ライフサイエンスコーパス: blue light

1 under equivalent intensities of both red and blue light.

2 gement of the three-dimensional genome using blue light.

3 go Z to E isomerization when excited with UV/blue light.

4 en light, while MpeZ attaches PUB to MpeA in blue light.

5 by fermented chickpea sprouts germinated in blue light.

6 d by one order of magnitude upon exposure to blue light.

7 r regulating transcription after exposure to blue light.

8 tin ligase to initiate photomorphogenesis in blue light.

9 eurotoxin B so that it can be activated with blue light.

10 ibly photochromic FP that responds to UV and blue light.

11 er that undergoes photolysis when exposed to blue light.

12 ithin microseconds upon photosolvolysis with blue light.

13 g CPT proteins, shows reduced sensitivity to blue light.

14 e model histidine kinase YF1 is activated by blue light.

15 of triphenylphosphine upon irradiation with blue light.

16 s observed in T. kotschyanus grown under red-blue light.

17 n establishing the antimicrobial activity of blue light.

18 d for stomatal responses to a low fluence of blue light.

19 ve mice regenerate rhodopsin more rapidly in blue light.

20 n end-binding protein-dependent manner using blue light.

21 enders them fluorescent when irradiated with blue light.

22 ltipodal microarchitectures under continuous blue light.

23 eased photosensitivity following exposure to blue light.

24 bolites following illumination of cells with blue light.

25 nly in the presence of protoporphyrin IX and blue light.

26 merizes from trans to cis in the presence of blue light.

27 activation of heterotrimeric G-proteins with blue light.

28 d using an n-AlGaN/p-CuI junction that emits blue light.

29 riboflavin combined with UV-A-light or with blue light.

30 xidant capacity (IC(50) = 176.8 ug/mL) under blue light.

31 that remain unchanged in response to red and blue light.

32 that oligomerizes rapidly in the presence of blue light.

33 Rho-family GTPase Cdc42 on stimulation with blue light.

34 ral tissue rupture at higher irradiance with blue light.

35 n the thalamofugal pathway when illuminating blue lights.

36 Herein, we develop a blue-light (365 nm) activation of NADH coupled to electr

37 on of the trans,cis and cis,cis-isomers with blue light (405 nm) affords the octahedral nitride compl

38 isomerization proceeds upon irradiation with blue light (405 nm).

39 the chiral molecular switch can be caused by blue light (440 nm).

40 Whole cell recording showed that blue light (470 nm) elicited the typical nonselective ca

41 estigated the effectiveness of antimicrobial blue light (aBL; wavelength, 405 nm), an innovative nonp

42 e the antimicrobial effects of antimicrobial blue light ([aBL] 405 nm wavelength) against multidrug-r

43 optogenetic experiments in combination with blue light absorbing cation conducting ChRs.

44 green-light absorbing phycoerythrobilin and blue-light absorbing phycourobilin.

45 rmits reversible photoconversion between the blue light-absorbing Pb and green light-absorbing Pg sta

46 -light-absorbing phycoerythrobilin (PEB) and blue-light-absorbing phycourobilin (PUB), within their l

47 ce of spectral crosstalk between Dr-Trks and blue-light-activatable LOV-domain-based translocation sy

48 ms and cultured sensory neurons, exposure to blue light activated TRPA1 and, to a lesser extent, TRPV

49 Phototropin (phot1) is a blue light-activated plasma membrane-associated kinase t

50 e-interacting beta helix-loop-helix (CIB), a blue light-activated protein-protein dimerization module

51 toxicity in zebrafish, we re-engineered the blue-light-activated EL222 system for minimal toxicity w

52 e spectral separation from green sensors and blue-light-activated optogenetic actuators.

53 We further found that blue light activation of inward-rectifying K(+) (K(+) (i

54 The blue light activation of K(+) (in) channels was also imp

55 Upon blue light activation, a covalent bond is formed between

56 ack MT plus ends and recruit tgRFP-SspB upon blue light activation.

57 chloroplast movement mechanism under excess blue light alongside the chloroplast unusual positioning

58 Here we show that both low blue light and a low-red to far-red light ratio are requ

59 ctor that is activated by the coincidence of blue light and a PPI.

