ライフサイエンスコーパス: red light

1 zymes' activity was promptly affected by the red light.

2 hing can be achieved using blue or green and red light.

3 tificially illuminated with white, green, or red light.

4 velengths of the visible spectrum, including red light.

5 have a sustained response to blue but not to red light.

6 ases accumulated the most in response to far-red light.

7 multicellular tumor spheroids with 2-photon red light.

8 hite light to an immobilized state under far-red light.

9 its them to thrive in niches enriched in far-red light.

10 is effectively triggered by blue, but not by red light.

11 al range for photosynthesis by absorbing far-red light.

12 in darkness even after illumination with far-red light.

13 light (VLFR) and high fluences (HIR) of far-red light.

14 thesis in two cyanobacteria that grow in far-red light.

15 d with peripheral test points in response to red light.

16 e measured in response to blue compared with red light.

17 assays, show hyposensitive responses to far-red light.

18 ast ratio on irradiation with ultraviolet or red light.

19 and the ots1/ots2 mutant is hyposensitive to red light.

20 gaseous SrO, which emits undesirable orange-red light.

21 intron retention (IR) events in response to red light.

22 anobacteria that is capable of utilizing far-red light.

23 e GAF domains were removed monomerizes under red light.

24 above 700 nm and enable cells to grow in far-red light.

25 ed that some cyanobacteria could utilize far-red light.

26 displayed PIF1-mediated enhanced response to red light.

27 meters) and enhances oxygen evolution in far-red light.

28 e of the transcriptome of the phyA mutant to red light.

29 expression of selected genes in response to red light.

30 etect using intrinsic signals from reflected red light.

31 hboring plants for photosynthetically active red light.

32 drives photosynthesis more efficiently than red light.

33 n of low-lying charge transfer states by far-red light.

34 ivation was demonstrated in HeLa cells using red light.

35 Z isomerization, which can be triggered with red light.

36 establishing a direct guard cell response to red light.

37 with near-infrared and inactivated with far-red light.

38 ceptor of photomorphogenic development under red light.

39 photopolymerization driven by visible to far-red light.

40 chable on and off with near-infrared and far-red light.

41 opsins for green light, and phytochromes for red light.

42 P-H1) in the nucleus, a process dependent on red light.

43 reas rod divisions predominate in red or far-red light.

44 ual life cycle of this alga by both blue and red light.

45 ller than those generated by blue, amber and red lights.

46 ignificantly less than white, blue, amber or red lights.

47 xposure to narrowband blue light (469 nm) or red light (631 nm) using a modified Ganzfeld dome.

48 activate classical photoCORM Mn2(CO)10 using red light (635 nm).

49 toswitching properties upon irradiation with red light (660 nm LED).

50 Methylene blue (4 muM) irradiated with red light (660 nm) catalyzes the rapid oxidation of a di

51 tects Synechocystis cells from strong orange-red light, a condition in which OCP is not photoactivate

52 The red/far red light absorbing photoreceptor phytochrome-B (phyB) c

53 otonation of FAD(*-) to form the long-lived, red-light absorbing FADH(*) species.

54 evaluate the effects of a papain-gel with a red-light absorbing pigment (methylene blue - MB) to med

55 We report that in the red light-absorbing (Pr) state, the bilin chromophore of

56 ht promotes the photoconversion to their far-red light-absorbing Pfr state or the red light-absorbing

57 d light-absorbing Pr state and an active far-red light-absorbing Pfr state.

58 interconvert between a biologically inactive red light-absorbing Pr state and an active far-red light

59 eir far-red light-absorbing Pfr state or the red light-absorbing Pr state, respectively.

60 images of the full-length BphP dimer in the red light-absorbing state and the photoactivated far-red

61 the bilin-binding pocket in the dark-adapted red light-absorbing state illuminated the intricate netw

62 t-absorbing state and the photoactivated far-red light-absorbing state revealed a large scale reorien

63 nsfer bands could be responsible for the far-red light absorption leading to PS I photochemistry at w

64 Upon red-light absorption, LAPD up-regulates hydrolysis of cA

65 overcome these problems, we prepared the far-red light-activatable prodrug of PTX by conjugating phot

66 ng factor39-1 (PpPRP39-1) in the presence of red light-activated phytochromes.

