ライフサイエンスコーパス: photosensitive

1 both the SP moieties and the BZ reaction are photosensitive.

2 ther fish horizontal cells are intrinsically photosensitive.

3 anglion cell in mammalian retina is directly photosensitive.

4 glion cells in mammals is also intrinsically photosensitive.

5 press melanopsin are no longer intrinsically photosensitive.

6 l-2, Bcl-xL must be membrane localized to be photosensitive.

7 We have developed novel photosensitive-2-nitrobenzyl esters that on irradiation

8 ABA and pyrabactin (a non-photosensitive ABA agonist) effects on red raspberry (Ru

9 n clock photoreceptor Vivid (VVD) contains a photosensitive allosteric light, oxygen, voltage (LOV) d

10 The ipRGCs, in addition to being directly photosensitive, also receive synaptic input from rod-con

11 iasmatic nuclei were no longer intrinsically photosensitive, although their number, morphology, and p

12 XP and 50% of TTD afflicted individuals are photosensitive and have a high susceptibility to develop

13 ssant/anti-inflammatory thiopurines are also photosensitive and have high rates of sun-related skin c

14 inal and, thus, in its absence, opsin is not photosensitive and no visual function exists.

15 Hypericin, a photosensitive and red-colored naphthodianthrone, has be

16 temic lupus erythematosus (SLE) patients are photosensitive and ultraviolet B light (UVB) exposure wo

17 ubset of retinal ganglion cells are directly photosensitive and utilize an opsin/vitamin A-based phot

18 mide-based materials are good candidates for photosensitive applications.

19 ina that, in addition to being intrinsically photosensitive, are strongly activated by rods and cones

20 debris in the skin, thereby predisposing to photosensitive autoimmune disease.

21 In this paper, we show that photosensitive azo-dye doped Blue-phase liquid crystals

22 ual-sensor, the specifically designed PTG (a photosensitive azobenzene derivative carrying one photoi

23 We quantify polyp retraction as a photosensitive behavioural response and show coral tissu

24 e modulated by the kinetic parameters of the photosensitive Belousov-Zhabotinsky reaction and the per

25 ions are applicable only to a small class of photosensitive biomolecules because of strong and ultraf

26 These cells are intrinsically photosensitive, but also receive inputs from rod and con

27 tissues or organisms that have been rendered photosensitive by genetic targeting of ChR2 or similar p

28 Photosensitive caged compounds have enhanced our ability

29 A photosensitive caged copper complex has been prepared fr

30 ility of converting inner retinal neurons to photosensitive cells as a possible strategy for impartin

31 Converting inner retinal neurons to photosensitive cells by expressing channelrhodopsin-2 (C

32 ver, it is still not clear how each class of photosensitive cells generates light responses in DACs.

33 light-insensitive retinal interneurons into photosensitive cells introduces an entirely new directio

34 ing retinal ganglion cells are intrinsically photosensitive cells that are involved in non-image form

35 and delivery modes, spatial distribution of photosensitive cells, and tissue illumination constraint

36 uld be controlled using light stimulation of photosensitive cells, which may offer a way to probe the

37 l soft materials by homogeneously dispersing photosensitive chiral material into an achiral soft syst

38 holesteric liquid crystal (CLC) containing a photosensitive chiral molecular switch with high helical

39 However, their photosensitive circadian clock had to adapt to extreme s

40 ght and blocked by TIMELESS (TIM), the major photosensitive clock component in Drosophila and a cruci

41 Studies have shown that bisretinoids are photosensitive compounds that undergo photooxidation and

42 rs by designing a mutant receptor that binds photosensitive compounds.

43 ied than contact allergy in this exquisitely photosensitive condition.

44 f cone cell function, but maintenance of non-photosensitive, cone opsin mRNA-expressing cells in the

45 copolymers are used to develop a platform of photosensitive core-shell nanoparticles.

46 s bionanocage) and co-polymeric shell of the photosensitive crosslinker protein.

47 transgenic flies have provided evidence that photosensitive Cryptochromes (Cry) are involved in the r

48 Intact photosensitive cyclometalated RuII derivatives of 2-phen

49 f several ER transmembrane proteins with the photosensitive degron (psd) module resulted in light-dep

50 Although rare in the pediatric population, photosensitive dermatoses may begin prior to adulthood.

51 ent sunburns, mitigate photoaging, and treat photosensitive dermatoses.

52 the clinical management of this disfiguring photosensitive disease.

