Projects per year
Project Details
Description
We will determine the molecular pathogenesis of CTDs by taking mouse genetics approaches. We propose that Tbxl genetic pathways are required for cardiac outflow tract development and when altered alters risk to CTDs in 22q11DS (Project 1) and more frequent non-syndromic forms (Project 2).
| Status | Finished |
|---|---|
| Effective start/end date | 9/24/11 → 6/30/16 |
Funding
- National Institute of Child Health and Human Development: $281,762.00
- National Institute of Child Health and Human Development: $359,287.00
- National Institute of Child Health and Human Development: $261,178.00
- National Institute of Child Health and Human Development: $271,357.00
- National Institute of Child Health and Human Development: $275,255.00
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Projects
- 1 Finished
-
Developmental mechanisms of human congenital heart disease
Morrow, B. E., Emanuel, B. S. & Goldmuntz, E.
National Institute of Child Health and Human Development
9/24/11 → 6/30/21
Project: Research project