ライフサイエンスコーパス: retinal ganglion cell

1 s location that stimulated the corresponding retinal ganglion cell.

2 h resulted in compromised differentiation of retinal ganglion cells.

3 t channels for transmission to the brain via retinal ganglion cells.

4 ersible blindness due to the degeneration of retinal ganglion cells.

5 tic transmission, which is propagated to the retinal ganglion cells.

6 associate with endosomes along the axons of retinal ganglion cells.

7 rizontal cells, as well as a small number of retinal ganglion cells.

8 s with intracellular recordings from macaque retinal ganglion cells.

9 tic transmission, which is propagated to the retinal ganglion cells.

10 immediately after axonal injury in purified retinal ganglion cells.

11 isely converging inputs from similarly tuned retinal ganglion cells.

12 wholemounts, we estimated a total of 353,000 retinal ganglion cells.

13 lycemia, particularly preserving survival of retinal ganglion cells.

14 Both RORalpha and SEMA3E were expressed in retinal ganglion cells.

15 by the innervation of the visual thalamus by retinal ganglion cells.

16 ed that arousal modulates the firing of some retinal ganglion cells.

17 that this interaction is present in primary retinal ganglion cells.

18 cells are one of the major types of primate retinal ganglion cells.

19 otoreceptor mediated stimulation in the same retinal ganglion cells.

20 mmatory mode of action or a direct impact on retinal ganglion cells.

21 to optically record optogenetically restored retinal ganglion cell activity in the fovea of the livin

22 e retina can produce saccadic suppression of retinal ganglion cell activity.

23 pletion impaired the removal of dead labeled retinal ganglion cells after optic nerve crush, but rema

24 cells, such that the densities of early-born retinal ganglion cells, amacrine and horizontal cells, a

25 ding to an overall decrease in the number of retinal ganglion cells, amacrine cells, and an increase

26 etinas displayed a massive postnatal loss of retinal ganglion cells and a large fraction of photorece

27 e (within 8 degrees of the central field) to retinal ganglion cells and associated central visual fie

28 we measured the topographic distribution of retinal ganglion cells and determined the spatial resolu

29 -unit recordings from synaptically connected retinal ganglion cells and LGN neurons and measured the

30 e recordings from monosynaptically connected retinal ganglion cells and LGN neurons in male/female ca

31 xpression of essentially the same markers of retinal ganglion cells and neuronal cells as seen in 661

32 of the midbrain, converging projections from retinal ganglion cells and neurons in visual cortex must

33 The progressive death of retinal ganglion cells and resulting visual deficits are

34 math5 nulls (math5(-/-)), mutants that lack retinal ganglion cells and retinofugal projections.

35 ic negative-response (PhNR; originating from retinal ganglion cells) and i-wave components were extra

36 , motoneurons, dorsal root ganglion neurons, retinal ganglion cells, and callosal projection neurons

37 expressed in several bipolar cell subtypes, retinal ganglion cells, and some amacrine cell subtypes

38 CYP2J2 overexpression on the attenuation of retinal ganglion cell apoptosis in a glaucoma rat model.

39 psin-expressing intrinsically photosensitive retinal ganglion cells are characterized by sluggish act

40 A small fraction of mammalian retinal ganglion cells are directly photoreceptive thank

41 Directional responses in retinal ganglion cells are generated in large part by di

42 Melanopsin-expressing retinal ganglion cells are intrinsically photosensitive

43 f gene regulatory reprogramming in zebrafish retinal ganglion cells at specific time points along the

44 inant viral overexpression of LOTUS enhances retinal ganglion cell axonal regeneration after optic ne

45 Retinal ganglion cell axons forming the optic nerve (ON)

46 e tool to automatically and accurately count retinal ganglion cell axons in optic nerve (ON) tissue i

47 Cue stimulation of growing Xenopus retinal ganglion cell axons induces rapid dissociation o

48 t arose in the developing Xenopus brain, and retinal ganglion cell axons turned to follow this gradie

49 thologic studies showing age-related loss of retinal ganglion cell axons, we showed a significant dec

50 and inner plexiform layers, the sites of the retinal ganglion cell bodies and dendrites, respectively

51 Retinal ganglion cells can be classified into more than

52 findings, we showed that, in rats, axons of retinal ganglion cells converge on hypothalamic neurons

53 The visual response properties of retinal ganglion cells correlated well with those of the

54 tudies that link visual field sensitivity to retinal ganglion cell count are discussed.

