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High Resolution Imaging Mass Spectrometry of Human Donor Eye: Photoreceptor Cells and Basal Laminar Deposits of Age-related Macular Degeneration
The non-canonical role of Complement Factor H in Retinal Pigment Epithelium (RPE) cells and implications for Age-related Macular Degeneration
Macular Pigment Carotenoids and Bisretinoid A2E
Disturbed matrix metalloproteinases activity in age-related macular degeneraton
Current views on Chr10q26 contribuiton to age-related macular degeneration
Untargeted lipidomic profiling of aged human retina with and without age-related macular degeneration (AMD)
Decoding Race and Age-Relation Macular Degeneration: GPR 143 Activity is the Key
Peroxisome proliferator-activated receptor gamma coactivator 1 alpha ( PGC-1x): a transcriptional regulator at the interface of aging and age-related macular degeneration?
Regulation of ABCA1 by miR-33 and miR-34a in the aging eye
The role of gene expression regulation on genetic risk of Age-related Macular Degeneration
Elastin layer in Bruch's membrane as a target for immunizatio or tolerization to modulate patthology in the mouse model of somke-induced ocular injury
Repuprosing drugs for treatment of age-relation macular degeneration
Extracellular Vesicle RNA Contents as Biomarkers for Ocular Diseases
Proteomics of retinal extracellular vesicles: a reviw inot an unexplored mechanism in retinal health and AMD pathogenesis
Prime Editing Strategy to Instally the PRHP2 c.828+1G A mutations
Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing
Generation of an Avian Myeloblastosis Virus (AMV) Reverse Transcriptase Prime Editor
Pre-existing neutralizing antibodies against different adeno-associated virus serotypes in humans and large animal models for gene therapy
Optimization of Capillary-based Western Blotting for MYO7A
AAV Serotypes and Their Suitability for Retinal Gene Therapy
Gene Augmentation ofautosomal dominant CRX-associated retinopathies
Txnip gene therapy of retinitis pigmentosa improves cone health Factors affecting readthrough of natural versus premature termination codons
Integrating Computational Approaches to Predict the Effect of Genetic Variants on Protein Stability in Retinal Degenerative Disease
Network biology and medcine to resuce: Applications for retinal disease mechanisms and therapy
Non-sydromic Retinal Degeneration Caused by Pathogenic Variants in Joubert Syndrome Genes
Exonic variants that affect splicing- an opportunity for "hidden" mutations causing inherited retinal diseases
Enhanced S-cone Syndrome, a Mini-Review
The role of microglia in Inherited Retinal Diseases
CD68: potential contributor to inflammation and RPE cell dystrophy
Gene Expression of Clusterin, Tissue Inhibitor of Metalloproteinase-1, and Their receptors in Retinal Pigment Epithelial Cells and Muller Glial Cells is Modulated by Inflammatory Stresses
Axonal Transport Defects in Retinal Ganglion Cells
Connexins biology in the pathophysiology of retinal diseases
Role of Nuclear NAD +in Retinal Homeostasis
Retinal pigmented epithelium-derived ectopic norrin does not promote intraretinal angiogenesis in transgenic mice
Caveolin-1 Muller glia exist as heat-resistant,high molecular weight complexes
Role of VLC-PUFAs in Retinal and Macular Degeneration
Ocular amyloid , condensates, and aggregates - higher order protein assemblies participate in both retinal degeneration and function
Photoreceptor ion channels in signaling and disease
The role of peripherin-2 /ROM1 complexes in photoreceptor outer segment disc morphogenesis
Human mutations in Arl3, a small GTPase involved inlipidated cargo delibery to the cilia cause retinatl dystropthy
Genotype-Phenotype Association in ABCA4-Associated Retinopathy
Retinal pathoconnectomics: A Window into Neurodegeneration
The role of Ceramide in Inherited Retinal Disease Pathology
Extracelluar Matix: the Unexplored Aspects of Retinal Pathologies and Regeneration
Role of TFEB in diseases assocaited with lysosomal dysfunction
Retinoic acid receptor -related oprhan receptors (RORs) in eye development and disease
A novel mouse model for Late-Onset Retinal Degeneration (L-ORD) devekios RPE abnormalities due to the loss of C1qtnf5/Ctrp5
Comparison of mouse models of autosomal dominant retinitis pigmentosa due to P23H muations of Rhodopsin
Compensatory Cone-Mediated Mechanisms in Inherited Retinal Degeneration Mouse Models: A Functional and Gene Expression Analsyis
