ライフサイエンスコーパス: photoresponse

1 18.4 nm) and stable defects with an extended photoresponse.

2 r solar light derives from the visible light photoresponse.

3 it is unclear what physics will dominate the photoresponse.

4 ovement and prolonged the termination of the photoresponse.

5 a critical level, essentially saturating the photoresponse.

6 that dPIS was essential for maintaining the photoresponse.

7 ching the photo-excited rhodopsin during the photoresponse.

8 g cascade to desensitize cones and speed the photoresponse.

9 DE6 by transducin, thereby desensitizing the photoresponse.

10 plitude, kinetics and reproducibility of the photoresponse.

11 the light sensitivity or the kinetics of the photoresponse.

12 psin in vivo and disrupts termination of the photoresponse.

13 s consistent with their participation in the photoresponse.

14 emical cascade that underlies the electrical photoresponse.

15 gamma-TRPL heteromultimers contribute to the photoresponse.

16 TP by Galphat and for normal recovery of the photoresponse.

17 ling complex is in rapid deactivation of the photoresponse.

18 nsduction cascade during the recovery from a photoresponse.

19 defects in adaptation and termination of the photoresponse.

20 that are dominated by ionic transport and no photoresponse.

21 photoisomerizations and >100 nm red shift of photoresponse.

22 le conductance and capacitance and broadband photoresponse.

23 to 2.62 eV, which are crucial for broadband photoresponse.

24 n be injected into phosphorene to induce its photoresponse.

25 preparation method to measure human ipRGCs' photoresponses.

26 ne photoreceptor (P3) cell components of ERG photoresponses.

27 found that the two pigments produced similar photoresponses.

28 iquitination by COP1, thereby enhancing phyA photoresponses.

29 mentary fly mutants with slow termination of photoresponses.

30 m signal transducer and thus enhancing plant photoresponses.

31 ors for regulating certain non-image forming photoresponses.

32 ith lambda(max) of 492 nm that supported rod photoresponses.

33 definitively linking phyA signaling to these photoresponses.

34 A mutant allele, cry(b), inhibits circadian photoresponses.

35 ng to circadian phase shifting and other NIF photoresponses.

36 ng and realize electrically tunable infrared photoresponse (1.15 to 1.47 mum).

37 transducin inactivation in the course of the photoresponse, a requisite for normal vision.

38 se range compression, sensitivity shift, and photoresponse acceleration.

39 ain > 1,000) and fast (response time < 1 ms) photoresponse allow us to study, for the first time, the

40 ng reduction in the amplification of the rod photoresponse, allowing rods to operate in illumination

41 stricted spots of light, the duration of the photoresponse along the OS does not increase linearly wi

42 The loss of photoresponse amplitude with age in the mutant mice para

43 receptor function (despite the low saturated photoresponse amplitude) and anomalous postreceptor reti

44 one morphology but reduced visual acuity and photoresponse amplitudes.

45 ations in NINAC have been shown to alter the photoresponse and compromise photoreceptor survival, the

46 ations in NINAC have been shown to alter the photoresponse and compromise photoreceptor survival.

47 as responsible for delaying the onset of the photoresponse and for attenuating its amplification.

48 e into perovskite absorbers to broaden their photoresponse and increase their photovoltaic efficiency

49 re classical preparations for studies of the photoresponse and its modulation by circadian clocks.

50 esent a class of carbon materials exhibiting photoresponse and many potential applications.

51 applications, it is desirable to obtain the photoresponse and positional sensitivity over a much lar

52 Combining the gate-tunable photoresponse and regression algorithm, we achieve spect

53 The rod photoresponse and rod recovery were derived by using a p

54 esponsivity exceeding 2600 A W(-1) with fast photoresponse and specific detectivity up to ~10(13) Jon

55 Few-layered CuIn7 Se11 has a strong photoresponse and the potential to serve as the active m

56 -activating proteins (GCAPs) regulate visual photoresponse and trigger congenital retinal diseases in

57 s after maturation of OS resulted in loss of photoresponse and vesiculation in the OS.

