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Titlebook: RNA Therapeutics; Function, Design, an Mouldy Sioud Book 2010 Humana Press 2010 DNA.Microarray.PCR.Transplantat.Tumor.cloning.gene expressi

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發(fā)表于 2025-3-21 19:26:28 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱RNA Therapeutics
副標(biāo)題Function, Design, an
編輯Mouldy Sioud
視頻videohttp://file.papertrans.cn/821/820203/820203.mp4
概述Collects in one single volume the most relevant RNA-based technologies, including ribozymes, RNA aptamers, and siRNAs, and mRNA-encoding therapeutic proteins.Features the translation of RNA-based ther
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: RNA Therapeutics; Function, Design, an Mouldy Sioud Book 2010 Humana Press 2010 DNA.Microarray.PCR.Transplantat.Tumor.cloning.gene expressi
描述.Central to the synthesis of proteins, the performance of catalysis, and many other physiological processes, the aberrant expression of which can be linked to human diseases including cancers, RNA has proven to be key target for therapeutics as well as a tool for therapy. In .RNA Therapeutics: Function, Design, and Delivery., expert contributors from a broad spectrum of scientific backgrounds highlight the roles that messenger RNAs and small RNAs can play in biology and medicine. While covering the five major RNA-based drugs, namely the use of ribozymes to cleave and/or correct mRNA transcript, the use of siRNA for targeted silencing of gene transcripts, the use of aptamers, like short RNA molecules, for neutralizing the protein functions, the use mRNA-transfected DCs to activate immune system against tumor cells, as well as the use of RNA to reprogram T and/or DC cell function, this extensive volume brings together the fields of coding (mRNA) and non-coding RNA such as ribozymes, RNAse P, siRNAs, and miRNAs into one convenient source. Written in the highly successful .Methods in Molecular Biology.? series format, the cutting-edge protocol chapters contain introductions to their re
出版日期Book 2010
關(guān)鍵詞DNA; Microarray; PCR; Transplantat; Tumor; cloning; gene expression; genes; hybridization; miRNAs; molecular b
版次1
doihttps://doi.org/10.1007/978-1-60761-657-3
isbn_softcover978-1-4939-6151-1
isbn_ebook978-1-60761-657-3Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2010
The information of publication is updating

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Mouldy Sioud,Lina Cekaitef these genes (Wong and Neumann, 1982; Neumann ., 1982; Potter ., 1984) has opened up new possibilities in molecular biology and genetic engineering research. Electric modification of cell membrane permeability, or “electroporation,” is believed to be the basis of the DNA entry. No less an accomplis
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Seungil Ro,Wei Yantic phenomena attributed to electroporation include rupture, reversible electrical breakdown, the transient high-permeability state, and electrical fusion. All are associated with transmembrane potentials significantly larger than cellular resting potentials. Generally, a theory of electroporation s
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Rui Song,Seungil Ro,Wei Yan recent years, dielectrophoresis has developed rapidly and its present-day field of application is broad and diverse both in inanimate and in biological systems. For example, using dielectrophoresis it may be possible to filter nonconductive liquids (Fielding ., 1975), to separate mineral powder mix
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Jet-Injection of Short Hairpin RNA-Encoding Vectors into Tumor Cells,e corresponding MDR1/P-gp protein is no longer detectable in the tumors after anti-MDR1 shRNA vector injection. Furthermore, combination of two intratumoral jet-injections of anti-MDR1 shRNA vectors with two intravenous administrations of doxorubicin is sufficient for a complete reversal of the MDR
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