Inhibition of Ryanodine Receptor 1 Reduces Endoplasmic Reticulum (ER) Sress and Promotes ER Protein Degradation in Cyclic Nucleotide-gated Channel Deficiency
Mouse choroid proteome revisited: foucs on aging
Morphological and functional comparison of mice models for retinitis pigmentosa
Current Advancements in Mouse Models of Retinal Disease
Single-cell Itrnacriptomic Profiling of Muller Glia in the rd10 Retina
Methods for in vivo characterization of proteostatis in the mouse retina
Absence or PRCD leads to dysregulation in lipie Homeostatis resulting in disorganizationof photorecptor outer segment structure
Expansion Microscopy of Mouse Photoreceptro Cilia
Rod photorecptor specific ablation of Metformin target, AMPK, in preclinical model of autosomal recessvie retinitis pigmentosa
TLR2 is highly overexpressed in retinal myeloid cells in the rd10 mouse model of retinitis pigmentosa
Environmental light has an essentail effrect on the diseasae expression in a dominant RPE65 mutation
Microglia Preserve Visual Function in A Mouse Model of Retinitis Pigmentosa with Rhodopsin-P23H Mutant
Measuring the release of lactate from wild-type and rd1 mouse retina
Aerobic glycolysis in photorecptors supports energy demand in the absence of mitochondrial coupling
Redox Status in Retinitis Pigmentosa
Perspectives on retinal dolichol metabolism and visual deficits in dolichol metalbolism-associated inherited disorders
Retinal metabolic profile on IMPG2 deficiency mice with subretinal lesions
Glutathione-coating of liposomes enhances the delivery of hydrophillic cargo to the inner nuclear layer in retinal cultures
Modification of Mueller glial cell fate and proliferation with the use of small molecules
A potential neuroprotective role for pyruvate kinase 2 in retinal degeneration
Critical role of VEGF as a direct regulator of photorecptor function
Lysine Ubiquitylation Drives Rhodopsin Protein Turnover
In-silico prediction of MYO!C Rhodopsin Interactions and its Significance in Protein Localization and Visual Function
A ciliary branched actin netowrk drives photoreceptor disc morphogenesis
Revisiting the daily timing of POS phagocytosis
Inhibition of Bacterial Peoptidoglycan Cytopahty by Retina Pigment Epithelial PGRP2 Amidase
Understanding ischemic retinopathies: the role of Succinate and its recpto^T mutation
Inducing neural regeneratio nfrom glia using proneural bHLH transcription factors.
The non-canonical role of Complement Factor H in Retinal Pigment Epithelium (RPE) cells and implications for Age-related Macular Degeneration
Macular Pigment Carotenoids and Bisretinoid A2E
Disturbed matrix metalloproteinases activity in age-related macular degeneraton
Current views on Chr10q26 contribuiton to age-related macular degeneration
Untargeted lipidomic profiling of aged human retina with and without age-related macular degeneration (AMD)
Decoding Race and Age-Relation Macular Degeneration: GPR 143 Activity is the Key
Peroxisome proliferator-activated receptor gamma coactivator 1 alpha ( PGC-1x): a transcriptional regulator at the interface of aging and age-related macular degeneration?
Regulation of ABCA1 by miR-33 and miR-34a in the aging eye
The role of gene expression regulation on genetic risk of Age-related Macular Degeneration
Elastin layer in Bruch's membrane as a target for immunizatio or tolerization to modulate patthology in the mouse model of somke-induced ocular injury
Repuprosing drugs for treatment of age-relation macular degeneration
Extracellular Vesicle RNA Contents as Biomarkers for Ocular Diseases
Proteomics of retinal extracellular vesicles: a reviw inot an unexplored mechanism in retinal health and AMD pathogenesis
Prime Editing Strategy to Instally the PRHP2 c.828+1G A mutations
Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing
Generation of an Avian Myeloblastosis Virus (AMV) Reverse Transcriptase Prime Editor
Pre-existing neutralizing antibodies against different adeno-associated virus serotypes in humans and large animal models for gene therapy
Optimization of Capillary-based Western Blotting for MYO7A
AAV Serotypes and Their Suitability for Retinal Gene Therapy
Gene Augmentation ofautosomal dominant CRX-associated retinopathies
Txnip gene therapy of retinitis pigmentosa improves cone health Factors affecting readthrough of natural versus premature termination codons
Integrating Computational Approaches to Predict the Effect of Genetic Variants on Protein Stability in Retinal Degenerative Disease
Network biology and medcine to resuce: Applications for retinal disease mechanisms and therapy
