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Titlebook: DNA Methylation and Cancer Therapy; Moshe Szyf Book 2005 Springer-Verlag US 2005 DNA.Expression.Microarray.Purine.enzymes.gene expression.

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書目名稱DNA Methylation and Cancer Therapy
編輯Moshe Szyf
視頻videohttp://file.papertrans.cn/261/260157/260157.mp4
概述DNA Methylation and Cancer Theraphy focuses on cancer therapy by thoroughly dissecting the basic principles of DNA methylation in cancer from molecular mechanisms to clinical trials..The chapters are
叢書名稱Medical Intelligence Unit
圖書封面Titlebook: DNA Methylation and Cancer Therapy;  Moshe Szyf Book 2005 Springer-Verlag US 2005 DNA.Expression.Microarray.Purine.enzymes.gene expression.
描述NA methylation has bewildered molecular biologists since Hotchkiss discovered it almost six decades ago (Hotchkiss RDJ. Biol Cem 1948; 175:315-332). The fact that the chemical structure of our D genome consists of two components that are covalently bound, the genetic information that is replicated by the DNA replication machinery ana DNA methylation that is maintainea by independent enzymatic machinery, has redictably stimulated the imagination and curiosity of generations of mo- Edular biologists. An obvious question was whether DNA methylation was a bearer of additional information to the genetic information and what was the nature of this information? It was tempting to speculate that DNA me- thylation applied some form of control over programming of the genome s expression profile. Once techniques to probe the methylation profile of whole genomes as well as specific genes became available, it became clear that DNA methylation patterns are gene and tissue specific and that patterns of gene expression correlate with patterns of methylation. DNA methylation pat- terns emerged as the only component of the chemical structure of DNA that exhibited tissue and cell specificity. This da
出版日期Book 2005
關(guān)鍵詞DNA; Expression; Microarray; Purine; enzymes; gene expression; gene therapy; protein; proteins; transcription
版次1
doihttps://doi.org/10.1007/b139080
isbn_softcover978-1-4419-3416-1
isbn_ebook978-0-387-27443-0
copyrightSpringer-Verlag US 2005
The information of publication is updating

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DNA Methylation in Urological Cancers,s has been described. In contrast, methylation of repetitive sequences is often diminished, resulting in decreased overall methylation levels (“global hypomethylation”). Altered imprinting is also found. Testicular tumors are derived from more or less immature germ cells whose methylation patterns t
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CpG Island Hypermethylation of Tumor Suppressor Genes in Human Cancer,methylation of CpG islands of tumor suppressor genes associated with their transcriptional silencing. The target genes are distributed in all cellular pathways (apoptosis, DNA repair, cell cycle, cell adherence, etc.). They are “classical” tumor suppressor genes with associated familial cancers (BRC
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Identifying Clinicopathological Association of DNA Hypermethylation in Cancers Using CpG Island Micility as molecular markers for cancer diagnosis. Here we describe a microarray-based technique, called differential methylation hybridization (DMH), for simultaneous screening of methylation alteration across thousands of CpG island loci in one tumor sample at a time. We also describe a second appro
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Regulation of DNA Methyltransferases in Cancer,aintaining the cell’s methylation pattern, as well for transcriptional repression through both methylation dependent and independent mechanisms. It is therefore fitting that the cell has evolved a number of layers of regulation to manage the appropriate expression of the DNMTs. While transcriptional
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