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1 ion cells (pRGCs) represent a third class of retinal photoreceptor.
2 t animals indicate a contribution from inner retinal photoreceptors.
3 ing protein family expressed specifically in retinal photoreceptors.
4 ransported, as earlier proposed, from distal retinal photoreceptors.
5 n of the circadian oscillator in the Xenopus retinal photoreceptors.
6 ession of these motors is highly enhanced in retinal photoreceptors.
7 uires neither rods nor cones, the only known retinal photoreceptors.
8          Ogre is required in the presynaptic retinal photoreceptors.
9  by these genes are expressed exclusively in retinal photoreceptors.
10 cleus is entrained to the day/night cycle by retinal photoreceptors.
11 t negative Xenopus CLOCK specifically in the retinal photoreceptors.
12 egment photocurrents of Lampetra fluviatilis retinal photoreceptors.
13 mplexed with GTP/Talpha in mature vertebrate retinal photoreceptors.
14 alized rhabdomeral membranes from Drosophila retinal photoreceptors.
15  the regulation of cGMP phosphodiesterase in retinal photoreceptors.
16 rons, including hippocampal mossy fibres and retinal photoreceptors.
17 tantially protected from light damage to the retinal photoreceptors.
18 here is a slowly progressive degeneration of retinal photoreceptors.
19 t mammals is thought be mediated entirely by retinal photoreceptors.
20 t/dark cycle is mediated exclusively through retinal photoreceptors.
21 dness result from the dysfunction or loss of retinal photoreceptors.
22 y, distribution, and spectral sensitivity of retinal photoreceptors.
23 s essential for the survival and function of retinal photoreceptors.
24 ted in inflammatory pathologic conditions in retinal photoreceptors.
25 vative bound to rhodopsin and cone opsins of retinal photoreceptors.
26 y sighted subjects can be supported by inner retinal photoreceptors.
27 disease characterized by progressive loss of retinal photoreceptors.
28 mately lead to blindness due to the death of retinal photoreceptors.
29 belief that rods and cones are the exclusive retinal photoreceptors.
30  the inner segment and synaptic terminals of retinal photoreceptors.
31 tenuated the detrimental influence of SNP to retinal photoreceptors.
32 viding cells and to the connecting cilium of retinal photoreceptors.
33  is crucial for the function and survival of retinal photoreceptors.
34 rriers targeted to the rod outer segments of retinal photoreceptors.
35                              Crocin protects retinal photoreceptors against light-induced cell death.
36                                           In retinal photoreceptors, amplification by the phototransd
37 y stereocilia of inner ear hair cells and to retinal photoreceptor and pigmented epithelium cells.
38  gamma) binding protein, highly expressed in retinal photoreceptor and pineal cells, yet whose physio
39     Mice with a 1.8-kb IRBP promoter develop retinal photoreceptor and pineal tumors.
40 transporter has been described in vertebrate retinal photoreceptors and bipolar cells, the molecular
41 els are crucial for synaptic transmission in retinal photoreceptors and bipolar neurons.
42  wide differences in DNA methylation between retinal photoreceptors and brain neurons.
43 o lead to the loss of temporal resolution in retinal photoreceptors and deficient synaptic transmissi
44 Da) matrix protein expressed specifically in retinal photoreceptors and developing cochlear hair cell
45 is required for the long-term maintenance of retinal photoreceptors and for the development of cochle
46 Both SMC1 and SMC3 localized to the cilia of retinal photoreceptors and Madin-Darby canine kidney cel
47 mfort and dazzling glare depend on different retinal photoreceptors and nociceptive brain pathways in
48            Specialized sensory cilia such as retinal photoreceptors and olfactory cilia use diverse i
49 yclic nucleotide-gated (CNG) ion channels of retinal photoreceptors and olfactory neurons are multime
50 tics of light-evoked responses in vertebrate retinal photoreceptors and ON-bipolar cells.
51  involved in differentiation and survival of retinal photoreceptors and photoentrainment of circadian
52 n protein that is expressed predominantly in retinal photoreceptors and pinealocytes.
