501 results on '"Naash, Muna I."'
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2. Effective intravitreal gene delivery to retinal pigment epithelium with hyaluronic acid nanospheres
3. Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization
4. The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1
5. The Role of Peripherin-2/ROM1 Complexes in Photoreceptor Outer Segment Disc Morphogenesis
6. Correction: Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones
7. Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones
8. Absence of retbindin blocks glycolytic flux, disrupts metabolic homeostasis, and leads to photoreceptor degeneration
9. Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration
10. The role of syntaxins in retinal function and health
11. Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival
12. Flavin Imbalance as an Important Player in Diabetic Retinopathy
13. The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis
14. Oxidative Stress, Diabetic Retinopathy, and Superoxide Dismutase 3
15. The Symbiotic Relationship between the Neural Retina and Retinal Pigment Epithelium Is Supported by Utilizing Differential Metabolic Pathways
16. Retbindin Is Capable of Protecting Photoreceptors from Flavin-Sensitized Light-Mediated Cell Death In Vitro
17. Role of Fibulins 2 and 5 in Retinal Development and Maintenance
18. Optimizing Non-viral Gene Therapy Vectors for Delivery to Photoreceptors and Retinal Pigment Epithelial Cells
19. ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims
20. ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims
21. Retention of Function without Normal Disc Morphogenesis Occurs in Cone but Not Rod Photoreceptors
22. The Potential Role of Flavins and Retbindin in Retinal Function and Homeostasis
23. Characterization of Ribozymes Targeting a Congenital Night Blindness Mutation in Rhodopsin Mutation
24. Therapeutic Approach of Nanotechnology for Oxidative Stress Induced Ocular Neurodegenerative Diseases
25. RDS Functional Domains and Dysfunction in Disease
26. Oxidative Stress, Diabetic Retinopathy, and Superoxide Dismutase 3
27. Flavin Imbalance as an Important Player in Diabetic Retinopathy
28. The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis
29. Nanoparticle-mediated miR200-b delivery for the treatment of diabetic retinopathy
30. PRPH2/RDS and ROM-1: Historical context, current views and future considerations
31. Episomal Maintenance of S/MAR-Containing Non-Viral Vectors for RPE-Based Diseases
32. Gene Therapy for Stargardt Disease Associated with ABCA4 Gene
33. Electrophysiological Characterization of Rod and Cone Responses in the Baboon Nonhuman Primate Model
34. Non-viral therapeutic approaches to ocular diseases: An overview and future directions
35. Optimizing Non-viral Gene Therapy Vectors for Delivery to Photoreceptors and Retinal Pigment Epithelial Cells
36. Retbindin Is Capable of Protecting Photoreceptors from Flavin-Sensitized Light-Mediated Cell Death In Vitro
37. Role of Fibulins 2 and 5 in Retinal Development and Maintenance
38. Nanoparticle-based technologies for retinal gene therapy
39. Mislocalization of Oligomerization-Incompetent RDS is Associated with Mislocalization of Cone Opsins and Cone Transducin
40. Overexpression of ROM-1 in the Cone-Dominant Retina
41. Gene Therapy in the Retinal Degeneration Slow Model of Retinitis Pigmentosa
42. RDS in Cones Does Not Interact with the Beta Subunit of the Cyclic Nucleotide Gated Channel
43. The Function of Oligomerization-Incompetent RDS in Rods
44. Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration
45. Genetic Supplementation of RDS Alleviates a Loss-of-function Phenotype in C214S Model of Retinitis Pigmentosa
46. In vitro Analysis of Ribozyme-mediated Knockdown of an ADRP Associated Rhodopsin Mutation
47. Transgenic Animal Studies of Human Retinal Disease Caused by Mutations in Peripherin/RDS
48. Light/Dark Translocation of Alphatransducin in Mouse Photoreceptor Cells Expressing G90D Mutant Opsin
49. Persistence of non-viral vector mediated RPE65 expression: Case for viability as a gene transfer therapy for RPE-based diseases
50. Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasis
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