• 1147 del A mutation in the arrestin gene in Japanese patients with Oguchi disease
• A 5-year-old Syrian female was born with Oguchi disease: a rare case report
• A case of Oguchi disease with disappearance of golden tapetal-like fundus reflex after vitreous resection
• A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene
• A compound heterozygous mutation in the S-Antigen Visual Arrestin SAG gene in a Chinese patient with Oguchi type one: a case report
• A Homozygote Mutation in <em>S-Antigen Visual Arrestin SAG</em> Gene in an Iranian Patient with Oguchi Type One: A Case Report
• A Mixture of U.S. Food and Drug Administration-Approved Monoaminergic Drugs Protects the Retina From Light Damage in Diverse Models of Night Blindness
• A non-stop S-antigen gene mutation is associated with late onset hereditary retinal degeneration in dogs
• A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease
• A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States
• A novel GRK1 mutation in an Italian patient with Oguchi disease
• A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses
• A novel missense mutation of the GRK1 gene in Oguchi disease
• A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
• A phase II randomized trial of metastasis-directed therapy with alpha emitter radium-223 in men with oligometastatic castration-resistant prostate cancer (MEDAL)
• A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene
• Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase
• Arrestin can act as a regulator of rhodopsin photochemistry
• Arrestin gene mutations in autosomal recessive retinitis pigmentosa
• Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease
• Association of Retinal Artery and Other Inner Retinal Structures With Distribution of Tapetal-like Reflex in Oguchi's Disease
• Bilateral Tapetal Reflex in a 12-Year-Old Girl
• Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the oguchi form of congenital stationary night blindness
• Clinical Findings in Four Siblings with Genetically Proven Oguchi Disease
• Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3
• Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms
• Control of rhodopsin activity in vision
• Dark adaptation and the retinoid cycle of vision
• Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
• Deletion of Protein Phosphatase 2A Accelerates Retinal Degeneration in GRK1- and Arr1-Deficient Mice
• Dietary polyphenols drive dose-dependent behavioral and molecular alterations to repeated morphine
• Ectopic transcription and the possibility of RNA editing of the human arrestin gene
• Electronegative Electroretinograms in the United Arab Emirates
• ERG rod a-wave in Oguchi disease
• Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness
• Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness
• Factors associated with carotid intima-media thickness progression in patients with asymptomatic hyperuricemia: insights from the PRIZE study
• Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease
• Genetic analysis and clinical features of three Chinese patients with Oguchi disease
• GRKs and arrestins: the therapeutic pathway?
• Gut microbiota-derived lipid metabolites facilitate regulatory T cell differentiation
• Hepatitis B Virus-related Membranous Nephropathy with Crescentic Formation in an Inactive Carrier of Positive Hepatitis B Surface Antigen with Undetectable DNA under Anti-viral Treatment: A Case Report
• Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness)
• Inflammasome-Mediated Neuronal-Microglial Crosstalk: a Therapeutic Substrate for the Familial C9orf72 Variant of Frontotemporal Dementia/Amyotrophic Lateral Sclerosis
• ISCEV extended protocol for the dark-adapted red flash ERG
• KMeyeDB: a graphical database of mutations in genes that cause eye diseases
• Light and inherited retinal degeneration
• Loss of sheen in Oguchi disease following short wavelength exposure
• Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene
• Mizuo phenomenon observed by scanning laser ophthalmoscopy in a patient with Oguchi disease
• Mizuo--Nakamura phenomenon with a negative waveform ERG
• Mizuo-Nakamura Phenomena
• Mizuo-Nakamura Phenomenon in a Middle-aged Woman
• Mizuo-Nakamura phenomenon in an Indian male
• Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene
• Molecular genetic study of congenital stationary night blindness
• Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture
• Mutation analysis reveals novel and known mutations in SAG gene in first two Egyptian families with Oguchi disease
• Neuroprotective Potential of Raloxifene via G-Protein-Coupled Estrogen Receptors in Aβ-Oligomer-Induced Neuronal Injury
• New variants and in silico analyses in GRK1 associated Oguchi disease
• NFIA in adipocytes reciprocally regulates mitochondrial and inflammatory gene program to improve glucose homeostasis
• Novel homozygous in-frame deletion of <em>GNAT1</em> gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family
• Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family
• Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease
• Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man
• Oguchi disease
• Oguchi Disease Associated with Keratoconus
• Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up
• Oguchi disease masked by retinitis pigmentosa
• Oguchi disease or stationary congenital night blindness: a case report
• Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene
• Oguchi disease with unusual findings associated with a heterozygous mutation in the SAG gene
• Oguchi Disease: The Chameleon in the Retina
• Oguchi type I caused by a homozygous missense variation in the SAG gene
• Oguchi's disease - Clinical image
• Omics Profiles of Non-GM Tubers from Transgrafted Potato with a GM Scion
• Optical coherence tomographic evaluation of the outer retinal architecture in Oguchi disease
• Pathophysiological roles of G-protein-coupled receptor kinases
• Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study
• Physiology and pathology of visual information processing
• Potential cellular functions of N-ethylmaleimide sensitive factor in the photoreceptor
• Progression from Classical Oguchi Disease to Retinitis Pigmentosa after 50 Years
• Rapid detection of SAG 926delA mutation using real-time polymerase chain reaction
• Retinal imaging in inherited retinal diseases
• Semi-Automated Isolation of the Stromal Vascular Fraction from Murine White Adipose Tissue Using a Tissue Dissociator
• Shortening of the rod outer segment in Oguchi disease
• Signs of Oguchi Disease and Pigmentary Degeneration from Early in Life
• Spectral-domain optical coherence tomography findings in the Mizuo-Nakamura phenomenon of Oguchi disease
• Structural Dynamics of Amyloid-β Protofibrils and Actions of Anti-Amyloid-β Antibodies as Observed by High-Speed Atomic Force Microscopy
• Subclinical C1q Nephropathy Combined with Possible Donor-Derived IgA Deposition in a 1-Year Kidney Allograft Biopsy: A Case Report
• Synergistic effects of immune checkpoint inhibitors in combination with stereotactic radiosurgery for patients with lung cancer and brain metastases: a propensity score-matched analysis
• Tertiary Lymphoid Tissues Are Microenvironments with Intensive Interactions between Immune Cells and Proinflammatory Parenchymal Cells in Aged Kidneys
• The effects of visual cues from optical stimulation devices on gait disturbance in patients with Parkinson's disease
• The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation
• The Mizuo phenomenon in Oguchi disease
• Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination
• Two novel compound heterozygous <em>SAG</em> mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging study
• Two novel compound heterozygous SAG mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging study
• Visual Arrestin 1 acts as a modulator for N-ethylmaleimide-sensitive factor in the photoreceptor synapse
• Wide-field true-colour imaging and clinical characterization of a novel GRK1 mutation in Oguchi disease