Ma'ayan Semo, Peter Coffey, Carlos Gias, Anthony Vugler. Invest Ophthalmol Vis Sci 2016
Times Cited: 8
Times Cited: 8
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Melanopsin and rod-cone photoreceptive systems account for all major accessory visual functions in mice.
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Inhibitory inputs tune the light response properties of dopaminergic amacrine cells in mouse retina.
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Melanopsin is required for non-image-forming photic responses in blind mice.
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Phototransduction by retinal ganglion cells that set the circadian clock.
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Photoentrainment and pupillary light reflex are mediated by distinct populations of ipRGCs.
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Synaptic influences on rat ganglion-cell photoreceptors.
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Two types of melanopsin retinal ganglion cell differentially innervate the hypothalamic suprachiasmatic nucleus and the olivary pretectal nucleus.
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Characterization of an ocular photopigment capable of driving pupillary constriction in mice.
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Melanopsin (Opn4) requirement for normal light-induced circadian phase shifting.
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Differential cone pathway influence on intrinsically photosensitive retinal ganglion cell subtypes.
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Light-induced c-fos in melanopsin retinal ganglion cells of young and aged rodless/coneless (rd/rd cl) mice.
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Rod photoreceptors drive circadian photoentrainment across a wide range of light intensities.
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Melanopsin cells are the principal conduits for rod-cone input to non-image-forming vision.
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Photoresponse diversity among the five types of intrinsically photosensitive retinal ganglion cells.
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Human melanopsin forms a pigment maximally sensitive to blue light (λmax ≈ 479 nm) supporting activation of G(q/11) and G(i/o) signalling cascades.
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Light acts through melanopsin to alter retinal waves and segregation of retinogeniculate afferents.
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