ライフサイエンスコーパス: photosensitive

1 ther fish horizontal cells are intrinsically photosensitive.

2 anglion cell in mammalian retina is directly photosensitive.

3 glion cells in mammals is also intrinsically photosensitive.

4 press melanopsin are no longer intrinsically photosensitive.

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

6 cells innervating the SCN are intrinsically photosensitive.

7 s possible pharmaceutical uses, to be rather photosensitive.

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

9 he side chain carboxylate was protected as a photosensitive 2,2'-dinitrobenzhydryl ester.

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

11 eventable when synthesis involves a directly photosensitive 5'-blocking group.

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

13 s were placed unilaterally near HVc or RA in photosensitive adult male white-crowned sparrows for one

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

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

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

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

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

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

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

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

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

23 One theory for the pathophysiology of photosensitive autoimmune skin diseases is that photoind

24 of apoptotic cells and could thereby lessen photosensitive autoimmunity.

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

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

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

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

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

30 Monocytic tumor cells were rendered photosensitive by infection with uroporphyric Leishmania

31 Photosensitive caged compounds have enhanced our ability

32 A photosensitive caged copper complex has been prepared fr

33 e herein a synthetic strategy that furnishes photosensitive caged diols and provides an entry into th

34 ight induction of plasmid expression using a photosensitive caging compound.

35 as previously determined not to injure these photosensitive cells and to fully induce gsa in wild-typ

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

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

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

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

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

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

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

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

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

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

46 ially involves the uptake or production of a photosensitive compound by tumor cells.

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

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

49 ied than contact allergy in this exquisitely photosensitive condition.

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

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

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

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

54 autosomal dominant trait are predisposed to photosensitive cutaneous lesions by various ecogenic fac

55 Intact photosensitive cyclometalated RuII derivatives of 2-phen

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

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

58 a tarda (PCT), a disorder characterized by a photosensitive dermatosis and hepatic siderosis.

59 The phenotype is characterized by a photosensitive dermatosis with hepatic accumulation and

60 s polymorphism with adult dermatomyositis, a photosensitive disease that exhibits some features in co

61 of xeroderma pigmentosum (XP), a hereditary, photosensitive disease with a high incidence of skin mal

62 the clinical management of this disfiguring photosensitive disease.

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

64 promoter polymorphism is associated with the photosensitive disorder subacute cutaneous lupus erythem

65 Among hereditary photosensitive disorders, including other xeroderma pigm

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

67 In photoangioplasty, light activation of a photosensitive drug offers the potential for treatment o

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

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

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

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

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

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

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

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

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

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

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

79 In photosensitive epilepsy, alpha-related blood oxygen leve

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

81 predictive of the pathological responses in photosensitive epilepsy.

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

83 inal ganglion cells (RGCs) are intrinsically photosensitive, express the opsin-like protein melanopsi

84 Photosensitive films incorporating molecular photoacid g

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

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

87 cutaneous lupus erythematosus, an extremely photosensitive form of cutaneous lupus erythematosus, bu

88 t not in discoid lupus erythematosus, a less photosensitive form.

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

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

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

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

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

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

95 Using a photosensitive hybrid hydrogel loaded with upconversion

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

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

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

99 triarylamine dialkylsulfonium salts that are photosensitive in the near-ultraviolet have been prepare

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

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

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

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

104 photopigment melanopsin and is intrinsically photosensitive (ipRGCs).

105 hotopigment melanopsin and are intrinsically photosensitive (ipRGCs).

106 hotopigment melanopsin and are intrinsically photosensitive (ipRGCs).

107 hotopigment melanopsin and are intrinsically photosensitive (ipRGCs).

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

109 because it is based on the illumination of a photosensitive layer through a "photomask" (a transparen

110 oxamic acid (SHAM) stimulated germination of photosensitive lettuce (Lactuca sativa L. cv Waldmann's

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

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

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

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

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

116 astructural changes in the rhodopsin-bearing photosensitive membrane (rhabdom) in Limulus ventral pho

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

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

119 cation of PKCalpha immunofluorescence to the photosensitive membrane, an effect that provides indepen

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

121 hibits rhodopsin transport to the developing photosensitive membrane.

