Retinal degenerative diseases : mechanisms and experimental therapy / edited by John D. Ash, Robert E. Anderson, Matthew M. LaVail, Catherine Bowes Rickman, Joe G. Hollyfield, Christian Grimm.
Ash, John D., editor.; Anderson, Robert E. (Robert Eugene), editor.; LaVail, Matthew M., editor.; Rickman, Catherine Bowes, editor.; Hollyfield, Joe G., editor.; Grimm, Christian, 1962- editor.
2018
RE661.D3
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Title Retinal degenerative diseases : mechanisms and experimental therapy / edited by John D. Ash, Robert E. Anderson, Matthew M. LaVail, Catherine Bowes Rickman, Joe G. Hollyfield, Christian Grimm.
ISBN 9783319754024 (electronic book)
3319754025 (electronic book)
9783319754017
3319754017
DOI https://doi.org/10.1007/978-3-319-75402-4
Published Cham, Switzerland : Springer, [2018]
Copyright ©2018
Language English
Description 1 online resource (xlii, 669 pages) : illustrations.
Item Number 10.1007/978-3-319-75402-4 doi
Call Number RE661.D3
Dewey Decimal Classification 617.7/35
Summary "The blinding diseases of inherited retinal degenerations have no treatments, and age-related macular degeneration has no cures, despite the fact that it is an epidemic among the elderly, with 1 in 3-4 affected by the age of 70. The RD Symposium will focus on the exciting new developments aimed at understanding these diseases and providing therapies for them. Since most major scientists in the field of retinal degenerations attend the biennial RD Symposia, they are known by most as the "best" and "most important" meetings in the field. The volume will present representative state-of-the-art research in almost all areas of retinal degenerations, ranging from cytopathologic, physiologic, diagnostic and clinical aspects; animal models; mechanisms of cell death; candidate genes, cloning, mapping and other aspects of molecular genetics; and developing potential therapeutic measures such as gene therapy and neuroprotective agents for potential pharmaceutical therapy. While advances in these areas of retinal degenerations will be described, there will be many new topics that either were in their infancy or did not exist at the time of the last RD Symposium, RD2014. These include the role of inflammation and immunity, as well as other basic mechanisms, in age-related macular degeneration, several new aspects of gene therapy, and revolutionary new imaging and functional testing that will have a huge impact on the diagnosis and following the course of retinal degenerations, as well as to provide new quantitative endpoints for clinical trials. The retina is an approachable part of the central nervous system (CNS), and there is a major interest in neuroprotective and gene therapy for CNS diseases and neurodegenerations, in general. It should be noted that with successful and exciting initial clinical trials in neuroprotective and gene therapy, including the restoration of sight in blind children, the retinal degeneration therapies are leading the way towards new therapeutic measures for neurodegenerations of the CNS. Many of the successes recently reported in these areas of retinal degeneration sprang from collaborations established at previous RD Symposia, and many of those will be reported at the RD2018 meeting and included in the proposed volume. We anticipate the excitement of those working in the field and those afflicted with retinal degenerations will be reflected in the volume"--Publisher's description.
Access Note Access limited to authorized users.
Digital File Characteristics text file PDF
Added Author Ash, John D., editor.
Anderson, Robert E. (Robert Eugene), editor.
LaVail, Matthew M., editor.
Rickman, Catherine Bowes, editor.
Hollyfield, Joe G., editor.
Grimm, Christian, 1962- editor.
Series Advances in experimental medicine and biology ; 1074.
Available in Other Form Retinal degenerative diseases.
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Age-related macular degeneration (AMD). Oxidative stress regulation and DJ-1 function in the retinal pigment epithelium: implications for AMD
Mitochondria: potential targets for protection in age-related macular degeneration
Toll-like receptors and age-related macular degeneration
Alterations in extracellular matrix/Bruch's membrane can cause the activation of the alternative complement pathway via tick-over
MicroRNA as therapeutics for age-related macular degeneration
Anaphylatoxin signaling in retinal pigment and choroidal endothelial cells: characteristics and relevance to age-related macular degeneration
Estimations of retinal blue-light irradiance values and melatonin suppression indices through clear and yellow-tinted intraocular lenses
Co-expression of wild-type and mutant S163R C1QTNF5 in retinal pigment epithelium
Gene therapies. Mini-review: cell type-specific optogenetic vision restoration approaches
Mutation-independent gene therapies for rod-cone dystrophies
Antisense oligonucleotide-based splice correction of a deep-intronic mutation in CHM underlying choroideremia
Gene therapy approaches to treat the neurodegeneration and visual failure in neuronal ceroid lipofuscinoses
Success of gene therapy in late-stage treatment
Optimizing non-viral gene therapy vectors for delivery to photoreceptors and retinal pigment epithelial cells
Nanoparticles as delivery vehicles for the treatment of retinal degenerative diseases
Overexpression of type 3 iodothyronine deiodinase reduces cone death in the Leber congenital amaurosis model mice
In-vivo diagnostics for structure and function. In vivo functional imaging of retinal neurons using red and green fluorescent calcium indicators
Optimizing ERG measures of scotopic and photopic critical flicker frequency