55 induces permanent visual dysfunction due to retinal ganglion cell damage in multiple sclerosis and e

56 Additionally, ST266 reduced retinal ganglion cell death in vitro.

57 e (IOP), which causes optic nerve damage and retinal ganglion cell death, is the primary risk factor

58 ration, oligodendrocyte loss, and subsequent retinal ganglion cell death.

59 ntified as a key proinflammatory mediator of retinal ganglion cell death.

60 Intraocular pressure-sensitive retinal ganglion cell degeneration is a hallmark of glau

61 ecies, we found a temporal area with maximum retinal ganglion cell density ( approximately 5,000-7,00

62 stimates of spatial resolution based on peak retinal ganglion cell density and eye size ( approximate

63 onfiguration of the retina (i.e., changes in retinal ganglion cell density from the retinal periphery

64 t to measure the topographic distribution of retinal ganglion cell density using stereology and retin

65 Retinal ganglion cell density was 33% lower in glaucoma

66 Retinal ganglion cell density was estimated at the same

67 crohabitats have a pronounced streak of high retinal ganglion cell density, whereas those favoring mo

68 ongation in myopia to compensate for reduced retinal ganglion cell density.

69 was not significantly associated with IOP or retinal ganglion cell density.

70 e, it is unknown whether direction-selective retinal ganglion cells (DSGCs) exist in primates and, if

71 eiving inputs from the melanopsin-containing retinal ganglion cells encode spatial information and th

72 Here, we identify a novel marker for retinal ganglion cells encoding directional motion that

73 (the vesicular GABA/glycine transporter) in retinal ganglion cells enhances the activity of inner re

74 These retinal ganglion cells express the photosensitive protei

75 KEY POINTS: A subpopulation of retinal ganglion cells expresses the neuropeptide vasopr

76 A small population of retinal ganglion cells expresses the photopigment melano

77 is hard-wired in the machinery of vertebrate retinal ganglion cell genesis.

78 In primates, over 17 morphological types of retinal ganglion cell have been distinguished by their d

79 ature, other important cell classes, such as retinal ganglion cells, have proven much more challengin

80 ociated with a loss of structural markers of retinal ganglion cell health in a multiethnic Asian popu

81 Muller glia, bipolar cells, amacrine cells, retinal ganglion cells, horizontal cells, astrocytes, an

82 inhibitor library in human stem cell-derived retinal ganglion cells (hRGCs).

83 use of cannabis could alter the function of retinal ganglion cells in humans.

84 t on central neurotransmission, studying the retinal ganglion cells in individuals who regularly use

85 For parasol retinal ganglion cells in macaque retina, estimated subu

86 Here, we identified calretinin positive retinal ganglion cells in the common marmoset Callithrix

87 We recorded from OFF delta retinal ganglion cells in the guinea pig retina and moni

88 e outgrowth in vitro and for the survival of retinal ganglion cells in vivo following optic nerve inj

89 ells, AII amacrine and melanopsin-containing retinal ganglion cells, in control and PD eyes from huma

90 een reported to occur only between homotypic retinal ganglion cells, in line with the concept of para

91 the spatial organization of cone signals in retinal ganglion cells, including how signals from cones

92 degenerated optic nerves as well as loss of retinal ganglion cells indicated optic atrophy.

