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The Journal of Cell Biology, ISSN 0021-9525, 05/2017, Volume 216, Issue 5, p. 1227
Formation of membrane discs in photoreceptor cells requires evagination of its ciliary plasma membrane by an unknown molecular mechanism. Salinas et al. (2017.... 
Physiological aspects | Cilia and ciliary motion | Photoreceptors
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 11/2011, Volume 51, Issue 10, pp. 1849 - 1860
Retinal mitochondria become dysfunctional and their DNA (mtDNA) is damaged in diabetes. The biogenesis of mitochondrial DNA is tightly controlled by... 
Diabetic retinopathy | Superoxide dismutase | Mitochondria | Free radicals | DNA damage | OXIDATIVE STRESS | ANTIOXIDANTS | CAPILLARY CELL-DEATH | BIOCHEMISTRY & MOLECULAR BIOLOGY | DAMAGE | DNA COPY NUMBER | ENDOCRINOLOGY & METABOLISM | RETINA | MICE | DYSFUNCTION | SUPEROXIDE-DISMUTASE | POTENTIAL ROLE | Electron Transport | Retina - metabolism | Superoxide Dismutase - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Transcriptional Activation | Diabetes Mellitus, Experimental - genetics | Diabetes Mellitus, Type 2 - metabolism | Mitochondria - ultrastructure | Nuclear Respiratory Factor 1 - genetics | DNA-Binding Proteins - metabolism | Endothelial Cells - ultrastructure | Mitochondria - genetics | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Nuclear Respiratory Factor 1 - metabolism | Trans-Activators - genetics | DNA Damage - genetics | Adult | Cell Growth Processes - genetics | Diabetes Mellitus, Experimental - metabolism | Diabetes Mellitus, Experimental - physiopathology | High Mobility Group Proteins - metabolism | Cells, Cultured | Oxidative Stress - genetics | Mice, Transgenic | Mitochondria - metabolism | DNA-Binding Proteins - genetics | Disease Progression | Animals | Diabetes Mellitus, Type 2 - physiopathology | Diabetes Mellitus, Experimental - pathology | Trans-Activators - metabolism | Aged | Mice | Transcription Factors | Diabetes Mellitus, Type 2 - pathology | Retina - pathology | Diabetic Retinopathy | High Mobility Group Proteins - genetics | Genes | Heat shock proteins | Development and progression | Mitochondrial DNA | Biosynthesis | Superoxide | Ophthalmology | Translocation | Transcription factors | Retinopathy | Diabetes mellitus | Transgenic mice | Retina | Hsp70 protein | Chaperones | Glucose | Electron microscopy | Endothelial cells | Replication | copy number | Communication | Pharmaceuticals | Index Medicus
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 05/2017, Volume 216, Issue 5, pp. 1227 - 1229
Journal Article
Journal Article
Journal Article
Molecular Biology of the Cell, ISSN 1059-1524, 07/2018, Volume 29, Issue 13, pp. 1590 - 1598
The outer segment (OS) of photoreceptor cells is an elaboration of a primary cilium with organized stacks of membranous disks that contain the proteins needed... 
TRANSPORT | MICROTUBULES | TRAFFICKING | REGULATOR (RPGR)-INTERACTING PROTEIN | MUTATIONS | BINDING | GTPASE | RPGR | REVEALS | DEGENERATION | CELL BIOLOGY | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 331 - 339
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
COMPLETE FORM | LIGHT RESPONSE | CHANNEL | MGLUR6 | SYNAPTIC-TRANSMISSION | MOUSE MODEL | GENETICS & HEREDITY | NYCTALOPIN | RICH REPEAT PROTEIN | MUTATIONS | CONE ELECTRORETINOGRAM | Electroretinography - methods | Night Blindness - metabolism | Humans | Dark Adaptation - genetics | Retinal Rod Photoreceptor Cells - metabolism | Gene Knockdown Techniques - methods | Myopia - metabolism | Receptors, Metabotropic Glutamate - genetics | Retinal Bipolar Cells - physiology | Chromosome Mapping - methods | Genetic Diseases, X-Linked | Night Blindness - genetics | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary | Signal Transduction | Mice, Inbred C57BL | Zebrafish | Mice, Inbred C3H | Myopia - genetics | Animals | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Retinal Rod Photoreceptor Cells - physiology | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Mutation | Chromosome mapping | Usage | Gene mutations | Retinal bipolar cells | Causes of | Physiological aspects | Night blindness | Genetic aspects | Research | Analysis | Genetic disorders | Proteins | Rodents | Blindness | Gene expression | Cells | Index Medicus | Animal models | Antibodies | Insertion | stationary night blindness | Retina | Guanine nucleotide-binding protein | Electroretinograms | Depolarization | Signal transduction | Vision | Bipolar cells | Gene mapping | DNA sequencing | Report
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 02/2019, Volume 116, Issue 9, pp. 3530 - 3535
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 12/2011, Volume 20, Issue 23, pp. 4569 - 4581
Defects in the photoreceptor-specific gene aryl hydrocarbon receptor interacting protein-like 1 (Aipl1) are associated with Leber congenital amaurosis (LCA), a... 
RETINAL DEGENERATION | ADENOASSOCIATED VIRAL VECTORS | CONE LOSS | PHOTORECEPTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE MODEL | GENETICS & HEREDITY | CGMP PHOSPHODIESTERASE | RPE65 MUTATIONS | ITALIAN PATIENTS | RETINITIS-PIGMENTOSA | AIPL1 MUTATIONS | Leber Congenital Amaurosis - pathology | Dependovirus - genetics | Genetic Therapy | Dependovirus - radiation effects | Retinal Rod Photoreceptor Cells - ultrastructure | Humans | Retinal Rod Photoreceptor Cells - metabolism | Vision, Ocular - radiation effects | Leber Congenital Amaurosis - complications | Behavior, Animal | Vision, Ocular - physiology | Retina - enzymology | Light | Eye Proteins - genetics | Capsid - metabolism | Carrier Proteins - therapeutic use | Leber Congenital Amaurosis - therapy | Retina - radiation effects | Cyclic Nucleotide Phosphodiesterases, Type 6 - metabolism | Leber Congenital Amaurosis - physiopathology | Eye Proteins - therapeutic use | Retinal Degeneration - physiopathology | Mutation - genetics | Carrier Proteins - genetics | Animals | Adaptor Proteins, Signal Transducing - deficiency | Retinal Degeneration - therapy | Mice | Adaptor Proteins, Signal Transducing - metabolism | Retinal Degeneration - pathology | Retina - pathology | Retinal Rod Photoreceptor Cells - pathology | Capsid Proteins - genetics | Retinal Degeneration - complications | Index Medicus
Journal Article