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1 vel G protein-mediated signaling cascades in photoreception.
2 tentially include signaling from non-retinal photoreception.
3 mal structural reactions as the basis of OCP photoreception.
4 ns that are essential for retinal health and photoreception.
5 ght, including those dependent on melanopsin photoreception.
6 ion of cell-cell signals, ion transport, and photoreception.
7 n HD mice is due to abnormalities in retinal photoreception.
8 ys tryptophan side chains to accomplish UV-B photoreception.
9 ing originates with inner-retinal melanopsin photoreception.
10 chromophore for light absorption during UV-B photoreception.
11 hotoreceptors that are involved in nonvisual photoreception.
12 icate several tryptophan amino acids in UV-B photoreception.
13  structures of mice with genetically altered photoreception.
14 anges in the sensitivity of circadian ocular photoreception.
15 valently bound flavin as the chromophore for photoreception.
16 ires both rod/cone- and melanopsin-dependent photoreception.
17 ing a role for cryptochrome in inner retinal photoreception.
18 clock modulates the sensitivity of nonvisual photoreception.
19  necessary and sufficient for this nonvisual photoreception.
20 o sensory inputs involved with olfaction and photoreception.
21 refore be a general phenomenon in vertebrate photoreception.
22 ial processes including the initial event in photoreception.
23 s are necessary and sufficient for circadian photoreception.
24 ent in the human eye that mediates circadian photoreception.
25 in mammals and may play a role in encephalic photoreception.
26  and likely involves a dedicated pathway for photoreception.
27 mer dissociates into monomers following UV-B photoreception, a process accompanied by conformational
28 ) to determine how the loss of cone-mediated photoreception affects light signaling pathways in the r
29 ides insight into the significance of dermal photoreception among color-changing animals.
30 a pleomorphic role for cryptochromes in both photoreception and central clock mechanism.
31 s assisting excitation and charge transport, photoreception and chemical sensing processes could be a
32 d theoretical studies suggest a link between photoreception and magnetoreception in some animals.
33 aluable teleost model for studying nonvisual photoreception and the basis of photoperiodism.
34  on signaling mechanisms mediating nonvisual photoreception and their physiological functions.
35 ndings in the expanding field of extraocular photoreception and their relevance for human physiology.
36                                         Both photoreception and ubiquitin conjugation may be associat
37              Mice lacking classical rod-cone photoreception, and thus entirely dependent on melanopsi
38               Multiple sites of extraretinal photoreception are present in vertebrates, but the molec
39 d molecular mechanism of animal cryptochrome photoreception are presently unknown.
40           This issue intersects with that of photoreception, because light is both an arousal signal
41  Despite the widespread prevalence of dermal photoreception, both its physiology and its function in
42 patial patterns is thought to originate with photoreception by rods and cones.
43 s is well documented, the function of direct photoreception by the CNS remains largely unknown.
44                   Cataract surgery increases photoreception by the photosensitive retinal ganglion ce
45   We suggest that disease-related changes in photoreception by the retina contribute to the progressi
46                                         UV-B photoreception by UVR8 is based on intrinsic tryptophan
47                                         UV-B photoreception causes rapid dissociation of dimeric UVR8
48 etic knockout animals suggest that circadian photoreception consists of an integration of multiple si
49 new possible routes through which melanopsin photoreception could contribute to reflex light response
50 nditions that incorporates dimer and monomer photoreception, dimer/monomer cycling, abundance of nati
51 stages indicates the importance of nonvisual photoreception early in development.
52                                   Melanopsin photoreception enhances retinal responses to variations
53                                              Photoreception for the image-forming pathway begins at t
54                                   Melanopsin photoreception has low temporal resolution, making it fu
55            Photopigments governing circadian photoreception have been localized to the inner retina.
56                        Receptor proteins for photoreception have been studied for several decades.
57 ct, OPN5-mediated extraocular and deep-brain photoreception have recently been described for the firs
58 the site and molecular basis of extraretinal photoreception have remained obscure.
59 ng pathways, the molecular mechanism of UVR8 photoreception, how the UVR8 protein initiates signaling
60                        This review addresses photoreception in cyanobacteria from the perception of l
61 intermediate provides a possible pathway for photoreception in halobacteria and a useful tool for stu
62 morphology, physiology, and optics of dermal photoreception in hogfish (Lachnolaimus maximus), we des
63 nt activity, one possible function of dermal photoreception in hogfish is to monitor chromatophores t
64  that cryptochromes have a role in circadian photoreception in mammals.
65                        We examined nonvisual photoreception in mice lacking RPE65, a protein that is
66 retinal-based pigments (opsins) in circadian photoreception in mice, animals mutated in plasma retino
67 lamus, both regions implicated in encephalic photoreception in nonmammalian vertebrates.
