ライフサイエンスコーパス: PL

1 PL activity during learning is required to initiate this

2 PL decay kinetics corroborated by DFT calculations revea

3 PL did not increase the peroxide values above the usual

4 PL excitation spectroscopy study unveils that PL enhance

5 PL inactivation disrupted active but not inhibitory avoi

6 PL lesions were also largest in the group of patients wi

7 PL levels measured before and during exposure demonstrat

8 PL spectra of anatase phase titania shows the peaks pres

9 PL-treated samples showed an increase in the concentrati

10 d induced PL from one-photon absorption (1PA-PL) suggests saturation of absorption and exciton-excito

11 Both 1PA- and 2PA-PL spatial mappings over large areas of single crystal p

12 e of IR excitation tuning, the origin of 2PA-PL excitation is suggested to arise from exciton dark st

13 ption induced exciton photoluminescence (2PA-PL) from these IO-MQWs, excited by infrared femtosecond

14 (ENG), 4% (FI), 12% (IT), 0% (NL), and 0.4% (PL) of residents; and "less frequently than daily" in 4%

15 ENG), 0.4% (FI), 6% (IT), 0% (NL), and 3.5% (PL) of residents.

16 aper highlights that not all networks with a PL degree distribution arise through a Barabasi-Albert (

17 lycans with linear poly-N-acetyllactosamine (PL) [-3Galbeta1-4GlcNAcbeta1-](n) extensions, which are

18 d the abundance of poly-N-acetyllactosamine (PL) [-3Galbeta1-4GlcNAcbeta1-](n) structures.

19 easily distinguished from amygdala activity, PL neurons could distinguish both valence and trial iden

20 To identify genes capable of affecting PL transport, we screened for genetic interactions with

21 s experimental approach is applicable to all PL-active materials to distinguish intrinsic defects fro

22 ity improvement in terms of antioxidants and PL enrichment without compromising total milk fat, sugge

23 the high levels of fatty acid elongation and PL-VLCFA accumulation that occur in HCMV-infected cells.

24 (photoreceptor length, OS length, FDI), and PL VA were obtained in preverbal children for comparison

25 lipin1 depletion required TG hydrolysis and PL synthesis.

26 a cued appetitive go/no-go task, both IL and PL inactivation impaired inhibitory but not active rewar

27 LFL and PL were associated with death (OR 13.20, 95%CI 5.21-33.7

28 and temperature-independent PL linewidth and PL lifetime (between room temperature and ~5 K).

29 erstanding of eicosanoid, prostaglandin, and PL biology in health and disease.

30 future VA than quantitative segmentation and PL testing.

31 that direct communication between the VH and PL during training is necessary for contextual fear memo

32 ns with mlaA*, a mutant in which anterograde PL transport causes the inner membrane (IM) to shrink an

33 d on the silver standard created by applying PL on unlabeled patient records, are comparable in perfo

34 Importantly, despite the closely arrayed PL units (~2 nm), the dyes behave as bright chromophores

35 r with ~20 % quantum yield and an attractive PL maximum of 450 nm.

36 rent PL methods indicated that TurboID-based PL provides more efficient levels of biotinylation than

37 and increased anatomical connections between PL and BLA.

38 veals that AB stacking possesses blueshifted PL peak positions, and broader peak widths, compared wit

39 We suggest that both PL enhancements are mainly attributed to the porous stru

40 Most importantly, bovine PL injection restored beta-cell proliferation and blood

41 ilar broad projections throughout the brain, PL neurons TRAPed later have a stronger functional recru

42 This broad PL presents the hypothesis of CTEs, verified by the excl

43 nge of energies, resulting in the very broad PL.

44 Bidirectional modulation of avoidance by PL projections to VS and BLA enables the animal to make

45 hase-separation domain sizes as evidenced by PL quenching and resonant soft X-ray scattering (R-SoXS)

46 veal grading was compared with prediction by PL, the current gold standard for visual assessment in i

47 by using a high spatial-resolution confocal PL system indicate that the two emissions origin from di

48 Scanning confocal PL measurements have been performed across BSFs regions

49 re importantly, the two-photon up-conversion PL is found to be sensitive to an external magnetic fiel

50 tic decrease in the two-photon up-conversion PL signal.

51 lta(E) = 1.5 +/- 0.2 eV with a corresponding PL peak centered at 1.25 +/- 0.07 eV.