58 n cone photoresponses, we have characterized photoresponses and GTPase regulatory components of cones

59 ignificantly shortened the duration of ipRGC photoresponses and reduced the number of light-evoked sp

60 eases in the magnitude of ocular type B cell photoresponses and the frequency of light-elicited actio

61 nificantly inhibited in vivo recovery of rod photoresponses and the rate of recovery of functional rh

62 black phosphorus, their electrically tunable photoresponse, and advanced computational algorithms for

63 Since superconductors rarely exhibit strong photoresponses, and optically sensitive materials are of

64 to near normal levels, restored dark-adapted photoresponses, and rescued rods from degeneration.

65 oreceptors can both contribute to non-visual photoresponses, and that both melanopsin and cryptochrom

66 er-dispersed SWCNTs demonstrated significant photoresponse, apparently due to photoinduced charge tra

67 Inner retinal photoresponses are mediated by melanopsin-expressing, in

68 These photoresponses are mediated by two phototropins, phot1 a

69 pRGCs) generate endogenous, melanopsin-based photoresponses as well as extrinsic, rod/cone-driven res

70 is not rate limiting for recovery of the rod photoresponse, as it is in Drosophila.

71 ollision-free phenomenon that yields a giant photoresponse at terahertz frequencies (1.9 THz), more t

72 pensions display interesting shape-dependent photoresponse behavior under white light illumination fr

73 course and pharmacology as the physiological photoresponse, but with a much shorter latency.

74 Substrate removal was found to enhance the photoresponse by four-fold compared to substrate-support

75 recovery phase abnormalities of rod-isolated photoresponses by electroretinography (ERG); photoactiva

76 onstrates high photoconductive gain and fast photoresponse can be achieved simultaneously and a clean

77 The same photoresponse changes occurred in exaggerated form in ce

78 These photoresponse changes were accompanied by increases and

79 he proposed photodetector has a bias-tunable photoresponse characteristic and can operate in the phot

80 ll-in-one OELG based on the bipolar spectral photoresponse characteristics of a self-powered perovski

81 rs exhibit spectrally tunable and narrowband photoresponses, circumventing the need for separate band

82 t good light-harvesting ability and enhanced photoresponses compared with the reverse rainbow photoca

83 de and slowed the kinetics of mouse M/L-cone photoresponses, cone adaptation in bright, steady light

84 ed with age-matched WT mice: recovery of the photoresponse, COX and SDH activity, retinal morphology,

85 erages existing visible and ultraviolet (UV) photoresponse data to predict more efficient material's

86 A basic model of photoresponse deactivation consistent with established p

87 Reduced AIPL1 delayed the photoresponse, decreased its amplification constant, slo

88 in, PIF4, in a pif4 null mutant, rescued the photoresponse defect in this mutant, whereas mutated PIF

89 , a universal method for evaluating material photoresponses, detailed illustrations of all instrument

90 on, which correlates with the performance of photoresponse devices.

91 highlight how the kinetics of the melanopsin photoresponse differentially regulate distinct light-med

92 the flexible detector arrays exhibit uniform photoresponse distribution, which is of much significanc

93 ndings is that the recovery phase of the rod photoresponse does not contribute significantly to visua

94 The photoresponse does not degrade for optical intensity mod

95 The devices exhibit a strong photoresponse down to the limit of a monolayer organic c

96 trates the photothermoelectric origin of the photoresponse due to gradients in the nanotube Seebeck c

97 In addition, the photoresponse due to the different photoexcited-charge-c

98 rating protein complex, which determines the photoresponse duration of photoreceptors, is composed of

99 One critical component which regulates the photoresponse duration on the molecular level is the com

100 the speed, sensitivity, and recovery of the photoresponse during visual signaling in vertebrate phot

101 bandgaps, the peak responsivity position and photoresponse edge of Se(x) Te(1-) (x) film-based photoc

102 The GFET shows a nonlocal photoresponse even when the SiC substrate is illuminated

103 addition to accelerating the recovery of the photoresponse, faster PDE6C deactivation may blunt the r

104 ncy by characterizing the sensitivity of rod photoresponses following exposure to bright bleaching li

105 -studied reduction in the sensitivity of rod photoresponses following pigment bleaching.

