150 results on '"Kostic, Corinne"'
Search Results
2. Fine-tuning FAM161A gene augmentation therapy to restore retinal function
3. Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia
4. Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa
5. PupilMetrics: a support system for preprocessing of pupillometric data and extraction of outcome measures.
6. Glutamylation imbalance leads to photoreceptor degeneration
7. Modeling the critical MCOR-causing deletion in mouse unveils aberrantSox21expression in developing and adult iris and ciliary body, and implicatesTgfβ2in MCOR-associated glaucoma and myopia
8. Quantification of the early pupillary dilation kinetic to assess rod and cone activity
9. A new mouse model for retinal degeneration due to Fam161a deficiency
10. Fine-tuning FAM161A gene augmentation therapy to restore retinal function
11. Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in non-human primates
12. Lentiviral mediated RPE65 gene transfer in healthy hiPSCs-derived retinal pigment epithelial cells markedly increased RPE65 mRNA, but modestly protein level
13. Occipital cortex activity in response to melanopsin in healthy humans
14. Lentiviral Gene Transfer-Mediated Cone Vision Restoration in RPE65 Knockout Mice
15. Lentiviral Vectors Containing a Retinal Pigment Epithelium Specific Promoter for Leber Congenital Amaurosis Gene Therapy : Lentiviral gene therapy for LCA
16. Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161aretinitis pigmentosa
17. Lentiviral Vectors for Ocular Gene Therapy
18. The connecting cilium inner scaffold provides a structural foundation that protects against retinal degeneration
19. Animal modelling for inherited central vision loss
20. The connecting cilium inner scaffold provides a structural foundation to maintain photoreceptor integrity
21. Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy
22. Notch signaling in the pigmented epithelium of the anterior eye segment promotes ciliary body development at the expense of iris formation
23. FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies
24. Isolation and characterization of sixteen novel p53 response genes
25. Reduction of choroidal neovascularization in mice by adeno-associated virus-delivered anti-vascular endothelial growth factor short hairpin RNA
26. An in vitro Model of Human Retinal Detachment Reveals Successive Death Pathway Activations
27. Lentiviral Vectors Containing a Retinal Pigment Epithelium Specific Promoter for Leber Congenital Amaurosis Gene Therapy
28. In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death
29. Maturation of the Pupil Light Reflex Occurs Until Adulthood in Mice
30. FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies
31. In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death
32. Rai1 frees mice from the repression of active wake behaviors by light
33. Author response: Rai1 frees mice from the repression of active wake behaviors by light
34. Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development
35. Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics
36. Determination of Rod and Cone Influence to the Early and Late Dynamic of the Pupillary Light Response
37. Animal modelling for inherited central vision loss
38. Multigenic lentiviral vectors for combined and tissue-specific expression of miRNA- and protein-based antiangiogenic factors
39. In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death
40. Rapid Cohort Generation and Analysis of Disease Spectrum of Large Animal Model of Cone Dystrophy
41. Retinal Degeneration Progression Changes Lentiviral Vector Cell Targeting in the Retina
42. Gene Therapy Regenerates Protein Expression in Cone Photoreceptors in Rpe65R91W/R91W Mice
43. Remaining Rod Activity Mediates Visual Behavior in AdultRpe65−/−mice.
44. [b]Ophtalmologie[/b]. Thérapie génique des rétinopathies héréditaires: premiers résultats
45. Lentiviral Gene Transfer of Rpe65 Rescues Survival and Function of Cones in a Mouse Model of Leber Congenital Amaurosis
46. High Yield of Cells Committed to the Photoreceptor Fate from Expanded Mouse Retinal Stem Cells
47. 419. Rescue of Cone Photoreceptors after Lentiviral Gene Transfer of Rpe65 cDNA in Knockout Mouse Models of Leber Congenital Amaurosis
48. Non-neural Regions of the Adult Human Eye: A Potential Source of Neurons?
49. Delivery of Ciliary Neurotrophic Factor via Lentiviral-Mediated Transfer Protects Axotomized Retinal Ganglion Cells for an Extended Period of Time
50. Lentiviral Gene Transfer-Mediated Cone Vision Restoration in RPE65 Knockout Mice.
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