68 e aim of this study was to examine circadian photoreception in RCS/N-rdy(+) (rdy(+)) rats homozygous
69                        Evidence is shown for photoreception in the absence of the dominant, and here
70  the brain that respond to such 'non-visual' photoreception in the human eye.
71 e Cryptochrome (CRY)- and compound-eye-based photoreception in the large LNvs while synergizing CRY-m
72                                              Photoreception in the mammalian retina is not restricted
73 within the brain and contribute to circadian photoreception in the retina.
74 he large LNvs while synergizing CRY-mediated photoreception in the small LNvs.
75 eration, no study has investigated circadian photoreception in these animals.
76 ant biological implications in understanding photoreception in vertebrates.
77 a previously unidentified form of deep-brain photoreception in Xenopus laevis frog tadpoles.
78 idence on a role of zeaxanthin in blue light photoreception, indicates that the guard cell and coleop
79                                         UV-B photoreception induces the conversion of the UVR8 dimer
80 at monomeric UVR8 has the potential for UV-B photoreception, initiating signal transduction and respo
81                                              Photoreception is a ubiquitous sensory ability found acr
82 n of these indirect projections to circadian photoreception is currently poorly understood.
83 sential for optimal rod and retinal ganglion photoreception is decreased by progressive age-related c
84 The effect of cryptochrome loss on nonvisual photoreception is due to loss of the circadian clock non
85                                              Photoreception is essential for the development of the v
86 is geniculohypothalamic pathway in circadian photoreception is poorly understood.
87 ystal structure of UVR8 reveals the basis of photoreception, it does not show how UVR8 initiates sign
88 euronal Ca2+ homeostasis and in invertebrate photoreception, little is known about their contribution
89          These data characterize a non-opsin photoreception mechanism in a vertebrate eye and suggest
90                  Accidentally, we identify a photoreception mechanism under strong continuous light,
91               Our data and analyses reveal a photoreception mechanism with implications for plant phy
92 mpted by earlier suggestions that melanopsin photoreception might be important for certain functions
93 , has conserved tryptophan residues for UV-B photoreception, monomerizes upon UV-B exposure, and inte
94 otransduction in these sites of extraretinal photoreception must be mediated by novel opsins.
95 used the most severe decrements of circadian photoreception observed so far.
96 lasma membrane, whereas secondary modulatory photoreception occurs in the cytoplasm and nucleus.
97                   Thus, nonclassical retinal photoreception occurs within diverse cell types and infl
98 carotenoid recently implicated in blue light photoreception of both guard cells and coleoptiles.
99 minantly mediated by melanopsin (OPN4)-based photoreception of photosensitive retinal ganglion cells
100 ignals required for sensory processes, e.g., photoreception, olfaction, and taste.
101  the effects of an evolutionary loss of cone photoreception on retinal organization.
102 er development and contain the machinery for photoreception (Opn4) and neurotransmitter release (Vglu
103     Even in the additional absence of visual photoreception, partial molecular and behavioral light s
104 ly undescribed genes with potential roles in photoreception, pathogenesis, and the regulation of deve
105 ings lead to a plausible model for circadian photoreception/phototransduction in Drosophila.
106  a broad role in the regulation of nonvisual photoreception, providing collateralized projections tha
107                                    Nonvisual photoreception (pupillary light responses, circadian ent
108                                    Nonvisual photoreception regulates numerous biological systems, in
109                                              Photoreception reversibly disrupts salt bridges, trigger
110                                         UV-B photoreception stimulates nuclear accumulation of UVR8 i
111 ce lacking melanopsin still retain nonvisual photoreception, suggesting that rods and cones could ope
112                     Given that the circadian photoreception system is maximally sensitive to short-wa
113 s and cognition, presumably acting through a photoreception system that heavily relies on the photopi
114              The complexity of the nonvisual photoreception systems in teleosts has just started to b
115                                  Extraocular photoreception, the ability to detect and respond to lig
116 ggest that despite the loss of cone-mediated photoreception, the associated cone signaling structures
117 ive contributions of inner and outer retinal photoreception to the pupillary light response.
118 ) that acts as the second messenger coupling photoreception to the zebrafish circadian clock.
119                                    Following photoreception, UVR8 interacts directly with multiple pr
120                      We present evidence for photoreception via the light-sensitive proteins opsin (O
121 is that has been repeatedly linked to dermal photoreception via the study of excised skin preparation
122 tion of three tryptophans implicated in UV-B photoreception, W233, W285, and W337, impairs photomorph
123 cally do not support a role for extraretinal photoreception with respect to direct circadian rhythm r

 
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