60 y of individuals on diurnal schedules, using blue light and a single temperature sensor.

61 oral resolution only in the presence of both blue light and calcium.

62 ption by SIG5 was predominantly dependent on blue light and cryptochrome.

63 odimer that dissociates when irradiated with blue light and demonstrated that by fusing each half of

64 terconnected photosynthetic cell networks by blue light and monitor the subsequent plasma membrane el

65 xpressing retinal ganglion cells that detect blue light and project to the thalamus.

66 kaemic cells, differentiate upon exposure to blue light and release paracrine factors that modulate n

67 to predict melatonin rhythms accurately from blue light and skin temperature recordings in individual

68 lants are hyposensitive to red, far-red, and blue light, and flower precociously.

69 rubinemia is easily treated with exposure to blue light, and phototherapy systems have been developed

70 calcium concentration when illuminating with blue light, and the fluorescence can be reset with viole

71 eversible NPQ (qE) is induced by high light, blue light, and UV light via increased expression of LHC

72 sterically controlled by either rapamycin or blue light, as well as experimental procedures to produc

73 recently benefited from the introduction of blue light assisted photodynamic diagnostic (PDD).

74 resulting in localized generation of visible blue light at the focal spot.

75 Exposure to blue-light at night leads to circadian misalignment that

76 Retinal imaging included OCT, blue-light autofluorescence imaging, fundus photography,

77 ultimately resulting in arrhythmicity, while blue light-based phase shifts show large deviations from

78 hototropism in a dose-dependent manner, with blue light being most effective, indicating that phytoch

79 It is established that blue-light (BL) photoactivation of CRY is sufficient to

80 by ARPE-19 cells, which was abrogated with a blue light - blocking filter.

81 With the addition of a blue light-blocking filter in normoxia, a significant in

82 lls to white light for 48 h with and without blue light-blocking filters (BLF) in different condition

83 After incubation, they were exposed to blue light (Blu-U, Dusa Pharmaceuticals) for 1000 second

84 , resulting in enhanced sleep in response to blue light but delayed sleep induction in response to gr

85 bit impaired stomatal opening in response to blue light but no deficits in other phototropin-mediated

86 is counterpart (long hypocotyls in white and blue light), but also several additional features such a

87 Irradiation with blue light cleaves DEACM from the CPP, allowing the CPP

88 vioral and electrophysiological responses to blue light coded by circadian and arousal neurons.

89 posure and more specifically the spectrum of blue light contribute to the oxidative stress in Age-rel

90 light-activated modules capable of imparting blue light control of biological processes.

91 Red-shifted sensors combined with blue light-controllable optogenetic modules achieved sim

92 uction of prolonged dark currents by intense blue light could be suppressed by a following intense gr

93 Blue light cystoscopy (BLC) with hexaminolevulinate (HAL

94 While blue light cystoscopy improves diagnostic sensitivity, i

95 have clearly shown that light, particularly blue light, delays sleep onset [2].

96 abcb19 mutants were analyzed for fluence and blue light-dependent changes in leaf positioning and mor

97 ressing lines demonstrate that PPKs catalyse blue light-dependent CRY2 phosphorylation to both activa

98 ), inhibit cryptochrome function by blocking blue light-dependent cryptochrome dimerization.

99 The blue light-dependent homooligomerization of Arabidopsis

100 CRY2 interact with the COP1/SPA complex in a blue light-dependent manner.

101 Plant cryptochromes undergo blue light-dependent phosphorylation to regulate their a

102 ngle crystal as Pb or after irradiation with blue light, detected photoconversion product(s) based on

103 In Abca4(-/-) mice, the acute blue light diminished the mean autofluorescence (AF) int

104 opherols, was more influenced by lower (16%) blue light dosage, increasing about 1.3 times.

105 er blue 33% treatment in comparison to lower blue light dosages.

106 The mechanism by which a blue-light driven covalent bond formation leads to a glo

107 complexes with naphthalenes, we demonstrate blue-light driven upconversion in water with unprecedent

108 ammals), and its spectral compatibility with blue-light-driven optogenetic systems.

