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6. Correction to: Retinal Degenerative Diseases

11. TLR2 Is Highly Overexpressed in Retinal Myeloid Cells in the rd10 Mouse Model of Retinitis Pigmentosa

12. Single-Cell Transcriptomic Profiling of Müller Glia in the rd10 Retina

13. Current Advancements in Mouse Models of Retinal Disease

14. Expansion Microscopy of Mouse Photoreceptor Cilia

15. Retinal Metabolic Profile on IMPG2 Deficiency Mice with Subretinal Lesions

16. Perspectives on Retinal Dolichol Metabolism, and Visual Deficits in Dolichol Metabolism-Associated Inherited Disorders

17. Aerobic Glycolysis in Photoreceptors Supports Energy Demand in the Absence of Mitochondrial Coupling

18. Redox Status in Retinitis Pigmentosa

19. Environmental Light Has an Essential Effect on the Disease Expression in a Dominant RPE65 Mutation

20. Rod Photoreceptor-Specific Ablation of Metformin Target, AMPK, in a Preclinical Model of Autosomal Recessive Retinitis Pigmentosa

21. Methods for In Vivo Characterization of Proteostasis in the Mouse Retina

22. Microglia Preserve Visual Function in a Mouse Model of Retinitis Pigmentosa with Rhodopsin-P23H Mutant

23. Measuring the Release of Lactate from Wild-Type and rd1 Mouse Retina

24. Absence of PRCD Leads to Dysregulation in Lipid Homeostasis Resulting in Disorganization of Photoreceptor Outer Segment Structure

25. A Novel Mouse Model for Late-Onset Retinal Degeneration (L-ORD) Develops RPE Abnormalities Due to the Loss of C1qtnf5/Ctrp5

26. Inhibition of Ryanodine Receptor 1 Reduces Endoplasmic Reticulum (ER) Stress and Promotes ER Protein Degradation in Cyclic Nucleotide-Gated Channel Deficiency

27. Retinoic Acid Receptor-Related Orphan Receptors (RORs) in Eye Development and Disease

28. Mouse Choroid Proteome Revisited: Focus on Aging

29. Comparison of Mouse Models of Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation of Rhodopsin

30. Compensatory Cone-Mediated Mechanisms in Inherited Retinal Degeneration Mouse Models: A Functional and Gene Expression Analysis

31. Morphological and Functional Comparison of Mice Models for Retinitis Pigmentosa

32. Extracellular Matrix: The Unexplored Aspects of Retinal Pathologies and Regeneration

33. Retinal Pathoconnectomics: A Window into Neurodegeneration

34. Role of TFEB in Diseases Associated with Lysosomal Dysfunction

35. Genotype–Phenotype Association in ABCA4-Associated Retinopathy

36. The Role of Ceramide in Inherited Retinal Disease Pathology

37. The Retinal Pigment Epithelium: Cells That Know the Beat!

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

39. Ocular Amyloid, Condensates, and Aggregates – Higher-Order Protein Assemblies Participate in Both Retinal Degeneration and Function

40. Role of Nuclear NAD+ in Retinal Homeostasis

41. Photoreceptor Ion Channels in Signaling and Disease

42. Human Mutations in Arl3, a Small GTPase Involved in Lipidated Cargo Delivery to the Cilia, Cause Retinal Dystrophy

43. Role of VLC-PUFAs in Retinal and Macular Degeneration

44. Connexins Biology in the Pathophysiology of Retinal Diseases

45. Revisiting the Daily Timing of POS Phagocytosis

46. Axonal Transport Defects in Retinal Ganglion Cell Diseases

47. Retinal Pigmented Epithelium-Derived Ectopic Norrin Does Not Promote Intraretinal Angiogenesis in Transgenic Mice

48. Caveolin-1 in Müller Glia Exists as Heat-Resistant, High Molecular Weight Complexes

49. Gene Expression of Clusterin, Tissue Inhibitor of Metalloproteinase-1, and Their Receptors in Retinal Pigment Epithelial Cells and Müller Glial Cells Is Modulated by Inflammatory Stresses

50. Understanding Ischemic Retinopathies: The Role of Succinate and Its Receptor in Retinal Pigment Epithelium

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