93 retinal nerve fiber layer (RNFL) and macular retinal ganglion cell-inner plexiform layer (GCIPL) chan

94 , sixth type of intrinsically photosensitive retinal ganglion cell (ipRGC) in the mouse-the M6 cell.

95 sin-expressing, intrinsically photosensitive retinal ganglion cell (ipRGC) subtypes are two RGC types

96 The intrinsically photosensitive M1 retinal ganglion cells (ipRGC) initiate non-image-formin

97 inally found in intrinsically photosensitive retinal ganglion cells (ipRGCs) [11-19].

98 is mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) and is critical for driv

99 Intrinsically photosensitive retinal ganglion cells (ipRGCs) are a subset of cells th

100 emonstrate that intrinsically photosensitive retinal ganglion cells (ipRGCs) are both resilient to ce

101 discovered that intrinsically photosensitive retinal ganglion cells (ipRGCs) are critical for this re

102 psin-containing intrinsically photosensitive retinal ganglion cells (ipRGCs) are thought to play a ro

103 Intrinsically photosensitive retinal ganglion cells (ipRGCs) combine direct photosens

104 Intrinsically photosensitive retinal ganglion cells (ipRGCs) control non-visual light

105 Intrinsically photosensitive retinal ganglion cells (ipRGCs) express the photopigment

106 Intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopigm

107 types of these intrinsically photosensitive retinal ganglion cells (ipRGCs) have emerged.

108 These intrinsically photosensitive retinal ganglion cells (ipRGCs) have well-established ro

109 Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate the pupillary li

110 sin-expressing, intrinsically photosensitive retinal ganglion cells (ipRGCs) synchronize our biologic

111 t (IGL) through intrinsically photosensitive retinal ganglion cells (ipRGCs)(4).

112 psin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs), but the relevant downst

113 mmalian retina, intrinsically photosensitive retinal ganglion cells (ipRGCs), has had a revolutionary

114 Intrinsically photosensitive retinal ganglion cells (ipRGCs), which express the photo

115 as well as the intrinsically photosensitive retinal ganglion cells (ipRGCs).

116 he trichromatic primate retina, the "midget" retinal ganglion cell is the classical substrate for red

117 ructural changes of the optic nerve head and retinal ganglion cells is the hallmark of glaucoma diagn

118 optic nerve atrophy resulting from death of retinal ganglion cells is the most prominent ocular mani

119 d of the M(1) receptor, neuron number in the retinal ganglion cell layer and axon number in the optic

120 itecture, specifically, the thickness of the retinal ganglion cell layer and inner plexiform layer (G

121 xygen species level was also elevated in the retinal ganglion cell layer of aged M(1) receptor-defici

122 ons of the retinal nerve fiber layer and the retinal ganglion cell layer with spectral-domain optical

123 ~1 million ganglion cells in the Nubian ibex retinal ganglion cell layer.

124 ads to age-dependent neuron reduction in the retinal ganglion cell layer.

125 tly in cones and combined at the bipolar and retinal ganglion cell level, creating parallel color opp

126 ion photoswitch that is capable of restoring retinal ganglion cell light responses to blue or white l

127 However, optic nerve crush injury-mediated retinal ganglion cell loss evokes neither peripheral mon

128 clusion, M(1) receptor deficiency results in retinal ganglion cell loss in aged mice via involvement

129 attenuated visual dysfunction, and prevented retinal ganglion cell loss in experimental optic neuriti

130 opsin cells may contribute to the melanopsin retinal ganglion cell loss previously described and to t

131 e retina, which is associated with increased retinal ganglion cell loss, retinal nerve fiber layer th

132 duration included capillary degeneration and retinal ganglion cell loss.

133 ptor gene knockout, reduced inflammation and retinal ganglion cell loss.

134 angle, ectropion uvea, retinal gliosis, and retinal ganglion cell loss.