Non-sydromic Retinal Degeneration Caused by Pathogenic Variants in Joubert Syndrome Genes
Exonic variants that affect splicing- an opportunity for "hidden" mutations causing inherited retinal diseases
Enhanced S-cone Syndrome, a Mini-Review
The role of microglia in Inherited Retinal Diseases
CD68: potential contributor to inflammation and RPE cell dystrophy
Gene Expression of Clusterin, Tissue Inhibitor of Metalloproteinase-1, and Their receptors in Retinal Pigment Epithelial Cells and Muller Glial Cells is Modulated by Inflammatory Stresses
Axonal Transport Defects in Retinal Ganglion Cells
Connexins biology in the pathophysiology of retinal diseases
Role of Nuclear NAD +in Retinal Homeostasis
Retinal pigmented epithelium-derived ectopic norrin does not promote intraretinal angiogenesis in transgenic mice
Caveolin-1 Muller glia exist as heat-resistant,high molecular weight complexes
Role of VLC-PUFAs in Retinal and Macular Degeneration
Ocular amyloid , condensates, and aggregates - higher order protein assemblies participate in both retinal degeneration and function
Photoreceptor ion channels in signaling and disease
The role of peripherin-2 /ROM1 complexes in photoreceptor outer segment disc morphogenesis
Human mutations in Arl3, a small GTPase involved inlipidated cargo delibery to the cilia cause retinatl dystropthy
Genotype-Phenotype Association in ABCA4-Associated Retinopathy
Retinal pathoconnectomics: A Window into Neurodegeneration
The role of Ceramide in Inherited Retinal Disease Pathology
Extracelluar Matix: the Unexplored Aspects of Retinal Pathologies and Regeneration
Role of TFEB in diseases assocaited with lysosomal dysfunction
Retinoic acid receptor -related oprhan receptors (RORs) in eye development and disease
A novel mouse model for Late-Onset Retinal Degeneration (L-ORD) devekios RPE abnormalities due to the loss of C1qtnf5/Ctrp5
Comparison of mouse models of autosomal dominant retinitis pigmentosa due to P23H muations of Rhodopsin
Compensatory Cone-Mediated Mechanisms in Inherited Retinal Degeneration Mouse Models: A Functional and Gene Expression Analsyis
Inhibition of Ryanodine Receptor 1 Reduces Endoplasmic Reticulum (ER) Sress and Promotes ER Protein Degradation in Cyclic Nucleotide-gated Channel Deficiency
Mouse choroid proteome revisited: foucs on aging
Morphological and functional comparison of mice models for retinitis pigmentosa
Current Advancements in Mouse Models of Retinal Disease
Single-cell Itrnacriptomic Profiling of Muller Glia in the rd10 Retina
Methods for in vivo characterization of proteostatis in the mouse retina
Absence or PRCD leads to dysregulation in lipie Homeostatis resulting in disorganizationof photorecptor outer segment structure
Expansion Microscopy of Mouse Photoreceptro Cilia
Rod photorecptor specific ablation of Metformin target, AMPK, in preclinical model of autosomal recessvie retinitis pigmentosa
TLR2 is highly overexpressed in retinal myeloid cells in the rd10 mouse model of retinitis pigmentosa
Environmental light has an essentail effrect on the diseasae expression in a dominant RPE65 mutation
Microglia Preserve Visual Function in A Mouse Model of Retinitis Pigmentosa with Rhodopsin-P23H Mutant
Measuring the release of lactate from wild-type and rd1 mouse retina
Aerobic glycolysis in photorecptors supports energy demand in the absence of mitochondrial coupling
Redox Status in Retinitis Pigmentosa
Perspectives on retinal dolichol metabolism and visual deficits in dolichol metalbolism-associated inherited disorders
Retinal metabolic profile on IMPG2 deficiency mice with subretinal lesions
Glutathione-coating of liposomes enhances the delivery of hydrophillic cargo to the inner nuclear layer in retinal cultures
Modification of Mueller glial cell fate and proliferation with the use of small molecules
A potential neuroprotective role for pyruvate kinase 2 in retinal degeneration
Critical role of VEGF as a direct regulator of photorecptor function
Lysine Ubiquitylation Drives Rhodopsin Protein Turnover
In-silico prediction of MYO!C Rhodopsin Interactions and its Significance in Protein Localization and Visual Function
A ciliary branched actin netowrk drives photoreceptor disc morphogenesis
Revisiting the daily timing of POS phagocytosis
Inhibition of Bacterial Peoptidoglycan Cytopahty by Retina Pigment Epithelial PGRP2 Amidase
Understanding ischemic retinopathies: the role of Succinate and its recpto^T mutation
Inducing neural regeneratio nfrom glia using proneural bHLH transcription factors.