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Application of Stem Cells in Disease and Gene Therapy

机译:干细胞在疾病和基因治疗中的应用

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Over the last two decades, a number of strategies have been devised with the aim to treat diseases with a genetic approach. Gene therapy or the genetic manipulation of nongerm line cells has emerged as one of most promising strategies for treating human diseases. There are two methods of gene therapy: direct gene therapy or in vivo and indirect gene therapy or in vitro. Both two gene transferring that are divided and are modified genetically. Stem cells have some specifications to transfer highlighted genes to patients. These include proliferation viability and renewing in long period of time and diferention to variety of host cells. The basis for gene therapy is based on treatment both genetic and multifactorial disorders like neoplasia, infectious disease and cardio-vascular disorders. Comparing to other genetics engineering fields, Stem cell gene therapy will only meet success when essential improvement developed in stem cell studies and transferred gene regulation
机译:在过去的二十年中,已经设计了许多策略,旨在通过遗传方法治疗疾病。基因疗法或非生殖系细胞的基因操作已成为治疗人类疾病的最有希望的策略之一。基因治疗有两种方法:直接基因治疗或体内和间接基因治疗或体外。这两个基因转移都是分开的,并且经过遗传修饰。干细胞具有将高亮基因转移给患者的某些规格。这些包括增殖活力和长时间更新以及对多种宿主细胞的分化。基因治疗的基础是治疗遗传性和多因素性疾病,例如瘤形成,传染病和心血管疾病。与其他遗传工程领域相比,干细胞基因疗法只有在干细胞研究和转移基因调控方面取得重大进步时才能取得成功。

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