Muscular Dystrophy Methods and Protocols /
| निगमित लेखक: | |
|---|---|
| अन्य लेखक: | , |
| सारांश: | XII, 458 p. text |
| भाषा: | अंग्रेज़ी |
| प्रकाशित: |
Totowa, NJ :
Humana Press : Imprint: Humana,
2001.
|
| संस्करण: | 1st ed. 2001. |
| श्रृंखला: | Methods in Molecular Medicine,
43 |
| विषय: | |
| ऑनलाइन पहुंच: | https://doi.org/10.1385/1592591388 |
| स्वरूप: | इलेक्ट्रोनिक पुस्तक |
विषय - सूची:
- Background
- 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.