ライフサイエンスコーパス: PL

1 PL exposure of cancer cells results in increased reactiv

2 PL reduced the activity of POD by more than 95% after ap

3 PL titrations, thermochemical cycles, and kinetic analys

4 PL-spectroscopy of PSi was performed at room temperature

5 Samples containing 0.2% PL and 0.03% GA and no salt had higher turbidity and inc

6 rements suggest the elastic behavior of 0.2% PL and 0.03% GA complex.

7 bcooled liquid vapor pressure (log PL) > -5 (PL in Pa), as well as the total suspended particle conce

8 reen, with an overall wavelength span of 73 (PL) and 67 (ECL) nm, respectively.

9 We are able to retain a PL efficiency of 20% in the solid state (vs. 30% in dilu

10 studies showed that binding to an activating PL ligand, such as dilauroylphosphatidylcholine, favors

11 d a photon correlation analysis of aggregate PL reveal that triplets are quenched by intermolecular i

12 m MS in positive (as [M + H](+) ions for all PL classes) and negative-ion mode (as [M - H](-) ions fo

13 ratures above 75 K, excitonic absorption and PL exhibit homogeneous broadening.

14 ve splitting of the excitonic absorption and PL into multiple regularly-spaced resonances every 40-46

15 Large blue-shifted UV-vis absorption and PL spectra have been observed due to strong two-dimensio

16 recorded neuronal activity from the BLA and PL while rats performed a task wherein competing shock-

17 ith PL dynamics of energy-accepting MoS2 and PL quenching data of the energy-donating NQDs.

18 efined white list of fatty acid residues and PL class-specific fragments.

19 ome tectal neurons could project to rUva and PL via branched axons.

20 The TA and PL data clearly illustrate the efficacy of MoS2 and like

21 ent HAstV-2-neutralizing monoclonal antibody PL-2 (MAb PL-2).

22 ound to the neutralizing monoclonal antibody PL-2.

23 th CD11b expression, through cell-associated PL-C and -D. mCD48 remained stable due to up-regulation

24 de (0.1 muM) or p50 siRNA (100 nM) augmented PL-induced inhibitory effect on cell growth and activati

25 metry (MS) analysis of the reactions between PL and GSTP1 confirmed that PL does not label GSTP1.

26 dSe and Cu(+):CdSe NCs display similar broad PL with large Stokes shifts, we demonstrate that both al

27 ins, which exhibit red-shifted and broadened PL compared to single-chain aggregates.

28 adiative decay ultimately leads to broadened PL.

29 en switched from Context A to Context B, but PL inactivation decreased responding only in Context A.

30 llenges in correlating defects identified by PL with those by PAS and DLTS methods.

31 dy indicates that the inactivation of POD by PL is an all-or-none process related to loss of helical

32 e (EL), photoluminescence (PL), and confocal PL mapping have been used to further understand the impo

33 recombination (~200 ns) causing considerable PL enhancement.

34 The prelimbic prefrontal cortex (PL) has consistently been found to be necessary for the

35 ulations of the prelimbic prefrontal cortex (PL).

36 icity in prelimbic medial prefrontal cortex (PL-mPFC) pyramidal neurons, a phenomenon that correlates

37 rats, inactivation of the prelimbic cortex (PL) attenuates renewal.

38 ne- and sucrose-seeking in prelimbic cortex (PL), infralimbic cortex (IL), BLA, and vSub neurons that

39 bitory transmission in the prelimbic cortex (PL).

40 Although the prelimbic cortex (PL, part of medial prefrontal cortex) has been implicate

41 auses stronger p53 degradation than SARS-CoV PL(pro) alone.

42 imbic (PL) cortex and activation of critical PL molecular mechanisms that are not required for extinc

43 also show very similar temperature-dependent PL lifetimes and magneto-luminescence.

44 We analyze the temperature-dependent PL to reveal the effective trion size, consistent with t

45 Time dependent PL spectral shifts provided the first kinetic data for e

46 observed for the lowly heritable traits DPR, PL, and SCS.

47 In turn, the sum of the QD and dye PL intensities, when adjusted for quantum yields, reflec

48 for memory consolidation, retrieval engages PL BDNF to regulate excitatory and inhibitory synaptic p

49 sport properties indicates that the enhanced PL due to increased Mo-O bonding leads to p-type compens

50 epsilon-Polylysine (epsilon-PL) is a broad-spectrum antimicrobial biopolymer, suitab

51 Hot exciton PL and time-resolved PL measurements show that vibration

52 nstrate a 10-fold increase of MoS2 excitonic PL enabled by nonradiative energy transfer (NRET) from a

53 cosecond timescale competitive with that for PL.