Repeatability and reproducibility of in vivo cone density measurements in the adult zebrafish retina
Normative retinal thicknesses in common animal models of eye disease using spectral domain optical coherence tomography
A novel approach for integrating AF-SLO and SDOCT imaging data demonstrates the ability to identify early retinal abnormalities in mutant mice and evaluate the effects of genetic and pharmacological manipulation
Inflammation and angiogenesis. The role of hypoxia, hypoxia-inducible factor (HIF), and VEGF in retinal angiomatous proliferation
Neuroinflammation in retinitis pigmentosa, diabetic retinopathy, and age-related macular degeneration: a minireview
Autoimmune retinopathy: an immunologic cellular-driven disorder
Inflammation-induced photoreceptor cell death
Sall1 regulates microglial morphology cell autonomously in the developing retina
Inherited retinal degenerations. Whole-exome sequencing identifies novel variants that co-segregates with autosomal recessive retinal degeneration in a Pakistani pedigree
Identification of novel deletions as the underlying cause of retinal degeneration in two pedigrees
Molecular findings in families with an initial diagnose of autosomal dominant retinitis pigmentosa (adRP)
Pleiotropic effects of risk factors in age-related macular degeneration and seemingly unrelated complex diseases
Mapping of canine models of inherited retinal diseases
A mini-review: Leber congenital amaurosis: identification of disease-causing variants and personalised therapies


Mechanisms of degeneration. Role of fibulins 2 and 5 in retinal development and maintenance
Identifying key networks linked to light-independent photoreceptor degeneration in visual arrestin 1 knockout mice
How excessive cGMP impacts metabolic proteins in retinas at the onset of degeneration
Protein carbonylation-dependent photoreceptor cell death induced by N-Methyl-N-nitrosourea in mice
Müller glia reactivity and development of gliosis in response to pathological conditions
Underdeveloped RPE apical domain underlies lesion formation in canine bestrophinopathies
Binary function of ARL3-GTP revealed by gene knockouts
Do cGMP levels drive the speed of photoreceptor degeneration?
Early endosome morphology in health and disease
The retinal circadian clock and photoreceptor viability
The role of c-Jun N-terminal kinase (JNK) in retinal degeneration and vision loss
The evaluation of BMI1 posttranslational modifications during retinal degeneration to understand BMI1 action on photoreceptor death execution
Primary rod and cone degeneration is prevented by HDAC inhibition
Impact of MCT1 haploinsufficiency on the mouse retina
The Leber congenital amaurosis-linked protein AIPL1 and its critical role in photoreceptors
Alternative splicing for activation of coagulation factor XIII-A in the fish retina after optic nerve injury
Bisretinoid photodegradation is likely not a good thing
Further characterization of the predominant inner retinal degeneration of aging Cln3[superscript][delta]ex7/8 knock-in mice
Differential exon expression in a large family of retinal genes is regulated by a single trans locus
Molecular chaperone ERp29: a potential target for cellular protection in retinal and neurodegenerative diseases
The role of microbiota in retinal disease
Neuroprotection. Current pharmacological concepts in the treatment of the retinitis pigmentosa
Valproic acid inhibits human retinal pigment epithelial (hRPE) cell proliferation via a P38 MAPK signaling mechanism
Pigment epithelium-derived factor protects retinal pigment epithelial cells against cytotoxicity “in vitro”
Brain-derived neurotrophic factor as a treatment option for retinal degeneration
VEGF as a trophic factor for Müller glia in hypoxic retinal diseases
Müller cell biological processes associated with leukemia inhibitory factor expression
Retbindin is capable of protecting photoreceptors from flavin-sensitized light-mediated cell death in vitro
Constitutive activation mutant mTOR promote cone survival in retinitis pigmentosa mice
Maintaining cone function in rod-cone dystrophies
PKG-dependent cell death in 661W cone photoreceptor-like cell cultures (experimental study)
Retinal cell biology. more than meets the eye: current understanding of RPGR function
Polarized exosome release from the retinal pigmented epithelium
The impact of adherens and tight junctions on physiological function and pathological changes in the retina
TRPV4 does not regulate the distal retinal light response
Role of sirtuins in retinal function under basal conditions
The retinol-binding protein receptor 2 (Rbpr2) is required for photoreceptor survival and visual function in the zebrafish
Opposite roles of MerTK ligands Gas6 and protein S during retinal phagocytosis
Redundant and nonredundant functions of Akt isoforms in the retina
Photoreceptor outer segment isolation from a single canine retina for RPE phagocytosis assay
Preservation of photoreceptor nanostructure for electron tomography using transcardiac perfusion followed by high-pressure freezing and freeze-substitution
Microtubule-associated protein 1 light chain 3 (LC3) Isoforms in RPE and retina
Stem cells. The iPSc-derived retinal tissue as a tool to study growth factor production in the eye
Stem cell-based RPE therapy for retinal diseases: engineering 3D tissues amenable for regenerative medicine
Validation of iPS cell-derived RPE tissue in animal models
Cell transplantation for retinal degeneration: transition from rodent to nonhuman primate models
Talaumidin promotes neurite outgrowth of staurosporine-differentiated RGC-5 cells through PI3K/Akt-dependent pathways.

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