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1 at results in proteolytic degradation of the photopigment.
2 press a human long-wavelength-sensitive cone photopigment.
3 activities and express the melanopsin (OPN4) photopigment.
4 ches too large a fraction of the rod or cone photopigment.
5 that bleached a significant fraction of cone photopigment.
6 also as a consequence of regeneration of the photopigment.
7 contain melanopsin, a putative ganglion cell photopigment.
8 enerated in some way by the bleaching of the photopigment.
9 ng an antiserum against melanopsin, a likely photopigment.
10 which bleached a negligible fraction of the photopigment.
11 ough to bleach a substantial fraction of the photopigment.
12 charge motion is consistent with a rhodopsin photopigment.
13 ing the immediate utility of acquiring a new photopigment.
14 transgenic mouse that expresses a human cone photopigment.
15 that is unrelated to spectral shifts of the photopigment.
16 it to all-trans-retinal, which activates the photopigment.
17 ated with 9-cis retinal before extraction of photopigment.
18 pends on the presence of three types of cone photopigment.
19 t with the predicted axial absorptance of th photopigment.
20 uggesting the involvement of another retinal photopigment.
21 atic theory, with no need to invoke a fourth photopigment.
22 All ipRGCs use melanopsin (Opn4) as their photopigment.
23 the rate of recovery of functional rhodopsin photopigment.
24 diate dim light vision and express rhodopsin photopigment.
25 istry share more in common with invertebrate photopigments.
26 nset of synaptogenesis and the expression of photopigments.
27 y random rule for assigning the L and M cone photopigments.
28 reased effective optical density of the cone photopigments.
29 a delay in the regeneration of cone and rod photopigments.
30 have been proposed to function as circadian photopigments.
31 tinin or by colabeling with antisera to cone photopigments.
32 absorptance differences among the three cone photopigments.
33 icantly, both isoforms form fully functional photopigments.
34 n that enhances the regeneration of rod/cone photopigments.
35 L and cVA) are capable of forming functional photopigments.
38 retinal that is generated after cone and rod photopigments absorb photons of light is recycled back t
39 otopigment gene sites responsible for tuning photopigment absorption spectra revealed differences tha
40 cone noise was not dominated by spontaneous photopigment activation or by quantal fluctuations in ph
41 receptor current, a linear manifestation of photopigment activation, indicated large expression of O
43 ough to bleach a significant fraction of the photopigment and is restricted to the part of the outer
44 ty of pigment distributions: central peak of photopigment and macular pigment, small foveal alteratio
46 ite conformations in the AppA (activation of photopigment and puc expression) BLUF domain before and
48 distinct genes encoding 10 classical visual photopigments and 32 nonvisual opsins, including 10 nove
49 sin, defines a new gene family of vertebrate photopigments and is expressed in a majority of parapine
51 th with restored regulated synthesis of both photopigments and ribulose-bisphosphate carboxylase/oxyg
52 ate intensity (bleaching 0.3-3% of the total photopigment) and duration (between 5 and 90 s) were rec
53 ous measurements of the regeneration of cone photopigment, and it seems highly probable that the redu
54 retinal ganglion cells use melanopsin as the photopigment, and mediate non-image-forming visual funct
55 9-cis-retinal generated isorhodopsin, a rod photopigment, and restored light sensitivity to the elec
56 light-attenuating macular pigment (MP), cone photopigment, and retinal pigment epithelial (RPE) pigme
57 eptors mediate vision in bright light, their photopigments are bleached at a rapid rate and require s
58 ven alterations in the complement of retinal photopigments are fundamental steps in the evolution of
59 In rodents, cones expressing different opsin photopigments are sensitive to middle (M, 'green') and s
60 centration suggest that the blue and near-UV photopigments are tautomeric forms of RGR, in which an a
62 prise a novel pathway that regenerates opsin photopigments at a rate 20-fold faster than the known vi
63 flashes, thereby quantifying the fraction of photopigment available at the time of delivery of each f
64 is an aerobic repressor of genes involved in photopigment biosynthesis and puc operon expression.
66 Disruption of aerR resulted in increased photopigment biosynthesis during aerobic growth to a lev
69 ogous expression of six genes, five encoding photopigment biosynthetic proteins and one encoding a PR
72 ostress is caused by excessive local retinal photopigment bleaching uncommon in ordinary situations.
