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020			_a9781592591381
024	7		_a10.1385/1592591388 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC _dES-MaUEC
050		4	_aRC925 _b2001 EB
245	0	0	_aMuscular Dystrophy : _bMethods and Protocols _cedited by Katherine M. D. Bushby, Louise V. B. Anderson
250			_a1st edition 2001
264		1	_aTotowa, NJ _bHumana Press _c2001
300			_a1 recurso en línea (XII, 458 páginas)
336			_atexto _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
347			_aarchivo de texto _bPDF
490	0		_aMethods in Molecular Medicine _x1940-6037 _v43
505	0		_aBackground -- Application of Molecular Methodologies in Muscular Dystrophies -- Clinical Examination as a Tool for Diagnosis -- Histopathological Diagnosis of Muscular Dystrophies -- Serum Creatine Kinase in Progressive Muscular Dystrophies -- The molecular approach -- Deletion and Duplication Analysis in Males Affected with Duchenne or Becker Muscular Dystrophy -- Point Mutation Detection in the Dystrophin Gene -- DNA-Based Techniques for Detection of Carriers of Duchenne and Becker Muscular Dystrophy -- Fluorescence In Situ Hybridization Analysis for Carrier Detection in Duchenne/Becker Muscular Dystrophy -- DNA- Based Prenatal Diagnosis for Duchenne and Becker Muscular Dystrophy -- Molecular Diagnosis and Genetic Counseling of the Manifesting Carrier of Duchenne Muscular Dystrophy -- Mutation Analysis of X-Linked Emery-Dreifuss Muscular Dystrophy Gene -- Analysis of LAMA2 Gene in Merosin- Deficient Congenital Dystrophy -- ?-Sarcoglycan Mutations -- Mutation Detection in ?- and ?-Sarcoglycan (LGMD2E and LGMD2C) -- Mutation Analysis in ?-Sarcoglycan (LGMD2F) -- Molecular Diagnosis of Calpainopathies -- Molecular Investigation of LGMD2B-Haplotype Analysis and Mutation Screening -- Molecular Analysis of Facioscapulohumeral Muscular Dystrophy (FSHD1) -- Protein Analysis in the Muscular Dystrophies -- Analysis of Protein Expression in Muscular Dystrophies -- Immunological Reagents and Amplification Systems -- Immunocytochemical Analysis -- Multiplex Western Blot Analysis of Muscular Dystrophy Proteins -- Fetal Muscle Biopsy -- Use of Animal Models to Understand Human Muscular Dystrophy -- Options for Development of Gene-Based Therapy for Muscular Dystrophy.
520			_aWith the molecular mechanisms underlying the various forms of muscular dystrophy now rapidly clarifying, precise diagnosis has become a reality, and even a requirement in clinical practice. In Muscular Dystrophy: Methods and Protocols, Katherine Bushby and Louise Anderson have assembled an outstanding collection of key techniques for the analysis of DNA and protein from patients suspected to suffer from muscular dystrophy. Each method is highly detailed to ensure success and is presented by a hands-on expert who uses it on a day-to-day basis. The various DNA techniques focus on both the X-linked muscular dystrophies and the autosomal recessive muscular dystrophies. The protein methods include expression analysis, multiplex western blot analysis, immunocytochemical analysis, and reviews of immunological reagants and of amplification systems. Also discussed are the use of animal models to understand human muscular dystrophy and the available options for gene-based therapy. Comprehensive and highly practical, Muscular Dystrophy: Methods and Protocols offers today,s diagnostic laboratories, basic and medical researchers, and active clinicians an authoritative collection of tools that will serve as exacting diagnostic tools as well as greatly empowering research on the novel therapeutics now beginning to emerge.
988			_aSpringer_Protocols_2001
650		7	_2embne _9181875 _aAparato locomotor _xEnfermedades
776	0	8	_iPrinted edition: _z9781617371400
776	0	8	_iPrinted edition: _z9780896036956
776	0	8	_iPrinted edition: _z9781489942319
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/1592591388 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
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998			_b01/2024 _dz _eb _zSI