106 A broadband photoresponse from 532 to 1850 nm with ultrahigh respons

107 It consistently shows broadband photoresponse from the ultraviolet (255 nm) to the mid-i

108 hotosensor, yet is a fundamental link in the photoresponses from blue light perceived by the conserve

109 Many plant photoresponses from germination to shade avoidance are m

110 we established a method for collecting flash photoresponses from zebrafish rods and cones by recordin

111 ed for the timely inactivation of mouse cone photoresponse, gradually increasing its expression progr

112 The underlying mechanism of the photoresponse has been a particular focus of recent work

113 channel subunits required for the Drosophila photoresponse; however, our understanding of the identit

114 al electric field can dynamically extend the photoresponse in a 5 nm-thick BP photodetector from 3.7

115 affects the post-bleach recovery of the rod photoresponse in ABCR-deficient (abcr-/-) mice.

116 ere, we report the spatial dependence of the photoresponse in backgated graphene field-effect transis

117 e one of the mechanisms mediating a stronger photoresponse in dark-adapted cells.

118 photovoltaic effect, dominates the intrinsic photoresponse in graphene.

119 y kinetics of the intrinsic melanopsin-based photoresponse in ipRGCs, the duration of the PLR, and th

120 rollable and wavelength-selective bolometric photoresponse in macroscale assemblies of chirality-sort

121 the DNA interfacial layer that enhances the photoresponse in n-type field-effect transistors (FET) a

122 of biliverdin (BV) chromophore triggers the photoresponse in native Agp1 bacteriophytochrome.

123 ht absorption leads to a remarkably enhanced photoresponse in PNCs/graphene nanohybrid photodetectors

124 conclude that the slower termination of the photoresponse in retin(1) resulted from a requirement fo

125 The photoresponse in retinal photoreceptors begins when a mo

126 The intensity dependence of the photoresponse in rods lacking arrestin further suggests

127 Impurity-mediated sub-band gap photoresponse in silicon is an alternative to these meth

128 Room-temperature infrared sub-band gap photoresponse in silicon is of interest for telecommunic

129 urity-mediated room-temperature sub-band gap photoresponse in single-crystal silicon-based planar pho

130 The photoresponse in the electrical conductivity of a single

131 ended with fullerene derivatives show a high photoresponse in the near-infrared (NIR) and good photov

132 A high photoresponse in the near-infrared (NIR) region with exc

133 eurotrophin expression, and it preserved the photoresponse in the phototoxicity model of retinal dege

134 proteins (GCAPs) control the recovery of the photoresponse in vertebrate photoreceptors, through thei

135 ential factor in determining the duration of photoresponse in vertebrate rods and cones.

136 transretinal recordings revealed normal cone photoresponses in all RDH10-deficient mouse lines.

137 y account for faster and less sensitive cone photoresponses in darkness, whereas a reduced rise of st

138 vated cryptochrome (CRY) regulates circadian photoresponses in Drosophila melanogaster.

139 The physiology of nonimage-forming (NIF) photoresponses in humans is not well understood; therefo

140 te collar-2 genes, both global regulators of photoresponses in Neurospora, encode DNA binding protein

141 aining photoreceptors that regulate numerous photoresponses in plants and microorganisms through thei

142 ship between phytochrome kinase activity and photoresponses in plants.

143 However, melanopsin photoresponses in RPE-separated rat retinas became more

144 Unexpectedly, the early activation phase of photoresponses in Rpe65(-/-) mice accelerated with age a

145 d-type rods and may explain the decay of rod photoresponses in the presence of nonhydrolyzable analog

146 Whole-cell patch-clamp recording showed photoresponses in these cells even after degeneration of

147 ant of decay of the rate-limiting species in photoresponse inactivation (activated rhodopsin or the a

148 nd INAD did not appear to have a role in the photoresponse independent of localization of multiple si

149 risingly, there was little change in the rod photoresponse, indicating that dynamic Ca2+-dependent re

150 mma dominantly suppressed the TRPL-dependent photoresponse, indicating that TRPgamma-TRPL heteromulti

151 gap of 1.7 eV and display an electrochemical photoresponse indicative of a p-type semiconductor.

