Subject Areas on Research
- An allele-specific hammerhead ribozyme gene therapy for a porcine model of autosomal dominant retinitis pigmentosa.
- Axotomized mouse retinal ganglion cells containing melanopsin show enhanced survival, but not enhanced axon regrowth into a peripheral nerve graft.
- Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin.
- De novo transcriptomics reveal distinct phototransduction signaling components in the retina and skin of a color-changing vertebrate, the hogfish (Lachnolaimus maximus).
- Evidence from opsin genes rejects nocturnality in ancestral primates.
- Histologic development of the human fovea from midgestation to maturity.
- Immunocytochemical localization of photopigments in cephalopod retinae.
- Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome.
- Interconversion of red opsin isoforms by the cyclophilin-related chaperone protein Ran-binding protein 2.
- Light-dependent magnetoreception: quantum catches and opponency mechanisms of possible photosensitive molecules.
- Opsin, G-protein and 48-kDa protein in normal and rd mouse retinas: developmental expression of mRNAs and proteins and light/dark cycling of mRNAs.
- Role of the Fas-signaling pathway in photoreceptor neuroprotection.
- Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.
- X-linked high myopia associated with cone dysfunction.
- mRNAs coding for proteins of the cGMP cascade in the degenerative retina of the rd mouse.