Retinitis pigmentosa (RP) is a form of retinal degeneration characterized by primary
degeneration of rod photoreceptors followed by a secondary cone loss that leads to vision …

Inherited and non-inherited retinopathies can affect distinct cell types, leading to progressive
cell death and visual loss. In the last years, new approaches have indicated exciting …

Over 100 mutations in the rhodopsin gene have been linked to a spectrum of retinopathies
that include retinitis pigmentosa and congenital stationary night blindness. Though most of …

Rhodopsin is a light-sensitive G protein-coupled receptor that initiates the phototransduction
cascade in rod photoreceptors. Mutations in the rhodopsin-encoding gene RHO are the …

The neuropeptide galanin receptor 3 (GALR3) is a class AG protein-coupled receptor
(GPCR) broadly expressed in the nervous system, including the retina. GALR3 is involved in …

When the eyes work intensively, it is easy to have eye discomfort such as blurred vision,
soreness, dryness, and tearing, that is, visual fatigue. Visual fatigue not only affects work and …

The majority of inherited retinal degenerative diseases and dry age-related macular
degeneration are characterized by decay of the outer retina and photoreceptors, which …

The correct expression of folded, functional rhodopsin (Rho) is critical for visual perception.
However, this seven-transmembrane helical G protein-coupled receptor is prone to …

Retinitis pigmentosa (RP) is a group of devastating inherited retinal diseases that leads to
visual impairment and oftentimes complete blindness. Currently no cure exists for RP thus …

The majority of inherited retinal degenerative diseases and dry age-related macular
degeneration are characterized by decay of the outer retina and photoreceptors, which …