73 nsitive and utilize an opsin/vitamin A-based photopigment called melanopsin maximally sensitive in th
74 direct demonstration that melanopsin forms a photopigment capable of activating a G-protein, but its
77 the potential deleterious effects related to photopigments consumption by Spectralis optical coherenc
78 different light regimes, and an analysis of photopigment content and photosynthetic rates along bori
79 ayed a pleiotropic phenotype with defects in photopigment content, photoautotrophic growth and carbon
80 uch conditions, melanopsin acts as a sensory photopigment, coupled to a native ion channel via a G-pr
86 opsins demonstrate that they form functional photopigments, each with unique chromophore-binding and
89 apparent in early chordates; the decrease in photopigment expression-and loss of the anatomical corre
90 9-cis retinal did not add absorbance to the photopigment extracts of dark-adapted retinas at any age
93 on and in most mammals express M and S opsin photopigments for sensitivity to medium-long and short l
96 The distinct absorbance spectra of the cone photopigments form the basis of color vision, but ultras
97 taloging the spectral properties of the cone photopigments found in retinas of a number of primate sp
102 ion in which the expression of a mutant cone photopigment gene leads to the loss of the entire corres
104 omparison of the sequence of the dolphin rod photopigment gene with that of the bovine rod suggests t
105 dolphin long-wavelength sensitive (LWS) cone photopigment gene with those of the human LWS cones sugg
109 e whether melanopsin is a functional sensory photopigment, here we transiently expressed it in HEK293
110 ichromatic image showing the distribution of photopigment if the retina could be viewed directly in w
112 a primary role for a novel short-wavelength photopigment in light-induced melatonin suppression and
113 light bleaches a significant fraction of the photopigment in rods and cones and produces a prolonged
115 d a human long-wavelength-sensitive (L) cone photopigment in the form of an X-linked polymorphism.
116 findings suggest that there is a novel opsin photopigment in the human eye that mediates circadian ph
120 ectance affect the light that passes through photopigment in the receptors rather than the stray ligh
122 s approach identified the full complement of photopigments in a highly light-sensitive model vertebra
125 se properties reflect the use of specialized photopigments in the primary process of magnetoreception
127 evealed a remarkable number and diversity of photopigments in zebrafish, the largest number so far di
128 ggest that single site mutations can convert photopigments into visual light sensors or nonvisual sen
129 termine whether a gene encoding a human cone photopigment introduced into the mouse genome would be e
133 rements, for which the bleaching of the cone photopigment is too small to affect flash kinetics, the
135 the middle- (M) wavelength-sensitive visual photopigments, is the most common single locus genetic d
139 within Lepidoptera of convergently evolved L photopigment lineages whose lambda(max) values were blue
140 igh-frequency alleles at the single X-linked photopigment locus, and that the spectral sensitivity pe
141 ost New World monkeys have only one X-linked photopigment locus, many species have three polymorphic
142 he results suggest that, in humans, a single photopigment may be primarily responsible for melatonin
143 that the spectral sensitivity of horse cone photopigments, measured as cone excitation ratios, was c
144 uble-knockout mice lacking the inner-retinal photopigment melanopsin (OPN4) and RPE65, a key protein
146 tinal ganglion cells (ipRGCs) expressing the photopigment melanopsin (OPN4), together with rods and c
148 mammalian retinal ganglion cells express the photopigment melanopsin and are intrinsically photosensi
149 on cells in the mammalian retina express the photopigment melanopsin and are intrinsically photosensi
150 on cells in the mammalian retina express the photopigment melanopsin and are intrinsically photosensi
151 These ganglion cells express the putative photopigment melanopsin and by signalling gross changes
152 retinal ganglion cells (ipRGCs) contain the photopigment melanopsin and drive subconscious physiolog
153 tion of retinal ganglion cells expresses the photopigment melanopsin and function as autonomous photo
155 retinal ganglion cells (RGCs) expresses the photopigment melanopsin and is intrinsically photosensit
156 tinal ganglion cells (ipRGCs), which use the photopigment melanopsin and mediate nonimage-forming vis
157 retinal ganglion cells (ipRGCs) express the photopigment melanopsin and mediate several non-image-fo
158 retinal ganglion cells (ipRGCs) express the photopigment melanopsin and regulate a wide array of lig
159 tinal ganglion cells (ipRGCs) expressing the photopigment melanopsin and the neuropeptide pituitary a
160 tinal ganglion cells (ipRGCs) expressing the photopigment melanopsin belong to a heterogenic populati