52 synapses in the prelimbic prefrontal cortex (PL-PFC).

53 cue-elicited firing in the prelimbic cortex (PL).

54 ys with the slowest component of the crystal PL absent.

55 f WT mice at trend level, but decreased D3KO PL area glial cell density.

56 Gate and magnetic-field dependent PL measurements unveil a circularly-polarized replica pe

57 measurements and excitation-power dependent PL measurements have been performed, further validating

58 Evaluation of different PL methods indicated that TurboID-based PL provides more

59 However, it is unknown how and when distinct PL afferents contribute to different associative compone

60 he most basic membrane building blocks, i.e. PLs, are shuttled across the cell envelope remain elusiv

61 eride acyltransferases (DGATs) and enhancing PL synthesis through the Kennedy pathway promoted axon r

62 ission wavelengths, yielding single ensemble PL dynamics.

63 scence (PL) peak energy, and non-exponential PL decay curves that varied across the PL spectra at 10

64 ectronic states resulting in reasonably fast PL decays (~1 ns), large vibrational energy spacing, sma

65 Using variable magnetic field PL spectroscopy, we resolved emission into each of the g

66 Like the crystals, the film PL decays as a single ensemble.

67 istence of a high-flux diffusive pathway for PL flow in Escherichia coli that is modulated by YhdP.

68 data further support a suppressive role for PL in cocaine seeking by implicating PL efferent project

69 e hypothesized that these opposing roles for PL may be supported by distinct efferent projections.

70 esting that VS receives opposing inputs from PL and BLA.

71 silateral and contralateral projections from PL to RMTg have an inhibitory influence on behavior.

72 dissymmetric factors of photoluminescence (g(PL) ) less than 10(-2) .

73 This combination increases the |g(PL) | of the superhelicene from approximately 3x10(-4) i

74 habit, clinical characteristics of gingival PL lesions, and location, tumor-node-metastasis (TNM) st

75 : group 1 included 33 patients with gingival PL that did not progress to cancer, and group 2 included

76 al characteristics of patients with gingival PL with and without progression to oral squamous cell ca

77 inferior to VA prediction by foveal grading (PL: r = 0.42, F = 3.12, P < 0.03).

78 ient conditions and exhibits two-fold higher PL emission compared with the pristine (HA)(2) (GA)Pb(2)

79 We conclude that the human PL contains excitatory neurons that remain immature for

80 lated PL terminals in VS and BLA to identify PL outputs regulating avoidance.

81 coeruleus mimics this shift in reciprocal IL-PL spike firing, increases the expression of conditioned

82 ole for PL in cocaine seeking by implicating PL efferent projections to RMTg in inhibiting cue-induce

83 teens may largely reflect circuit defects in PL-PFC networks communicating through endocannabinoid-re

84 Synaptic drive in PL was increased in both TMT and H(2)O mice following ba

85 Thus, fear-encoding ensembles in PL cortex drive long-term fear expression in a sex and f

86 unveil the impact of DB-position isomers in PL metabolism.

87 A narrowing in PL linewidth with increasing NWs diameter is correlated

88 ces in basal theta and gamma oscillations in PL and IL.

89 iton annihilation, with typical reduction in PL radiative relaxation times from 270 ps to 190 ps upon

90 itiate this time-dependent reorganization in PL ensembles underlying memory retrieval.

91 s the maximal solubility reported for TGs in PL bilayers (2.8%).

92 In contrast, adiponectin treatment increased PL expression in human placenta explants and JEG3 tropho

93 ll Stokes shift, and temperature-independent PL linewidth and PL lifetime (between room temperature a

94 However, the published data on individual PL classes in the pig muscle are inconsistent.

95 clude that the two-photon absorption induced PL is highly sensitive to the self-assembly process of f

96 High intensity femtosecond induced PL from one-photon absorption (1PA-PL) suggests saturati

97 ool to visualize PL distributions, inferring PL identities from MSI experiments is challenging.