53 ecoverin expressed in tumor cells may damage retinal photoreceptors and play a role in the pathogenes
54  the retina, is driven synaptically, because retinal photoreceptors and second-order cells tonically
55                Synaptic transmission between retinal photoreceptors and second-order neurones is cont
56 nerating the electrical response to light in retinal photoreceptors and to odorants in olfactory rece
57  The confocal IOS predominantly results from retinal photoreceptors, and can be used to map localized
58 ve is the light-induced hyperpolarization of retinal photoreceptors, and the b-wave is the depolariza
59                   prCAD is expressed only in retinal photoreceptors, and the prCAD protein is localiz
60 at following an intraocular injection of SNP retinal photoreceptors are affected.
61                                              Retinal photoreceptors are highly metabolic and their en
62 fects of drusen on the synaptic machinery of retinal photoreceptors are investigated.
63                                              Retinal photoreceptors are susceptible to mitochondrial
64                         The photoresponse in retinal photoreceptors begins when a molecule of rhodops
65                              When applied to retinal photoreceptors, bicarbonate enhanced the circula
66 visually driven signals as they flow through retinal photoreceptor, bipolar, and ganglion cells.
67 -ATPase ("flippase") located in membranes of retinal photoreceptors, brain cells, and testis, where i
68 gene fusion expressed high levels of FGF2 in retinal photoreceptors but developed no retinal neovascu
69 cked the membranous stacks characteristic of retinal photoreceptors but were ciliated and contained n
70 es are being developed to bypass degenerated retinal photoreceptors by directly activating retinal ne
71 5 to inner ear hair cell stereocilia, and to retinal photoreceptors by immunocytochemistry.
72 dition to rods and cones, mammals have inner retinal photoreceptors called intrinsically photosensiti
73 sion of beta-galactosidase (beta gal) on the retinal photoreceptor cell arrestin promoter, in conjunc
74                        Circadian shedding of retinal photoreceptor cell discs with subsequent phagocy
75                                        Mouse retinal photoreceptor cell generation and morphogenesis
76  maintain the blood-retinal barrier, sustain retinal photoreceptor cell health and function, and may
77               Retinal pigment epithelial and retinal photoreceptor cell lines were treated with TP de
78 esis and cohesion of stereocilia bundles and retinal photoreceptor cell maintenance or function.
79 ramide metabolism plays an important role in retinal photoreceptor cell survival and apoptosis.
80 th transgenic mice that expressed betagal in retinal photoreceptor cells (arrbetagal mice).
81                    Several proteins found in retinal photoreceptor cells (guanylate cyclase activatin
82                  Melatonin is synthesized in retinal photoreceptor cells and acts as a neuromodulator
83 ns-retinal triggers phototransduction in the retinal photoreceptor cells and causes ultimately the se
84 gene promoter are hypomethylated in DNA from retinal photoreceptor cells and pineal gland compared to
85 sorders characterized by degeneration of the retinal photoreceptor cells and progressive loss of visi
86  of Hmgb1 at the protein level occurs in rat retinal photoreceptor cells and to a lesser extent in bi
87                                              Retinal photoreceptor cells are particularly vulnerable
88  vertebrates is triggered when light strikes retinal photoreceptor cells causing photoisomerization o
89           In vivo, AANAT activity in chicken retinal photoreceptor cells exhibits a circadian rhythm
90 c factors (NTFs) are effective in protecting retinal photoreceptor cells from the damaging effects of
91 ses selective irreversible apoptotic loss of retinal photoreceptor cells in vivo.
