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Retinal Degenerative Diseases
other
Editor(s):
John D. Ash
,
Christian Grimm
,
Joe G. Hollyfield
,
Robert E. Anderson
,
Matthew M. LaVail
,
Catherine Bowes Rickman
Publication date
(Print):
2014
Publisher:
Springer New York
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Book
ISBN (Print):
978-1-4614-3208-1
ISBN (Electronic):
978-1-4614-3209-8
Publication date (Print):
2014
DOI:
10.1007/978-1-4614-3209-8
SO-VID:
07dfc4b5-fca1-462f-8fa2-40faab788387
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http://www.springer.com/tdm
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Book chapters
pp. 3
Cell Type-Specific Epigenetic Signatures Accompany Late Stages of Mouse Retina Development
pp. 9
Programmed Cell Death During Retinal Development of the Mouse Eye
pp. 15
Spatial and Temporal Localization of Caveolin-1 Protein in the Developing Retina
pp. 23
Glutathione S-Transferase Pi Isoform (GSTP1) Expression in Murine Retina Increases with Developmental Maturity
pp. 31
RETINA-Specific Expression of Kcnv2 Is Controlled by Cone-Rod Homeobox (Crx) and Neural Retina Leucine Zipper (Nrl)
pp. 43
AIPL1 Protein and its Indispensable Role in Cone Photoreceptor Function and Survival
pp. 49
Primate Short-Wavelength Cones Share Molecular Markers with Rods
pp. 57
Exploration of Cone Cyclic Nucleotide-Gated Channel-Interacting Proteins Using Affinity Purification and Mass Spectrometry
pp. 67
Electrophysiological Characterization of Rod and Cone Responses in the Baboon Nonhuman Primate Model
pp. 77
Animal Models, in “The Quest to Decipher RPE Phagocytosis”
pp. 85
In Vivo and in Vitro Monitoring of Phagosome Maturation in Retinal Pigment Epithelium Cells
pp. 91
Lack of Effect of Microfilament or Microtubule Cytoskeleton-Disrupting Agents on Restriction of Externalized Phosphatidylserine to Rod Photoreceptor Outer Segment Tips
pp. 97
Vacuolar ATPases and Their Role in Vision
pp. 105
Rescue of Compromised Lysosomes Enhances Degradation of Photoreceptor Outer Segments and Reduces Lipofuscin-Like Autofluorescence in Retinal Pigmented Epithelial Cells
pp. 113
The Role of Bestrophin-1 in Intracellular Ca2+ Signaling
pp. 123
Application of Next-Generation Sequencing to Identify Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa (adRP)
pp. 131
Digital Quantification of Goldmann Visual Fields (GVFs) as a Means for Genotype–Phenotype Comparisons and Detection of Progression in Retinal Degenerations
pp. 139
Simplified System to Investigate Alteration of Retinal Neurons in Diabetes
pp. 145
What is the Nature of the RGC-5 Cell Line?
pp. 157
Modeling Retinal Dystrophies Using Patient-Derived Induced Pluripotent Stem Cells
pp. 165
Mutation K42E in Dehydrodolichol Diphosphate Synthase (DHDDS) Causes Recessive Retinitis Pigmentosa
pp. 171
IROme, a New High-Throughput Molecular Tool for the Diagnosis of Inherited Retinal Dystrophies—A Price Comparison with Sanger Sequencing
pp. 177
Genetic Heterogeneity and Clinical Outcome in a Swedish Family with Retinal Degeneration Caused by Mutations in CRB1 and ABCA4 Genes
pp. 185
FAM161A, a Novel Centrosomal-Ciliary Protein Implicated in Autosomal Recessive Retinitis Pigmentosa
pp. 193
Molecular Pathology of Macrophages and Interleukin-17 in Age-Related Macular Degeneration
pp. 199
The Role of Monocytes and Macrophages in Age-Related Macular Degeneration
pp. 207
Microglia in the Aging Retina
pp. 213
The Role of Complement Dysregulation in AMD Mouse Models
pp. 221
Prolonged Src Kinase Activation, a Mechanism to Turn Transient, Sublytic Complement Activation into a Sustained Pathological Condition in Retinal Pigment Epithelium Cells
pp. 229
Inflammation in Age-Related Macular Degeneration
pp. 237
Impairment of the Ubiquitin-Proteasome Pathway in RPE Alters the Expression of Inflammation Related Genes
pp. 251
Inflammatory Biomarkers for AMD
pp. 259
Oxidized Low-Density-Lipoprotein-Induced Injury in Retinal Pigment Epithelium Alters Expression of the Membrane Complement Regulatory Factors CD46 and CD59 through Exosomal and Apoptotic Bleb Release
pp. 267
Should I Stay or Should I Go? Trafficking of Sub-Lytic MAC in the Retinal Pigment Epithelium
pp. 275
Hypoxia-Inducible Factor (HIF)/Vascular Endothelial Growth Factor (VEGF) Signaling in the Retina
pp. 283
Is Age-Related Macular Degeneration a Microvascular Disease?