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

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

124 hibits NIR response without any conventional photosensitive moieties.

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

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

127 The photosensitive molecules, visual pigments, can be synthe

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

129 l, these opsins regenerate the corresponding photosensitive molecules, visual pigments.

130 l, these opsins regenerate the corresponding photosensitive molecules, visual pigments.

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

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

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

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

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

136 y of the photoreceptor adherens junction and photosensitive organ, or rhabdomere.

137 light-dark rhythm presented to one of three photosensitive organs (the pineal gland and both eyes) c

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

139 thmicity and metabolism through unexpectedly photosensitive pathways.

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

141 n two independent families that included two photosensitive patients that were identified as xeroderm

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

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

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

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

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

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

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

149 rom x 2 microm x 210 nm) on fused quartz and photosensitive polyimide surfaces.

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

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

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

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

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

155 An investigation of potential photosensitive protecting groups for diazeniumdiolates (

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

157 Chromophores absorb light in photosensitive proteins and thereby initiate fundamental

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

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

160 which is typically associated with a severe photosensitive rash.

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

162 ut not the 50-kDa subunit, interacted with a photosensitive residue of a substrate oligonucleotide.

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

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

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

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

167 Intrinsically photosensitive retinal ganglion cells (ipRGCs) and their

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

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

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

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

172 Intrinsically photosensitive retinal ganglion cells (ipRGCs) are recen

173 Intrinsically photosensitive retinal ganglion cells (ipRGCs) combine d

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

175 Intrinsically photosensitive retinal ganglion cells (ipRGCs) contain t

176 Intrinsically photosensitive retinal ganglion cells (ipRGCs) convey ro

177 Intrinsically photosensitive retinal ganglion cells (ipRGCs) express t

178 Intrinsically photosensitive retinal ganglion cells (ipRGCs) express t

179 Intrinsically photosensitive retinal ganglion cells (ipRGCs) expressin

180 Intrinsically photosensitive retinal ganglion cells (ipRGCs) expressin

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

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

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

184 These intrinsically photosensitive retinal ganglion cells (ipRGCs) generate

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

186 Intrinsically photosensitive retinal ganglion cells (ipRGCs) have been

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

236 Mammalian intrinsically photosensitive retinal ganglion cells are involved in th

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

238 These intrinsically photosensitive retinal ganglion cells express the putati

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

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

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

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

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

244 A subset of intrinsically photosensitive retinal ganglion cells transduce informat

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

246 Intrinsically photosensitive retinal ganglion cells use melanopsin as

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

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

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

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

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

252 ood functions directly through intrinsically photosensitive retinal ganglion cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

270 ceptor, including the region occupied by the photosensitive rhabdom.

271 , and calmodulin are all concentrated at the photosensitive rhabdomeral membrane, which is consistent

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

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

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

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

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

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

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

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

280 ren with complete congenital heart block and photosensitive skin lesions.

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

282 three-dimensional cytoarchitecture in highly photosensitive specimens such as mammalian embryos.

283 ent modality that uses light excitation of a photosensitive substance to produce oxygen-related cytot

284 finding that mice lacking the Ro protein are photosensitive suggests that loss of Ro function could c

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

286 1q have been observed to develop early-onset photosensitive systemic lupus erythematosus (SLE).

287 A photosensitive TA analogue was designed and synthesized

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

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

290 accumulation of PER is also dependent on the photosensitive TIMELESS (TIM) protein, long photoperiods

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

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

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

294 l, the ligand necessary for the formation of photosensitive visual pigments.

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

296 t, demonstrating that the pineals had become photosensitive while in culture.

297 Photosensitive white-crowned sparrows were exposed to on

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