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Testing the Efficacy of New NF1 Gene Therapy Candidates in Human Cell Types
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Exon Skipping to Treat NF1 – Phase B
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Targeted Delivery of Full Length NF1 cDNA Using Non-Viral Vectors
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Exploring Nonsense Suppression as a Treatment for NF1 – Phase B
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Disrupting FBXW11-Mediated Degradation of NF1 to Rescue Haploinsufficiency
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RAFT-Polymerized Nanoparticles for Delivery of NF1 cDNA to Schwann Cells
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Genome Editing for the Treatment of Neurofibromatosis Type I
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Evaluating a Next Generation AAV Capsid for Targeted Transduction of Schwann Cells
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Development of Targeted Gene Therapy Platform for Neurofibromatosis Type I
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Detroit Future City Releases New Report: “Keeping Your Family Home: Addressing the Challenges of Inherited Properties in Detroit”
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