67 lopmental Cell, Shi et al. (2016a) show that red-light-activated phytochrome B interacts with transcr

68 at intermediate R2 and causes an alternative red light-adapted state.

69 d indicated an absence of cross-talk between red light and ABA.

70 cally with OST1 during stomatal responses to red light and altered [CO2 ].

71 ific functionality as a voltage sensor under red light and as an inhibitory actuator under green ligh

72 Phytochromes sense red/far-red light and control many biological processes in plant

73 cumulation of SUMOylated phyB is enhanced by red light and displays a diurnal pattern in plants grown

74 The nanoparticles are excitable by red light and emit in the near-infrared spectra region w

75 Gene expression is only activated under red light and remains inactive under white light or in d

76 hrough the appropriate combination of violet/red light and temperature, results that highlight the po

77 o interact genetically with OST1 both during red light- and low [CO2 ]-induced stomatal opening.

78 In aquatic environments, red and far-red light are rapidly attenuated with depth; therefore,

79 n activity before and after irradiation with red light at 652 nm, showcasing the effective "activatio

80 reinhardtii, which is controlled by blue and red light at the steps of gametogenesis along with its r

81 viation in LMCV parameter in response to the red light between different test point was significantly

82 range light combined with a weak emission of red light both in solution and in the crystalline state.

83 High levels of red light but not of blue light were enough to restrain

84 yB enhanced the long-term growth response to red light but reduced the expression of selected genes i

85 s were induced only by blue light or only by red light, but not both.

86 e relative tissue transmissibility of orange-red light, but their dependence on illumination limits t

87 Sensing of red and far-red light by bacteriophytochromes involves intricate int

88 ining photoreceptors that detect red and far-red light by photointerconversion between a dark-adapted

89 s finding was explained by the absorption of red light by the flavin neutral radical as the dark stat

90 cAMP and cGMP by up to sixfold, whereas far-red light can be used to down-regulate activity.

91 light intensities and ratios of red and far-red light caused by shading and neighbor proximity.

92 inally we show that both shaded, low red/far-red light conditions and high temperature induce more ve

93 tion of photomorphogenesis under red and far-red light conditions involves both positively and negati

94 uple mutant pifq both in the dark and in far-red light conditions.

95 esulting CDots gradually shifts from blue to red light, covering the entire light spectrum.

96 Discussion: The results show that saturated red light delivered through closed eyelids at levels tha

97 (the control), exposure to long-wavelength (red) light delivered to closed eyelids during sleep (red

98 aks at dusk, binds phytochrome B (phyB) in a red light-dependent manner, and co-localizes with phyB i

99 In both cases, they act as sensitive red light detectors.

100 ose reared in white light, B6 mice reared in red light developed relative hyperopia, principally char

101 Our analysis revealed that illumination with red light effectively terminates VT in diseased, ChR2-ex

102 Finally, red light elevates PphnRNP-F1 protein levels via PpPHY4,

103 electrically-driven GaN:Eu based device for red light emission is analyzed in the framework of a cur

104 than the state-of-the-art GaN:Eu system for red light emission.

105 Red-light emission based solely on transient SrOH(g) has

106 anic/h-BN vdW solid arrays are patterned for red-light emission.

107 IQE in the electrically-driven GaN:Eu based red light emitters.

108 n solid state thin films, and the fabricated red light emitting diodes exhibited high brightness (125

109 eral advantages such as being excitable with red light, emitting in the near-infrared spectral region

110 they can operate with low-power density far-red light-emitting diode light.

111 ere photo-irradiated for 15 min with visible red light-emitting diodes with a light-fluence of 0.54 J

112 0 s of irradiation using green, red, and far-red light-emitting diodes.