135 valent eye disease characterized by death of retinal ganglion cells; lowering IOP is the only proven

136 tatory and disinhibitory inputs to a type of retinal ganglion cell maximizes the signal-to-noise rati

137 asses-rods, cones, and melanopsin-containing retinal ganglion cells (mRGCs)-have been shown to provid

138 uses vision loss through the degeneration of retinal ganglion cell neurons and their axons in the opt

139 mitted to the brain by dimming-sensitive OFF retinal ganglion cells (OFF-RGCs) that respond to light

140 the four subtypes of ON direction-selective retinal ganglion cells (ON-DS RGCs), those preferring ve

141 While we focused our efforts on the retinal ganglion cells, our transcriptomes of developing

142 nd intrinsically-photosensitive (melanopsin) retinal ganglion cell pathways.

143 open-angle glaucoma with structural macular retinal ganglion cell plus inner plexiform layer (RGC+IP

144 Unlike DENAQ, DAD acts upstream of retinal ganglion cells, primarily conferring light sensi

145 These retinal ganglion cells project predominately to our biol

146 the midbrain is the primary region to which retinal ganglion cells project their axons in the chick.

147 Introduction of miR-223-3p in vivo in mouse retinal ganglion cells protects their axons from degener

148 pression of ephrin-A3 (Efna3) in a subset of retinal ganglion cells, quantitatively altering the reti

149 s significant because chemical synapses on a retinal ganglion cell require the probabilistic release

150 RNFL thickness near birth, implying that the retinal ganglion cells reserve is affected by intrauteri

151 retina, extensive work has revealed how the retinal ganglion cells respond to extracellular electric

152 Pou5f1), Sox2 and Klf4 genes (OSK) in mouse retinal ganglion cells restores youthful DNA methylation

153 deferiprone, preserves vision and attenuates retinal ganglion cell (RGC) and axonal loss during EAE o

154 Also, there was worse retinal ganglion cell (RGC) and axonal loss in EAE femal

155 Early progression involves retinal ganglion cell (RGC) axon dysfunction that preced

156 small fraction of Xenopus tadpoles, a single retinal ganglion cell (RGC) axon misprojects to the ipsi

157 In the developing mouse optic tract, retinal ganglion cell (RGC) axon position is organized b

158 Binocular vision depends on retinal ganglion cell (RGC) axon projection either to th

159 in-like growth factor-1 (IGF1) by initiating retinal ganglion cell (RGC) axon regeneration after axot

160 In mammals with binocular vision, retinal ganglion cell (RGC) axons from each eye project

161 For example, degeneration of retinal ganglion cell (RGC) axons in glaucoma leads to i

162 NS axon regeneration, and we have shown that retinal ganglion cell (RGC) axons regenerate in the liza

163 This study explored why lesioned retinal ganglion cell (RGC) axons regenerate successfull

164 tood, the mechanisms promoting the growth of retinal ganglion cell (RGC) axons toward visual targets

165 MAP1B and CRMP2 was expectedly increased in retinal ganglion cell (RGC) axons upon enhanced GSK3 act

166 ion is relayed from the eye to the brain via retinal ganglion cell (RGC) axons.

167 The retinal ganglion cell (RGC) competence factor ATOH7 is d

168 licated in developing LHON phenotype such as retinal ganglion cell (RGC) death and loss of vision.

169 genetic deficits, which are characterized by retinal ganglion cell (RGC) death and ON degeneration.

170 n is believed to be the major contributor to retinal ganglion cell (RGC) death, the endpoint of optic

171 an increase in oxidative damage, leading to retinal ganglion cell (RGC) death.

172 rldwide, and is characterized by progressive retinal ganglion cell (RGC) death.

