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1 essing amacrine cells (VG3-ACs) in the mouse retina.
2 ge related macular degeneration, AMD) in the retina.
3 -dihydroxyphenylacetic acid (DOPAC) in mouse retina.
4 sustained alpha ganglion cells in the mouse retina.
5 stinct set of feature detectors in the mouse retina.
6 ne telodendria in adult and larval zebrafish retina.
7 ritic stratification of neurons in the inner retina.
8 eliably measure DA turnover in the mammalian retina.
9 ible for long-range coherent activity in the retina.
10 ter towards the dorso-temporal region of the retina.
11 is predominantly expressed in the brain and retina.
12 equal double cones compared with the ventral retina.
13 ecordings from 62 ON-OFF DSGCs in the rabbit retina.
14 or their spatial distribution throughout the retina.
15 tina and highest densities in the peripheral retina.
16 visual cortex while visually stimulating the retina.
17 gment epithelium (RPE) to support the neural retina.
18 ion of vasomotor response in the nondiabetic retina.
19 to ganglion cell connection in the mammalian retina.
20 endritic branches in both dorsal and ventral retina.
21 activated CD4(+) T cells that infiltrate the retina.
22 d synaptic markers in fetal human and Macaca retina.
23 in adult rabbits while preserving the inner retina.
24 structural and functional alterations of the retina.
25 nglion cells extend dendrites into the outer retina.
26 nsive study of K2P channel expression in the retina.
27 ossibly mispositioning of cone nuclei in the retina.
28 one photoreceptor mosaic in the living human retina.
29 reporter mouse peaked in the mid-peripheral retina.
30 ow non-uniform distribution across the mouse retina.
31 ed to the apical side and is taken up by the retina.
32 it-level encoding of motion direction in the retina.
33 s to process visual information in the inner retina.
34 organism to study the function of EYS in the retina.
35 somata and arborize in various levels of the retina.
36 the neuronal and vascular components of the retina.
37 ss in the eye occurring entirely outside the retina.
38 nd cell body, and increased apoptosis in the retina.
39 Visual processing starts in the retina.
40 erent cell types and subcellular location of retina.
41 n reducing the amount of VEGF present in the retina.
42 port between photoreceptors and cells in the retina.
43 A1) was the only chromophore detected in the retina.
44 en implicated in impaired development of the retina.
45 ear the fovea) to 1,000 microm in peripheral retina.
46 opment in the fovea compared with peripheral retina.
47 photothermal signal from the melanin in the retina.
48 and co-localizes with S-opsin in the ventral retina.
49 ants derived from different quadrants of the retina.
50 of features available simultaneously on the retina.
51 ates to the apical side to nourish the outer retina.
52 spanning the inner two layers of the rabbit retina.
53 " condition but one that involves the entire retina.
54 t immediately associated with the stomatopod retina.
55 s been shown to start at later stages in the retina.
56 f visual impairment that affects the central retina.
57 rcuit-level neuronal plasticity in the adult retina.
58 re also detected in the RPE of healthy human retina.
59 s in the peripheral nervous system (PNS) and retina.
60 testinal organoids (HIOs), colon mucosa, and retina.
61 nsmission via Gbetagamma in tiger salamander retinas.
62 Stargardt disease and is evidenced in human retinas.
63 increased ERp29 and calreticulin in diabetic retinas.
64 l ganglion cell (RGC) fate in the developing retina?
65 We conclude that RDH10 is not the dominant retina 11-cis-RDH, leaving its primary function in the r
66 ; OCT angiography of the 6 x 6-mm perifoveal retina; 30 degrees and 12 degrees central visual fields;
67 -selective ganglion cells (ooDSGCs) in mouse retina acquire their bistratified dendrites, in which re
71 markable feature of human vision is that the retina and brain have evolved circuitry to extract usefu
74 in the iris in cases 1, 3, and 4; the neural retina and choroid in case 1; and in the optic nerve in
76 se 2C promote neovascularization in both the retina and choroid, which suggests that inhibition of th
77 ates, nonuniform opsin expression across the retina and coexpression in single cones creates a mostly
78 , freely moving mice and at the level of the retina and dorsal lateral geniculate nucleus (dLGN).
