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Titlebook: Differential Display Methods and Protocols; Peng Liang,Jonathan D. Meade,Arthur B. Pardee Book 2006Latest edition Humana Press 2006 DNA.Mi

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發(fā)表于 2025-3-21 18:48:49 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Differential Display Methods and Protocols
編輯Peng Liang,Jonathan D. Meade,Arthur B. Pardee
視頻videohttp://file.papertrans.cn/279/278660/278660.mp4
概述Includes supplementary material:
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Differential Display Methods and Protocols;  Peng Liang,Jonathan D. Meade,Arthur B. Pardee Book 2006Latest edition Humana Press 2006 DNA.Mi
描述Since the first edition of this book dedicated to differential display (DD) technology was published in 1997, we have witnessed an explosive interest in studying differential gene expression. The gene-hunting euphoria was initially powered by the invention of DD, which was gradually overtaken by DNA microarray technology in recent years. Then why is there still the need for second edition of this DD book? First of all, DD still enjoys a substantial lead over DNA microarrays in the ISI citation data (see Table 1), despite the h- dreds of millions of dollars spent each year on arrays. This may come as a surprise to many, but to us it implies that many of the DNA microarray studies went unpublished owing to their unfulfilled promises (1). Second, unlike DNA microarrays, DD is an “open”-ended gene discovery method that does not depend on prior genome sequence information of the organism being studied. As such, DD is applicable to the study of all living organisms—from bacteria, fungi, insects, fish, plants, to mammals—even when their genomes are not sequenced. Second, DD is more accessible technically and financially to most cost-conscious “cottage-industry” academic laboratories. So c
出版日期Book 2006Latest edition
關(guān)鍵詞DNA; Microarray; PCR; fungi; gene expression; genes; transcription
版次2
doihttps://doi.org/10.1385/1592599680
isbn_softcover978-1-61737-503-3
isbn_ebook978-1-59259-968-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2006
The information of publication is updating

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ROBOT2013: First Iberian Robotics Conferenced constitutes an independent sampling of the mRNA population. The large number of reactions performed allows the repeated sampling of the targeted polycistronic mRNA, which is clearly identified among possible false positives.
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https://doi.org/10.1007/978-3-7091-2666-0or-suppression function. p53 is a transcription factor that binds to DNA in a sequence-specific manner to activate transcription of target genes. In this chapter, we describe the application of differential display to identify p53-regulated genes.
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L. Beji,A. Abichou,P. Joli,M. Pascalkine, which we named IL-24, is a member of IL-10 family of cytokines, and it signals through two hetorodimeric receptors, whose expression is also upregulated by ras oncogenes. Thus, IL-24 and its receptors may represent a novel autocrine loop coordinately activated by ras oncogenes.
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Identification of p53-Regulated Genes by the Method of Differential Displayor-suppression function. p53 is a transcription factor that binds to DNA in a sequence-specific manner to activate transcription of target genes. In this chapter, we describe the application of differential display to identify p53-regulated genes.
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Identification by Differential Display of IL-24 Autocrine Loop Activated by Ras Oncogeneskine, which we named IL-24, is a member of IL-10 family of cytokines, and it signals through two hetorodimeric receptors, whose expression is also upregulated by ras oncogenes. Thus, IL-24 and its receptors may represent a novel autocrine loop coordinately activated by ras oncogenes.
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