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1. DNA nanoparticles are safe and nontoxic in non-human primate eyes

3. Differential composition of DHA and very-long-chain PUFAs in rod and cone photoreceptors

5. Downregulation of rhodopsin is an effective therapeutic strategy in ameliorating peripherin-2-associated inherited retinal disorders.

6. Effective intravitreal gene delivery to retinal pigment epithelium with hyaluronic acid nanospheres.

7. The role of syntaxins in retinal function and health.

8. ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims.

10. Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization.

11. Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones.

12. The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1.

13. The Role of Peripherin-2/ROM1 Complexes in Photoreceptor Outer Segment Disc Morphogenesis.

14. Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasis.

15. The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural Retina.

16. Prph2 disease mutations lead to structural and functional defects in the RPE.

17. Modulation of SOD3 Levels Is Detrimental to Retinal Homeostasis.

18. Co-Injection of Sulfotyrosine Facilitates Retinal Uptake of Hyaluronic Acid Nanospheres Following Intravitreal Injection.

19. Photoreceptor Disc Enclosure Is Tightly Controlled by Peripherin-2 Oligomerization.

20. Gene Therapy to the Retina and the Cochlea.

21. Absence of retbindin blocks glycolytic flux, disrupts metabolic homeostasis, and leads to photoreceptor degeneration.

22. Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration.

23. ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal disease.

24. Flavins Act as a Critical Liaison Between Metabolic Homeostasis and Oxidative Stress in the Retina.

25. Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival.

26. Pluripotent Stem Cells for the Treatment of Retinal Degeneration: Current Strategies and Future Directions.

27. Elimination of a Retinal Riboflavin Binding Protein Exacerbates Degeneration in a Model of Cone-Rod Dystrophy.

28. Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds Oligomerization.

29. The Symbiotic Relationship between the Neural Retina and Retinal Pigment Epithelium Is Supported by Utilizing Differential Metabolic Pathways.

30. The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases.

31. The Intersection of Serine Metabolism and Cellular Dysfunction in Retinal Degeneration.

32. Novel molecular mechanisms for Prph2-associated pattern dystrophy.

33. Prph2 initiates outer segment morphogenesis but maturation requires Prph2/Rom1 oligomerization.

34. The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis.

35. Flavin Imbalance as an Important Player in Diabetic Retinopathy.

36. Oxidative Stress, Diabetic Retinopathy, and Superoxide Dismutase 3.

37. Flavin homeostasis in the mouse retina during aging and degeneration.

38. Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation.

39. Differential composition of DHA and very-long-chain PUFAs in rod and cone photoreceptors.

40. Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration.

41. Role of Fibulins 2 and 5 in Retinal Development and Maintenance.

42. Retbindin Is Capable of Protecting Photoreceptors from Flavin-Sensitized Light-Mediated Cell Death In Vitro.

43. Optimizing Non-viral Gene Therapy Vectors for Delivery to Photoreceptors and Retinal Pigment Epithelial Cells.

44. Ablation of the riboflavin-binding protein retbindin reduces flavin levels and leads to progressive and dose-dependent degeneration of rods and cones.

45. Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa.

46. Nanoparticle-mediated miR200-b delivery for the treatment of diabetic retinopathy.

47. The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function.

48. PRPH2/RDS and ROM-1: Historical context, current views and future considerations.

49. Role of RDS and Rhodopsin in Cngb1-Related Retinal Degeneration.

50. Characterization of Ribozymes Targeting a Congenital Night Blindness Mutation in Rhodopsin Mutation.

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