113 y concerns, the development of lithium-based red-light-emitting pyrotechnic compositions of high puri

114 The development of a red-light-emitting pyrotechnic illuminant has garnered i

115 nsitizer (PS) with the photoCORM and shining red light, energy transfer occurs from triplet excited-s

116 ity and shade (i.e. to the perception of far-red light-enriched light filtered through or reflected f

117 of their contrasting growth responses to far-red light enrichment.

118 le in sustaining robust clock function under red light, even in the absence of photosynthesis or exog

119 Surprisingly, dCRY appears to mediate red-light-evoked depolarization in wild-type flies, abse

120 ve uroporphyrin (URO) and their loading with red light excitable phthalocyanines (PC) that was cation

121 Under biotissue-penetrable red-light excitation, we found that such nanocrystals po

122 ies have examined the efficacy of low dosage red light exposure for cellular repair and increasing sp

123 Vegetation-induced reduction in the red light:far-red light ratio provides a competition sig

124 results confirmed that cells grown under far-red light form biofilms with a significantly increased a

125 Far-red light (FR) pretreatment and transfer to white light

126 sponses to the ratio of red light (R) to far-red light (FR; an indicator of competition) by suppressi

127 cidiopsis thermalis PCC 7203 grown under far-red light (FRL; >725 nm) contains both chlorophyll a and

128 Performance scores in the red light goggles condition improved significantly after

129 ed light mask) and to eyes open upon waking (red light goggles) reduced sleep inertia.

130 considerably larger (20%, visualized as dark red -> light green in the TOC).

131 enhanced phytochrome B protein abundance in red light-grown MEcPP-accumulating ceh1 mutant Arabidops

132 and uncover differential hypocotyl growth of red light-grown seedlings in response to these phytohorm

133 plete recovery of the etiolated phenotype of red light-grown seedlings of the tomato phytochrome-defi

134 In red-light-grown seedlings PIF4 ubiquitination was reduce

135 from white light D2O-seawater medium to far-red light H2O-seawater medium, the observed deuteration

136 Red light has the advantages of low energy, less health

137 such that axillary buds growing in added far-red light have greatly increased receptor transcript abu

138 Arg)-YFP photoreceptor are hypersensitive to red light, (ii) light-induced SUMOylation of the mutant

139 2.6 s, which is present already 1 mus after red light illumination of the flavin radical.

140 ct measurement of curvilinear velocity under red light illumination.

141 nate hydrochloride incubation and subsequent red light illumination.

142 Under red-light illumination, the photosensitizer produces sin

143 This was due to the deeper penetration of red light in cardiac tissue compared with blue light, wh

144 ue light enhanced voltage signals excited by red light in cultured neurons that expressed paQuasAr3 (

145 with those genes showing hyper-promotion by red light in phyA.

146 mbered the genes showing reduced response to red light in phyA.

147 sential oil yield (4.17%) was observed under red light in T. migricus, while the lowest (1.05%) was o

148 ard cell metabolic signatures in response to red light in the absence of the mesophyll.

149 gated concentration range, and doing so with red light in the therapeutic window.

150 hmania spp., to take up diamino-PC (PC2) for red light inactivation.

151 Red light induced a hyperopic shift in mouse refractive

152 SIVE GATA FACTOR1 as well as that of SPCH is red light induced but the induction of SPCH is compromis

153 We characterized red light-induced clustering localization and adjustable

154 Further analysis reveals that far-red light-induced phosphorylation and degradation of PIF

155 m (strain Shark) and engineered to result in red light-induced photocurrents three times those of ear

156 esults demonstrate that HT1 is essential for red light-induced stomatal opening and interacts genetic

157 The question of whether red light-induced stomatal opening is mediated by a phot

158 ere, we report a strong impairment in ht1 in red light-induced stomatal opening whereas blue light wa

159 imentally showed that ABA is able to inhibit red light-induced stomatal opening, and our model offers

160 low [Ci ]-dependent pathway may function in red light-induced stomatal opening.

