23 results on '"Boye, Shannon E."'
Search Results
2. Intravitreal injection of a rationally designed AAV capsid library in non-human primate identifies variants with enhanced retinal transduction and neutralizing antibody evasion
3. Dual-AAV vector-mediated expression of MYO7A improves vestibular function in a mouse model of Usher syndrome 1B
4. Development of an AAV-CRISPR-Cas9-based treatment for dominant cone-rod dystrophy 6
5. Preclinical studies in support of phase I/II clinical trials to treat GUCY2D-associated Leber congenital amaurosis
6. Post-developmental plasticity of the primary rod pathway allows restoration of visually guided behaviors
7. Night vision restored in days after decades of congenital blindness
8. Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutations
9. Current Clinical Applications of In Vivo Gene Therapy with AAVs
10. Novel AAV44.9-Based Vectors Display Exceptional Characteristics for Retinal Gene Therapy
11. Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutations
12. A Drug-Tunable Gene Therapy for Broad-Spectrum Protection against Retinal Degeneration
13. Rationally Engineered AAV Capsids Improve Transduction and Volumetric Spread in the CNS
14. Optimization of Retinal Gene Therapy for X-Linked Retinitis Pigmentosa Due to RPGR Mutations
15. Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations
16. Gene Therapy With the Caspase Activation and Recruitment Domain Reduces the Ocular Inflammatory Response
17. Targeted Gene Delivery to the Enteric Nervous System Using AAV: A Comparison Across Serotypes and Capsid Mutants
18. Targeted CNS delivery using human MiniPromoters and demonstrated compatibility with adeno-associated viral vectors
19. A Comprehensive Review of Retinal Gene Therapy
20. Virally delivered Channelrhodopsin-2 Safely and Effectively Restores Visual Function in Multiple Mouse Models of Blindness
21. Long-term Retinal Function and Structure Rescue Using Capsid Mutant AAV8 Vector in the rd10 Mouse, a Model of Recessive Retinitis Pigmentosa
22. 620. Use of Transgenic Mice to Quantify Transduction Efficiency and Specificity of Novel AAV Vectors in Retina
23. 498. Optimization of rAAV Targets ON Bipolar Cells and Rescues the nobnyx Mouse Model of X-Linked Congenital Stationary Night Blindness
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