98 ow cytometry and cross-polarised light (ISX(+PL)) to rapidly and reliably visually isolate and quanti

99 trol mice (baseline and posttreatment mean k(PL), 0.011 and 0.017 sec(-1), respectively, P = .91; bas

100 e with glioma (baseline and treatment mean k(PL), 0.027 and 0.018 sec(-1), respectively, P = .01; bas

101 t an approach referred to as polar labeling (PL), to create silver standard for training machine lear

102 Here, we used proximity labeling (PL) to identify the proteome proximal to N, which is an

103 By contrast, smaller N-glycans lack PL and are enriched in alpha2,6-linked sialic acids.

104 Addition of pyruvate and L-lactate (+PL) to RN at 50% of standard concentrations restored bla

105 It was reported that placental lactogen (PL) plays a crucial role in pregnancy-induced maternal b

106 fluor fixed into a masked porphyrin lantern (PL) state, due to intramolecular host-guest interactions

107 egree distribution that follows a power-law (PL) pattern.

108 tional breakdown theory using Paschen's law (PL), driven by Townsend avalanche, fails for gap distanc

109 depolarizing response to NMDA in deep-layer PL-PFC neurons analyzed by current-clamp recordings.

110 seen: Large focal leak (LFL), punctate leak (PL) and vessel leak.

111 ecently coined as proliferative leukoplakia (PL), is associated with a strong tendency to recur after

112 The efficacy of pulsed light (PL) for the surface decontamination of ready-to-eat dry-

113 monolayer surface (SURF-TG) are ordered like PLs with the glycerol moiety exposed to water, creating

114 al hazards (Cox PH) model and product-limit (PL) estimator.

115 (GSL)-glycans, which also consists of linear PL, terminating in mainly alpha2,3-linked sialic acid.

116 Dairy polar lipids (PL) seem to exhibit antiplatelet effects.

117 l memory deficit and the disruption of local PL firing during optogenetic silencing of VH-PL suggest

118 such as monolayer MoS(2), often exhibit low PL QY for as-processed samples, which has typically been

119 ase, beta-amylase, chitinase, pectate lyase (PL), pectinesterase (PE) and polygalacturonase (PG)), en

120 ciences, fall into ten polysaccharide lyase (PL) families.

121 y to PCer, suggesting that the ceramide/lyso-PL interaction was not sensitive to structural alteratio

122 It is concluded that ceramides and lyso-PLs associated with each other both in binary bilayers a

123 Other saturated lyso-PLs (e.g., palmitoyl lyso-phosphatidylethanolamine and l

124 large-headgroup co-lipid, and saturated lyso-PLs were preferred co-lipids over DOPC because of the na

125 posed that the interaction of PCer with lyso-PLs was driven by the need of ceramide to obtain a large

126 The levels of many PL-VLCFAs were lower in subUL37x1-infected cells than in

127 and activity of NMDA receptors in the mature PL-PFC.

128 MFGM-PL treatment to HFD dams decreased the body weight gain

129 MFGM-PL+HFD offspring showed promoted thermogenic function in

130 In adulthood, maternal MFGM-PL supplementation reduced adiposity and increased oxyge

131 In conclusion, maternal MFGM-PL treatment activated thermogenesis in offspring, which

132 ids-enriched milk fat globule membrane (MFGM-PL) supplementation to high-fat diet (HFD) rats during p

133 pregnancy and lactation with or without MFGM-PL.

134 In TMT mice, but not vanilla or H(2)O mice, PL layers 2/3 showed heightened spontaneous excitatory p

135 Milk PL content-20% higher in the CPE-supplemented group-was

136 the antithrombotic properties of ovine milk PL.

137 Here, we optogenetically modulated PL terminals in VS and BLA to identify PL outputs regula

138 In children, most PL cells are immature (DCX+PSA-NCAM+), and during adoles

139 The mRNA levels of mouse PL genes were robustly decreased in the placentas of Adi

140 At 37 degrees C, N&PL by itself forms coexisting L(alpha) and L(beta) phase

141 Mixtures with different ratios of N&PL and CLSE provided the same set of lipids with differe

142 The mixed samples of N&PL with CLSE show that increasing amounts of the protein

143 contained the nonpolar and phospholipids (N&PL) obtained from calf lung surfactant extract (CLSE), w

144 immature neurons in the paralaminar nuclei (PL), suggesting protracted development and possibly neur

145 Using BPh, PB product ions of numerous PL classes are readily generated to pinpoint the locatio

146 We simultaneously observe PL brightness, emission spectrum, and in-plane excitatio

147 G) are disordered and increase the amount of PL packing defects and the PL tail order.

148 ic pH was 4, the average bioaccessibility of PL, PN, and PM were 38%, 67%, and 36%, respectively.