161 pen question concerning the effect of ABA on red light-induced stomatal opening.

162 n demonstrated by successful applications in red-light-induced aerobic oxidative hydroxylation of ary

163 as been debate regarding the extent to which red-light-induced stomatal opening arises from direct gu

164 Within the visible light spectrum, red light induces stomatal opening in intact leaves.

165 ines a blue-light-regulated repressor with a red-light-inducible switch.

166 ght versus indirect responses as a result of red light influences on mesophyll photosynthesis.

167 ternode length, enhanced hypocotyl length in red light, inhibited primary root growth under different

168 This reaction is a new example of red-light-initiated atmospheric chemistry that may help

169 the YHB mutation is sufficient to phenocopy red light input into the circadian mechanism and to sust

170 nities because of the deep penetrance of far-red light into mammalian tissue and the small size of th

171 ght-regulated histidine kinases that convert red light into signaling events.

172 edox catalyst, pheophorbide a (PheoA), under red light irradiation (lambdamax = 635 nm, 0.4 mW/cm(2))

173 Combination of (13)CO gas exposure, blue or red light irradiation, and controlled hydration of three

174 ymerization of a methacrylate backbone under red light irradiation.

175 lated Arabidopsis seedlings before and after red-light irradiation, we identified a number of influen

176 rsion efficiency of 5.4% under low-intensity red-light irradiation.

177 (1) O(2) at the cell surface in response to red-light irradiation.

178 discovered that stomatal opening response to red light is correlated with a decrease in guard cell ab

179 Visible red light is observed when pumped with a telecommunicati

180 odopsins and can enable experiments in which red light is preferred.

181 We further show that blue (but not red) light is necessary and sufficient to activate photo

182 as also agravitropic but when adapted to dim red light it displayed a reversed gravitropic response.

183 chemical water splitting under broadband and red light (lambda > 590 nm) illumination in a dye-sensit

184 tions and photooxidations in the presence of red light (lambda(max) = 640 nm).

185 r of the excited states formed upon blue- or red-light laser excitation.

186 posing liquid-stored boar semen to different red light LED regimens on sperm quality and reproductive

187 anging R:FRs or lowering R:FRs by adding far-red light led to the appearance of small nuclear bodies

188 re dimeric photoreceptor proteins that sense red light levels in plants, fungi, and bacteria.

189 iberated upon irradiation with low-intensity red light (</=36 mW 635 nm).

190 f some tasks was significantly better in the red light mask condition than in the dim light condition

191 ht delivered to closed eyelids during sleep (red light mask) and to eyes open upon waking (red light

192 ere demonstrate that HOS1 is involved in the red light-mediated degradation of CO that takes place in

193 We show that PphnRNP-H1 is involved in red light-mediated phototropic responses in P. patens an

194 display strong hyposensitive response to far-red light-mediated seed germination and light-regulated

195 It has catalyzed red-light-mediated dual transition-metal/photo-redox-cat

196 toredox catalyst (helical carbenium ion) for red-light-mediated photoredox reactions has been develop

197 The red-light-modulated guard cell metabolome reported here

198 These red-light-modulated metabolites participate in the trica

199 A narrowband red-light nanocomposite photodetector with gain is prese

200 Dye 700Dx, and then activated by near infra-red light (NIR) to specifically target tumors.

201 ular peroxy decomposition is promoted by the red-light or near-IR radiation excitation.

202 nm or 613 nm wavelength narrow-band green or red light, or wide-spectrum white light, and thereby pro

203 ite light or blue light, over 60%, and under red light, over 90% of all simulated knockouts had simil

204 Red light penetrates deeper into tissue than other visib

205 Because red light penetrates tissue more deeply than light of sh

206 t manner, thereby increasing the response to red light perceived by phyB.

207 t cannot be attributed to changes in red/far-red light perception alone.

208 terconversion between red light (Pr) and far-red light (Pfr)-absorbing states.

