Several mouse models of muscular dystrophy will be used extensively by all investigators. Much of this work can be most efficiently handled by a core that provides various services, including maintenance of the mouse colonies, breeding, and genotyping. In addition, muscle physiology studies important for testing rescue of the dystrophic phenotype will be carried out in the core, as will injection of both viral vectors and transduced stem cells. Finally, the core will perform creatine kinase and/or pyruvate kinase assays for identification of suppressor mutations following mutagenesis of the mdx mice.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
1P01NS046788-01A1
Application #
6803775
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Project Start
2004-04-01
Project End
2009-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
1
Fiscal Year
2004
Total Cost
$89,872
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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