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93 Retinol binding protein 3 is increased in the retina of patients with diabetes resistant to diabetic retinopathy.

92 Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids.

91 Soluble CX3CL1 gene therapy improves cone survival and function in mouse models of retinitis pigmentosa.

90 Intein-mediated protein trans-splicing expands adeno-associated virus transfer capacity in the retina.

89 Mammalian Near-Infrared Image Vision through Injectable and Self-Powered Retinal Nanoantennae.

88 Single-cell-based analysis provides a comprehensive molecular and cellular taxonomy of the primate retina.

87 Loss of MPC1 reprograms retinal metabolism to impair visual function.

86 Ocular fluids from patients with retinal detachment show iron accumulation, and transferrin can be used as a therapeutic adjuvant.

85 A swarm of slippery micropropellers penetrates the vitreous body of the eye.

84 Antisense oligonucleotides targeting mutant Ataxin-7 restore visual function in a mouse model of spinocerebellar ataxia type 7.

83 Thyroid hormone signaling specifies cone subtypes in human retinal organoids.

82 Restoration of vision after de novo genesis of rod photoreceptors in mammalian retinas.

81 Cholesterol sulfate is a DOCK2 inhibitor that mediates tissue-specific immune evasion in the eye.

80 Artificial Rod and Cone Photoreceptors with Human‐Like Spectral Sensitivities.

79 Phase 1 clinical study of an embryonic stem cell–derived retinal pigment epithelium patch in age-related macular degeneration.

78 BEST1 gene therapy corrects a diffuse retina-wide microdetachment modulated by light exposure.

77 Molecular Anatomy of the Developing Human Retina.

76 Inhibition of soluble epoxide hydrolase prevents diabetic retinopathy.

75 A reversible thermoresponsive sealant for temporary closure of ocular trauma.

74 Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapy.

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