53 CS) and xeroderma pigmentosum (XP) are human photosensitive diseases with mutations in the nucleotide

54 version efficiency of an interesting type of photosensitive DNA nanomotor through coupling with incor

55 for cancer that involves administration of a photosensitive drug or photosensitizer that localizes at

56 The ch1 mutant is highly photosensitive due to a selective increase in the releas

57 loid precursor protein mouse models with the photosensitive dye Rose bengal, and monitored plaque for

58 of polarization is imprinted into a layer of photosensitive dye that is protected against dissolution

59 sessions of adjunctive PAD (red LED, 635 nm, photosensitive dye, 0.01% tolonium chloride), whereas th

60 Approach (ANADOLUCA) method, which utilizes photosensitive electron transfer based microemulsion co-

61 unique variants in the 580 individuals with photosensitive epilepsies and 128 unique variants in the

62 tosensitivity in common epilepsies, specific photosensitive epilepsies and individuals with photosens

63 seizure activity in observational studies of photosensitive epilepsy and Dravet syndrome.

64 features that increase seizure likelihood in photosensitive epilepsy are linked to narrowband gamma o

65 a risk factor for seizures in patients with photosensitive epilepsy is engagement of the circuitry t

66 entified cause of the archetypal generalized photosensitive epilepsy syndrome, eyelid myoclonia with

67 CHD2 variants (3/36 cases) in the archetypal photosensitive epilepsy syndrome, eyelid myoclonia with

68 In photosensitive epilepsy, alpha-related blood oxygen leve

69 res or pre-seizure activity in patients with photosensitive epilepsy.

70 icker, can trigger seizures in patients with photosensitive epilepsy.

71 predictive of the pathological responses in photosensitive epilepsy.

72 on is developed, where 32 x 32 = 1024 MoS(2) photosensitive field-effect transistors manifesting pers

73 Through the exposure of photosensitive films placed a finite and known distance

74 ed with patterned UV light to polymerize the photosensitive fluid, creating particles with multi-scal

75 earance of apoptotic debris in patients with photosensitive forms of DM.

76 The photosensitive functions of Opn3 in mammals are poorly u

77 Rhodopsin is a canonical class A photosensitive G protein-coupled receptor (GPCR), yet re

78 ent found in a small subset of intrinsically photosensitive ganglion cells (ipRGCs) of the mammalian

79 Primary outcome was activation of intrinsic photosensitive ganglion cells using post-illumination pu

80 paminergic amacrine cells, (2) intrinsically photosensitive ganglion cells, and (3) bistratified divi

81 ivity of melanopsin containing intrinsically photosensitive ganglion retinal cells (ipRGC) can be ass

82 KAR(1), and TMB regulate seed germination in photosensitive 'Grand Rapids' lettuce (Lactuca sativa),

83 messengers can be "caged" by adding a single photosensitive group that can be photolyzed by a light f

84 Herein, by artificial design of photosensitive heterostructures with desired band alignm

85 dine kinase PPHK (phosphorylation-responsive photosensitive histidine kinase) that operates a molecul

86 Using a photosensitive hybrid hydrogel loaded with upconversion

87 ayer technique, cells are patterned within a photosensitive hydrogel fiber to mimic physiological cel

88 ecursors in subsurface of fused silica (e.g. photosensitive impurities, scratches and redeposited sil

89 C, a conventional RGC type, is intrinsically photosensitive in mammals.

90 ptochrome 1 (DpCry1) belongs in the class of photosensitive insect cryptochromes.

91 e activity-dependent gene arc to express the photosensitive ion channel, channelrhodopsin, in neurons

92 cells (M1-ipRGCs), which are by far the most photosensitive ipRGC subtype and also have the largest r

93 lation of RGCs are in addition intrinsically photosensitive (ipRGCs) and project to unique targets in

94 anopsin, rendering these cells intrinsically photosensitive (ipRGCs).

95 photopigment melanopsin and is intrinsically photosensitive (ipRGCs).

96 hotopigment melanopsin and are intrinsically photosensitive (ipRGCs).

97 hotopigment melanopsin and are intrinsically photosensitive (ipRGCs).

98 hotopigment melanopsin and are intrinsically photosensitive (ipRGCs).

99 ein melanopsin, rendering them intrinsically photosensitive (ipRGCs).

