22 results on '"Léveillard Thierry"'
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2. Shedding light on myopia by studying complete congenital stationary night blindness
3. Modulating antioxidant systems as a therapeutic approach to retinal degeneration
4. The metabolic signaling of the nucleoredoxin-like 2 gene supports brain function
5. Assessing Photoreceptor Status in Retinal Dystrophies: From High-Resolution Imaging to Functional Vision
6. The role of RdCVFL in a mathematical model of photoreceptor interactions
7. The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte Elimination
8. Otx2-Genetically Modified Retinal Pigment Epithelial Cells Rescue Photoreceptors after Transplantation
9. Rod-Derived Cone Viability Factor Promotes Cone Survival by Stimulating Aerobic Glycolysis
10. Therapeutic strategy for handling inherited retinal degenerations in a gene-independent manner using rod-derived cone viability factors
11. The Thioredoxin-like Protein Rod-derived Cone Viability Factor (RdCVFL) Interacts with TAU and Inhibits Its Phosphorylation in the Retina
12. Rétinopathies pigmentaires : de la thérapie cellulaire à la signalisation intercellulaire
13. Inherited retinal degenerations: therapeutic prospects
14. Differential Proteomic Analysis of the Mouse Retina: The Induction of Crystallin Proteins by Retinal Degeneration in the rd1 Mouse
15. Rod–Cone Interactions:: Developmental and Clinical Significance
16. Chapter 47 Rod-cone interdependence: implications for therapy of photoreceptor cell diseases
17. Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy
18. Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
19. TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness
20. Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
21. MDM2 expression during mouse embryogenesis and the requirement of p53
22. The MDM2 C-terminal Region Binds to TAFII250 and Is Required for MDM2 Regulation of the Cyclin A Promoter
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