54 n substrate binding with strong affinity for PLs, and modulates ATP hydrolytic activity.

55 , rather than attenuating renewal generally, PL inactivation specifically affects ABA renewal by redu

56 Therefore, the BLA-->PL circuit is critical in governing the selection of beh

57 orrelated firing primarily displayed a BLA-->PL directionality during the shock-associated cue.

58 Finally photostimulation of the BLA-->PL projection increased freezing, whereas both chemogene

59 y, longer charge carrier lifetimes, and high PL yields and was rationalized as a consequence of the d

60 For all compounds, we observed a very high PL quantum yield (79-89%) and formation of stable radica

61 These data highlight PL neurons that project to NAcC, and their regulation by

62 While absorption remains homogeneous, PL becomes inhomogeneous below 75K, which we speculate i

63 ch whereby dopamine signaling was blocked in PL and glutamate signaling was blocked in the contralate

64 lane sapphire can yield >100x enhancement in PL and carrier lifetime due to increased molybdenum-oxyg

65 midal neurons; a cocaine-induced increase in PL excitability was decreased by riluzole, and a cocaine

66 on energy results in a four-fold increase in PL intensity.

67 resynaptic and postsynaptic modifications in PL-mPFC and causes long-lasting memory impairments.

68 Neurons in PL, BLA, and vSub that project to NAcC, but not NAcSh, e

69 l that cocaine-evoked synaptic plasticity in PL-mPFC is reversible in vivo, and suggest a novel strat

70 pothesized that cocaine-evoked plasticity in PL-mPFC may underlie cocaine-associated memory retrieval

71 The lens position in PL was greater than in CR and LS (p < 0.05 and <0.01, re

72 Polyunsaturated fatty acids predominated in PL of all tissues (52.2-55.8% of total FA); monounsatura

73 sfer to surface plasmons (SPs), resulting in PL suppression.

74 Second, in PL, unlike in PR, the promoter distal operator site, OL3

75 To determine what information PL-NAc neurons convey, we selectively recorded from them

76 eaflavin-3-gallate, and theaflavin inhibited PL with IC50 of 1.9, 4.2, 3.0, and >10mumol/L.

77 med reinstatement was recapitulated by intra-PL injection of corticosterone, the CB1R agonist WIN 55,

78 ts on reinstatement were attenuated by intra-PL injections of either the CB1R antagonist, AM251, or t

79 cocaine seeking were determined using intra-PL microinfusions.

80 "bare" CNP with high luminescence loses its PL when positively charged macromolecules are wrapped ar

81 icients: two permutation (Lasso-Ayers, Lasso-PL) and one analytic approach (Lasso-AL) to select the p

82 However, Lasso-PL and Lasso-AL remain fast and powerful tools for condu

83 posed permutation selection procedure (Lasso-PL) and the analytic selection method (Lasso-AL) are fas

84 r [AL], central layer [CL], posterior layer [PL], and total layer [TL]) and 2 annuli (central annular

85 les, utilizing enzyme-modified pencil leads (PL) as effective electrochemical biosensors for robotic

86 Pulsed light (PL) is a non-thermal preservation method in which foods

87 Pancreatic lipase (PL) plays a central role in fat metabolism and is a vali

88 Polar lipids (PL) were less influenced by captivity since the fatty ac

89 separated into four fractions: polar lipids (PL), diacylglycerols, free fatty acids and triacylglycer

90 Infants in the LNS-PL group had higher birth weights (2629 +/- 408 compared

91 LNS-PLs reduced the risk of newborn stunting (18.7% compared

92 mug folic acid) and 16 clusters received LNS-PLs (20 g/d, 118 kcal) containing essential fatty acids

93 ements for pregnant and lactating women (LNS-PLs) on birth outcomes.

94 0 and a subcooled liquid vapor pressure (log PL) > -5 (PL in Pa), as well as the total suspended part

95 2-neutralizing monoclonal antibody PL-2 (MAb PL-2).

96 lly blocks binding and neutralization by MAb PL-2.

97 the molecular basis for resistance from MAb PL-2 neutralization, we determined the 1.35-A-resolution

98 ne permits loop flexibility and recovers MAb PL-2 binding.

