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Muscular Dystrophy: Pathogenesis and Therapies (R01)
Release Date: December 12, 2006
Announcement Number: PA-07-125
Application Receipt Date:
February 5, 2007
June 5, 2007
October 5, 2007
Funding Contact: John Porter, Ph.D.
Program Area: Channels, Synapses and Neural Circuits
Brief Description:
A principal goal of this initiative is to promote research that will lead to better treatment for all muscular dystrophies.
The NIAMS, NINDS, NICHD and NHLBI encourage investigator-initiated research grant applications to study therapeutic and pathogenic
approaches. Special emphasis is on areas discussed in the MDCC Action Plan for the Muscular Dystrophies. Important research
priorities include studies on gene and stem cell therapies, pharmacological and molecular approaches to treatment, and clarification
of the role of inflammatory mechanisms. Topics for research projects can include screening and/or diagnosis, understanding
disease mechanisms, treatment strategies, and improving quality of life, and can include studies in appropriate animal models
or preclinical or clinical studies in patients. Program staff must be contacted prior to submitting a proposal that includes
a clinical trial or interventional study in humans.
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