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Retinal Degenerative Diseases

Overview of attention for book
Cover of 'Retinal Degenerative Diseases'

Table of Contents

  1. Altmetric Badge
    Book Overview
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    Chapter 1 Apolipoprotein E Isoforms and AMD.
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    Chapter 2 Role of Chemokines in Shaping Macrophage Activity in AMD.
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    Chapter 3 Biology of p62/sequestosome-1 in Age-Related Macular Degeneration (AMD).
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    Chapter 4 Retinal Degenerative Diseases
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    Chapter 5 Retinal Degenerative Diseases
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    Chapter 6 Therapeutic Approaches to Histone Reprogramming in Retinal Degeneration.
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    Chapter 7 A Brief Discussion on Lipid Activated Nuclear Receptors and their Potential Role in Regulating Microglia in Age-Related Macular Degeneration (AMD).
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    Chapter 8 Extracellular Matrix Alterations and Deposit Formation in AMD
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    Chapter 9 The NLRP3 Inflammasome and its Role in Age-Related Macular Degeneration
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    Chapter 10 Oxidative Stress and the Nrf2 Anti-Oxidant Transcription Factor in Age-Related Macular Degeneration
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    Chapter 11 Aging Changes in Retinal Microglia and their Relevance to Age-related Retinal Disease
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    Chapter 12 VEGF-A and the NLRP3 Inflammasome in Age-Related Macular Degeneration
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    Chapter 13 Interrelation Between Oxidative Stress and Complement Activation in Models of Age-Related Macular Degeneration
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    Chapter 14 Gene-Diet Interactions in Age-Related Macular Degeneration.
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    Chapter 15 Challenges in the Development of Therapy for Dry Age-Related Macular Degeneration
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    Chapter 16 Nanoceria: a Potential Therapeutic for Dry AMD
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    Chapter 17 β-amyloidopathy in the Pathogenesis of Age-Related Macular Degeneration in Correlation with Neurodegenerative Diseases.
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    Chapter 18 Different Mutations in ELOVL4 Affect Very Long Chain Fatty Acid Biosynthesis to Cause Variable Neurological Disorders in Humans
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    Chapter 19 Mouse Models of Stargardt 3 Dominant Macular Degeneration
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    Chapter 20 Current Progress in Deciphering Importance of VLC-PUFA in the Retina
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    Chapter 21 Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy: Similarities to Age-Related Macular Degeneration and Potential Therapies
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    Chapter 22 Hsp90 as a Potential Therapeutic Target in Retinal Disease
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    Chapter 23 Leber Congenital Amaurosis: Genotypes and Retinal Structure Phenotypes
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    Chapter 24 A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects
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    Chapter 25 Ablation of Chop Transiently Enhances Photoreceptor Survival but Does Not Prevent Retinal Degeneration in Transgenic Mice Expressing Human P23H Rhodopsin
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    Chapter 26 Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP).
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    Chapter 27 FAM161A and TTC8 are Differentially Expressed in Non-Allelelic Early Onset Retinal Degeneration
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    Chapter 28 Retinal Degenerative Diseases
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    Chapter 29 RDS Functional Domains and Dysfunction in Disease
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    Chapter 30 TULP1 Missense Mutations Induces the Endoplasmic Reticulum Unfolded Protein Response Stress Complex (ER-UPR)
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    Chapter 31 Understanding Cone Photoreceptor Cell Death in Achromatopsia
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    Chapter 32 Geranylgeranylacetone Suppresses N -Methyl- N -nitrosourea-Induced Photoreceptor Cell Loss in Mice
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    Chapter 33 My Retina Tracker(™): An On-line International Registry for People Affected with Inherited Orphan Retinal Degenerative Diseases and their Genetic Relatives - A New Resource.
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    Chapter 34 A Mini-review: Animal Models of GUCY2D Leber Congenital Amaurosis (LCA1)
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    Chapter 35 A Comprehensive Review of Mutations in the MERTK Proto-Oncogene
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    Chapter 36 New Developments in Murine Imaging for Assessing Photoreceptor Degeneration In Vivo
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    Chapter 37 Reliability and Repeatability of Cone Density Measurements in Patients with Congenital Achromatopsia
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    Chapter 38 Quantitative Fundus Autofluorescence in Best Vitelliform Macular Dystrophy: RPE Lipofuscin is not Increased in Non-Lesion Areas of Retina
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    Chapter 39 Interpretation of Flood-Illuminated Adaptive Optics Images in Subjects with Retinitis Pigmentosa.
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    Chapter 40 Retinal Degenerative Diseases
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    Chapter 41 Wide-Field Fundus Autofluorescence for Retinitis Pigmentosa and Cone/Cone-Rod Dystrophy
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    Chapter 42 The Development of a Cat Model of Retinal Detachment and Re-attachment.
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    Chapter 43 The Role of X-Chromosome Inactivation in Retinal Development and Disease
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    Chapter 44 A Non-Canonical Role for β-Secretase in the Retina
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    Chapter 45 The Consequences of Hypomorphic RPE65 for Rod and Cone Photoreceptors
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    Chapter 46 The Rate of Vitamin A Dimerization in Lipofuscinogenesis, Fundus Autofluorescence, Retinal Senescence and Degeneration.
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    Chapter 47 Can Vitamin A be Improved to Prevent Blindness due to Age-Related Macular Degeneration, Stargardt Disease and Other Retinal Dystrophies?
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    Chapter 48 Class I Phosphoinositide 3-Kinase Exerts a Differential Role on Cell Survival and Cell Trafficking in Retina
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    Chapter 49 Cell Cycle Proteins and Retinal Degeneration: Evidences of New Potential Therapeutic Targets.
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    Chapter 50 Nitric Oxide Synthase Activation as a Trigger of N-methyl-N-nitrosourea-Induced Photoreceptor Cell Death
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    Chapter 51 Molecular Principles for Decoding Homeostasis Disruptions in the Retinal Pigment Epithelium: Significance of Lipid Mediators to Retinal Degenerative Diseases
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    Chapter 52 Aging and Vision
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    Chapter 53 Retinal Degenerative Diseases
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    Chapter 54 Retinal Degenerative Diseases
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    Chapter 55 Photoreceptor Neuroprotection: Regulation of Akt Activation Through Serine/Threonine Phosphatases, PHLPP and PHLPPL
