Blue cone function in the retina of the cat

Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.

Gene therapy·2015

Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy.

Journal of medical genetics·2005

Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX.

Human mutation·2001

Novel frameshift mutations in CRX associated with Leber congenital amaurosis.

Human mutation·2001

Melanoma-associated retinopathy and recurrent exudative retinal detachments in a patient with choroidal melanoma.

American journal of ophthalmology·2001

Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.

Investigative ophthalmology & visual science·2001

Pupillometric evidence favors an active attentional zoom lens account over passive filtering.

Vision research·2026

Apparent-length expansion in whole contours and isolated parts: evidence for configuration-dependent processing.

Vision research·2026

Discovering flexible codes for prediction across timescales in the retina.

Vision research·2026

Gait kinematics during walking in children with impaired binocular vision due to amblyopia or strabismus.

Vision research·2026

Perceptual ocular dominance plasticity is resilient to concurrent attentional demands in working memory.

Vision research·2026

A new oculomotor model demystifies "Remarkable Saccades".

Vision research·2026

Prevalence and Causes of Visual Impairment and Blindness in the Qassim Region, Saudi Arabia: A Retrospective Study.

Cureus·2026

Migration of perivenous opacities during retinal vasculopathy and retinal vasculitis.

American journal of ophthalmology case reports·2026

Reactivation of Choroidal Neovascularization in Bilateral Punctate Inner Choroidopathy: A Case Report.

Cureus·2026

Incidence and Recovery of 15-Letter Loss of Visual Acuity in Patients With Neovascular Age-Related Macular Degeneration on Antivascular Endothelial Growth Factor Therapy.

Journal of vitreoretinal diseases·2026

Severe visual impairment as a complication of autism spectrum disorder.

Documenta ophthalmologica. Advances in ophthalmology·2026

Aqueous Humor Proteomics Reveals the Molecular Basis for Differential Treatment Responses in nAMD and pmCNV.

Investigative ophthalmology & visual science·2026

Related Experiment Videos

Blue cone function in the retina of the cat

Related Concept Videos

Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.

Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy.

Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX.

Novel frameshift mutations in CRX associated with Leber congenital amaurosis.

Melanoma-associated retinopathy and recurrent exudative retinal detachments in a patient with choroidal melanoma.

Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.

Pupillometric evidence favors an active attentional zoom lens account over passive filtering.

Apparent-length expansion in whole contours and isolated parts: evidence for configuration-dependent processing.

Discovering flexible codes for prediction across timescales in the retina.

Gait kinematics during walking in children with impaired binocular vision due to amblyopia or strabismus.

Perceptual ocular dominance plasticity is resilient to concurrent attentional demands in working memory.

A new oculomotor model demystifies "Remarkable Saccades".

Prevalence and Causes of Visual Impairment and Blindness in the Qassim Region, Saudi Arabia: A Retrospective Study.

Migration of perivenous opacities during retinal vasculopathy and retinal vasculitis.

Reactivation of Choroidal Neovascularization in Bilateral Punctate Inner Choroidopathy: A Case Report.

Incidence and Recovery of 15-Letter Loss of Visual Acuity in Patients With Neovascular Age-Related Macular Degeneration on Antivascular Endothelial Growth Factor Therapy.

Severe visual impairment as a complication of autism spectrum disorder.

Aqueous Humor Proteomics Reveals the Molecular Basis for Differential Treatment Responses in nAMD and pmCNV.

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Blue cone function in the retina of the cat

Related Concept Videos

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