92 ngly, an eye with restored cornea, iris, and retinal photoreceptor cells is formed when a surface fis
93 era) visual system contains three classes of retinal photoreceptor cells that are maximally sensitive
94 is a canonical G protein-mediated cascade of retinal photoreceptor cells that transforms photons into
95  links photoactivation of visual pigments in retinal photoreceptor cells to a change in their membran
96                   LEDGF enhanced survival of retinal photoreceptor cells under serum starvation and h
97 ects of LEDGF on survival of embryonic chick retinal photoreceptor cells under serum starvation and h
98 hed transgenic mice expressing human E2F1 in retinal photoreceptor cells under the regulation of the
99 pression pattern of LEDGF in embryonic chick retinal photoreceptor cells was investigated with protei
100 vels were both high in the inner segments of retinal photoreceptor cells where energy-demanding activ
101         Melatonin receptors are expressed in retinal photoreceptor cells, and this study was undertak
102 showed that both GCAP genes are expressed in retinal photoreceptor cells, but GCAP2 was nearly undete
103 oA are used as alternative Nmt substrates in retinal photoreceptor cells, even though they do not exh
104 ythmically expressed in the cytoplasm of the retinal photoreceptor cells, the only other described ve
105       Notably, expression is not observed in retinal photoreceptor cells, the opsin-containing cells
106 urnin is rhythmically transcribed in Xenopus retinal photoreceptor cells, which contain endogenous ci
107 r responsible for the capture of a photon in retinal photoreceptor cells.
108 ransduction in olfactory sensory neurons and retinal photoreceptor cells.
109 rtant during phototransduction in vertebrate retinal photoreceptor cells.
110 laevis its mRNA is specifically expressed in retinal photoreceptor cells.
111 -sensitive regulator of phototransduction in retinal photoreceptor cells.
112 MD) leads to dysfunction and degeneration of retinal photoreceptor cells.
113  to adaptation to background illumination in retinal photoreceptor cells.
114 pe voltage-gated Ca(2+) channels (Cav1.4) in retinal photoreceptor cells.
115 te and continuously supply 11-cis-retinal to retinal photoreceptor cells.
116 ion and proper development of hair cells and retinal photoreceptor cells.
117 ndition characterized by progressive loss of retinal photoreceptor cells.
118 n nuclear receptor expressed specifically by retinal photoreceptor cells.
119 such asymmetry in any bird and suggests that retinal photoreceptor composition should be assessed dur
120  While luminance adaptation can begin at the retinal photoreceptors, contrast adaptation has been sho
121                                           In retinal photoreceptors, coupling plays important roles i
122 right light can cause visual dysfunction and retinal photoreceptor damage in humans and experimental
123 activation of this gene in zebrafish induced retinal photoreceptor defects that were rescued by human
124 ammatory response was associated with marked retinal photoreceptor degeneration and massive neuronal
125 is pigmentosa comprises a group of inherited retinal photoreceptor degenerations that lead to progres
126 eptor gene, NR2E3, cause a disorder of human retinal photoreceptor development characterized by hyper
127 progenitor cell marker, in the biogenesis of retinal photoreceptor disk arrays.
128 ayer morphology, large areas of RPE atrophy, retinal photoreceptor dysfunction, and microglial cell a
129                                              Retinal photoreceptors entrain the circadian system to t
130                                  These novel retinal photoreceptors express the photopigment melanops
131 onses to Arm signaling that specify distinct retinal photoreceptor fates.
132 mon causes of blindness involve the death of retinal photoreceptors, followed by progressive inner re
133 ead throughout the CNS and is observed among retinal photoreceptors from essentially all vertebrates.
134 functional cell monolayer that separates the retinal photoreceptors from the choroid, are prevalent i
135 -expressing ipRGCs, showing that these inner retinal photoreceptors function as retinal irradiance de
136                                           In retinal photoreceptors, highly polarized organization of
137 dimension to an essential role for LPCAT1 in retinal photoreceptor homeostasis.
138 sed on the differential color sensitivity of retinal photoreceptors, however the developmental progra
139                                              Retinal photoreceptors in Cep290(ko/ko) mice lack connec
140 E) performs specialized functions to support retinal photoreceptors, including regeneration of the vi
141 ory light avoidance behavior in mice lacking retinal photoreceptors, indicating reconstitution of lig
142 age formation, the light that is detected by retinal photoreceptors influences subcortical functions,
143 al photoreceptors (rods and cones) and inner retinal photoreceptors (intrinsically photosensitive ret
144 The cGMP-specific phosphodiesterase (PDE) of retinal photoreceptors is a central regulatory enzyme in
145 n vivo, the circadian clock localized in the retinal photoreceptors is necessary for its rhythmicity.
