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Titlebook: Antisense Research and Application; Stanley T. Crooke Book 1998 Springer-Verlag Berlin Heidelberg 1998 Anti-Sense.Antisense.Oligonuclotide

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期刊全稱(chēng)Antisense Research and Application
影響因子2023Stanley T. Crooke
視頻videohttp://file.papertrans.cn/159/158675/158675.mp4
發(fā)行地址A concise, up-to-date report on this important area
學(xué)科分類(lèi)Handbook of Experimental Pharmacology
圖書(shū)封面Titlebook: Antisense Research and Application;  Stanley T. Crooke Book 1998 Springer-Verlag Berlin Heidelberg 1998 Anti-Sense.Antisense.Oligonuclotide
影響因子Antisense technology may result in dramatic changes in the therapy of many diseases and may provide tools to dissect pharmacological processes and to confirm the roles of various genes. In this volume, progress in the understanding of antisense technology and its use in creating new drugs is discussed. Potential caveats, pitfalls and limitations of the technology are also presented. In the next few years the pace at which new molecular targets will be identified will increase exponentially as the sequencing of the human genome and of other genomes proceeds.
Pindex Book 1998
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https://doi.org/10.1007/b115596means to study various neurobiological events, antisense compounds have the potential to be used as therapeutic agents in the management of neuropsychiatric and neurodegenerative disorders. An antisense strategy to reduce the function of neuroreceptors might have a further distinct advantage over tr
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https://doi.org/10.1007/b115596r suppressers, encode proteins that are crucial regulators for both intra-and intercellular signal transduction (.;.;.;.;.;.). This conceptual framework has provided a basis for the development of novel anticancer strategies and therapeutic modalities aimed at inhibiting cancer growth either by bloc
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Antisense Medicinal Chemistry,his, certain limitations as antisense agents have become apparent. While it appears certain that PS drugs will soon become available, in order to continually improve the oligonucleotide drug class and to overcome certain limitations, structural changes to PS are required. To date, a diverse range of
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Use of Antisense Oligonucleotides to Modify Inflammatory Processes,d that it was possible to attenuate an immune response without causing generalized myelosuppression, thus identifying methods for selectively modulating an immune response. These findings, combined with our vastly increased understanding of how the immune system functions, has opened up tremendous o
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