100 -mammalian vertebrates have an intrinsically photosensitive iris and thus a local pupillary light ref

101 heterodimerization modules and engineered a photosensitive kinesin-3, which is activated upon blue l

102 The intrinsically photosensitive M1 retinal ganglion cells (ipRGC) initiat

103 object by illuminating a rotating volume of photosensitive material with a dynamically evolving ligh

104 g the unique multiphoton effect of UCNPs for photosensitive materials of biomedical interest.

105 artificial photosynthesis, photovoltaics and photosensitive materials.

106 ry light reflex is mediated by intrinsically photosensitive melanopsin-containing retinal ganglion ce

107 e events to light detection by intrinsically photosensitive melanopsin-expressing retinal ganglion ce

108 that target the rod, cone, and intrinsically-photosensitive (melanopsin) retinal ganglion cell pathwa

109 ght induces the migration of arrestin to the photosensitive membrane in both vertebrate and invertebr

110 ules migrates to the cytoplasmic face of the photosensitive membrane organelle, the rhabdomere, where

111 the apical membrane skeleton that builds the photosensitive membrane, the rhabdomere.

112 ocytosed rhodopsin is trafficked back to the photosensitive membranes if animals are shifted back to

113 The various strategies for synthesizing photosensitive metal nitrosyls have been discussed to es

114 hibits NIR response without any conventional photosensitive moieties.

115 Like rods, cones use the photosensitive molecule 11-cis-retinal to detect light,

116 Currently, the need to synthesize complex photosensitive molecules hampers the applicability of th

117 e their fundamental importance, the roles of photosensitive molecules, visual pigments, in arrhythmic

118 Here, we report that a photosensitive mouse model of acute stress-induced photo

119 In this paper, we show that anisotropic photosensitive nematic liquid crystals (PNLC) made by in

120 in-depth generation of action potentials in photosensitive neurons both in vitro and in vivo, but th

121 ich express the photopigment melanopsin, are photosensitive neurons in the retina and are essential f

122 although pineals in culture were shown to be photosensitive, night-time melatonin levels were much lo

123 The potential of these photosensitive nitrosyl-dye conjugates as (i) biological

124 vable BAPTA-based Ca(2+) cage containing two photosensitive o-nitrobenzhydryl groups attached to the

125 Patients were usually highly photosensitive on EEG.

126 esis of the rhabdomere, the microvilli-based photosensitive organelle of Drosophila photoreceptor cel

127 To enable dynamic imaging of this photosensitive organism at different scales, we develope

128 nvasive continuous dynamic imaging of highly photosensitive organisms with sizes between 1 mm(3) and

129 calize exclusively to the plasma membrane of photosensitive outer segments of rod photoreceptors wher

130 thmicity and metabolism through unexpectedly photosensitive pathways.

131 the hallmark of the brain resting state, in photosensitive patients and in people without photosensi

132 Although most of the TTD patients are photosensitive, patients with TTDN1 mutations were repor

133 uce controlled chemical modifications of non-photosensitive peptides and proteins in polar liquids un

134 latory role for the C terminus of CRY on the photosensitive, photolyase-like part of the protein.

135 Rhodopsin is the photosensitive pigment in the rod photoreceptor cell.

136 by itself, as well as other agents that form photosensitive pigments, will not be good therapeutic ca

137 nd extraretinal cell types, along with other photosensitive pigments.

138 ectronic device represents an easy-to-handle photosensitive platform for the study of the photo respo

139 cess; active electrode area was defined by a photosensitive polyimide mask.

140 Here, we show that 3D cell-laden photosensitive polymer hydrogels can be bioprinted acros

141 also realized by a self-writing process in a photosensitive polymer resin.

142 ymmetric microparticles from the epoxy-based photosensitive polymer SU-8.

143 nufacturing (AM) technology, starting with a photosensitive preceramic precursor.

144 atforms are used to deterministically deform photosensitive precursor fluid streams.

145 ion cells has been identified to be directly photosensitive (pRGCs), modulating a range of behavioral

146 Utilizing the photosensitive protein Arabidopsis thaliana cryptochrome

147 The photosensitive protein bacteriorhodopsin (bR) has been s

148 These retinal ganglion cells express the photosensitive protein melanopsin, rendering them intrin

149 ctric response in tissue modified to express photosensitive proteins (opsins).

150 Chromophores absorb light in photosensitive proteins and thereby initiate fundamental

151 rs and for the rational design of artificial photosensitive proteins.

152 h chronic plaque psoriasis exhibits severely photosensitive psoriasis (PP) with a pronounced seasonal

153 sed to pattern an approximately 10 mum thick photosensitive recording medium.

