Alzheimer's Disease: Methods and Protocols
With 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 outstandi...
Gespeichert in:
| Weitere Verfasser: | |
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| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Totowa, NJ
Humana Press
2000
|
| Schriftenreihe: | Methods in Molecular Medicine™
32 |
| Schlagworte: | |
| Online-Zugang: | UBR01 TUM01 Volltext |
| Zusammenfassung: | With 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 |
| Beschreibung: | 1 Online-Ressource (XIV, 408 p) |
| ISBN: | 9781592591954 |
| DOI: | 10.1385/1592591957 |
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| 520 | |a With 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 | ||
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| spelling | Alzheimer's Disease Methods and Protocols edited by Nigel M. Hooper Totowa, NJ Humana Press 2000 1 Online-Ressource (XIV, 408 p) txt rdacontent c rdamedia cr rdacarrier Methods in Molecular Medicine™ 32 With 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 Medicine & Public Health Neurology Medicine Hooper, Nigel M. edt Erscheint auch als Druck-Ausgabe 9780896037373 https://doi.org/10.1385/1592591957 Verlag URL des Erstveröffentlichers Volltext |
| spellingShingle | Alzheimer's Disease Methods and Protocols Medicine & Public Health Neurology Medicine |
| title | Alzheimer's Disease Methods and Protocols |
| title_auth | Alzheimer's Disease Methods and Protocols |
| title_exact_search | Alzheimer's Disease Methods and Protocols |
| title_full | Alzheimer's Disease Methods and Protocols edited by Nigel M. Hooper |
| title_fullStr | Alzheimer's Disease Methods and Protocols edited by Nigel M. Hooper |
| title_full_unstemmed | Alzheimer's Disease Methods and Protocols edited by Nigel M. Hooper |
| title_short | Alzheimer's Disease |
| title_sort | alzheimer s disease methods and protocols |
| title_sub | Methods and Protocols |
| topic | Medicine & Public Health Neurology Medicine |
| topic_facet | Medicine & Public Health Neurology Medicine |
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