164 how retinal ganglion cells that express the photopigment melanopsin, also known as OPN4, contribute
165 nal ganglion cells (ipRGCs) that express the photopigment melanopsin, but also receive input from rod
167 l subset of retinal output cells express the photopigment melanopsin, rendering them intrinsically li
168 retinal ganglion cells (RGCs) expresses the photopigment melanopsin, rendering these cells intrinsic
179 In bright light, mammals use a distinct photopigment (melanopsin) to measure irradiance for cent
181 We sought to determine how a newly added photopigment might impact vision by studying a transgeni
184 elanopsin resembles invertebrate rhabdomeric photopigments more than vertebrate ciliary pigments and
187 which the mouse OPN4 replaced the native Rh1 photopigment of Drosophila R1-6 photoreceptors, resultin
188 ctional sensory photopigment, that it is the photopigment of ganglion-cell photoreceptors, and that t
195 id sites are under positive selection in the photopigments of both butterflies and primates, spanning
196 lts have established that mice have two cone photopigments, one peaking near 350 nm (UV-cone pigment)
198 propose that mammals have a vitamin A-based photopigment (opsin) for vision and a vitamin B2-based p
200 ponses, the question arises whether a single photopigment or a greater diversity of proteins within t
201 erations in the distributions of foveal cone photopigment or macular pigment were found that varied a
203 trometric analysis of subnanomolar levels of photopigments or other integral membrane proteins either
204 nall nomograms generated for rhodopsin-based photopigments over the lambda(max) range 420-480 nm show
205 New World monkeys that show sex-linked cone photopigment polymorphism, whereby all males and some fe
206 asure of the product of the fraction of cone photopigment present, and the amplification constant of
209 etinal significantly increases the amount of photopigment recovered without reducing the variance in
211 recovery time and the time constant of cone photopigment regeneration among the patients was quantif
213 omophore and in understanding the process of photopigment regeneration in photoreceptors that are not
214 s also measured their time constants of cone photopigment regeneration with a video imaging fundus re
217 t RppA is a regulator of photosynthesis- and photopigment-related gene expression, is involved in the
228 ed than would be expected for a single opsin photopigment, suggesting the expression of multiple phot
231 Action spectra implicated an opsin-based photopigment system, but further identification based on
234 s melanopsin (Opn4), a putative opsin-family photopigment that has been shown to play a role in media
235 xtremely rapid regeneration and reuse of the photopigment that is essential for cone function at high
237 adian rhythms are generated, but the retinal photopigment that mediates circadian entrainment has rem
238 part of the spectrum is reduced because the photopigments that mediate discrimination in this range
239 the degree of similarity among the residual photopigments that serve vision in the color-anomalous e
240 mammalian melanopsin is a functional sensory photopigment, that it is the photopigment of ganglion-ce
241 ight bleaching a significant fraction of the photopigment, the circulating current was initially supp
242 the changes caused by the presence of novel photopigments, this study was designed to determine whet
243 lor afterimages range from bleaching of cone photopigments to cortical adaptation [4-9], but direct n
246 -wave data were fitted with a model based on photopigment transduction to obtain values for log Rmax
247 -wave data were fitted with a model based on photopigment transduction to obtain values for the param
250 t, published action spectra suggest that the photopigment underlying the intrinsic light sensitivity
255 ed that large quantities of a blue absorbing photopigment were expressed, having a dark stable blue i
256 for the human long wavelength-sensitive (L) photopigment were generated by microinjection of fertili
258 nes arose from spontaneous activation of the photopigment, which is a million-fold less stable than t
259 t to exist since the rhodopsins are bistable photopigments, which consist of a chromophore that norma
260 tion signatures of diatom and cyanobacterial photopigments, which were confirmed by HPLC-analysis.
263 is driven by a single opsin/vitamin A-based photopigment with peak sensitivity around 479 nm (opsin
264 t even if melanopsin functions as a bistable photopigment with photo-regenerative activity native mel
266 tinal and formed two long-lived pH-dependent photopigments with absorption maxima of 469 +/- 2.4 and
267 ddle- (M) and long-wavelength- (L) sensitive photopigments with overlapping absorbance spectrum maxim
268 also a RPE-independent visual cycle for cone photopigment within the neurosensory retina may contribu
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