173 Interestingly, time course and extent of retinal ganglion cell (RGC) degeneration after optic ner

174 Optic atrophy resulting from retinal ganglion cell (RGC) degeneration is a prominent

175 s study describes a novel paradigm to reduce retinal ganglion cell (RGC) degeneration underlying glau

176 bition onto cone bipolar cell (BC) axons and retinal ganglion cell (RGC) dendrites, but makes the maj

177 Considerable between-individual variation in retinal ganglion cell (RGC) density exists in healthy in

178 Regulated retinal ganglion cell (RGC) differentiation and axonal g

179 evation of intraocular pressure (IOP) causes retinal ganglion cell (RGC) dysfunction and death and is

180 ocular pressure (IOP) but are protected from retinal ganglion cell (RGC) dysfunction and neuroglial c

181 s and fusion protein optic atrophy 1 (Opa1), retinal ganglion cell (RGC) dysfunction and visual loss

182 What pathways specify retinal ganglion cell (RGC) fate in the developing retin

183 vely investigated flicker-induced changes of retinal ganglion cell (RGC) function in common inbred mo

184 The visual message conveyed by a retinal ganglion cell (RGC) is often summarized by its s

185 t the individual somas of neurons within the retinal ganglion cell (RGC) layer can be imaged with a m

186 total number of Nissl-stained neurons in the retinal ganglion cell (RGC) layer in the Caribbean and C

187 ate that female Nf1-OPG mice exhibit greater retinal ganglion cell (RGC) loss and only females have r

188 of CYP2J2 (tie2-CYP2J2-Tr) protects against retinal ganglion cell (RGC) loss induced by glaucoma and

189 x 1-driven ATP synthesis, and cause specific retinal ganglion cell (RGC) loss.

190 eversible vision loss is due to the death of retinal ganglion cell (RGC) neurons.

191 ll size has previously been used to stratify Retinal Ganglion Cell (RGC) populations in histological

192 In adult rodents, Rbfox2 is expressed in all retinal ganglion cell (RGC) subtypes, horizontal cells,

193 analyzed dendritic morphogenesis in a single retinal ganglion cell (RGC) type in mouse called J-RGC.

194 oding emerged in which the three most common retinal ganglion cell (RGC) types captured much of the v

195 Visual information is encoded in distinct retinal ganglion cell (RGC) types in the eye tuned to sp

196 Multiple retinal ganglion cell (RGC) types in the mouse retina me

197 ctionally and anatomically-distinct types of retinal ganglion cell (RGC).

198 Injury to retinal ganglion cells (RGC), central nervous system neu

199 progressive degeneration of optic nerve and retinal ganglion cells (RGC).

200 ve an established role in the development of retinal ganglion cell (RGCs) types, the main transducers

201 ochemistry, single cell electrophysiology of retinal ganglion cells (RGCs) and by immunohistochemistr

202 eath signaling secondary to axonal damage in retinal ganglion cells (RGCs) and other neurons.

203 tials increase the background firing rate of retinal ganglion cells (RGCs) and overlay the stimulated

204 Precise connectivity between retinal ganglion cells (RGCs) and thalamocortical (TC) r

205 ic SSBP1 mitochondria-associated function in retinal ganglion cells (RGCs) and the resulting optic ne

206 The damage or loss of retinal ganglion cells (RGCs) and their axons accounts f

207 for glaucoma, a sight threatening disease of retinal ganglion cells (RGCs) and their axons.

208 Retinal ganglion cells (RGCs) are a heterogeneous popula

209 Retinal ganglion cells (RGCs) are frequently divided int

210 Retinal ganglion cells (RGCs) are tasked with transmitti

211 Midget retinal ganglion cells (RGCs) are the most common RGC ty

212 ted IOP on the retina.SIGNIFICANCE STATEMENT Retinal ganglion cells (RGCs) are the obligate output ne

213 Retinal ganglion cells (RGCs) are the sole projecting ne

214 egins in the retina, where distinct types of retinal ganglion cells (RGCs) are tuned to specific visu

215 We compared acutely isolated retinal ganglion cells (RGCs) at various developmental s

216 Retinal ganglion cells (RGCs) convey visual signals to 5

217 the diagnostic ability of OCT parameters and retinal ganglion cells (RGCs) count in identify glaucoma

218 Retinal ganglion cells (RGCs) drive diverse, light-evoke

219 we studied the selective resilience of mouse retinal ganglion cells (RGCs) following optic nerve crus

220 onical model to describe receptive fields of retinal ganglion cells (RGCs) for decades.