99 ying nitroalkenes derivatives of three major PL classes found in living systems: phosphatidylcholines

100 pressure window (7-17 GPa) with flat maximum PL yielding and sharp edges at both ends, which may prov

101 Both micro-PL and micro-reflectance reveal the spectral characteris

102 gated through pump intensity-dependent micro-PL measurements, whereby relatively large local inhomoge

103 In xenograft mice model, PL (2.5-5 mg/kg) suppressed tumor growth of NSCLC dose-d

104 l vertical sizes is responsible for a narrow PL, strong excitonic absorption, and a blue shift of the

105 Activation of NAc-projecting PL neurons (PL-NAc), but not the other subpopulations, decreased the

106 pical MS/MS fragmentation pattern of all NO2-PL included a neutral loss of HNO2, product ions arising

107 origin, or role of nitro phospholipids (NO2-PL) was reported up to now.

108 NO2-PLs were generated by NO2BF4 in hydrophobic environment,

109 Identified NO2-PLs were further analyzed by tandem MS in positive (as [

110 The NO2-PLs were then detected by electrospray ionization (ESI-M

111 tran amine into the lateral pontine nucleus (PL), and led to extensive retrograde labeling of tectal

112 a affected by antibiotics a faster occurring PL maximum, compared with growing bacteria, is observed.

113 Comprehensive analysis of PL data in combination with theoretical calculations of

114 hedron in the 2D layer and the broadening of PL emission, with the most distorted structure having th

115 Experiment 2a examined the effects of PL inactivation on ABC renewal in the same rats.

116 s concentration results in an enhancement of PL emission due to electrostatic image charge effect.

117 er 13 tectal neurons, retrograde labeling of PL neurons, and anterograde labeling of PL.

118 g of PL neurons, and anterograde labeling of PL.

119 Some insights related to the mechanism of PL-signal generation are proposed and discussed.

120 ti-cancer effects and possible mechanisms of PL on non-small cell lung cancer (NSCLC) cells in vivo a

121 C8 olefin of PL, whereas the C2-C3 olefin of PL was postulated to react with GSH.

122 lent adduct formation at the C7-C8 olefin of PL, whereas the C2-C3 olefin of PL was postulated to rea

123 tructure showed that a hydrolysis product of PL (hPL) was conjugated to glutathione at the C7-C8 olef

124 The rats exhibited ACD renewal regardless of PL inactivation.

125 In contrast to these, results of PL spectra are rather unexpected, as distinct room tempe

126 Moreover, co-treatment of PL with NF-kappaB inhibitor phenylarsine oxide (0.1 muM)

127 e study suggests that complex coacervates of PLs could be one feasible ways of incorporating amino ac

128 a also indicated that nucleophilic attack on PL at the C2-C3 olefin led to PL hydrolysis.

129 he effects of stress-level corticosterone on PL neurotransmission and cocaine seeking were determined

130 the influence of triplet-quenching oxygen on PL and a photon correlation analysis of aggregate PL rev

131 ve measurable influence on the absorption or PL line widths, produce small (+/-0.05), nonmonotonic ch

132 de tracers into four different face patches (PL, ML, AL, AM) to characterize their anatomical connect

133 The peak PL intensity was found to be highest for ZnO: graphene n

134 ncreatic fistula/pancreatic leak/abscess (PF/PL/A) (21.9% to 9.2%).

135 variable perioperative mortality, rate of PF/PL/A, and readmission rates did not significantly alter

136 pasireotide is administered, the cost per PF/PL/A avoided is approximately $300,000.

137 The resultant cost per PF/PL/A avoided was $301,628.

138 th or without inhibitors for phospholipases (PL) (-C or -D), or cycloheximide, or brefeldin A.

139 d fragmentation rules for each phospholipid (PL) class.

140 Methylation of phospholipids (PL) leads to increased uniformity in positive electrospr

141 hey may also be esterified to phospholipids (PL).

142 Phospholipids (PLs) are a major, diverse constituent of cell membranes.

143 Phospholipids (PLs) are unusual signaling hormones sensed by the nuclea

144 sport of aberrantly localized phospholipids (PLs) from the OM to the inner membrane (IM).

145 Photoluminescence (PL) and time-resolved PL measurements indicated the latt

146 Photoluminescence (PL) studies show a correlation between the distortion of

147 Photoluminescence (PL) was used to estimate the concentration of point defe

148 ngle X-ray scattering and photoluminescence (PL) probes, the NC-SL structural transformations are cor

149 emits strong visible blue photoluminescence (PL) upon UV excitation.