79 primate visual system, where neurons in the retina and dorsal lateral geniculate nucleus of the thal
80 raphy with very low densities in the central retina and highest densities in the peripheral retina.
81 erent developmental time points in the mouse retina and identified five types of ORDs originating fro
82 lliculus (SC) receives direct input from the retina and integrates it with information about sound, t
83 e specific neural circuits that begin in the retina and mediate this important behaviour remain uncle
84 lta retinal ganglion cells in the guinea pig retina and monitored synaptic currents that were evoked
87 characteristics of combined hamartoma of the retina and retinal pigment epithelium (CHRRPE) involving
89 sfunction, and angiogenesis, its role in the retina and the factors that regulate its actions are not
90 etinal pigment epithelium, outer part of the retina and the optic nerve head within 24-hours, in both
95 2 deletion, PKM1 is upregulated in the outer retina and there is increased expression of genes involv
96 trol distribution of drugs from blood to the retina and thereby influence drug efficacy and toxicity.
97 nd sub-cellular localization of IFT43 in the retina and transiently transfected cells was examined by
99 athogenic variants in genes expressed in the retina and/or brain and consistent with the pattern of i
100 biallelic RPE65 mutations, sufficient viable retina, and ability to perform standardised multi-lumina
102 ed eye tissues from the conjunctiva, cornea, retina, and sclera were performed to determine the distr
103 ed in AII amacrine cells in the mature mouse retina, and which conjointly identify this retinal cell
104 l Zeiss Meditec) and the modified Heidelberg Retina Angiograph (Heidelberg Engineering) (HRA) at 0.98
106 and RPE changes were seen in the peripheral retina, anterior to the vortex veins, in 21.8% of eyes.
108 t regenerated neurons of the adult zebrafish retina are capable of restoring complex morphologies and
112 SH1 and USH2 proteins in the cochlea and the retina as well as the disease mechanisms underlying USH1
113 olds in the retina and a crease in the outer retina associated with papilledema owing to idiopathic i
114 ants of Houston, Houston, Texas; New England Retina Associates, Guilford, Connecticut; Elman Retina G
116 Eyes with retinitis involving >/=25% of the retina at presentation detached at nearly 12 times the r
117 yzed for percent of areas of avascular/total retina (AVA) and of intravitreal neovascular/total retin
118 ycoprotein (ABCB1) is expressed at the blood-retina barrier (BRB), where it may control distribution
119 ar antigens are sequestered behind the blood-retina barrier and the ocular environment protects ocula
120 n the retina, endothelial cells form a blood-retina barrier by virtue of tight junctions and low tran
124 t LXA4 and LXB4 are synthesized in the inner retina, but their levels are reduced following injury.
125 e types of thorny ganglion cells in marmoset retina can be identified with antibodies against calreti
126 from January 1 to June 30, 2016, at medical retina clinics at the Singapore National Eye Center amon
128 gments, were significantly lower in diabetic retinas compared to those in controls, suggesting a reti
129 performed in a clinical/surgical setting at Retina Consultants of Houston and Houston Methodist Hosp
130 n Eye Institute, Houston Methodist Hospital, Retina Consultants of Houston, Houston, Texas; New Engla
131 nd one female retina revealed that the human retina contains 7283 +/- 237 melanopsin-ir (0.63-0.75% o
132 esions," the OCT showed a cleft in the outer retina, creating an apical and basal separation of retin
135 of 2 to 4 distinct vascular plexuses in the retina, depending on location relative to the optic disc
136 t in mouse and rat, and the structure of the retina differs substantially between humans and Drosophi
137 Fluorescence microscopy of wild-type mouse retina disclosed a strong DNM1L expression in the gangli
138 Furthermore, ERG traces from regenerated retinas displayed waveforms matching those of controls,
141 alized individual rod bipolar cells in mouse retina during postnatal development and quantified the n
142 -AAV2 demonstrated deeper penetration in the retina, efficiently reaching the inner nuclear and outer
143 o the size, speed, and type of motion on the retina, enabling them to occupy different niches in stim
145 had no effect on the ex-vivo isolated mouse retina ERG where the RPE is not attached to the isolated
149 trans-retinol (all-trans-ROL)) in the neural retina following a photobleach and 5-fold lower retinyl
150 , teleost fish functionally regenerate their retina following injury, and Muller glia (MG) are the so
151 ersists in restoring visual responses to the retina for almost 1 month after a single intraocular inj
152 ertebrates, it is required not only for lens/retina formation but also for the development of the CNS
153 RGCs and polyaxonal amacrine cells in mouse retina forms the synaptic mechanism responsible for long
154 inhibition prevents progenitor cells of the retina from exiting the cell cycle and differentiating.