pp. 291
Genetic Risk Models in Age-Related Macular Degeneration
pp. 301
A Mechanistic Review of Cigarette Smoke and Age-Related Macular Degeneration
pp. 309
Measuring Cone Density in a Japanese Macaque (Macaca fuscata) Model of Age-Related Macular Degeneration with Commercially Available Adaptive Optics
pp. 317
Nuclear Receptors as Potential Therapeutic Targets for Age-Related Macular Degeneration
pp. 323
Utilizing Stem Cell-Derived RPE Cells as A Therapeutic Intervention for Age-Related Macular Degeneration
pp. 333
Microglia-Müller Cell Interactions in the Retina
pp. 339
Isolation and Ex Vivo Characterization of the Immunophenotype and Function of Microglia/Macrophage Populations in Normal Dog Retina
pp. 347
Müller Cells and Microglia of the Mouse Eye React Throughout the Entire Retina in Response to the Procedure of an Intravitreal Injection
pp. 355
Subretinal Infiltration of Monocyte Derived Cells and Complement Misregulation in Mice with AMD-Like Pathology
pp. 365
Ambiguous Role of Glucocorticoids on Survival of Retinal Neurons
pp. 373
Microglia-Müller Glia Crosstalk in the rd10 Mouse Model of Retinitis Pigmentosa
pp. 381
The Neuroprotective Potential of Retinal Müller Glial Cells
pp. 389
Leukemia Inhibitory Factor Signaling in Degenerating Retinas
pp. 395
In Vivo Function of the ER-Golgi Transport Protein LMAN1 in Photoreceptor Homeostasis
pp. 401
Investigating the Role of Retinal Müller Cells with Approaches in Genetics and Cell Biology
pp. 409
An Overview of the Involvement of Interleukin-18 in Degenerative Retinopathies
pp. 417
Chronic Intraocular Inflammation and Development of Retinal Degenerative Disease
pp. 427
The Relevance of Chemokine Signalling in Modulating Inherited and Age-Related Retinal Degenerations
pp. 435
The Complement Regulatory Protein CD59: Insights into Attenuation of Choroidal Neovascularization
pp. 441
Regeneration-Associated Genes on Optic Nerve Regeneration in Fish Retina
pp. 447
Dominant Stargardt Macular Dystrophy (STGD3) and ELOVL4
pp. 455
Modulation of the Rate of Retinal Degeneration in T17M RHO Mice by Reprogramming the Unfolded Protein Response.
