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008			100301s2004 xxu| o |||| 0|eng d
020			_a9781592598281
024	7		_a10.1385/1592598285 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC _dES-MaUEC
050		4	_aQH599 _b2004 EB
245	0	0	_aEpigenetics Protocols _cedited by Trygve O. Tollefsbol
250			_a1st edition 2004
264		1	_aTotowa, NJ _bHumana Press _c2004
300			_a1 recurso en línea (XII, 304 páginas)
336			_atexto _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
347			_aarchivo de texto _bPDF
490	0		_aMethods in Molecular Biology _x1940-6029 _v287
505	0		_aMethods of Epigenetic Analysis -- Chromatin Immunoprecipitation Assays -- Native Chromatin Immunoprecipitation -- Q-PCR in Combination With ChIP Assays to Detect Changes in Chromatin Acetylation -- Restriction Endonuclease Accessibility as a Determinant of Altered Chromatin Structure -- Measuring Changes in Chromatin Using Micrococcal Nuclease -- DNaseI Hypersensitivity Analysis of Chromatin Structure -- Inhibition of Histone Deacetylases -- Site-Specific Analysis of Histone Methylation and Acetylation -- Analysis of Mammalian Telomere Position Effect -- Activity Assays for Poly-ADP Ribose Polymerase -- Multigenerational Selection and Detection of Altered Histone Acetylation and Methylation Patterns -- Profiling DNA Methylation by Bisulfite Genomic Sequencing -- Methylation-Sensitive Single-Strand Conformation Analysis -- SIRPH Analysis -- Real-Time PCR-Based Assay for Quantitative Determination of Methylation Status -- Denaturing Gradient Gel Electrophoresis to Detect Methylation Changes in DNA -- Photocrosslinking Oligonucleotide Hybridization Assay for Concurrent Gene Dosage and CpG Methylation Analysis -- Methylation-Specific Oligonucleotide Microarray -- Methylation-Specific PCR In Situ Hybridization -- Relative Quantitation of DNA Methyltransferase mRNA by Real-Time RT-PCR Assay -- DMB (DNMT-Magnetic Beads) Assay.
520			_aRecent advances in epigenetic research as well as the development of exciting new technologies have helped greatly in unraveling the many mysteries of nontraditional genetic processes. In Epigenetics Protocols, hands-on researchers describe state-of-the-art methods for epigenetic analysis, including recent breakthrough techniques that have great potential in the rapidly expanding field of non-Mendelian genetics. The authors provide techniques for the analysis of chromatin remodeling, such as histone acetylation and methylation. In addition, methods in newly developed and especially promising areas of epigenetics, such as telomere position effects, quantitative epigenetics, and ADP ribosylation are covered. There is also an updated analysis of techniques involving DNA methylation and its role in the modification, as well as the maintenance, of chromatin structure. Of special interest are potentially revolutionary techniques. These include methods for determining changes in native chromatin, methods of microarray analysis applied to epigenetics, and methylation-sensitive single-strand conformation techniques. The methods are suitable not only for studying fundamental biological processes, but also for investigating possible therapeutic interventions and such diseases as cancer. The protocols follow the successful Methods in Molecular Biology™ series format, each one offering step-by-step laboratory instructions, an introduction outlining the principle behind the technique, lists of the necessary equipment and reagents, and tips on troubleshooting and avoiding known pitfalls. Comprehensive and easy to use, Epigenetics Protocols offers investigators readily reproducible techniques that will further promote progress in this critically important field.
988			_aSpringer_Protocols_2004
650		7	_2embne _9688615 _aTelómeros
650		7	_2embne _9526531 _aEpigenética
650		7	_2embne _9144121 _aCromatina
776	0	8	_iPrinted edition: _z9781617375019
776	0	8	_iPrinted edition: _z9781489939326
776	0	8	_iPrinted edition: _z9781588293367
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/1592598285 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942			_2lcc _cLE
998			_b01/2024 _dz _eIG _zSI