效明确，但长期疗效不显著。

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the adult bone marrow derived msc is useful in bioengineering, cell and gene therapy;

成人骨髓MSC在组织工程、细胞治疗、基因治疗等领域具有广阔的临床应用前景；

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these characteristics of mscs make them ideal engineering cells in cell and gene therapies.

这些特性使MSCs成为在细胞治疗、基因治疗中有效发挥作用的理想工程细胞。

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the experimental study of ct-guided hepatocyte growth factor gene therapy for cerebral ischemic diseases

CT导引下肝细胞生长因子基因治疗脑缺血的实验研究

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in this study, stable and highly repetitive rabbit models of unilateral mandibular distraction osteogenesis were successfully established which were suitable for high-volume animal experiments and would provide a good experimental platform for cell and gene therapy. 3.

本实验成功建立了稳定的兔单侧下颌骨牵张成骨的动物模型，重复性高，适合大批量动物实验，为细胞和基因治疗提供了良好的实验平台。

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shoukhrat mitalipov, director of the oregon health& science university's center for embryonic cell and gene therapy, reportedly led the new research.

据报道，俄勒冈卫生科学大学胚胎干细胞与基因治疗中心主任舒赫拉特？米塔利波夫是这项新研究的领头人。

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objective: to study the mechanism of exogenous eukaryotic gene expression and the possibility of keratinocytes as a target of gene therapy.

目的：探讨外源性基因真核表达的机理及角朊细胞作为基因治疗靶细胞的可能性。

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objective: to study systematically the role of skeletal muscle cells in synthesizing, processing and secreting recombinant proteins in vitro.

目的：研究骨骼肌细胞作为基因治疗靶细胞，其合成、加工和分泌外源性蛋白质的功能。

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objective to evaluate the feasibility of oral cytokine gene therapy against tumor using live attenuated salmonella as a vector.

目的探讨以减毒鼠伤寒沙门氏菌为载体的口服细胞因子基因治疗防治小鼠肿瘤的可行性。

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application of cationic liposome adeno associated virus based plasmid complexes for gene therapy of hepatocellular cancer

阳离子脂质体&病毒增强质粒复合物在肝细胞癌基因治疗中的应用

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genetic treatment of tumor with cytokines

肿瘤的细胞因子基因治疗

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experimental study of gene therapy for colon cancer by replication-defective recombinant adenovirus harboring human endostatin

复制缺陷型重组腺病毒介导人内皮细胞抑制素基因治疗结肠癌的实验研究

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study of suicide gene therapy controlled by a novel chimeric promoter for lung cancer cells

新型嵌合启动子介导的肺癌细胞自杀基因治疗的研究

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meanwhile, we also searched the cnki full-text database for the same articles published between january 2000 and june 2006, with the key words of "marrow mesenchymal stem cells, gene therapy, gene vector" in chinese.

同时检索中文CNKI全文数据库2000-01/2006-06与骨髓间充质干细胞在基因治疗中研究进展相关的文章，检索词为“骨髓间充质干细胞，基因疗法，基因载体”，并限定文章语言种类为中文。

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the vhl gene may be useful as a marker gene for the diagnosis of rcc and as a target gene for molecular therapy.

VHL基因可作为临床诊断指标，并可望成为肾透明细胞癌基因治疗的重要目的基因。

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conclusions these findings showed that nscs engineered to release il-12 could have a strong anti-tumor effect. neural stem/ precursor cells could be useful vectors in genetic approaches to brain tumors.

结论表达IL-12的NSCs有很强的抗肿瘤效果，神经干细胞是基因治疗的良好载体。

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