109 zii, specifically avoid ultraviolet (UV) and blue light during the day.

110 Recent data indicate that high-intensity blue light effectively removes bacteria from surfaces, b

111 arge dispersion of the reaction products the blue light emission is confined to discrete bands clearl

112 ct itself unless irradiated with a low-power blue light emitting diode (LED), resulting in local anes

113 e single-protein sensors that consist of the blue-light emitting luciferase NanoLuc connected via a s

114 al to develop ultrastable and efficient deep-blue light-emitting conjugated polymers (LCPs).

115 the presence of a photoredox catalyst under blue light-emitting diode (LED) irradiation.

116 then paced electrically or optically with a blue light-emitting diode, with activation spread record

117 r, semi-polar (20[Formula: see text]1) InGaN blue light-emitting diodes (LEDs) were fabricated and co

118 -stilbene to cis-stilbene in the presence of blue light-emitting diodes with broad substrate scope vi

119 e successful growth of p-type GaN by VPE for blue light-emitting diodes.

120 rmed when anilines reacted with thiols under blue light-emitting-diode (LED) irradiation at room temp

121 into polyfluorene-the benchmark wide-bandgap blue-light-emitting polymer organic semiconductor.

122 Yet, the monochromatic high intensity blue light enhanced the synthesis of total phenolic cont

123 b, Photoactivation by blue light enhanced voltage signals excited by red light

124 ial analysis shows that dCRY mediates UV and blue-light-evoked depolarizations that are long lasting,

125 We go on to show that blue light evokes higher Fos induction in the SCN compar

126 uorescent background, and compatibility with blue-light-excitable channelrhodopsins.

127 Upon blue-light excitation, the dominant tryptophan populatio

128 green alga Chlamydomonas reinhardtii evolved blue light-excited channelrhodopsins (ChR1, 2) to naviga

129 ign principle in solid-state materials for a blue-light-excited Eu(2+) -doped red-emitting oxide-base

130 -8] and gives rise to the popular view that "blue" light exerts the strongest effects on the clock.

131 cell layer, the same procedure is applied to blue light exposure experiment.

132 Pain during the blue light exposure was not significantly different betw

133 get-inhibiting actuation trains with minimal blue-light exposure, and context-based optimisation can

134 marker gene in the presence of dopamine and blue-light exposure, both in vitro and in vivo.

135 Our findings support the position that blue light filtering affects the secretion of angiogenic

136 urpose of the study was to establish whether blue light filtering could modify proangiogenic signalin

137 h statistical significance was not achieved, blue light filters reduce light-induced secretion of bFG

138 a phase III prospective multicentre study of blue light flexible cystoscopy (BLFC) in surveillance of

139 utput light, accessing both orange light and blue light from low-energy infrared light, by pairwise m

140 ulating animals of either sex with polarized blue light from zenithal direction and an unpolarized gr

141 Ultraviolet and blue light generates singlet oxygen, which oxidizes and

142 polymerization process is photoinitiated by blue light granting complete control of the reaction, in

143 Thus blue light holds promise for the sterilization of clinic

144 In late-stage STGD1-like patient and blue light-illuminated Abca4(-/-) mice, lipofuscin and m

145 This blue light-illuminated pigmented Abca4(-/-) mouse model

146 s an orange, inactive state known as OCP(O); blue light illumination results in the red active state,

147 l chloroplasts during light-to-low-intensity blue light illumination transition.

148 he tissue level after light-to-low-intensity blue light illumination transitions, but monitor transie

149 ment on the visual analog scale (VAS) during blue light illumination was not significantly different

150 educed neutral form of its FAD cofactor upon blue light illumination.

151 salt via organic photoredox catalysis under blue light illumination.

152 ignals rapidly, locally, and reversibly upon blue light illumination.

153 f interest can be enhanced or inhibited upon blue light illumination.

154 d-type mice showed no RPE degeneration after blue light illumination.

155 Blue-light illumination at the embryonic termini for 90

156 Optimized blue-light illumination triggered the co-localization of

157 to create E-hexafluorobutenes (E-HFBs) under blue light in a single step.

158 any TOC and TIC genes are rapidly induced by blue light in both WT and the ppi2 mutant.