209 In addition, the long hypocotyl in far-red light phenotype of the laf6 mutant could not be resc

210 art of an extensive acclimation process, far-red light photoacclimation (FaRLiP), which occurs in man

211 Far-red light photoacclimation appears to be controlled by a

212 iproteins and minor amounts of Chl d via far-red light photoacclimation in a range of cyanobacteria,

213 Far-red light photoacclimation leads to substantial remodell

214 Here we propose that the red/far-red light photoreceptor HvPHYTOCHROME C (HvPHYC), carryi

215 Phytochrome B (phyB) is the primary red light photoreceptor in plants, and regulates both gr

216 Moreover, the red/far-red light photoreceptor phyB interacts with SPA1 through

217 The red/far-red light photoreceptor phytochrome participates in ligh

218 ated by plant photoreceptors [3-5], with the red-light photoreceptor phytochrome B (phyB) having a do

219 hat interact physically with the red and far-red light photoreceptors, phytochromes, are called PHYTO

220 ar-red photosystem II (FR-PSII) supports far-red light photosynthesis.

221 nd abscisic acid treatments and enhanced far-red light/phyA-mediated photomorphogenesis.

222 e light through photointerconversion between red light (Pr) and far-red light (Pfr)-absorbing states.

223 Excitation of the holoproteins by red or far-red light promotes the photoconversion to their far-red

224 haliana) branching responses to the ratio of red light (R) to far-red light (FR; an indicator of comp

225 ights (RGB) during the day and to: darkness; red light (R); combined red-green LED (RG) lights; and c

226 eptors perceive reduced ratios of red to far-red light (R:FR) and initiate stem elongation to enable

227 receptor that senses the ratio of red to far-red light (R:FR) to regulate the shade-avoidance respons

228 tion of light quality, including the red/far-red light ratio (R/FR) that informs plants about proximi

229 hat both low blue light and a low-red to far-red light ratio are required to rapidly enhance phototro

230 The influence of red/far-red light ratio on the fibre length prompted us to exami

231 ation-induced reduction in the red light:far-red light ratio provides a competition signal sensed by

232 ight quality (as crowding and the red-to-far-red light ratio) and phosphate availability, such that t

233 flowering via physical interactions with the red-light receptor phytochrome B (phyB).

234 ied nine independent causal mutations in the red-light receptor phytochrome B (phyB).

235 jor thermosensory role for the phytochromes (red light receptors) during the night.

236 Phytochromes, red/far-red light receptors, are believed to regulate light-resp

237 Phytochrome-mediated detection of far-red light reflection from neighboring plants activates g

238 eir constitutive photomorphogenic phenotype, red light-regulated thermomorphogenesis, and input of ph

239 on of PIF4 expression by SHB1 and CCA1 under red light represents a desensitization step.

240 s that affect photosynthesis, flowering, and red light response are described.

241 ream photoreceptor, implements a "long-pass" red light response distinct from those accomplished by c

242 identified the Ser/Arg-like protein REDUCED RED-LIGHT RESPONSES IN CRY1CRY2 BACKGROUND1 (RRC1).

243 , AS of the putative splicing factor REDUCED RED-LIGHT RESPONSES IN CRY1CRY2 BACKGROUND1, previously

244 limitations, we report the development of a red light responsive initiator capable of polymerizing a

245 ontrol gene expression from blue, green, and red light responsive optogenetic tools in bacteria, yeas

246 rabidopsis guard cells, with 104 found to be red light responsive.

247 tion and higher transcriptional induction of red-light responsive genes compared with plantlets expre

248 be an exonic splicing silencer that controls red light-responsive IR.

249 both phyB and PCH1 generate stable, yet far-red light-reversible PBs that persisted for days.

250 hereas cells are smaller and spherical under red light (RL).

251 ed farther through seawater than the red/far-red light sensed by land plant phytochromes.

