Epigenetic methods in neuroscience research / edited by Nina N. Karpova.
Material type:
TextSeries: Neuromethods ; 105.Publisher: New York : Springer, [2015]Copyright date: ©2016Description: 1 online resource (xii, 258 pages) : illustrationsContent type: text Media type: computer Carrier type: online resourceISBN: 9781493927548; 149392754X; 1493927531; 9781493927531Subject(s): Neurogenetics | Epigenetics | Epigenomics -- methods | Medical -- Neuroscience | Neurosciences | Epigenetics | NeurogeneticsGenre/Form: Electronic books. Additional physical formats: Print version:: Epigenetic methods in neuroscience research.DDC classification: 612.8 LOC classification: QP356.22Online resources: Click here to access online Summary: Epigenetic Methods in Neuroscience Research guides readers through methods for the analyses of chromatin remodeling, transposable elements, non-coding RNAs, such as miRNAs, and circadian oscillations, including: analysis of DNA methylation in neuronal and glial cells or small tissue samples; sensitive method for quantification of alternative methylated forms of cytosines by liquid chromatography/mass spectrometry; affinity-based detection of modified cytosines by immunohistochemistry or methylated DNA immunoprecipitation; chromatin immunoprecipitation, or ChIP; miRNA high-throughput profiling and the in situ detection of miRNA subtle expression in the brain; analysis of genes with alternative 3'UTRs; and the cite-specific delivery of chromatin-modifying drugs.
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Includes bibliographical references and index.
Online resource; title from PDF title page (SpringerLink, viewed December 23, 2015).
Epigenetic Methods in Neuroscience Research guides readers through methods for the analyses of chromatin remodeling, transposable elements, non-coding RNAs, such as miRNAs, and circadian oscillations, including: analysis of DNA methylation in neuronal and glial cells or small tissue samples; sensitive method for quantification of alternative methylated forms of cytosines by liquid chromatography/mass spectrometry; affinity-based detection of modified cytosines by immunohistochemistry or methylated DNA immunoprecipitation; chromatin immunoprecipitation, or ChIP; miRNA high-throughput profiling and the in situ detection of miRNA subtle expression in the brain; analysis of genes with alternative 3'UTRs; and the cite-specific delivery of chromatin-modifying drugs.