146 nes constitute approximately 1% of adult rat retinal photoreceptors, it was estimated that the relati
147                                           In retinal photoreceptors, L-VGCCs are responsible for neur
148      SNP caused an increase in the number of retinal photoreceptors labeled for DNA breakdown by the
149 o have potential for success but only if the retinal photoreceptor layer is intact, as in the early-d
150 pically, patients lose vision when the outer retinal photoreceptor layer is lost, and so the therapeu
151 ian rhythm of melatonin synthesis in Xenopus retinal photoreceptor layers is driven by rhythmic chang
152  in the circadian system in cultured Xenopus retinal photoreceptor layers.
153 eins of the EF-hand superfamily that inhibit retinal photoreceptor membrane guanylyl cyclase (retGC)
154 ,5'-monophosphate phosphodiesterase (PDE) in retinal photoreceptors, must be deactivated for the ligh
155 ion is achieved by comparing the inputs from retinal photoreceptor neurons that differ in their wavel
156          In contrast, neither RH5-expressing retinal photoreceptors nor RH2-expressing ocellar photor
157 ning electron microscopy to characterize the retinal photoreceptors of spine-bellied (Lapemis curtus)
158          A circadian clock is located in the retinal photoreceptors of the African clawed frog Xenopu
159 degeneration of cerebellar Purkinje neurons, retinal photoreceptors, olfactory bulb mitral neurons, a
160                       Visual transduction in retinal photoreceptors operates through a dynamic interp
161      These results indicate that a rhythm of retinal photoreceptor outer segment disk shedding exists
162 acts access to the confined space within the retinal photoreceptor outer segment signaling compartmen
163  (TLRs) in the innate immune response causes retinal photoreceptor oxidative stress and mitochondrial
164 sion, when mutated can result in an isolated retinal photoreceptor phenotype.
165                                              Retinal photoreceptor phosphodiesterase (PDE6) is unique
166                                In vertebrate retinal photoreceptors, photoisomerization of opsin-boun
167  study was undertaken to investigate whether retinal photoreceptor (PR) cells lacking MTs are more su
168                     Circadian oscillators in retinal photoreceptors provide a mechanism that allows p
169                Despite the loss of all known retinal photoreceptors, rd/rd cl mice showed normal supp
170  Timely termination of the light response in retinal photoreceptors requires rapid inactivation of th
171                                           In retinal photoreceptors, RGS9.Gbeta5 is bound to the memb
172                                   Both outer retinal photoreceptors (rods and cones) and inner retina
173 on within the protein-coding region of a new retinal photoreceptor-specific gene, ELOVL4, in all affe
174 acterize transgenic protein localization and retinal photoreceptor structure and function.
175                             Gap junctions in retinal photoreceptors suppress voltage noise and facili
176                     Transplantation of fetal retinal photoreceptor suspensions into the subretinal sp
177 ion cells (ipRGCs) comprise a third class of retinal photoreceptors that are known to mediate physiol
178 Light produces a graded hyperpolarization in retinal photoreceptors that decreases their release of s
179 In mammals, pineal function is influenced by retinal photoreceptors that project to the suprachiasmat
180                                In vertebrate retinal photoreceptors, the absorption of light by rhodo
181  the intrinsic ability of regenerating adult retinal photoreceptors to reconstitute properly differen
182             The outer segments of vertebrate retinal photoreceptors undergo periodic shedding of memb
183                                              Retinal photoreceptors use the heterotrimeric G protein
184                                           In retinal photoreceptors, vectorial transport of cargo is
185 al visual structures by receiving input from retinal photoreceptors via bipolar and amacrine cells.
186 to supply 11-cis-retinal from the RPE to the retinal photoreceptors was accompanied by a massive accu
187                       To stimulate different retinal photoreceptors, we used a 1-second 640-nm flash
188                                           In retinal photoreceptors where rootlets appear particularl
189    Rac1 is expressed abundantly in mammalian retinal photoreceptors, where it is activated in respons
190  observations, we show here that adult mouse retinal photoreceptors, which are terminally differentia
191 occur through either extraretinal (brain) or retinal photoreceptors, which mediate sensitivity to blu
192 ataract removal, we have found evidence that retinal photoreceptors will swiftly realign towards the

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