252 rate a role for phytochrome C as part of the red light sensing network that modulates phytochrome B s

253 Phytochromes are red/far-red light sensing photoreceptors employing linear tetrap

254 Red light-sensing bacteriophytochromes are attractive ta

255 iple photoreceptors, among which the red/far-red light-sensing phytochromes have been extensively stu

256 Phytochromes are a major family of red-light-sensing kinases that control diverse cellular

257 ive sweep centered on the adjacent blue- and red-light sensitive opsins SWS2 and LWS.

258 r results suggest that cardiac expression of red light-sensitive ion channels is necessary for the de

259 successfully terminated VF, illumination of red light-sensitive ion channels with dense arrays of im

260 imeric proteins that function as red and far-red light sensors influencing nearly every phase of the

261 highlight opportunities for using additional red-light sensors in artificial sensor-effector systems.

262 vivo, optimized the conditions for using the red-light-shifted halorhodopsin Jaws in primates, and de

263 and abi mutants indicates that ZFP3 enhances red light signaling by photoreceptors other than phytoch

264 CRY2 BACKGROUND1, previously identified as a red light signaling component, was shifted to the functi

265 undamental information concerning autonomous red light signaling pathways in guard cells.

266 odule in leaves strongly linking red and far-red light signaling to drought responses in a TOC1-depen

267 phyB pool after light exposure, potentiating red-light signaling and prolonging memory of prior illum

268 ight-to-dark) switch, the blue, red, and far-red light signals, and UV-B irradiation.

269 shade or neighbor proximity (low red to far-red light), some plant species exhibit shade-avoiding ph

270 ion channels with dense arrays of implanted red light sources resulted in successful defibrillation.

271 Recruitment of SHB1 by CCA1 modulates red light-specific induction of PIF4 expression thus int

272 Here we identify conditions that result in red-light-stimulated stomatal opening in isolated epider

273 tion phase response following cessation of a red light stimulus.

274 e photoacclimative response to growth in far-red light that includes the synthesis of chlorophylls d

275 h reduction in the ratio between red and far-red light that triggers the shade avoidance syndrome, in

276 When stimulated by far-red light, the intense TTA upconversion blue emission in

277 However, once illuminated with far-red light, the prodrug effectively killed SKOV-3 ovarian

278 as photoisomerization under irradiation with red light to a [2.1.0]-housane-type species.

279 Land plant phytochromes perceive red and far-red light to control growth and development, using the l

280 odimers that translocate into the nucleus in red light to mediate photomorphogenic responses.

281 ablated tumors by the illumination with far-red light to the mice, presumably through the combined e

282 We then assess the safety of red light treatment of sperm by analyzing, (1) the level

283 Soon after red-light treatment, PhyA becomes the dominant ubiquityl

284 osure and to complete this process under far-red light (typical of dense vegetation canopies).

285 obleaching and constitutes the brightest far-red light-up aptamer system known to date owing to its f

286 ing arises from direct guard cell sensing of red light versus indirect responses as a result of red l

287 Bright red light was observed with the addition of ODI and H2O2

288 e to the relative proportions of red and far red light was regulated by SIG5 through phytochrome and

289 oid shading through sensing of both blue and red light wavelengths.

290 nts showing altered photomorphogenesis under red light, we identified a mutant with dramatically enha

291 Pupillary responses to blue light and red light were compared between control subjects and tho

292 rkably, RR enhancement occurs with low-toxic red light, which is close to maximum transparency in the

293 tissue penetrable and clinically useful far-red light, which kills the cancer cells through the comb

294 ime to be photochromic upon irradiation with red light, which should be advantageous for many applica

295 sitivity was better under polychromatic than red light, which was significant at 3 frequencies.

296 s that operate in the near-infrared and deep-red light window, enabling deeper tissue penetration.

297 Here we present clear evidence that even far-red light with wavelengths beyond 800 nm, clearly outsid

298 disease severity compared with responses to red light, with a significant linear correlation observe

299 een the binding and non-binding states under red light, with the light intensity determining the cycl

300 radiation with green/yellow light as well as red light within the biooptical window.