159 the account the scattering and absorption of blue light in brain tissue together with the relative de

160 Complex II activity was inactivated by blue light in mitochondria from strains expressing activ

161 erved stomatal responses to a low fluence of blue light in Regnellidium diphyllum and Marsilea minuta

162 Two new studies highlight the importance of blue light in the regulation of stem elongation and bend

163 f circadian period and uncovered the role of blue light in the response of the circadian oscillator t

164 This may lead to novel applications using blue light induced oxidative bursts to prime crop plants

165 Blue light-induced RPE cellular damage preceded the phot

166 her experiments indicated a role for ERA1 in blue light-induced stomatal opening.

167 ) consisting of split antibody fragments and blue-light inducible heterodimerization domains.

168 cantly reduce dark leak activity and improve blue-light induction developing our new version, PA-Cre

169 e 1 (CRY1) and cryptochrome 2 (CRY2) mediate blue light inhibition of hypocotyl elongation and long-d

170 ive regulators of Arabidopsis cryptochromes, Blue light Inhibitors of Cryptochromes 1 and 2 (BIC1 and

171 to become physiologically active, and BICs (blue-light inhibitors of CRYs) suppress homo-oligomeriza

172 gments may be achieved using higher (16-33%) blue light intensities.

173 Ambulatory wrist blue light irradiance and skin temperature data were col

174 After blue light irradiation for 10 min at 470 nm, the sample

175 Blue light irradiation, a [Ru] or [Ir] photocatalyst, an

176 The reaction is performed under blue-light irradiation and catalyzed by photoactive Lewi

177 Chain walking combined with blue-light irradiation functions as the mechanistic swit

178 oom temperature is reported to proceed under blue-light irradiation.

179 For growth under a canopy, where blue light is diminished, CRY1 and CRY2 perceive this ch

180 re pathogenic to humans and demonstrate that blue light is effective against some, but not all, funga

181 The stomatal response to blue light is highly sensitive, rapid, and not driven by

182 By contrast, avoidance of blue light is primarily mediated by multidendritic neuro

183 The biochemical changes induced by LED Blue Light (LBL) (450 nm) in Lane Late oranges were inve

184 The objective was to investigate whether LED Blue Light (LBL) induces changes in phenolics and ethyle

185 Red, far-red, and blue light lead to negative phototropism in a dose-depen

186 auxin signaling reporter, indicates that low blue light leads to enhanced auxin signaling in the hypo

187 ation of such a "click-armed" photocage with blue light leads to fast and efficient release of a set

188 Blue light levels commonly needed for actuation can be c

189 vy rosette leaves that are less sensitive to blue light-mediated leaf flattening.

190 ell movement requires components involved in blue light-mediated stomatal opening, suggesting cross t

191 le cross-linking with riboflavin and UV-A or blue light might be a clinical approach in future.

192 While illumination with blue light never successfully terminated VF, illuminatio

193 antly reduces the biological responsivity to blue light of the cryptochrome receptor cry1 in Arabidop

194 ere is altered transcript accumulation under blue light of the strictly light-dependent, gamete-speci

195 White Collar proteins and cryptochromes for blue light, opsins for green light, and phytochromes for

196 exemplified by its implementation under UV, blue light or even sunlight irradiation as well as in bu

197 and bundle sheath genes were induced only by blue light or only by red light, but not both.

198 Pupil responses to red and blue light (peak, 485 and 625 nm, respectively) presente

199 fundamental link in the photoresponses from blue light perceived by the conserved White Collar compl

200 nificant quantitative changes in response to blue light percentage were obtained for both directly an

201 gh the guard-cell-signaling pathway coupling blue light perception to ion channel activity is relativ

202 d interruption of fciB causes a constitutive blue light phenotype.