149 Comparison of PL and SIMS data has revealed that apparently high conce

150 Functional disconnection of PL-RMTg via contralateral inactivation markedly increase

151 Tr-OxPL generation by ectopic expression of PL-specific platelet-activating factor acetylhydrolase 2

152 so observed with ipsilateral inactivation of PL and RMTg, but not with unilateral inactivation of PL

153 MTg, but not with unilateral inactivation of PL or RMTg alone, indicating that both ipsilateral and c

154 of transcription 5, a downstream molecule of PL signaling, was observed in islets from Adipoq (-/-) d

155 mation, we compared the coding properties of PL and amygdala neurons during a task that requires rats

156 permeability barrier, modulates the rate of PL transport during mlaA*-mediated lysis.

157 sly showed that inhibitory tone responses of PL neurons correlate with avoidability of shock (Diehl e

158 o expose local isomer-specific metabolism of PLs.

159 Thus, when the supply of PLs is limited, SURF-TG may reduce surface tension by be

160 ading to the formation of truncated oxidized PL products (Tr-OxPLs), which exhibit deleterious effect

161 maneuver (LRM) in the presence of elevated P(PL) on hemodynamics, left and right ventricular pressure

162 We hypothesized that elevated P(PL) protects the cardiovascular system against high airw

163 EPs in a model of swine with ARDS and high P(PL) (n=9) versus healthy swine with normal P(PL) (n=6).

164 ARDS swine with high P(PL) demonstrated unchanged transmural left ventricle pre

165 PL) (n=9) versus healthy swine with normal P(PL) (n=6).

166 haracterized by elevated pleural pressure (P(PL)) and worsening atelectasis during mechanical ventila

167 In particular, PL analysis supplemented by reactive ion etching up to t

168 s and is highly correlated with the area per PL or the expansion of the monolayer.

169 Thus, high-luminescent efficiencies (Phi(PL) = 0.61 and 0.77) along with short lifetimes (tau < 2

170 sterol esters, surrounded by a phospholipid (PL) monolayer.

171 but very little is known about phospholipid (PL) transport.

172 at content-fatty acid (FA) and phospholipid (PL) composition-were monitored.

173 l partitions between different phospholipid (PL) environments using different methods based on choles

174 Nevertheless, several phospholipid (PL) subclasses involved in stabilizing brain membranes w

175 TG) storage lipids rather than phospholipid (PL) membrane lipids in neurons.

176 ing dry-cured ham processing, phospholipids (PL) are the main substrates of lipolysis and oxidation.

177 tional isomers of unsaturated phospholipids (PL) in tissue sections by use of refined matrix-assisted

178 ding in the outer leaflet and phospholipids (PLs) in the inner leaflet.

179 ell membranes and circulating phospholipids (PLs), leading to the formation of truncated oxidized PL

180 The location and identity of phospholipids (PLs) within tissues can serve as diagnostic markers for

181 Photoactivating PL-VS projections reduced avoidance, whereas photoactiva

182 s reduced avoidance, whereas photoactivating PL-BLA projections increased avoidance.

183 Photoluminescence (PL) imaging and the spatial-resolved PL intensity and li

184 Photoluminescence (PL) was used to estimate the concentration of carbon in

185 Here, a photoluminescence (PL) measurement of single-crystal BAs at different tempe

186 ced by UV-vis absorption, photoluminescence (PL) spectroscopies, thermal analysis, and grazing incide

187 ) Br(5) , its bandgap and photoluminescence (PL) origin have generated intense debate and remained co

188 unneling spectroscopy and photoluminescence (PL) reveal that the electronic gap is Delta(E) = 1.5 +/-

189 gap (1.88 +/- 0.5 eV) and photoluminescence (PL) spectrum of CdSe QDs with a peak intensity at 556 nm

190 icated that the broadband photoluminescence (PL) from (110) perovskites arises from a distribution of

191 two-photon up-conversion photoluminescence (PL) by directly exciting the gap states with continuous-

192 ns that exhibit efficient photoluminescence (PL).

193 pite the strong excitonic photoluminescence (PL) of monolayer transition metal dichalcogenides (TMDs)

194 hibit unique blueshift in photoluminescence (PL) upon compression, which is in contrast to many other

195 ted narrow, near-infrared photoluminescence (PL) from a spin-singlet excited state.

