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Insights into the Activation and Self-Association of Arrestin-1.
Biochemistry
December 2024
Gavin Herbert Eye Institute - Center for Translational Vision Research, Department of Ophthalmology, University of California, Irvine, Irvine, California 92697, United States.
Arrestins halt signal transduction by binding to the phosphorylated C-termini of activated G protein-coupled receptors. Arrestin-1, the first subtype discovered, binds to rhodopsin in rod cells. Mutations in , the gene encoding Arrestin-1, are linked to Oguchi disease, characterized by delayed dark adaptation.
View Article and Find Full Text PDFLoss of sheen in Oguchi disease following short wavelength exposure.
Eye (Lond)
November 2024
UCL Institute of Ophthalmology, University College London, London, UK.
Oguchi's disease - Clinical image.
Oman J Ophthalmol
May 2023
Department of Ophthalmology, Rajan Eye Care Hospital Pvt Ltd, Chennai, Tamil Nadu, India.
A 5-year-old Syrian female was born with Oguchi disease: a rare case report.
Ann Med Surg (Lond)
April 2023
Marashi Eye Clinic, Aleppo, Syrian Arab Republic.
Unlabelled: Oguchi disease is a rare autosomal recessive disease that causes congenital stationary blindness, which is distinguished by the Mizuo-Nakamura phenomenon and caused by mutations of rhodopsin kinase gene or the arrestin gene.
Case Presentation: A 5-year-old Syrian female complains of stationary night blindness, investigated by fundus photo and optical coherence photograph and diagnosed as Oguchi disease.
Discussion: Oguchi disease is an autosomal recessive retinal disorder causing stationary nyctalopia.
Bilateral Tapetal Reflex in a 12-Year-Old Girl.
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