203 for all-optical electrophysiology, although blue light photoactivation of the FlicR1 chromophore pre

204 Ectopic clocks also require the blue light photoreceptor CRYPTOCHROME (CRY), which is re

205 adation of the clock protein TIMELESS by the blue light photoreceptor Cryptochrome is considered the

206 In Drosophila, the blue-light photoreceptor CRYPTOCHROME (CRY) synchronizes

207 Finally, we identify the circadian blue-light photoreceptor CRYPTOCHROME as a molecular reg

208 Fc1 that impairs its capacity to bind to the blue-light photoreceptor FKF1 in yeast two-hybrid assays

209 The blue-light photoreceptor FLAVIN-BINDING, KELCH REPEAT, F

210 ese processes are primarily modulated by the blue light phototropin photoreceptors phot1 and phot2.

211 limits the expression of PIF4, while in low blue light, PIF4 expression increases, which contributes

212 pH-values ranging from 2.6 to 4.6, purplish-blue, light pink, magenta, brick-red, and intense red hu

213 Under blue light, plant chloroplasts relocate to different are

214 Emmetropization was not affected by blue light, possibly because the reduction in vitreous c

215 hotosynthetic bacterium that swims away from blue light, presumably in an effort to evade photons ene

216 n of alcohols via an S(N)2 pathway, in which blue light-promoted iodination is used to form alkyl iod

217 INDING KELCH REPEAT, F-BOX 1 (FKF1), another blue light receptor and well-known photoperiodic floweri

218 Recently, the blue light receptor CRYPTOCHROME 1 (CRY1) was shown to p

219 sum, our data demonstrate that pCRY is a key blue light receptor in Chlamydomonas that is involved in

220 Phototropins (phot1 and phot2) are plant blue light receptor kinases that function to mediate pho

221 Phototropin blue light receptors (phot1 and phot2) optimize photosyn

222 dance, and this involves the PHOT1 and PHOT2 blue light receptors [3].

223 ght, oxygen, or voltage (LOV) domains of the blue light receptors aureochrome and phototropin reveale

224 Cryptochromes are known as flavin-binding blue light receptors in bacteria, fungi, plants, and ins

225 omes are flavin-binding proteins that act as blue light receptors in bacteria, fungi, plants, and ins

226 chromes constitute a group of flavin-binding blue light receptors in bacteria, fungi, plants, and ins

227 ive manner, similar to the regulation by the blue light receptors phototropin and plant cryptochrome

228 Cryptochromes are blue light receptors that regulate various light respons

229 Cryptochromes are evolutionarily conserved blue light receptors with many roles throughout plant gr

230 the four remaining genes encode for putative blue light receptors.

231 Plant cryptochromes (cry) act as UV-A/blue light receptors.

232 ty in the same NBs that can also contain the blue-light receptors CRYPTOCHROME 1 and CRYPTOCHROME 2.

233 Cross-linking with riboflavin/blue light reduced the degradation by MMP1 to 77% +/- 13

234 MacTel patients, macular pigment (MP), OCT, blue light reflectance, fluorescein angiography, as well

235 s with their maximum emission limited at the blue-light region.

236 PULSE combines a blue-light-regulated repressor with a red-light-inducibl

237 Blue light regulates multiple processes that optimize li

238 cryptochrome (CRY) photoreceptors to mediate blue light regulation of development or the circadian cl

239 lets disassemble and reassemble under UV and blue light, respectively, due to azobenzene trans/cis ph

240 4, featuring yellow, lime-green, green, and blue light, respectively.

241 arbohydrate metabolism, cold stimulation and blue-light response were identified using GO and KEGG da

242 ration than to humidity, suggesting that the blue light responses of Marsileaceae stomata differ from

243 However, blue light-responsive photoreceptors are, in principle,

244 lustrate herein the incorporation of various blue light-responsive photoreceptors into modular domain

245 ily exposure of differentiated adipocytes to blue light resulted in decreased lipid droplet size, inc

246 Animals were subjected to combined red-green-blue lights (RGB) during the day and to: darkness; red l

247 Cherenkov radiation (CR), the blue light seen in nuclear reactors, is emitted by some

248 tional changes upon activation of a minimal, blue-light-sensing histidine kinase from Erythrobacter l

249 In this regard, we discovered a novel blue light-sensitive current in human scWAT that is medi

250 otoactivatable Dab1 (opto-Dab1) by using the blue light-sensitive dimerization/oligomerization proper

251 sensitive kinesin-3, which is activated upon blue light-sensitive homodimerization.