154 ntified a novel, sixth type of intrinsically photosensitive retinal ganglion cell (ipRGC) in the mous

155 and M5 melanopsin-expressing, intrinsically photosensitive retinal ganglion cell (ipRGC) subtypes ar

156 Intrinsically photosensitive retinal ganglion cell (ipRGC) types can b

157 rd class of photoreceptor, the intrinsically photosensitive retinal ganglion cell (ipRGC).

158 opsin [5], originally found in intrinsically photosensitive retinal ganglion cells (ipRGCs) [11-19].

159 These cells have been termed intrinsically photosensitive retinal ganglion cells (ipRGCs) and compr

160 photoreceptors is mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) and is cr

161 Intrinsically photosensitive retinal ganglion cells (ipRGCs) and their

162 sine on the light responses of intrinsically photosensitive retinal ganglion cells (ipRGCs) and to de

163 Intrinsically photosensitive retinal ganglion cells (ipRGCs) are a sub

164 and the melanopsin-containing, intrinsically photosensitive retinal ganglion cells (ipRGCs) are activ

165 onal fate, we demonstrate that intrinsically photosensitive retinal ganglion cells (ipRGCs) are both

166 dian clock and discovered that intrinsically photosensitive retinal ganglion cells (ipRGCs) are criti

167 These intrinsically photosensitive retinal ganglion cells (ipRGCs) are more

168 Intrinsically photosensitive retinal ganglion cells (ipRGCs) are recen

169 hile the melanopsin-containing intrinsically photosensitive retinal ganglion cells (ipRGCs) are thoug

170 Intrinsically photosensitive retinal ganglion cells (ipRGCs) combine d

171 Melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs) comprise

172 Intrinsically photosensitive retinal ganglion cells (ipRGCs) contain t

173 Intrinsically photosensitive retinal ganglion cells (ipRGCs) control n

174 Intrinsically photosensitive retinal ganglion cells (ipRGCs) convey ro

175 Intrinsically photosensitive retinal ganglion cells (ipRGCs) express t

176 Intrinsically photosensitive retinal ganglion cells (ipRGCs) express t

177 ronmental light/dark cycle via intrinsically photosensitive retinal ganglion cells (ipRGCs) expressin

178 Intrinsically photosensitive retinal ganglion cells (ipRGCs) expressin

179 Intrinsically photosensitive retinal ganglion cells (ipRGCs) expressin

180 direct retinal input from the intrinsically photosensitive retinal ganglion cells (ipRGCs) for circa

181 Melanopsin-expressing, intrinsically photosensitive retinal ganglion cells (ipRGCs) form a li

182 These intrinsically photosensitive retinal ganglion cells (ipRGCs) generate

183 ypes of melanopsin-expressing, intrinsically photosensitive retinal ganglion cells (ipRGCs) have been

184 Intrinsically photosensitive retinal ganglion cells (ipRGCs) have been

185 following, many types of these intrinsically photosensitive retinal ganglion cells (ipRGCs) have emer

186 These intrinsically photosensitive retinal ganglion cells (ipRGCs) have well

187 These intrinsically photosensitive retinal ganglion cells (ipRGCs) help to s

188 ent melanopsin is expressed in intrinsically photosensitive retinal ganglion cells (ipRGCs) in the ma

189 Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate n

190 Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate n

191 Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate t

192 4 (Opn4)/melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs) play a ma

193 psin photopigment expressed in intrinsically photosensitive retinal ganglion cells (ipRGCs) plays a c

194 mammals, a small population of intrinsically photosensitive retinal ganglion cells (ipRGCs) plays a k

195 The intrinsically photosensitive retinal ganglion cells (ipRGCs) provide a

196 ere used to probe responses of intrinsically photosensitive retinal ganglion cells (ipRGCs) recorded

197 g the photopigment melanopsin, intrinsically photosensitive retinal ganglion cells (ipRGCs) respond d

198 Melanopsin-expressing, intrinsically photosensitive retinal ganglion cells (ipRGCs) synchroni

199 The SCN receives input from intrinsically photosensitive retinal ganglion cells (ipRGCs) that expr

200 a relies on light detection by intrinsically photosensitive retinal ganglion cells (ipRGCs) to drive

201 at such order is necessary for intrinsically photosensitive retinal ganglion cells (ipRGCs) to functi

202 activated by rods, cones, and intrinsically photosensitive retinal ganglion cells (ipRGCs) upon illu

203 niculate leaflet (IGL) through intrinsically photosensitive retinal ganglion cells (ipRGCs)(4).