152 Fundamentally, the unique photoresponse induced by oxidation-related defects in 2D

153 ubstitutes equally for rTalpha in generating photoresponses initiated by either rhodopsin or S-cone o

154 nal studies, these data demonstrate the CarH photoresponse integrates B(12) photo- and redox-chemistr

155 -night (dawn), indicating that the circadian photoresponse is a network property and therefore non-ce

156 Activation of the Drosophila photoresponse is a rapid process that results in plasma

157 whether PKC-mediated desensitization of the photoresponse is accompanied by ultrastructural changes

158 Tunable photoresponse is achieved by controlling the nature of s

159 Rapid termination of the photoresponse is achieved in part by shuttling proteins

160 s on top of perovskite to further extend its photoresponse is considered as a simple and promising wa

161 yclic GMP concentration is decreased and the photoresponse is initiated.

162 Broadband sensitive photoresponse is realized at room temperature, with exce

163 Moreover, the photoresponse is studied at the heterointerface of the W

164 ole of phyA in mediating the blue light/UV-A photoresponses is a new function for phyA in chloroplast

165 rse transcription factors to modulate common photoresponses is an intriguing question in plant biolog

166 The reduction in photoresponses is due to defective association of crucia

167 n the membrane sets the rate of onset of the photoresponse, it was later argued that the subsequent p

168 candidate, did not substantially affect the photoresponse kinetics but did cause a significant reduc

169 k in this mechanism by establishing that rod photoresponse kinetics limit temporal sensitivity during

170 Cone photoresponse kinetics limit visual temporal sensitivity

171 vo recording revealed that R-econazole slows photoresponse kinetics, whereas S-econazole decreased th

172 e for GTPase acceleration in obtaining rapid photoresponse kinetics.

173 nt lines showed normal flash sensitivity and photoresponse kinetics.

174 Their synaptically driven photoresponses lack direction selectivity and show highe

175 amatic increase in the frequency of discrete photoresponse-like events.

176 external quantum efficiency of 25% and fast photoresponse <15 mus.

177 d dysfunction, detectable as reduced rod ERG photoresponse maximum amplitude, even in heterozygotes w

178 catalyst/electrolyte interfaces, and surface photoresponse measurements also demonstrated slow carrie

179 Photoresponse measurements on interfaces between perylen

180 m30a in adult mice led to a reduced scotopic photoresponse, mislocalization of ATP8A2 to the inner se

181 [Ca2+]i, PKC activators did not speed up the photoresponse, nor did PKC inhibitors antagonize the acc

182 A spectacular improvement of the photoresponse observed experimentally for mixed pyrite/m

183 me, temperature, and power dependence of the photoresponse of a bi-metal contacted graphene photodete

184 twork to recover the full nonlinear spectral photoresponse of a single GeSe-InSe p-n heterojunction d

185 resulted in a maximum power-producing ionic photoresponse of approximately 100 muA/cm(2) and approxi

186 bit enhanced current stability and a maximal photoresponse of approximately 860 microA cm(-2) , a fiv

187 esonance frequencies selectively amplify the photoresponse of graphene to light of different waveleng

188 unprecedented ambipolar (positive/negative) photoresponse of MCC-capped InAs NC solids that changed

189 fects, which may be exploited to enhance the photoresponse of nanoscale optoelectronic devices.

190 The photoresponse of suspended SWNT films is sufficiently hi

191 We compared the photoresponse of the as-exfoliated device with annealed

192 copy to assess the role of coherences in the photoresponse of the bacterial reaction center of Rhodob

193 function, it is necessary to understand the photoresponse of the chromophore.

194 The photoresponse of the coating is induced by a small amoun

195 pectra show that the Ti(3+) here extends the photoresponse of TiO(2) from the UV to the visible light

196 We have measured the photoresponse of two purple nonsulfur bacteria, Rhodobac

197 2% with a small energy loss of 0.53 eV and a photoresponse of up to 870 nm.

