Yingbin Fu

Role of visual pigment properties in rod and cone phototransduction.

Intrinsically photosensitive retinal ganglion cells detect light with a vitamin A-based photopigment, melanopsin.

Non-image-forming ocular photoreception in vertebrates.

Molecular properties of rhodopsin and rod function.

Phototransduction in mouse rods and cones.

Quantal noise from human red cone pigment.

Study of cytoskeletal changes induced by okadaic acid in HL-7702 liver cells and development of a fluorimetric microplate assay for detecting diarrhetic shellfish poisoning.

Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.

Increased expression of multifunctional serine protease, HTRA1, in retinal pigment epithelium induces polypoidal choroidal vasculopathy in mice.

Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis.

[A fluorimetric microplate assay for detecting diarrheic shellfish poisoning toxins].

A Phe-rich region in short-wavelength sensitive opsins is responsible for their aggregation in the absence of 11-cis-retinal.

Photoreceptor avascular privilege is shielded by soluble VEGF receptor-1.

Dimerization of visual pigments in vivo.

AIBP Limits Angiogenesis Through γ-Secretase-Mediated Upregulation of Notch Signaling.

Proteolytic Degradation and Inflammation Play Critical Roles in Polypoidal Choroidal Vasculopathy.

Characterization of Retinal Ganglion Cell and Optic Nerve Phenotypes Caused by Sustained Intracranial Pressure Elevation in Mice.

Disruption of Rhodopsin Dimerization in Mouse Rod Photoreceptors by Synthetic Peptides Targeting Dimer Interface.

Author Correction: Characterization of Retinal Ganglion Cell and Optic Nerve Phenotypes Caused by Sustained Intracranial Pressure Elevation in Mice.

Deletion of M-Opsin Prevents M Cone Degeneration in a Mouse Model of Leber Congenital Amaurosis.

Combination of apolipoprotein-A-I/apolipoprotein-A-I binding protein and anti-VEGF treatment overcomes anti-VEGF resistance in choroidal neovascularization in mice.

Visual pigment-deficient cones survive and mediate visual signaling despite the lack of outer segments.

Age differential response to bevacizumab therapy in choroidal neovascularization in rabbits.

Combination of AIBP, apoA-I, and Aflibercept Overcomes Anti-VEGF Resistance in Neovascular AMD by Inhibiting Arteriolar Choroidal Neovascularization.

Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degeneration.