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Journal Article
by Dai, T and Wu, XJ and Zhou, SN and Wang, QQ and Li, DN
BMC INFECTIOUS DISEASES, ISSN 1471-2334, 06/2016, Volume 16, Issue 1, pp. 245 - 245
Journal Article
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 04/2016, Volume 100, Issue 4, pp. 495 - 500
BackgroundThe GNAT1 gene encodes the α subunit of the rod transducin protein, a key element in the rod phototransduction cascade. Variants in GNAT1 have been... 
Genetics | Retina | Degeneration | CGMP-PHOSPHODIESTERASE | NOUGARET FORM | DATABASE | TRANSDUCIN ALPHA-SUBUNIT | ROD TRANSDUCIN | RECESSIVE RETINITIS-PIGMENTOSA | OPHTHALMOLOGY | UPDATE | GENOME | STATIONARY NIGHT BLINDNESS | Humans | Middle Aged | Molecular Sequence Data | Eye Diseases, Hereditary - diagnosis | Male | Heterotrimeric GTP-Binding Proteins - genetics | Base Sequence | Myopia - diagnosis | Aged, 80 and over | Adult | Female | Genetic Diseases, X-Linked - genetics | Eye Proteins - genetics | Night Blindness - genetics | Retinitis Pigmentosa - physiopathology | Genetic Diseases, X-Linked - physiopathology | Siblings | Electroretinography | Amino Acid Sequence | Eye Diseases, Hereditary - physiopathology | Tomography, Optical Coherence | Night Blindness - diagnosis | Retina - physiopathology | Retinitis Pigmentosa - genetics | Codon, Nonsense | Genetic Diseases, X-Linked - diagnosis | Eye Diseases, Hereditary - genetics | Retinitis Pigmentosa - diagnosis | Myopia - genetics | DNA - isolation & purification | Myopia - physiopathology | Night Blindness - physiopathology | Aged | High-Throughput Nucleotide Sequencing | Genetically modified mice | Retinal degeneration | Care and treatment | Research | Gene mutations | Risk factors | Proteins | Diabetic retinopathy | Genes | Tomography | Photoreceptors | Mutation | Patients | Age | Deoxyribonucleic acid--DNA | Index Medicus | Clinical Science | 1506
Journal Article
Vision Research, ISSN 0042-6989, 06/2015, Volume 111, Issue Pt B, pp. 149 - 160
Journal Article
Journal Article
The Journal of Comparative Neurology, ISSN 0021-9967, 01/2007, Volume 500, Issue 2, pp. 222 - 238
Retinal degeneration 10 (rd10) mice are a model of autosomal recessive retinitis pigmentosa (RP), identified by Chang et al. in 2002 (Vision Res. 42:517–525).... 
retinitis pigmentosa | immunocytochemistry | bipolar cell | ERG | confocal microscopy | horizontal cell | Confocal microscopy | Horizontal cell | Immunocytochemistry | Retinitis pigmentosa | Bipolar cell | RAT RETINA | ROD BIPOLAR CELLS | MODEL | RD/RD MOUSE | NEUROSCIENCES | PHOTOTRANSDUCTION | ZOOLOGY | ACTIVATION STEPS | NEURONS | GENE-THERAPY | RETINITIS-PIGMENTOSA | PHOTORECEPTOR DEGENERATION | Immunohistochemistry | Dendrites - pathology | Retinal Bipolar Cells - pathology | Electroretinography - methods | Retina - metabolism | Cell Count | Retinal Horizontal Cells - pathology | Nerve Degeneration - physiopathology | Nerve Degeneration - genetics | Retinal Rod Photoreceptor Cells - metabolism | Mice, Mutant Strains | Nerve Degeneration - diagnosis | Retinitis Pigmentosa - physiopathology | Disease Models, Animal | Biomarkers - metabolism | Dendrites - metabolism | Retinal Bipolar Cells - metabolism | Mice, Inbred C57BL | Retina - physiopathology | Retinitis Pigmentosa - genetics | Membrane Potentials - physiology | Mutation - genetics | Retinitis Pigmentosa - diagnosis | Nerve Tissue Proteins - metabolism | Microscopy, Confocal | Animals | Mice | Retinal Horizontal Cells - metabolism | Apoptosis - physiology | Retina - pathology | Retinal Rod Photoreceptor Cells - pathology | Retinal Rod Photoreceptor Cells - physiopathology | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2013, Volume 110, Issue 4, pp. 1500 - 1505
Advances in human genetics are leading to the discovery of new disease-causing mutations at a remarkable rate. Many such mutations, however, occur in genes... 
Brain | Enzymes | Nervous system diseases | Disease models | Neurodegenerative diseases | Lipids | Mice | Lipid metabolism | Genotypes | Microglia | TOLL-LIKE-RECEPTOR-2 | neuroinflammation | MICROGLIA | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | MAST-CELLS | PHENOTYPE | CHEMOTACTIC MIGRATION | MICE | GENERATION | RECEPTORS | lipidomics | Lysophospholipids - metabolism | Microglia - metabolism | Humans | Cataract - pathology | Monoacylglycerol Lipases - deficiency | Polyneuropathies - metabolism | Monoacylglycerol Lipases - genetics | Brain - metabolism | Monoacylglycerol Lipases - metabolism | Ataxia - genetics | Ataxia - metabolism | Retinitis Pigmentosa - physiopathology | Ataxia - pathology | Disease Models, Animal | Ataxia - physiopathology | Mice, Inbred C57BL | Retinitis Pigmentosa - genetics | Retinitis Pigmentosa - metabolism | Behavior, Animal - physiology | Lipid Metabolism | Polyneuropathies - physiopathology | Cataract - metabolism | Mice, Knockout | Phenotype | Animals | Metabolic Networks and Pathways | Polyneuropathies - pathology | Brain - pathology | Polyneuropathies - genetics | Cataract - genetics | Models, Neurological | Mutation | Cataract - physiopathology | Retinitis Pigmentosa - pathology | Gene mutations | Serine | Genomics | Physiological aspects | Nervous system | Development and progression | Genetic aspects | Degeneration | Research | Health aspects | Proteins | Genotype & phenotype | Neurodegeneration | Rodents | Genetics | Neuropsychology | Index Medicus | Biological Sciences
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 07/2008, Volume 106, Issue 1, pp. 158 - 169
Journal Article
Journal Article