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    Chapter 56 The Role of AMPK Pathway in Neuroprotection.
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    Chapter 57 Tauroursodeoxycholic Acid Protects Retinal Function and Structure in rd1 Mice
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    Chapter 58 Near-Infrared Photobiomodulation in Retinal Injury and Disease.
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    Chapter 59 Exercise and Cyclic Light Preconditioning Protect Against Light-Induced Retinal Degeneration and Evoke Similar Gene Expression Patterns
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    Chapter 60 Small Molecules that Protect Mitochondrial Function from Metabolic Stress Decelerate Loss of Photoreceptor Cells in Murine Retinal Degeneration Models
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    Chapter 61 Retinal Degenerative Diseases
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    Chapter 62 Therapeutic Approach of Nanotechnology for Oxidative Stress Induced Ocular Neurodegenerative Diseases
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    Chapter 63 Transscleral Controlled Delivery of Geranylgeranylaceton Using a Polymeric Device Protects Rat Retina Against Light Injury
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    Chapter 64 Targeting the Proteostasis Network in Rhodopsin Retinitis Pigmentosa.
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    Chapter 65 Gene Therapy for MERTK -Associated Retinal Degenerations
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    Chapter 66 Tamoxifen-Containing Eye Drops Successfully Trigger Cre -Mediated Recombination in the Entire Eye
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    Chapter 67 Retinal Degenerative Diseases
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    Chapter 68 Characterization of Ribozymes Targeting a Congenital Night Blindness Mutation in Rhodopsin Mutation
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    Chapter 69 Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies
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    Chapter 70 Functional Rescue of Retinal Degeneration-Associated Mutant RPE65 Proteins
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    Chapter 71 Evaluation of Ocular Gene Therapy in an Italian Patient Affected by Congenital Leber Amaurosis Type 2 Treated in Both Eyes.
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    Chapter 72 Retinal Degenerative Diseases
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    Chapter 73 Personalized Medicine: Cell and Gene Therapy Based on Patient-Specific iPSC-Derived Retinal Pigment Epithelium Cells.
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    Chapter 74 Human Retinal Pigment Epithelium Stem Cell (RPESC)
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    Chapter 75 Embryonic Stem Cell-Derived Microvesicles: Could They be Used for Retinal Regeneration?
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    Chapter 76 Intravitreal Implantation of Genetically Modified Autologous Bone Marrow-Derived Stem Cells for Treating Retinal Disorders.
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    Chapter 77 Gliosis Can Impede Integration Following Photoreceptor Transplantation into the Diseased Retina
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    Chapter 78 Interkinetic Nuclear Migration in the Regenerating Retina
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    Chapter 79 Use of a Machine Learning-Based High Content Analysis Approach to Identify Photoreceptor Neurite Promoting Molecules
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    Chapter 80 A Novel Approach to Identify Photoreceptor Compartment-Specific Tulp1 Binding Partners
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    Chapter 81 Thyroid Hormone Signaling and Cone Photoreceptor Viability.
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    Chapter 82 In-Depth Functional Diagnostics of Mouse Models by Single-Flash and Flicker Electroretinograms without Adapting Background Illumination.
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    Chapter 83 The Role of Intraflagellar Transport in the Photoreceptor Sensory Cilium
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    Chapter 84 Regulation of Retinal Development via the Epigenetic Modification of Histone H3.
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    Chapter 85 The Potential Role of Flavins and Retbindin in Retinal Function and Homeostasis
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    Chapter 86 Identification of Tyrosine O Sulfated Proteins in Cow Retina and the 661W Cell Line
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    Chapter 87 The Function of Arf-like Proteins ARL2 and ARL3 in Photoreceptors
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    Chapter 88 Characterization of Antibodies to Identify Cellular Expression of Dopamine Receptor 4
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    Chapter 89 A Possible Role of Neuroglobin in the Retina After Optic Nerve Injury: A Comparative Study of Zebrafish and Mouse Retina
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    Chapter 90 JNK Inhibition Reduced Retinal Ganglion Cell Death after Ischemia/Reperfusion In Vivo and after Hypoxia In Vitro.
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    Chapter 91 Cell Fate of Müller Cells During Photoreceptor Regeneration in an N -Methyl- N -nitrosourea-Induced Retinal Degeneration Model of Zebrafish
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    Chapter 92 Polymodal Sensory Integration in Retinal Ganglion Cells
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    Chapter 93 Retinal Degenerative Diseases
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    Chapter 94 The mTOR Kinase Inhibitor INK128 Blunts Migration of Cultured Retinal Pigment Epithelial Cells
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    Chapter 95 Live Imaging of LysoTracker-Labelled Phagolysosomes Tracks Diurnal Phagocytosis of Photoreceptor Outer Segment Fragments in Rat RPE Tissue Ex Vivo
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    Chapter 96 Cre Recombinase: You Can’t Live with It, and You Can’t Live Without It
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    Chapter 97 Efficiency of Membrane Protein Expression Following Infection with Recombinant Adenovirus of Polarized Non-Transformed Human Retinal Pigment Epithelial Cells
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    Chapter 98 Retinal Degenerative Diseases
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    Chapter 99 Lysosomal Trafficking Regulator (LYST)
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    Chapter 100 Live-Cell Imaging of Phagosome Motility in Primary Mouse RPE Cells
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    Chapter 101 RPE Cell and Sheet Properties in Normal and Diseased Eyes
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    Chapter 102 Valproic Acid Induced Human Retinal Pigment Epithelial Cell Death as Well as its Survival after Hydrogen Peroxide Damage is Mediated by P38 Kinase.
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    Chapter 103 Blockade of MerTK Activation by AMPK Inhibits RPE Cell Phagocytosis
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    Chapter 104 Modulation of V-ATPase by βA3/A1-Crystallin in Retinal Pigment Epithelial Cells.
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    Chapter 105 Proteomic Profiling of Cigarette Smoke Induced Changes in Retinal Pigment Epithelium Cells
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    Chapter 106 Reduced Metabolic Capacity in Aged Primary Retinal Pigment Epithelium (RPE) is Correlated with Increased Susceptibility to Oxidative Stress
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    Chapter 107 Erratum to: The Potential Use of PGC-1α and PGC-1β to Protect the Retina by Stimulating Mitochondrial Repair
Attention for Chapter 87: The Function of Arf-like Proteins ARL2 and ARL3 in Photoreceptors
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (55th percentile)
  • Good Attention Score compared to outputs of the same age and source (65th percentile)

