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Mendeley readers
Chapter title |
Probing the Pathogenesis of Duchenne Muscular Dystrophy Using Mouse Models
|
---|---|
Chapter number | 8 |
Book title |
Duchenne Muscular Dystrophy
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Published in |
Methods in molecular biology, January 2018
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DOI | 10.1007/978-1-4939-7374-3_8 |
Pubmed ID | |
Book ISBNs |
978-1-4939-7373-6, 978-1-4939-7374-3
|
Authors |
Alexander Morrison-Nozik, Saptarsi M. Haldar |
Abstract |
Investigations using mouse models have provided seminal insights into the pathogenesis of Duchenne muscular dystrophy and the development of novel therapeutics. Several important methods have been considered standard-in-the-field for analyses of skeletal muscle weakness, strength, endurance, and histopathology, as well as responses to therapeutics such as glucocorticoids, disease modifying drugs which are part of the current standard of care for patients with this disease. Here we describe optimized genetic, genomic, and physiologic assays to probe dystrophic pathobiology in the mdx mouse and related strains. |
Mendeley readers
The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 11 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Master | 2 | 18% |
Student > Ph. D. Student | 2 | 18% |
Student > Doctoral Student | 1 | 9% |
Student > Bachelor | 1 | 9% |
Professor | 1 | 9% |
Other | 2 | 18% |
Unknown | 2 | 18% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 4 | 36% |
Nursing and Health Professions | 2 | 18% |
Biochemistry, Genetics and Molecular Biology | 1 | 9% |
Computer Science | 1 | 9% |
Pharmacology, Toxicology and Pharmaceutical Science | 1 | 9% |
Other | 0 | 0% |
Unknown | 2 | 18% |