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of cysteamine for a rare disease, cystinosis. It's an exciting time to join our research group which currently has 4 members, 3 PhD students and a post-doctoral researcher and plans to hire 2 more PhD students by
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types in vitro. We will also assess novel IFN-I inhibitors developed in partnership with medicinal chemistry collaborators. This project will shed light on direct and indirect pathogenic properties of IFN
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