160 ina Associates, Guilford, Connecticut; Elman Retina Group, Baltimore, Maryland; and Retina Research I
161 mental sequence of plexiform layers in human retina has been characterized, the molecular steps of sy
164 system, which projects from the brain to the retina, has been intensively studied in several Neognath
165 emically, cone ERG(absent) RPGRIP1 (ins/ins) retinas have extensive L/M-opsin mislocalization, lack C
166 r glia, the most abundant glia of vertebrate retina, have an elaborate morphology characterized by a
168 acy results of the Retina Implant Alpha AMS (Retina Implant AG, Reutlingen, Germany) for partial rest
169 o report the initial efficacy results of the Retina Implant Alpha AMS (Retina Implant AG, Reutlingen,
170 on cycle reformats the flow impinging on the retina in a way that initiates coarse-to-fine processing
171 quantify the microstructural changes of the retina in CZS and compare these changes with those of co
172 lliculus (SC) receives visual input from the retina in its superficial layers (sSC) and induces eye/h
173 with thinning of the GCL + IPL sector of the retina in the eyes of patients with MS, particularly tho
175 of anesthesia on DA and DOPAC levels in the retina in vivo and find that basal dark-adapted concentr
176 umulation of iron-rich ferritin in the outer retina in-vivo and retinal-pigment-epithelial (RPE) cell
178 reocilia and for melanosome transport in the retina, in line with the phenotypic outcomes observed in
180 e important features reminiscent of a mature retina, including exuberant outgrowth of outer segment-l
181 Brn3b single- and Dlx1/Dlx2 double-knockout retinas, including near total RGC loss with a marked inc
185 degeneration of photoreceptors in the adult retina, interneurons, including bipolar cells, exhibit a
186 hird type of photoreceptors in the mammalian retina, intrinsically photosensitive retinal ganglion ce
189 he view that inhibition of TR locally in the retina is a therapeutic strategy for retinal degeneratio
191 e it is known that the number of ORDs in the retina is developmentally regulated, little is known abo
192 e) and the internal limiting membrane of the retina is essential to understanding the cause of rhegma
193 ent vision loss, and once 25% or more of the retina is involved the risk of RD and visual loss increa
194 me of neuronal organization in the mammalian retina is the segregation of ON and OFF pathways in the
197 d gamma oscillations with a peak at 60 Hz in retina, lateral geniculate, and primary visual cortex of
198 clature system that is consistent with human retina layer designations to standardize murine OCT, whi
199 mediating lateral inhibition in the central retina, likely horizontal cells, establish functional co
201 ld amacrine cells span large segments of the retina, making them uniquely equipped to normalize and o
203 ding that glucose enters mouse and zebrafish retinas mostly through photoreceptors support a conceptu
207 sible to infer some of the properties of the retina of early vertebrate progenitors by comparing lamp
209 Less VEGF staining was observed within the retina of the eyes treated with ranibizumab when compare
210 I amacrine-->RGC synaptic connections in the retina of the guinea pig (Cavia porcellus) by recording
213 tional-related proteins were observed in the retinas of diabetic rats, which were significantly chang
218 lotting were significantly down-regulated in retinas of STZ-rats and in human diabetic retinas (postm
219 antioxidant and anti-inflammatory effects in retinas of the treated rats, as shown by up-regulation o
220 avitated lamellar separation of neurosensory retina on spectral-domain optical coherence tomography (
222 ut DR showed a thicker choroid and a thinner retina, particularly in inner layers, after 1 year of fo
223 in retinas of STZ-rats and in human diabetic retinas (postmortem) compared with their respective cont
224 Standard models of stimulus encoding in the retina postulate that image presentations activate neuro
229 ptic to the ON sustained alpha cell of mouse retina provide currents with a higher signal-to-noise po