221 Retinal ganglion cells (RGCs) form an array of feature d

222 tial changes in transected axons of purified retinal ganglion cells (RGCs) from wild-type and Wld(S)

223 Using purified adult retinal ganglion cells (RGCs) in culture, we demonstrate

224 Counts of Brn3a-expressing retinal ganglion cells (RGCs) in implanted eyes were ind

225 the close interaction between astrocytes and retinal ganglion cells (RGCs) in the eye to characterize

226 ma is characterized by a progressive loss of retinal ganglion cells (RGCs) in the eye, which ultimate

227 tomography (OCT) measures the most critical retinal ganglion cells (RGCs) in the human eye.

228 Loss of retinal ganglion cells (RGCs) is a key pathological proc

229 In retinal ganglion cells (RGCs) of blind rd1 mice, photosw

230 e intense TBK1 labelling was detected in the retinal ganglion cells (RGCs) of Tg-TBK1 mice than in wi

231 ABSTRACT: How retinal ganglion cells (RGCs) process and integrate syna

232 we show unequivocally that a small subset of retinal ganglion cells (RGCs) project to the opposite re

233 In higher vertebrates, the circuit formed by retinal ganglion cells (RGCs) projecting ipsilaterally (

234 Retinal ganglion cells (RGCs) receive convergent input f

235 Retinal ganglion cells (RGCs) serve as a crucial communi

236 en in other mammals, the majority of injured retinal ganglion cells (RGCs) survive with relatively hi

237 Here we identify a subset of retinal ganglion cells (RGCs) that controls mouse loomin

238 on the rods and cones of the retina, but on retinal ganglion cells (RGCs) that detect the ambient li

239 We show in macaque monkeys that retinal ganglion cells (RGCs) that express this marker c

240 isual circuit is comprised of projections of retinal ganglion cells (RGCs) to ipsilateral and contral

241 The number of retinal ganglion cells (RGCs) underlying Ricco's area or

242 TRPV1 is expressed in a subset of mouse retinal ganglion cells (RGCs) with peak expression in th

243 or pulvinar (PIm) is innervated by widefield retinal ganglion cells (RGCs), and this pathway is not a

244 E STATEMENT: The output cells of the retina, retinal ganglion cells (RGCs), are a diverse group of ap

245 at give origin to its 1.2 million axons, the retinal ganglion cells (RGCs), are particularly vulnerab

246 In chick retinal ganglion cells (RGCs), downregulation of Arl8B r

247 Ret is initially expressed in retinal ganglion cells (RGCs), followed by horizontal ce

248 lar terminals then drive the output neurons, retinal ganglion cells (RGCs), following light increment

249 st amacrine cells (SACs), propagating across retinal ganglion cells (RGCs), further through visual ce

250 ration of optic nerve axons and apoptosis of retinal ganglion cells (RGCs), however, the precise mech

251 coma, a chronic neurodegenerative disease of retinal ganglion cells (RGCs), is a leading cause of irr

252 ic neuropathies are associated with death of retinal ganglion cells (RGCs), neurons that project thei

253 s that modulate input from photoreceptors to retinal ganglion cells (RGCs), rendering each RGC type s

254 Retinal ganglion cells (RGCs), the neurons that connect

255 Retinal ganglion cells (RGCs), the output neurons of the

256 nterneurons, and synaptically transmitted to retinal ganglion cells (RGCs), which send information to

257 relatively even topographic distribution of retinal ganglion cells (RGCs)-the output neurons of the

258 development of cell-specific morphologies in retinal ganglion cells (RGCs).

