Retinal Degenerative Diseases and Experimental Therapy
To create a forum for scientists and clinicians interested in degenerative retinal diseases, we began in 1984 to organize a biennial symposium on Retinal Degeneration as a satellite meeting of the International Congress of Eye Research. The timing and varying location of these meetings provides an i...
| Other Authors: | , , |
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| Format: | eBook |
| Language: | English |
| Published: |
New York, NY
Springer US
1999, 1999
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| Edition: | 1st ed. 1999 |
| Subjects: | |
| Online Access: | |
| Collection: | Springer Book Archives -2004 - Collection details see MPG.ReNa |
Table of Contents:
- Intraocular Pressure in Tapetoretinal Degenerations
- Gene Therapy for Photoreceptor Rescue
- Ribozymes Directed Against Messenger RNAs Associated With Autosomal Dominant Retinitis Pigmentosa
- Ribozyme-Mediated Gene Therapy for Autosomal Dominant Retinal Degeneration
- Targeting Müller Cells for Gene Therapy
- The Involvement of Light in Retinal Degeneration
- Dark Adaptation is Impaired in Diabetics before Photopic Visual Losses Can be Seen
- Age and Monocular Enucleation as Potential Determinants of Light Damage in the Mouse Retina
- Ultraviolet Light Damage and Reversal by Retinoic Acid in Juvenile Goldfish Retina
- A Comparison of Light-Induced Rod Degeneration in Two Teleost Models
- Regulation of Light Absorption in the Pigmented Rat Retina
- An Uncoupling Effect of Reactive Oxygen Species on the Retinal Horizontal Cells
- Animal Models with Photoreceptor Degeneration
- Animal Model for Retinitis Pigmentosa
- Specific Gene Defects Cause Photoreceptor Degeneration
- Evidence for Myosin VIIa-Driven Transport of Rhodopsin in the Plasma Membrane of the Photoreceptor-Connecting Cilium
- Blindness in Usher Syndrome 1B
- Different Mutations in RPE65 Are Associated with Variability in the Severity of Retinal Dystrophy
- The RPE65-Deficient Mouse as a Model for RPE65-Associated Leber’s Congenital Amaurosis and Related Disorders
- CRALBP and Inherited Retinal Degeneration
- Guanylyl Cyclase Genes and Their Role in Retinal Degeneration
- Loss of Cone and Reduction in Rod ERG Responses in the Guanylyl Cyclase-E (GC-E) Deficient Mouse
- Guanylyl Cyclase Gene is the Disease Locus in the rd Chicken
- Leber’s Congenital Amaurosis
- Retinal Degeneration is Accelerated when a Mutant Rhodopsin Transgene is Expressed on a Haploid or Null Rhodopsin Background
- Rhodopsin C-Terminal Sequence Qvs(A)Pa Directs Its Sorting To The Ros In Retinal Photoreceptors
- Development Of Rat Models For Choroidal Neovascularisation (CNV)
- Identification of Degeneration-Specific Genes in the Rcs Rat Retina By Subtractive Hybridization Techniques
- Analysis of Field Potentials and Spike Patterns Evoked by Local Electrical Stimulation of the Chicken Retina
- Molecular and Cell Biological Studies
- Antisense Inactivation of Rds/Peripherin in Xenopus Laevis Embryonic Retinal Cultures
- Phosducin-Like Protein 1 (Phlp1) and Phosducin-Like Orphan Protein 1 (Phlop1)
- Organization of The Interphotoreceptor Matrix
- Diverse Localization of Cyclic Nucleotide Gated Channels in the Outer Segments of Rods and Cones
- Retinal Prosthesis as a Replacement for Photoreceptors
- Development of an Epiretinal Electronic Visual Prosthesis
- ResponseCharacteristics of Subretinal Microphotodiode-Based Implant-Mediated Cortical Potentials
- Electrical Stimulation of the Human Retina
- Goals,Concepts,and Current State of the Retina Implant Project
- The Cytoplasmic Tail of Rhodopsin Acts as a Sorting Signal in Polarized Photoreceptors and MDCK Cells
- A Homozygous 1-Base Pair Deletion (1147dela) in the Arrestin Gene in Autosomal Recessive Retinitis Pigmentosa
- mRNA Analysis of Oguchi Patients with the Frequent 1147delA Mutation in the Arrestin Gene
- Mutation Spectrum in the Rep-1 Gene of Japanese Choroideremia Patients
- Phenotype-Genotype Correlations in Retinal Degenerations Caused by Abcr gene Mutations
- Autosomal Dominant Macular Degeneration Localized to Chromosome 6q by Linkage Analysis
- The Gene Product of IMPG1 is the Glycoprotein SPACR, not an IPM Proteoglycan
- Bardet-Biedl Syndrome
- Genetic Mapping and Evaluation of PDE6A in 49 Spanish Families with Autosomal Recessive Retinitis Pigmentosa
- Grading Device for Light Perception with Retinitis Pigmentosa
- Blue ConeMonochromacy
- The Peripherin/rds Gene
- Autosomal Dominant Retinitis Pigmentosa and Hyperopia
- Are Subretinal Microphotodiodes Suitable as a Replacement For Degenerated Photoreceptors?
- Neuroprotective Agents Romote Photoreceptor Survival
- Rods Produce a Diffusible Factor Promoting Cone Photoreceptor Survival In Vivo and in Vitro
- Pigment Epithelium-Derived Factor (PEDF) in the Retina
- Retinal Neurons in Primary Cell Culture
- Melatonin Receptor Blockers Enhance Photoreceptor Survival and Function in Light Damaged Rat Retina
- Transplantation Studies
- IRIS Pigment Epithelial Cell Transplantation in Monkey Eyes
- The Retinal Pigment Epithelial Cell Differentiation and Cell Marker Expression Following Cryopreservation at -80°C and under Liquid Nitrogen at -196°C.