204 or neurotransmitter output of intrinsically photosensitive retinal ganglion cells (ipRGCs), a critic

205 uire the melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs), but the

206 ptors in the mammalian retina, intrinsically photosensitive retinal ganglion cells (ipRGCs), has had

207 the eye, melanopsin-containing intrinsically photosensitive retinal ganglion cells (ipRGCs), in addit

208 riven by melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs), includin

209 eceive gap-junction input from intrinsically photosensitive retinal ganglion cells (ipRGCs), recently

210 ated by melanopsin-expressing, intrinsically photosensitive retinal ganglion cells (ipRGCs), suggesti

211 -forming pathway also involves intrinsically photosensitive retinal ganglion cells (ipRGCs), which ex

212 Intrinsically photosensitive retinal ganglion cells (ipRGCs), which ex

213 in is exclusively expressed in intrinsically photosensitive retinal ganglion cells (ipRGCs), which pl

214 diate visual function, and (2) intrinsically photosensitive retinal ganglion cells (ipRGCs), which pr

215 retinal photoreceptors called intrinsically photosensitive retinal ganglion cells (ipRGCs), which us

216 eceptor cones and rods and the intrinsically photosensitive retinal ganglion cells (ipRGCs)-converged

217 sense light: rods, cones, and intrinsically photosensitive retinal ganglion cells (ipRGCs).

218 ilar to signaling in mammalian intrinsically photosensitive retinal ganglion cells (ipRGCs).

219 reflexes that are mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs).

220 anopsin is the photopigment of intrinsically photosensitive retinal ganglion cells (ipRGCs).

221 nput from the eyes conveyed by intrinsically photosensitive retinal ganglion cells (ipRGCs).

222 onse (PIPR) is produced by the intrinsically photosensitive retinal ganglion cells (ipRGCs).

223 and the melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs).

224 and the melanopsin-containing intrinsically photosensitive retinal ganglion cells (ipRGCs).

225 rods and cones, as well as the intrinsically photosensitive retinal ganglion cells (ipRGCs).

226 ly development are mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs).

227 to be the photopigment of the intrinsically photosensitive retinal ganglion cells (ipRGCs); these ph

228 Melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs, with five

229 lls and melanopsin-containing, intrinsically photosensitive retinal ganglion cells (M1 ipRGCs) proces

230 type of melanopsin-expressing, intrinsically photosensitive retinal ganglion cells (M1-ipRGCs), which

231 sponses involve melanopsin (OPN4)-expressing photosensitive retinal ganglion cells (pRGCs) in additio

232 Melanopsin-expressing photosensitive retinal ganglion cells (pRGCs) represent

233 distinct pathway, originating in a subset of photosensitive retinal ganglion cells (pRGCs) that utili

234 gnalling pathways present in rods, cones and photosensitive retinal ganglion cells (pRGCs), and are t

235 by melanopsin (OPN4)-based photoreception of photosensitive retinal ganglion cells (pRGCs).

236 as recently been identified in intrinsically photosensitive retinal ganglion cells (RGCs) that projec

237 ce that melanopsin-containing, intrinsically photosensitive retinal ganglion cells (RGCs), signaling

238 The mammalian retina contains directly photosensitive retinal ganglion cells (RGCs), which use

239 inner retinal photoreceptors (intrinsically photosensitive retinal ganglion cells [ipRGCs]) are suff

240 Melanopsin-expressing intrinsically photosensitive retinal ganglion cells are characterized

241 Mammalian intrinsically photosensitive retinal ganglion cells are involved in th

242 Indeed, intrinsically photosensitive retinal ganglion cells are present from b

243 These intrinsically photosensitive retinal ganglion cells express the putati

244 The discovery of intrinsically photosensitive retinal ganglion cells has overthrown the

245 The involvement of intrinsically photosensitive retinal ganglion cells in this reconfigur

246 We also know that these photosensitive retinal ganglion cells mediate a broad ra

247 is detected by the retina and intrinsically photosensitive retinal ganglion cells project this infor

248 ensity-dependent discharges of intrinsically photosensitive retinal ganglion cells projecting axons t

249 A subset of intrinsically photosensitive retinal ganglion cells transduce informat

250 nes, and melanopsin-expressing intrinsically photosensitive retinal ganglion cells upon illumination.