252 plasma membrane recruitment of RAF1 based on blue light-sensitive protein dimerizer CRY2/CIB1.

253 simultaneous manipulation of common red- and blue-light-sensitive optogenetic probes.

254 ation with green-fluorescent sensors or with blue-light-sensitive sensors and rhodopsins.

255 photoreceptor co-action mechanism to sustain blue light sensitivity of plants under the broad spectra

256 tional and biochemical studies implicate the blue-light sensor cryptochrome (CRY) as an endogenous li

257 PP7 is thought to transduce a blue-light signal perceived by crys and phy a that induc

258 t effective, indicating that phytochrome and blue light signaling control AR system architecture.

259 der the control of the phototropin-dependent blue-light signaling cascade and correlated with the act

260 tion phase response following cessation of a blue light stimulus was compared with the photoreceptor-

261 Following an aversive mechanical or blue light stimulus, worms respond first by briefly movi

262 Blue light stomatal responses may have contributed to th

263 ulation with unpolarized green and polarized blue light suggested that the two compasses interact in

264 teraction with the light-responsive Cry2-CIB blue-light switch, referred to hereafter as the CofActor

265 s synthesize 11cRAL chromophore faster under blue light than in darkness.

266 renkov radiation (CR) is the ultraviolet and blue light that is produced by a charged particle travel

267 ferences between the responses under red and blue light, the chloroplast movement mechanism had no ef

268 Under blue light, the iLID + tdnano system recruits two copies

269 When A2E-loaded cells are exposed to blue light, the model parameters indicate, as expected,

270 Light-oxygen-voltage (LOV) domains sense blue light through the photochemical formation of a cyst

271 tivity of these receptors from ultraviolet A/blue light to almost the complete visible spectrum.

272 cally and illuminates it with red, green and blue light to control its colour as it quickly scans the

273 benula pathway is involved in the ability of blue light to influence a circadian behavior.

274 s in anesthetized mice following delivery of blue light to the pancreas.

275 rotease proximal to its cleavage peptide and blue light to uncage the cleavage site.

276 However, prolonged low blue light treatments are sufficient to promote phototro

277 In R. diphyllum, blue light triggered stomatal oscillations.

278 tely, the molecular parameters necessary for blue-light-triggered Pd-C bond homolysis from this alpha

279 ompounds reported here exhibited emission of blue light upon irradiation in EtOH in the region of 404

280 Moreover, far-red and blue light upregulate the expression of PCH1 and PCHL in

281 ging because CsChrimson is also sensitive to blue light used to activate green fluorescent protein, a

282 Blue Light Using Flavin (BLUF) domains are increasingly

283 Blue light using flavin (BLUF) photoreceptor proteins ar

284 Blue light using flavin adenine dinucleotide (BLUF) prot

285 Blue-light using flavin (BLUF) photoreceptor proteins ar

286 The flavin chromophore in blue-light-using FAD (BLUF) photoreceptors is surrounded

287 The LMCV in response to blue light was relatively constant throughout the VF.

288 drives absorption and emission peaks toward blue-light wavelengths.

289 By stimulating PdCMs selectively with blue light, we were able to control cardiac rhythm in th

290 isomerization is induced by irradiation with blue light, whereas switching back to the Z isomer is ac

291 a luciferase with luciferin generates bright blue light which can be readily detected and analyzed sp

292 vation by high energy UV or short wavelength blue light, which can limit their use as a consequence o

293 of red light in cardiac tissue compared with blue light, which resulted in more widespread light-indu

294 ) ends until their instantaneous release via blue light, which results in full restoration of their e

295 ted cytosolic calcium and externally applied blue light, which together produce translocation of a me

296 ol (66%) was found in T. migricus exposed to blue light, while the least (1.69%) was observed in T. k

297 When directly challenged with blue light, wild-type l-LNvs responded with increased fi

298 lamp, AFB1 molecules absorb photons and emit blue light with peak wavelength of 432 nm.

299 d more potent photocytotoxicity (IC50 3 muM, blue light) with a photocytotoxic index >5.

300 Cis human ovarian cancer cells (IC50 74 muM, blue light) with a photocytotoxic index <2, whereas Pt-G