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4. Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia

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

10. Fine-tuning FAM161A gene augmentation therapy to restore retinal function

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

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

27. Lentiviral Vectors Containing a Retinal Pigment Epithelium Specific Promoter for Leber Congenital Amaurosis Gene Therapy

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

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

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

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