251 Intrinsically photosensitive retinal ganglion cells use melanopsin as

252 t, and in vitro sensitivity of intrinsically photosensitive retinal ganglion cells) were studied in w

253 onse of melanopsin-containing, intrinsically photosensitive retinal ganglion cells, has previously be

254 the photopigment of mammalian intrinsically photosensitive retinal ganglion cells, where it contribu

255 ract surgery increases photoreception by the photosensitive retinal ganglion cells.

256 ation of melanopsin-expressing intrinsically photosensitive retinal ganglion cells.

257 ght cycle in animals that lack intrinsically photosensitive retinal ganglion cells.

258 ood functions directly through intrinsically photosensitive retinal ganglion cells.

259 ivating melanopsin-expressing, intrinsically photosensitive retinal ganglion cells.

260 t confers light sensitivity on intrinsically photosensitive retinal ganglion cells.

261 ediated responses to light, possibly through photosensitive retinal ganglion cells.

262 nal to convert opsin receptor molecules into photosensitive retinoid pigments of the eye.

263 unctional assay, we show that 2-APB inhibits photosensitive RGC activity in vivo.

264 g dopaminergic amacrine cells, intrinsically photosensitive RGCs (ipRGCs) and calbindin-positive cell

265 ablated melanopsin-expressing intrinsically photosensitive RGCs (ipRGCs) and showed deficits in noni

266 These intrinsically photosensitive RGCs (ipRGCs) drive circadian-clock reset

267 ubset of melanopsin-expressing intrinsically photosensitive RGCs (ipRGCs) in mice that release the in

268 s were from non-image-forming, intrinsically photosensitive RGCs (ipRGCs).

269 ucidate the phototransduction pathway in the photosensitive RGCs and demonstrate that 2-APB can be us

270 n extremely potent in vitro inhibitor of the photosensitive RGCs and that its effect is independent o

271 e photoreceptive properties of intrinsically photosensitive RGCs confer resistance to bleaching and/o

272 Until now, the study of photosensitive RGCs has lacked an acute inhibitor.

273 lls (RGCs), predominantly from intrinsically photosensitive RGCs, the principle conduit of non-image-

274 Moreover, M1 intrinsically photosensitive RGCs, which functionally are On RGCs but

275 e-forming targets, and include intrinsically photosensitive RGCs.

276 lular location of Aaop1 and reorganize their photosensitive rhabdomeric membranes on a daily basis.

277 edding and rebuilding of the photoreceptor's photosensitive rhabdomeric membranes.

278 awless vertebrates with the advent of highly photosensitive rod-like photoreceptors.

279 ds enable fast multi-electron injection from photosensitive [Ru(bpy)3](2+) units to redox-active WD-P

280 h a copolymer gel consisting of NIPAAm and a photosensitive ruthenium catalyst.

281 by coordination of its thioether group to a photosensitive ruthenium complex.

282 ied 580 individuals with epilepsy and either photosensitive seizures or abnormal photoparoxysmal resp

283 We employ a model of a photosensitive self-oscillating gel, in which chemical p

284 ture in order to study the photo-response of photosensitive semiconducting layers or patterns in an e

285 ha is central to the pathogenesis of several photosensitive skin diseases and certain forms of immune

286 ch enables the SP-to-MC isomerization of the photosensitive species.

287 We use a model of a photosensitive stimulus-responsive gel that supports the

288 vesicles (GUVs) in the presence of AzoTAB, a photosensitive surfactant.

289 1q have been observed to develop early-onset photosensitive systemic lupus erythematosus (SLE).

290 A photosensitive TA analogue was designed and synthesized

291 Cones are typically 100 times less photosensitive than rods and their response kinetics are

292 of poly(N-isopropylacrylamide)-which is not photosensitive-thus demonstrating the robustness and rel

293 The vertebrate retina is a specialized photosensitive tissue comprised of six neuronal and one

294 The photosensitive tissue is located in a small region of ca

295 es have been found to be associated with non-photosensitive TTD (NPS-TTD); these include MPLKIP (also

296 This active site is photosensitive: visible light has been shown to induce t

297 fly photoreceptors, light is focused onto a photosensitive waveguide, the rhabdomere, consisting of

298 recently been discovered to be intrinsically photosensitive, with melanopsin as the pigment.

299 Many animal tissues/cells are photosensitive, yet only two types of photoreceptors (i.

300 The UV light generates free carriers in a photosensitive ZnO spacer layer, which changes the metam