198 stand their functions better, we studied the photoresponses of all five cell types, by whole-cell rec

199 ype rcaE gene can rescue red and green light photoresponses of an rcaE null mutant, a gene in which t

200 The intrinsic photoresponses of M1 cells were lower threshold, higher

201 Photoresponses of mouse rods expressing lowered amounts

202 Melanopsin-based photoresponses of rat ipRGCs were remarkably sustained w

203 (IsPadC)) and characteristic differences in photoresponses of the two homologs, we identify an impor

204 Spectrally resolved photoresponses of these devices reveal a weakly conducti

205 We compare the photoresponses of wild-type cones with those of cones th

206 In this study, the photoresponses of Xenopus rods rendered constitutively a

207 with designable bandgap energy and enhanced photoresponse offer an attractive solution for on-chip i

208 sed photodetectors demonstrated to date, the photoresponse only comes from specific locations near gr

209 fied this parameter as rate-limiting for the photoresponse onset.

210 on, may play a role in the activation of the photoresponse or a component thereof, probably in synerg

211 ing to realize photodetectors with ultrafast photoresponse over a wide spectral range from far-infrar

212 response parameters were compared to the rod photoresponse parameters (S(ROD) and R(ROD)) in the same

213 Attenuation of the rod photoresponse parameters does not result simply from sho

214 The cone photoresponse parameters were compared to the rod photor

215 The mean rod photoresponse parameters were considerably less mature,

216 idual suspended VO(2) nanobeams we observe a photoresponse peaked at the metal-insulator boundary but

217 Because these photoresponse processes are recoverable following the re

218 rols, in part, the cGMP-triggered changes in photoresponse properties during light adaptation.

219 aps at the interface can dominate the device photoresponse properties.

220 asured spatial and density dependence of the photoresponse, provide strong evidence that nonlocal hot

221 -ZISe-Mo is mainly attributed to its widened photoresponse range and effective carrier separation bec

222 ight, and by controlling defects in GaS, the photoresponse range can be changed from vis-to-UV to UV-

223 a variety of conjugated polymers covering a photoresponse range from UV to NIR.

224 increased functionality in the form of fast photoresponse rates and the low defect density suggest C

225 The photoresponse reaches up to 50% external quantum efficie

226 king amacrine interneurons with sustained ON photoresponses receive gap-junction input from intrinsic

227 ransduction activation contributes to faster photoresponse recovery after a moderate pigment bleach i

228 Therefore, the speed of photoresponse recovery can affect temporal resolution an

229 GS9 anchor protein) proteins mediating rapid photoresponse recovery impair patients' ability to see m

230 nism for feedback control of the kinetics of photoresponse recovery in both rods and cones, with this

231 However, in brighter light, slow photoresponse recovery in rods and cones impaired visual

232 Electroretinography demonstrates that photoresponse recovery in zebrafish is delayed in the ev

233 eveal that the dominant time constant of rod photoresponse recovery is 1/(V(max)/K(m)) for the RGS9 r

234 ovide strong physiological evidence that rod photoresponse recovery is shaped by the sequential recru

235 Surprisingly, speeding up rod photoresponse recovery kinetics in transgenic mice impro

236 rprisingly, RGS9-2 not only supported normal photoresponse recovery under moderate light conditions b

237 ssing R9AP in rods, which causes accelerated photoresponse recovery.

238 ing functional performance, and facilitating photoresponse recovery.

239 n of the GPCR rhodopsin but has no effect on photoresponse recovery.

240 The melanopsin photoresponse relies on the presence of cis-isoforms of

241 /rd3GCAPs (-/-) hybrid photoreceptors, whose photoresponses remained drastically suppressed compared

242 , but their physiologic contribution to cone photoresponses remains unknown.

243 Before changes in photoresponse, removal of ARL13B led to mislocalization

244 for the first time, resulting in the fastest photoresponse reported for any solid-state material to d

245 Photoresponses revealed that the lifetime of R* is signi

246 tebrate cone photoreceptors, Ca(2+) controls photoresponse sensitivity, kinetics, and light adaptatio

247 Retinal photoresponses severely declined with age in beta5-/- mi

248 or quantum dots sensitizers, obtaining fast photoresponse simutaneously remains a challenge that mus

249 ed, but previous attempts to account for the photoresponse solely in terms of downstream products of

250 Photoresponse studies reveal that photoresponsivity in o

251 nses was comparable to that of the intrinsic photoresponse, suggesting that synaptic contacts are mad

252 has less effect on the cone than on the rod photoresponses, suggesting that cones are more resistant

253 es responsible for both vision and circadian photoresponse systems.