150 d GQDs show distinct blue photoluminescence (PL) with excellent quantum yield (QY) up to 12% as well

151 The NWs have bright photoluminescence (PL) with a photoluminescence quantum yield (PLQY) of abo

152 eir device performance by photoluminescence (PL) microscopy has now been studied.

153 e combination of confocal photoluminescence (PL) microscopy and chemical imaging to correlate the loc

154 A rapid and low cost photoluminescence (PL) immunosensor for the determination of low concentrat

155 nd polarization dependent photoluminescence (PL) spectra.

156 bright and size dependent photoluminescence (PL).

157 electroluminescence (EL), photoluminescence (PL), and confocal PL mapping have been used to further u

158 of bacteria by employing photoluminescence (PL) emission of photocorroding GaAs/AlGaAs quantum well

159 ca. 2.5-100 nm) with high photoluminescence (PL) quantum yield (QY; ca. 15-55 %) and product yield ha

160 ave demonstrated improved photoluminescence (PL) line widths for cadmium chalcogenide-based nanocryst

161 ignificant enhancement in photoluminescence (PL) due to localized surface plasmon (LSP) interactions.

162 s achieved for tuning its photoluminescence (PL).

163 Time-resolved micro photoluminescence (PL) measurements have been performed in order to further

164 The morphology, photoluminescence (PL) spectra and UV-vis spectra of these nanostructures w

165 tematic quench of the NGO photoluminescence (PL) by Ce doping.

166 Reversible switching of photoluminescence (PL) of carbon nanoparticles (CNP) can be achieved with c

167 e present paper we report photoluminescence (PL) based immunosensor for the detection of OTA.

168 we report high resolution Photoluminescence (PL) attributed to emission from individual Ge nanocrysta

169 e the first time-resolved photoluminescence (PL) data for any corannulene-based compounds in the soli

170 Raman spectroscopy, photoluminescence (PL), x-ray photoelectron spectroscopy (XPS), Fourier tra

171 ce, both the steady-state photoluminescence (PL) intensity and the time-resolved PL decay lifetime in

172 lved variable-temperature photoluminescence (PL) spectroscopy, magnetic circularly polarized luminesc

173 gion and room temperature photoluminescence (PL) with long tau > 100 ns excited state lifetimes.

174 ed for fine-tuning of the photoluminescence (PL) and ECL emission from blue to green, with an overall

175 in P3HT by analyzing the photoluminescence (PL) from isolated single-chain aggregates and multichain

176 Here, we show that the photoluminescence (PL) of QD bioconjugates can also be modulated by a combi

177 oncentrations (10 muM) to photoluminescence (PL)-relevant concentrations (0.1 muM) and the consequenc

178 ng in an asymmetric trion photoluminescence (PL) peak with a long low-energy tail and peak position t

179 The typical photoluminescence (PL) of monolayer MoS2 is however known to suffer very lo

180 lasmonic resonators using photoluminescence (PL) and excitation spectroscopy along with kinetic model

181 terials are studied using photoluminescence (PL), and we find that 1 and 2 act as efficient electron-

182 iffraction (XRD), UV-vis, photoluminescence (PL) spectroscopy, FT-IR, and cyclic voltammetry techniqu

183 pressure-induced visible photoluminescence (PL) above 2 GPa near 2 eV is observed.

184 UV-Visible absorption and Photoluminiscence (PL) techniques.

185 target of the plant compound piperlongumine (PL), which contains two reactive olefins and inhibits pr

186 rs 2-3 and 5-6 of the anterior and posterior PL and in the population of neurons projecting to poster

187 in nuclear pERK expression in the posterior PL in rats given instrumental training.

188 Comparison between single-crystal and powder PL decay curves of 1 suggests inherently high defect tol

189 The choice of cheap and practical PL enzyme biosensors and simple nonmicrofluidic measurem

190 nucleus of the amygdala (BLA) and prelimbic (PL) medial prefrontal cortex have been implicated in rew

191 ions in intrinsic excitability of prelimbic (PL) and infralimbic (IL) pyramidal neurons; a cocaine-in

192 Inactivation of the prelimbic (PL) region of the medial prefrontal cortex by baclofen/m

193 croinjection of ketamine into the prelimbic (PL) region of the medial prefrontal cortex duplicated th

194 ctions from dorsal hippocampus to prelimbic (PL) cortex and activation of critical PL molecular mecha

195 The high-pressure PL results demonstrate a well-defined pressure window (7

196 Activation of NAc-projecting PL neurons (PL-NAc), but not the other subpopulations, d

197 ng the transcription at two lytic promoters, PL and PR, and auto-regulating the promoter, PRM, which

198 Four pronounced PL peaks were identified below a temperature of 60 K at

199 nique domain (SUD) and papain-like protease (PL(pro)), and, as a consequence, the involvement of cell

200 Notably, the dye/QD PL intensity ratio reflected changes in the relative rat

201 (II) phenanthroline complex that quenched QD PL through electron transfer.