196 The long photoluminescence (PL) lifetime enables time-gated (TG) detection without a

197 The emission has a long photoluminescence (PL) lifetime of 582 ns, while the intensity is constant

198 Cryogenic single-particle photoluminescence (PL) spectroscopy has been used with great success to dir

199 Polarized photoluminescence (PL) reveals that AB stacking possesses blueshifted PL pe

200 g in an enhancement of QD photoluminescence (PL).

201 tism (AFM) and strong red photoluminescence (PL).

202 Here we report photoluminescence (PL) emission from tBLG after resonant 2-photon excitatio

203 by polarization-resolved photoluminescence (PL) spectroscopy.

204 ermittency of solid-state photoluminescence (PL) can be used to probe chemical transformations on the

205 compounds exhibit strong photoluminescence (PL) at room temperature.

206 ion patterns of the SWCNT photoluminescence (PL).

207 erature dependence of the photoluminescence (PL) peak energy, and non-exponential PL decay curves tha

208 s substantially lower the photoluminescence (PL) quantum yield (QY), a key metric of optoelectronic p

209 h manifests itself as the photoluminescence (PL) quenching to PL enhancement transition.

210 gths was calculated using photoluminescence (PL) spectroscopy.

211 d green luminophore with a photoluminescent (PL) efficiency up to 93%.

212 Local photoluminescent (PL) images obtained with an immersion oil objective lens

213 Moreover, photosilencing PL-BLA or BLA-VS projections reduced avoidance, suggesti

214 Here, we show that the dorsal, prelimbic (PL) region of the medial PFC aids active avoidance in si

215 eld potentials were recorded from prelimbic (PL) and infralimbic (IL) mPFC during retrieval.

216 This avoidance requires prelimbic (PL) PFC, basolateral amygdala (BLA), and ventral striatu

217 Specifically, the rodent prelimbic (PL) prefrontal cortex drives fear expression during both

218 The prelimbic (PL) and infralimbic (IL) regions of the medial prefronta

219 cortex (mPFC), we found that the prelimbic (PL) and infralimbic (IL) subregions of the mPFC had elev

220 The prelimbic (PL) area and basolateral amygdala (lateral [LA] and baso

221 The prelimbic (PL) region of prefrontal cortex has been implicated in b

222 rve almost perfectly polarization-preserving PL emission from chiral excitons.

223 High-pressure PL spectra show that the donor level with respect to the

224 Intravenously administered procoagulant PL caused clotting factor activation and depletion, indu

225 Thus, procoagulant PL regulate AAA development through complex interactions

226 induced beta-cell proliferation by promoting PL expression in trophoblast cells.

227 eries of polyunsaturated phospholipids (PUFA-PLs), specifically phosphatidylinositol (-PI) lipids lin

228 of CsPb(2) Br(5) ; pressure-dependent Raman-PL with a diamond anvil cell as a dynamic probe further

229 Same-spot Raman-PL as a static property-structure probe reveals that CsP

230 volume in both WT and D3KO mice, and reduced PL area volume in D3KO mice both at trend level.

231 A remarkable PL enhancement by 12 fold is achieved using pressure to

232 scence (PL) imaging and the spatial-resolved PL intensity and lifetime scanning confirm the electroni

233 Time-resolved PL measurements reveal an increase in excited-state life

234 In addition, blastocysts produced in RN + PL contained more ICM cells and ATP than blastocysts cul

235 in driving reinstatement of cocaine seeking, PL projections to the rostromedial tegmental nucleus (RM

236 Importantly, males also showed PL/IL theta activation during safety signalling by the C

237 Steady-state PL spectra show a broad strong emission centered at ~700

238 functional theory (DFT) calculations suggest PL transitions arise from defects within a CuAl(5) S(8)

239 ipids with very-long-chain fatty acid tails (PL-VLCFAs) that contain 26 or more carbons in one of the

240 is stable and determines the width of the TG-PL overlap, whereas that caused by SURF-TG fluctuates an

241 We demonstrate that PL is a very sensitive and reliable tool to determine th

242 After the discovery that PL centers occupy only specific morphological structures

243 ation of mlaA*-mediated lysis suggested that PL transport can occur via a high-flux diffusive flow me

244 L excitation spectroscopy study unveils that PL enhancement arises from the blockage of the optically

245 The PL data were compared with profiles of the impurities ob

246 The PL emission of the LSCs is centered at about 700 nm with

247 The PL emission of these centers is extremely bright-50 time

248 ntial PL decay curves that varied across the PL spectra at 10 K.

249 using specific starter cultures altered the PL composition.

