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Titlebook: Genomic Mosaicism in Neurons and Other Cell Types; José María Frade,Fred H. Gage Book 2017 Springer Science+Business Media LLC 2017 FISH.n

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书目名称Genomic Mosaicism in Neurons and Other Cell Types
编辑José María Frade,Fred H. Gage
视频video
概述Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
丛书名称Neuromethods
图书封面Titlebook: Genomic Mosaicism in Neurons and Other Cell Types;  José María Frade,Fred H. Gage Book 2017 Springer Science+Business Media LLC 2017 FISH.n
描述.This volume presents methods for the analysis of genomic variability in vertebrate neurons and broadens our knowledge in the ways we understand the brain and its neurons. The chapters in this book are divided into 5 parts, and cover the following topics: principles and approaches for discovery of somatic mosaicism in the brain, aneuploidy and ploidy variation, DNA copy number variation, LINE-1 retrotransposition, and genetic and genomic mosaicism in aging and disease. In .Neuromethods. series style, chapters include the kind of detail and key advice from the specialists needed to get successful results in your laboratory..Cutting-edge and authoritative, .Genomic Mosaicism in Neurons and Other Cell Types. is a valuable resource for learning about the latest techniques for the analysis of genome and genetic mosaicism in vertebrate neurons..
出版日期Book 2017
关键词FISH; neuronal aneuploidy; Flow cytometric; cytometry; somatic L1 insertions
版次1
doihttps://doi.org/10.1007/978-1-4939-7280-7
isbn_softcover978-1-4939-8440-4
isbn_ebook978-1-4939-7280-7Series ISSN 0893-2336 Series E-ISSN 1940-6045
issn_series 0893-2336
copyrightSpringer Science+Business Media LLC 2017
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Giant Cell Reparative Granulomation, some populations of vertebrate neurons can also show double the normal amount of DNA, a condition referred to as somatic tetraploidy. These neurons are generated during early stages of development, as they migrate to their adult locations in the adult nervous system, and constitute subpopulati
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Poor-Prognosis Germ Cell Tumoursution of neurons with DNA content variation (DCV) in the context of preserved tissue architecture. The method had been optimized for DNA quantification of identified neurons but could easily be adapted to other tissues. It had been validated against chromogenic in situ hybridization (CISH) with chro
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Steven P. Rowe,Yafu Yin,Michael A. Gorins to isolate neuronal nuclei from human brain and identify megabase-scale copy number variants (CNVs) in single nuclei. The approach detailed herein includes use of CellRaft technology for single-nucleus isolation, the PicoPLEX approach to whole-genome amplification and library preparation, and a po
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R. Curtis Ellison,Peter F. Cohned to examine the genome at single-cell resolution. Here we describe the recent progress in the development of single-cell whole-genome amplification methods and the state of art for analyzing one of the major forms of genomic variations—copy number of variations (CNVs). Robust detection of CNVs in
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G. Schley,W. Hengstebeck,K. D. Bockwn to cause particular neurodegenerative diseases. We developed a dNTP-limited, competitive PCR technique to identify relative copy number differences between a reference and one or more target genes. Suitable fragments with single melting domains, well-separated melting temperatures, and no common
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