202 th either a fluorescent dye that quenched QD PL through FRET or a ruthenium(II) phenanthroline comple

203 ynaptic and postsynaptic transmission in rat PL-mPFC pyramidal neurons.

204 inhibitory synaptic transmission in the rat PL were determined using whole-cell recordings in layer

205 responsible for the dominant defect-related PL bands in this material are found.

206 Defect-related PL intensity in undoped GaN grown by hydride vapor phase

207 -0.05), nonmonotonic changes in the relative PL quantum yield, and produce small, nonmonotonic change

208 site, OL3, is sufficient to directly repress PL.

209 significantly reduced the levels of residual PLs as well as the TBA number.

210 Interestingly, the levels of residual PLs showed a proportionate relationship with thiobarbitu

211 escence (PL) intensity and the time-resolved PL decay lifetime increase after electrical stress, indi

212 Photoluminescence (PL) and time-resolved PL measurements indicated the lattice-mismatch induced s

213 Hot exciton PL and time-resolved PL measurements show that vibrational relaxation occurs

214 x participates in ensuring active retrograde PL transport to maintain OM lipid asymmetry.

215 hildren Present and Lifetime version (K-SADS-PL).

216 olayer of QD multilayers exhibit significant PL enhancement mainly through long-range exciton-SP coup

217 study of CoFe2O4@CdSe has shown significant PL quenching by the formation of CoFe2O4 core inside CdS

218 The active Mn oxidase in Bacillus sp. PL-12, Mnx, is a complex composed of a multicopper oxida

219 Steady state PL studies were carried out to measure the PL response o

220 A SUD-PL(pro) fusion interacts with RCHY1 more intensively and

221 Furthermore, while sustained PL brain-derived neurotrophic factor (BDNF) expression i

222 llary block (PB), and plateau iris syndrome (PL).

223 Study of room temperature PL was performed in both single-crystal and polycrystall

224 Ce concentration and their room temperature PL was studied using 325 nm laser.

225 other information led to the conclusion that PL inhibits GSTP1, which forms covalent bonds between GS

226 eactions between PL and GSTP1 confirmed that PL does not label GSTP1.

227 Experiment 2b demonstrated that PL inactivation attenuated the ABA renewal effect in the

228 We found that PL contains anatomically and molecularly distinct subpop

229 as shown by Clarke in pigeons, we found that PL projects to caudal cerebellar folia.

230 Therefore, these results indicated that PL could inhibit lung cancer cell growth via inhibition

231 However, we report that PL inactivation after training attenuates responding in

232 plasmon resonance (SPR) analysis showed that PL binds to p50 concentration-dependently.

233 ocking model and pull down assay showed that PL directly binds to the DNA binding site of nuclear fac

234 The PL emission of the heterostructures was monitored with a

235 The PL has a lifetime of 50 ns, almost 2 orders of magnitude

236 The PL intensity increases six-fold, while the PL peak shift

237 The PL is recovered in the presence of a higher energy repum

238 The PL line width of HgTe NPLs (40 nm full width at half-max

239 The PL quench was attributed to the novel concept of super h

240 The PL spectroscopy study of CoFe2O4@CdSe has shown signific

241 The PL thus has a more specific role in controlling contextu

242 unctionalized diatom frustule biosilica, the PL emission from the biosilica was partially quenched du

243 At higher concentrations, the PL intensity associated with individual defects tends to

244 growth of these bacteria further delays the PL maximum.

245 decreased below 22.1 GPa, thus enhancing the PL quantum yield leading to Sn (3) P1 --> (1) S0 photons

246 recombination center are responsible for the PL quenching.

247 Our results highlight a role for the PL-NAcC pathway in cocaine seeking and show that these g

248 To confirm a functional role for the PL-NAcC pathway, and to test the hypothesis that this pa

249 not activate DRN-projecting neurons from the PL, IS did so after ketamine, suggesting that the prophy

250 re infused with either B/M or vehicle in the PL and tested in the acquisition context (A) and in a di

251 ng in distinct layers and populations in the PL and this signaling underlies the consolidation of goa

252 lectrostatic field induced blue shift in the PL energy of the rGO-QDs.