230 s diagnosed with primary DLBCL of the eye or retina (PVRL) or the eyelid, conjunctiva, choroid, cilia
234 ts diagnosed with PEVAC were identified at 4 retina referral centers worldwide and underwent complete
238 tal cell counts from one male and one female retina revealed that the human retina contains 7283 +/-
239 OFF responses to light, but not in wild-type retinas, revealing selectivity for RGCs that have lost p
241 sources and allows for an examination of the retina's early morphologic changes that are not generall
245 Surgery (ASCRS) and the American Society of Retina Specialists (ASRS) formed a joint task force to d
246 untarily reported to the American Society of Retina Specialists Research and Safety in Therapeutics (
249 to target the Nrl gene, encoding for Neural retina-specific leucine zipper protein, a rod fate deter
251 ased rhodopsin aggregation in the P23H-1 rat retina, suggesting enhanced P23H misfolding and aggregat
252 Muller glia pERK expression in the detached retina, suggesting that Muller survival pathways might u
254 tivity patterns were restored in regenerated retinas, suggesting that regenerated BPs recover accurat
255 wever, that these cells remain in the ageing retina suggests the potential for functional restoration
258 notype was found in the Dlx1/Dlx2/Brn3b-null retinas than was predicted by combining features of the
259 c immunocytochemistry, we show in the rabbit retina that bright-light-induced activation of dopamine
260 The fovea is a specialized region of the retina that dominates the visual perception of primates
261 from the retinal vasculature into the inner retina that replenishes the local myeloid cell populatio
262 only a fraction of diseased cells, yielding retinas that are a mosaic of treated and untreated rods,
264 ree differentially growing compartments: the retina, the ciliary margin (CM), and the retinal pigment
265 ed on the central rod-free region of primate retina, the fovea, to specifically investigate the devel
266 masomes in fully differentiated cells in the retina, the removal of the damaged and dysfunctional mit
269 re emphasize the peculiar sensitivity of the retina to perturbations of this pathway, which is highli
271 ation of endogenous microglia from the inner retina to the RPE layer, followed by (2) subsequent mono
272 ess corneal imaging by a LS-IVCM (Heidelberg Retina Tomograph 3 with Rostock Cornea Module; Heidelber
273 mpleted within 3 d, and we present data from retinas treated with laser-induced choroidal neovascular
275 ed JN expression and functional roles in the retina using fluorescence histochemistry, confocal micro
278 linics between November 2012 and March 2015 (Retina-Vitreous Associates Medical Group, Beverly Hills,
281 dark adaptation both in vivo and in isolated retina was unaffected, indicating that RDH10 is not requ
283 Using large-scale recordings in the rat retina, we show that a homogeneous population of fast OF
284 00 bipolar cell axon terminals in the intact retina, we show that bipolar cell functional diversity i
285 Cs) in rod differentiation in neonatal mouse retinas, we used a pharmacological approach that showed
289 NF-kappaB and Nrf2 signaling pathways in the retina which may contribute to ameliorating retinal dama
290 erall cone density was greater in the dorsal retina which was also characterized by a larger proporti
291 eptor found in the rod outer segments in the retina, which triggers a visual response under dim light
294 cells, unlike neurons, are spread across the retina with homogenous density, and their arbor sizes ch
295 the ellipsoid zone, thinning of the central retina with increased backscatter, and severe structural
296 ectrode recordings in the peripheral primate retina with single-electrode and several types of multi-
298 by which hPSCs can be differentiated into 3D retinas with at least some important features reminiscen
299 pression of IRX1 and ADAMTS16 in human fetal retina, with IRX1 preferentially expressed in fetal macu
300 P channels are widely expressed in the mouse retina, with variations in expression detected at differ
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