Associated Papers
Development and Validation of a Commercially Available Two Color Dark Adapted Perimetry to Assess Inherited Retinal Degenerations.
Pennesi ME et al.
American Journal of Ophthalmology, 2026
The role of arrestin-1 N-edge in rhodopsin binding.
Vishnivetskiy SA et al.
Cellular Signalling, 2025
Novel founder variant in the S-antigen visual arrestin gene SAG is the most prevalent cause of autosomal dominant retinitis pigmentosa in Singaporean Chinese.
Quinodoz M et al.
Journal of Medical Genetics, 2025
Advancements and future directions in Oguchi disease research.
Fan F et al.
International Ophthalmology, 2025
Spectrum of variants associated with inherited retinal dystrophies in Northeast Mexico.
Villafuerte-de la Cruz RA et al.
Bmc Ophthalmology, 2024
Two novel compound heterozygous SAG mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging study.
Pilotto E et al.
European Journal of Ophthalmology, 2022
Genetic dissection of non-syndromic retinitis pigmentosa.
Bhardwaj A et al.
Indian Journal of Ophthalmology, 2022
Progressive sector retinitis pigmentosa due to c.440G>T mutation in SAG in an Australian family.
Pappalardo J et al.
Ophthalmic Genetics, 2021
Arrestin mutations: Some cause diseases, others promise cure.
Gurevich VV et al.
Progress in Molecular Biology and Translational Science, 2019
Molecular Defects of the Disease-Causing Human Arrestin-1 C147F Mutant.
Vishnivetskiy SA et al.
Investigative Ophthalmology & Visual Science, 2018
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.
Sullivan LS et al.
Investigative Ophthalmology & Visual Science, 2017
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