The Orphan Disease Center's JumpStart program serves to establish and progress research agendas in emerging and neglected rare diseases. The JumpStart program works closely with patient groups and foundations, pharma and biotech, and the academic community to drive therapeutic development for rare diseases. We offer a tailor approach to disease groups with limited expertise and resources. We can help overcome obstacles to progress research and bridge gaps for future success.
The JumpStart program connects patients and foundations to researchers and key opinion leaders, encouraging scientific collaboration. Through the JumpStart Biorepository, we provide research tools for researchers, which are essential for clinical development programs.
iPSCs in this catalog represent cell lines from patients with different mutations in diseases represented by the JumpStart Program.