250 ase the amount of PL packing defects and the PL tail order.

251 fast compared to the PL, which averages the PL decay at all emission wavelengths, yielding single en

252 This study determined the PL class contents and composition in biceps femoris of I

253 nnection approach to temporarily disrupt the PL-RMTg pathway during cue- or cocaine-induced reinstate

254 ual valence plays a critical role in how the PL is recruited in initiating or suppressing actions, wh

255 of ventral hippocampal (VH) terminals in the PL of adult male Long-Evans rats selectively during pair

256 ynaptic function in layer 2/3 neurons in the PL, which are consistent with previous findings that CRF

257 Electron microscopic immunolabeling in the PL-PFC of adult mice that had received Delta9-THC only d

258 rast, the TGs that intercalate just into the PL tail region (CORE-TG) are disordered and increase the

259 CLZ increased volume of the PL area of WT mice at trend level, but decreased D3KO PL

260 Based on the dependences of the PL spectra on the energy and polarization of incident ph

261 ed, as well as a surprising splitting of the PL spectrum into two bands with an average energy separa

262 ine and evaluate the bioaccessibility of the PL, PN, and PM forms of vitamin B(6) in cereal-based bab

263 Here, we report on the PL properties of Molecular Beam Epitaxy grown, SC InAs N

264 In this study, the PL, PN, and PM forms of vitamin B(6) were determined usi

265 sorption microscopy results suggest that the PL drop may derive from a higher concentration of traps

266 We show that the PL QY of as-processed MoS(2) and WS(2) monolayers reache

267 necessity of direct hippocampal input to the PL for the acquisition of trace-cued fear memory and the

268 ronments on time scales fast compared to the PL, which averages the PL decay at all emission waveleng

269 suggest that the VH continuously updates the PL with the current contextual state of the animal, whic

270 erentiate between their smells utilizing the PL response pattern.

271 Thus, PL has greater representational capacity.

272 ry nanometer scale structural information to PL spectroscopy, but the two techniques have not been co

273 Among the prominent inputs to PL, the hippocampus shares with PL a role in both workin

274 f as the photoluminescence (PL) quenching to PL enhancement transition.

275 nimum; at lower pressures, the transition to PL occurs to the left of the minimum.

276 these parameters cause V(B) to transition to PL to the left of the Paschen minimum, which would yield

277 e of the Paschen minimum V(B) transitions to PL as pressure approaches atmospheric pressure while fie

278 At atmospheric pressure, V(B) transitions to PL near the product of pressure and gap distance, pd, co

279 Total PL and PC, PE, phosphatidylinositol + phosphatidylserine

280 ehyde composition, mainly in PE and in total PL.

281 synthesis away from TG synthesis and toward PL synthesis may promote axon regeneration.

282 Pathways that transport PLs across the bacterial cell envelope are fundamental t

283 Chemogenetic inhibition of TRAPed PL cortex ensembles reduced conditioned suppression of f

284 s offers a high promise to deeper understand PL metabolism and isomer-specific functions in health an

285 basis of our analysis, we find an unexpected PL increase (~ 540 nm) at the oil/shell interface.

286 baclofen/muscimol (1/0.1 mM) into unilateral PL and the AMPA receptor antagonist NBQX (1 mM) into con

287 regation in a ternary bilayer of unsaturated PL/N-palmitoyl-D-erythro-sphingomyelin and cholesterol.

288 holesterol was for the different unsaturated PLs, the more cholesterol stimulated lateral segregation

289 that allows functionalization of unsaturated PLs during the MALDI process via a laser-light driven Pa

290 PL firing during optogenetic silencing of VH-PL suggest that the VH continuously updates the PL with

291 demonstrating the biomarker recognition via PL.

292 or I) is responsible for the strong visible PL in CsPb(2) Br(5-) (x) X(x) .

293 s a powerful bioanalytical tool to visualize PL distributions, inferring PL identities from MSI exper

294 Whereas PL and BL neurons represented many different parameters

295 However, it remains unclear whether PL cortex neuronal ensembles that encode fear memory con

296 While PL projections to nucleus accumbens core have been shown

297 ancer, and group 2 included 30 patients with PL who developed malignant transformation during follow-

298 ciated with gingival cancer in patients with PL.

299 nt inputs to PL, the hippocampus shares with PL a role in both working memory and contextual processi

300 ed antithrombotic properties of the yoghurts PL fractions against platelet-activating factor (PAF) an