253 0 min, suggesting that ERK expression in the PL is necessary for the consolidation of goal-directed l

254 ppearance of a characteristic maximum in the PL plot collected over time.

255 ue that the spread of the nc-Ge peaks in the PL spectrum is due to different confinement energies ari

256 ibutions of endocannabinoid signaling in the PL to the effects of stress-level corticosterone on PL n

257 ated inhibitory synaptic transmission in the PL via cannabinoid receptor type 1 (CB1R)- and 2-arachid

258 Following infusions of B/M or vehicle in the PL, responding was tested in Context C and another new c

259 by mobilizing 2-arachidonoylglycerol in the PL, resulting in CB1R-mediated attenuation of inhibitory

260 AstV-2 capsid genes reveals mutations in the PL-2 epitope within the capsid's spike domain.

261 show one single band that almost matches the PL band.

262 e PL studies were carried out to measure the PL response of the fabricated fluorescent bioprobe as a

263 Under a repump of 2.33 eV (532 nm), the PL increases rapidly, with a time constant 30 mus.

264 r an energy below 1.3 eV (above 950 nm), the PL is suppressed by more than two orders of magnitude.

265 n the degree of circular polarization of the PL at increasing temperatures indicating a relatively st

266 ase in pERK expression in all regions of the PL both at 5 and 60 min, and this was accompanied by an

267 The position of the PL maximum depends on the photocorrosion rate which, in

268 A significant red-shift of the PL peak for Eu(3+) was observed.

269 However, only activation of the PL-NAcC pathway positively correlated with cocaine reins

270 evented by pharmacological inhibition of the PL.

271 ntrast, when the repump is switched off, the PL decreases first within 100-200 mus, followed by a muc

272 The detuning quenches the PL emission from rGO-QDs at higher concentration of Ag N

273 ptured on the surface of biochips retard the PL maximum, while growth of these bacteria further delay

274 It was found that the PL intensity shows a systematic quench with increasing C

275 o experiments tested the hypothesis that the PL is important in context-dependent responding learned

276 ional functional experiments showed that the PL-NAcC pathway was recruited by drug-associated cues in

277 -lasting upregulation of pERK throughout the PL and specifically within neurons that project to the p

278 hat SiHx species obviously contribute to the PL emission of NPSi, and the introduce of oxidization st

279 nzyme so as to attach glucose oxidase to the PL surface.

280 e PL intensity increases six-fold, while the PL peak shifts from 1.92 eV to 1.97 eV during the laser

281 c conformational change in a loop within the PL-2 epitope due to a serine-to-proline mutation, lockin

282 of social and spatial information within the PL-NAc may contribute to social behavior by supporting s

283 he X-ray crystal structure of GSTP1 bound to PL and GSH at 1.1 A resolution to rationalize previously

284 In contrast to PL spectroscopy, TA can detect even non-emissive exciton

285 ilic attack on PL at the C2-C3 olefin led to PL hydrolysis.

286 optogenetically identified as projecting to PL more accurately predicted behavioral responses during

287 in vitro, treatment of cells susceptible to PL with hPL did not have significant anti-proliferative

288 l DeltaEST of 0.03 and 0.04 eV and transient PL characteristics indicating that they are thermally ac

289 time the temperature-dependence of the trion PL has been analyzed with such detail in any system.

290 The asymmetry of the trion PL peak and resulting peak red-shift depends both on the

291 formational dynamics that drive this unusual PL-mediated nuclear hormone receptor activation.

292 The feasibility of using PL to inactivate POD was tested and results explained ba

293 ese mechanistically different pathways using PL measurements at both the ensemble and the single part

294 zation (ESI) efficiencies across the various PL subclasses.

295 followed by bandgap opening and the visible PL appearing at the point of the gap reversal, which is

296 The emergence of unusual visible PL behavior is associated with the seriously trigonal la

297 Altogether, our data suggest a model wherein PL is a prodrug whose intracellular hydrolysis initiates

298 primarily of TAG (96.9% of total FA), while PL were the major component of both male (67.6%) and fem

299 , Ehrlich S, Meeker JD, Calafat AM, Williams PL, for the EARTH Study Team.

300 e kinetics in TA features is consistent with PL dynamics of energy-accepting MoS2 and PL quenching da