259 Cs) and postsynaptic densities (PSD95-FP) of retinal ganglion cells (RGCs).

260 sf1 receptor results in increased density of retinal ganglion cells (RGCs).

261 olume under normal and injury conditions, in retinal ganglion cells (RGCs).

262 , respectively, and to distinguish them from retinal ganglion cells (RGCs).

263 ic neuropathies, is characterized by loss of retinal ganglion cells (RGCs).

264 and visual field loss caused by the death of retinal ganglion cells (RGCs).

265 ontogeny of light-driven responses in mouse retinal ganglion cells (RGCs).

266 om the eye to the brain by distinct types of retinal ganglion cells (RGCs).

267 on blinding disease characterized by loss of retinal ganglion cells (RGCs).

268 egulate axon growth in CNS neurons including retinal ganglion cells (RGCs).

269 th the signal and noise among populations of retinal ganglion cells (RGCs).

270 ON and OFF receptive subfields in F-mini-ON retinal ganglion cells (RGCs).

271 about what their eyes send to the brain via retinal ganglion cells (RGCs).

272 ck proteins 72 (HSP72) induction behavior in retinal ganglion cells (RGCs-5) to provide a possible so

273 e revealed increased mitochondrial length in retinal ganglion cell soma and axon, but no degeneration

274 ification and the anatomical location of the retinal ganglion cell soma.

275 ent confocal imaging of genetically targeted retinal ganglion cell sub-populations in the mouse.

276 l line expressed certain markers specific to retinal ganglion cells such as Rbpms, Brn3b (Pou4f2), Br

277 hosphodiesterase is demonstrated to increase retinal ganglion cell survival in vivo in mice of both s

278 may become therapeutically useful to promote retinal ganglion cell survival.

279 ondrial fusion and fission, similarly affect retinal ganglion cell survival.

280 lamina-specific, and topographically ordered retinal ganglion cell synaptic inputs.

281 ells (TWIK-1, TASK-3, TRAAK, and TREK-2) and retinal ganglion cells (TASK-1, TREK-1, TWIK-1, TWIK-2 a

282 mice, which exhibit elevated IOP and loss of retinal ganglion cells, Tek(+/-);Ptprb(+/-) mice have el

283 We then image activity of retinal ganglion cell terminals and pretectal neurons.

284 mice, masking requires melanopsin-expressing retinal ganglion cells that detect blue light and projec

285 initiated transsynaptic tracing to label the retinal ganglion cells that provide input to individual

286 nding disease due to the degeneration of the retinal ganglion cells, the axons of which form the opti

287 have been shown to restore the responses of retinal ganglion cells to light in mouse models of retin

288 hypothalamic pathway, connecting a subset of retinal ganglion cells to the circadian pacemaker in the

289 he excitatory synaptic inputs and outputs of retinal ganglion cells to understand how such dynamic pr

290 he human eye, followed by neural sampling by retinal ganglion cells, to demonstrate the perceptual ef

291 f innate behaviors, receiving input from >30 retinal ganglion cell types and projecting to behavioral

292 The functions of the diverse retinal ganglion cell types in primates and the parallel

293 uman CSF and the response characteristics of retinal ganglion cells under a broad range of conditions

294 psin-expressing intrinsically photosensitive retinal ganglion cells upon illumination.

295 ere next most central and amacrine cells and retinal ganglion cells were on the outside.

296 n, specific subtypes of horizontal cells and retinal ganglion cells were overrepresented, suggesting

297 aim to confer intrinsic light sensitivity to retinal ganglion cells when photoreceptors have degenera

298 Axotomy elevated lipin1 in retinal ganglion cells, which contributed to regeneratio

299 four morphologically distinct types of mouse retinal ganglion cells with overlapping excitatory synap

300 Neural sampling by retinal ganglion cells with receptive field size and spa