Mentioned by

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15 Mendeley
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Chapter title
The Function of Arf-like Proteins ARL2 and ARL3 in Photoreceptors
Chapter number 87
Book title
Retinal Degenerative Diseases
Published in
Advances in experimental medicine and biology, January 2016
DOI 10.1007/978-3-319-17121-0_87
Pubmed ID
Book ISBNs
978-3-31-917120-3, 978-3-31-917121-0
Authors

Christin Hanke-Gogokhia, Houbin Zhang, Jeanne M. Frederick, Wolfgang Baehr, Hanke-Gogokhia, Christin, Zhang, Houbin, Frederick, Jeanne M., Baehr, Wolfgang

Abstract

Arf-like proteins (ARLs) are ubiquitously expressed small G proteins of the RAS superfamily. In photoreceptors, ARL2 and ARL3 participate in the trafficking of lipidated membrane-associated proteins and colocalize in the inner segment with UNC119A and PDEδ. UNC119A and PDEδ are acyl- and prenyl-binding proteins, respectively, involved in trafficking of acylated (transducin-α subunit, nephrocystin NPHP3) and prenylated proteins (GRK1, PDE6). Germline Arl3 knockout mice do not survive beyond postnatal day 21 and display ciliary defects in multiple organs (kidney, liver and pancreas) as well as retinal degeneration. Conditional knockouts will be necessary to delineate mechanisms of protein transport in retina disease.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 27%
Professor 3 20%
Student > Postgraduate 2 13%
Researcher 2 13%
Lecturer 1 7%
Other 2 13%
Unknown 1 7%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 47%
Medicine and Dentistry 2 13%
Agricultural and Biological Sciences 1 7%
Nursing and Health Professions 1 7%
Neuroscience 1 7%
Other 1 7%
Unknown 2 13%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 May 2022.
All research outputs
#7,553,524
of 23,041,514 outputs
Outputs from Advances in experimental medicine and biology
#1,236
of 4,969 outputs
Outputs of similar age
#123,833
of 394,754 outputs
Outputs of similar age from Advances in experimental medicine and biology
#126
of 444 outputs
Altmetric has tracked 23,041,514 research outputs across all sources so far. This one is in the 44th percentile – i.e., 44% of other outputs scored the same or lower than it.
So far Altmetric has tracked 4,969 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.1. This one has gotten more attention than average, scoring higher than 65% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 394,754 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 55% of its contemporaries.
We're also able to compare this research output to 444 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 65% of its contemporaries.