254 To explain the residual photoresponse that remains in the trp mutant, a third TR

255 ght receptor kinases that control a range of photoresponses that serve to optimize the photosynthetic

256 r ipRGC photosensitivity and for behavioural photoresponses that survive disrupted rod and cone funct

257 ontrol of visual temporal sensitivity to rod photoresponses themselves.

258 ndings reveal that the modification of ipRGC photoresponses through a cAMP/PKA pathway is a general f

259 are blue light receptors that mediate plant photoresponses through regulating gene expressions.

260 d reveals the different contributions to our photoresponse, thus paving the way for further improveme

261 Ts play an important role in controlling the photoresponse time and photocurrent improvement.

262 nd adaptation, suggesting that modulation of photoresponse time course may involve a separate Ca2+-de

263 ultra-high carrier mobility and ultra-short photoresponse time has shown remarkable potential in ult

264 , we study the light-intensity-dependent OPD photoresponse time with two small-molecule donors (plana

265 current, a higher sensitivity, and a faster photoresponse time, exhibiting a promising candidate usi

266 of expression of RGS9 is required for normal photoresponse timing.

267 t-adapted conditions and the recovery of the photoresponse to a bright flash.

268 as, thus indicating the reversibility of the photoresponse to charging effects.

269 The circadian photoresponse to constant light was impaired in rh7 muta

270 in the BHJ layer not only need to have broad photoresponse to increase JSC , but also possess suitabl

271 phototransduction deactivation, causing rod photoresponses to appear light adapted, with reduced dar

272 However, its photoresponses to different wavelengths have not been th

273 We show that NCKX4 shapes the cone photoresponse together with the cone-specific NCKX2: NCK

274 Mutations that affect termination of the photoresponse typically lead to a reduction in levels of

275 s of (3AMPY)Pb(2)I(6) crystals exhibit clear photoresponse under ambient light without applied bias,

276 Such photoresponse was attributed to photothermal effect inst

277 Photoresponse was detected with compatible binding prote

278 Its effect on the photoresponse was investigated by dialyzing the recombin

279 We found that the temporal loss of the photoresponse was paralleled by a gradual decline in the

280 The onset of the rising phase of the photoresponse was significantly delayed (P < 0.004) at 9

281 Prior to the onset of cell death, rod photoresponse was significantly reduced along with a rob

282 nock-out rods to regulate retGC and generate photoresponses was tested.

283 in GTP hydrolysis kinetics in mammalian cone photoresponses, we have characterized photoresponses and

284 The extended photoresponse, well-matched energy levels, and high hole

285 nd saturated amplitude (R(CONE)) of the cone photoresponse were calculated by fit of a model of the a

286 Analogous to bleaching adaptation, the photoresponses were desensitized (10- to 20-fold) and fa

287 The rod photoresponses were desensitized, and the response time

288 e were exposed to continuous light, and cone photoresponses were recorded.

289 Photoresponses were unaffected when arrestin expression

290 Electroretinogram (ERG) photoresponses were used to investigate activation kinet

291 d to allow isolated recording of cone-driven photoresponses, were bred with platelet-derived growth f

292 ed that single PDI fibers exhibit the higher photoresponse when compared to more poorly organized fil

293 The RP structures show strong photoresponse, whereas the SL materials exhibit resistiv

294 significantly decreases recovery of the cone photoresponse, which is mediated by Grk7a rather than Gr

295 amic range over 100 decibels (dB) and a fast photoresponse with 3-dB bandwidth up to 3 MHz.

296 l irradiation, this p-n diode shows a strong photoresponse with an external quantum efficiency of 52.

297 Intracellular IBMX enhanced the photoresponse with little effect on the baseline current

298 oelectronic characterizations show prominent photoresponse, with a fast response time of 500 mus, fas

299 ee unannealed films displays a strong p-type photoresponse, with up to 0.1 mA/cm(2) measured under mi

300 he junction to create the narrowest NIR-band photoresponses yet demonstrated.