pp. 463
Expression of Poly(ADP-Ribose) Glycohydrolase in Wild-Type and PARG-110 Knock-Out Retina
pp. 471
Current Therapeutic Strategies for P23H RHO-Linked RP
pp. 477
Pathogenesis of X-linked RP3: Insights from Animal Models
pp. 487
Unc119 Gene Deletion Partially Rescues the GRK1 Transport Defect of Pde6d - /- Cones
pp. 495
Retinal Function in Aging Homozygous Cln3 Δex7/8 Knock-In Mice
pp. 503
Synergistic Interaction of Tubby and Tubby-Like Protein 1 (Tulp1)
pp. 511
Interaction of Tubby-Like Protein-1 (Tulp1) and Microtubule-Associated Protein (MAP) 1A and MAP1B in the Mouse Retina
pp. 519
CEP290 and the Primary Cilium
pp. 527
Usher Syndrome Protein Network Functions in the Retina and their Relation to Other Retinal Ciliopathies
pp. 535
The Phenotype of the Good Effort Mutant Zebrafish is Retinal Degeneration by Cell Death and is Linked to the Chromosome Assembly Factor 1b Gene
pp. 543
Knock-Down DHDDS Expression Induces Photoreceptor Degeneration in Zebrafish
pp. 551
Spectral Domain Optical Coherence Tomography Findings in CNGB3-Associated Achromatopsia and Therapeutic Implications
pp. 559
Photoreceptor Pathology in the X-Linked Retinoschisis (XLRS) Mouse Results in Delayed Rod Maturation and Impaired Light Driven Transducin Translocation
pp. 567
Mouse Models for Cone Degeneration
pp. 575
How Long Does a Photoreceptor Cell Take to Die? Implications for the Causative Cell Death Mechanisms
pp. 585
Endoplasmic Reticulum Stress in Vertebrate Mutant Rhodopsin Models of Retinal Degeneration
pp. 593
Bisretinoid Degradation and the Ubiquitin-Proteasome System
pp. 601
Analysis of Mouse RPE Sheet Morphology Gives Discriminatory Categories
pp. 609
High Glucose Activates ChREBP-Mediated HIF-1α and VEGF Expression in Human RPE Cells Under Normoxia
pp. 623
Sphingolipids in Ocular Inflammation
pp. 631
Biosynthesis of Very Long-Chain Polyunsaturated Fatty Acids in Hepatocytes Expressing ELOVL4
pp. 637
Very Long Chain Polyunsaturated Fatty Acids and Rod Cell Structure and Function
pp. 649
Oxidative Stress Regulation by DJ-1 in the Retinal Pigment Epithelium
pp. 655
The Role of Reactive Oxygen Species in Ocular Malignancy
pp. 661
The Effects of IRE1, ATF6, and PERK Signaling on adRP-Linked Rhodopsins
pp. 669
Role of Endothelial Cell and Pericyte Dysfunction in Diabetic Retinopathy: Review of Techniques in Rodent Models
pp. 677
Autophagy Induction Does Not Protect Retina Against Apoptosis in Ischemia/Reperfusion Model
pp. 687
Advances in AAV Vector Development for Gene Therapy in the Retina
pp. 695
Cone Specific Promoter for Use in Gene Therapy of Retinal Degenerative Diseases
pp. 703
Episomal Maintenance of S/MAR-Containing Non-Viral Vectors for RPE-Based Diseases
pp. 711
Gene Therapy in the Rd6 Mouse Model of Retinal Degeneration
pp. 719
Gene Therapy for Stargardt Disease Associated with ABCA4 Gene
pp. 725
Assessment of Different Virus-Mediated Approaches for Retinal Gene Therapy of Usher 1B
pp. 733
Gene Therapy Restores Vision and Delays Degeneration in the CNGB1−/− Mouse Model of Retinitis Pigmentosa
pp. 741
Therapy Strategies for Usher Syndrome Type 1C in the Retina
pp. 751
Nipradilol Promotes Axon Regeneration Through S-Nitrosylation of PTEN in Retinal Ganglion Cells
pp. 759
Reciprocal Changes in Factor XIII and Retinal Transglutaminase Expressions in the Fish Retina During Optic Nerve Regeneration
pp. 765
N-Acetylserotonin: Circadian Activation of the BDNF Receptor and Neuroprotection in the Retina and Brain
pp. 773
A High Content Screening Approach to Identify Molecules Neuroprotective for Photoreceptor Cells
pp. 783
Antioxidant Therapy for Retinal Disease
pp. 791
Pathophysilogical Mechanism and Treatment Strategies for Leber Congenital Amaurosis
pp. 797
Current and Emerging Therapies for Ocular Neovascularisation
pp. 805
Targeting the PI3K/Akt/mTOR Pathway in Ocular Neovascularization
pp. 813
Pigment Epithelium-Derived Factor Protects Cone Photoreceptor-Derived 661W Cells from Light Damage Through Akt Activation
pp. 821
Nanoceria as Bona Fide Catalytic Antioxidants in Medicine: What We Know and What We Want to Know…
pp. 829
Nanoceria and Thioredoxin Regulate a Common Antioxidative Gene Network in tubby Mice
pp. 837
Intrascleral Transplantation of a Collagen Sheet with Cultured Brain-Derived Neurotrophic Factor Expressing Cells Partially Rescues the Retina from Damage due to Acute High Intraocular Pressure
pp. 845
Neuroprotective Effects of Low Level Electrical Stimulation Therapy on Retinal Degeneration
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