ライフサイエンスコーパス: LPP

1 LPP and palladin expression was markedly decreased, in c

2 LPP and simultaneous external urethral sphincter electro

3 LPP blunting during positive ER mediated the association

4 LPP children were less likely to have been ill recently

5 LPP expression in FAK-null fibroblasts enhanced cell spr

6 LPP expression was also markedly decreased in focal adhe

7 LPP frequency filtering is modified by the unique presyn

8 LPP immunotherapy, but not placebo, was associated with

9 LPP silencing with short interfering RNA significantly d

10 LPPs to positive pictures did not change across treatmen

11 LPPs to positive pictures did not change across treatmen

12 inhibition of lipid phosphate phosphatase-1 (LPP-1) by propranolol or inhibition of the phosphatidylc

13 Positivity for GADA was associated with 3q28/LPP, for IA-2A with 1q23/FCRL3 and 11q13/RELA, and for P

14 es (P=4.50x10(-34)), PTPN22 (P=1.31x10(-7)), LPP (P=1.01x10(-11)), IL2RA (P=2.78x10(-9)), UBASH3A (P=

15 Once localized to the adhesions, LPP was required for TGFbeta-induced increases in cell m

16 analyzed for prevalence, 241 patients had an LPP diagnosis (222 [92.1%] female; median [IQR] age, 64

17 the treatment analysis, 991 patients had an LPP diagnosis (907 [91.5%] female; median (IQR) age, 60

18 As predicted, performance on an LPP-dependent episodic memory task declined by late adul

19 h as myosin, actin, caldesmon, calponin, and LPP, were down-regulated in embryoid bodies (EBs) derive

20 t expansion and proliferation of HPP-CFC and LPP-CFC.

21 FAP5), focal adhesion kinase (FAK), ERK, and LPP.

22 The HPP and LPP had kwashiorkor prevalence of 4.5% and 1.7%, respect

23 ive potential colony-forming cells (HPP- and LPP-CFCs) indicates an expansion of stem cells which wil

24 Recombinant LiGGPPS, LiFPPS and LPP synthase (LPPS) proteins were active individually.

25 the dorsal premotor cortex to both P200 and LPP.

26 sponses, while women exhibited larger P3 and LPP amplitudes.

27 h larger positive ERP responses (P2, P3, and LPP).

28 ants showed significantly decreased P300 and LPP amplitudes to pleasant and unpleasant stimuli, espec

29 ytoskeletal proteins, including paxillin and LPP.

30 mpared to placebo, LSD-13 increased RewP and LPP amplitudes for reward (vs.

31 th a functional interaction between SHCA and LPP, TGFbeta-induced LPP localization to cellular adhesi

32 mily composed of zyxin, migfilin, TRIP6, and LPP.

33 Zyxin and LPP are implicated in cellular signaling and tumorigenes

34 cell adhesion, we demonstrate that zyxin and LPP function to increase the rate of early cell-cell jun

35 data implicate the LIM domains of zyxin and LPP in regulating cell-cell junction assembly through VA

36 We also identify the LIM region of zyxin and LPP to be a regulatory domain that blocks function of th

37 faster N170 latency to faces, and attenuated LPP amplitude to facial emotions, particularly subtle fa

38 Further, greater baseline LPP responses to positive pictures was associated with a

39 Further, greater baseline LPP responses to positive pictures were associated with

40 hange across treatment, but greater baseline LPPs to positive pictures predicted a higher likelihood

41 hange across treatment, but greater baseline LPPs to positive pictures predicted a higher likelihood

42 e direct peptide-protein association between LPP and BMP-RII.

43 h heightened amygdala activation and blunted LPPs to negative pictures showed the greatest increases

44 negative stimuli in combination with blunted LPPs could indicate overvaluation of threatening stimuli

45 Both LPP and palladin enhanced cell migration and spreading.

46 The expression of both LPP and palladin, like smooth muscle alpha-actin, was in

47 Here, we present an in-depth study of CSC by LPP, focusing on the complex interplay of the fundamenta

48 ex regulatory signaling cascade initiated by LPP and suggest that LPP may be a useful therapeutic sub

49 erm potentiation, which increases release by LPP terminals, enhanced within-train depression.

50 he conversion of extracellular S1P to Sph by LPP-1, which facilitates Sph uptake, followed by the int

51 es in syngeneic tumor-bearing FVB mice and C-LPP liposomes reduced doxorubicin accumulation in the sk

52 ockdown resulting from doxorubicin-loaded, C-LPP liposomes was similar to non-targeted liposomes in s

53 The binding of C-LPP liposomes conjugated with 0.63mol% of the peptide wa

54 carboxyl-terminated CRPPR peptide (termed C-LPP liposomes) bound to the NRP-positive primary prostat

55 Binding of the C-LPP liposomes was receptor-limited, with saturation obse

56 lar internalization was also enhanced with C-LPP liposomes, with 80% internalized following 3h incuba

57 cular and high molecular weight carbonylated LPP with 7-(diethylamino)coumarin-3-carbohydrazide (CHH)

58 Third, within each picture category, LPP-BOLD coupling revealed category-specific differences

59 In conclusion, LPP appears to be a myocardin-, RhoA/ROK-dependent SMC d

60 ion of FPPase activity for synthesis of CPP, LPP, and MPP.

61 (eq) and k(p) biases, which arise during CSC-LPP of comonomer mixtures.

62 ters, which enable the unique ability of CSC-LPP to precisely control comonomer sequences across a va

63 Seven of these genes (ARHGEF12, CTNNB1, LPP, MLLT4, PTEN, TCF12, and TFRC) harbored LoF variants

64 l diphosphate (CPP), lavandulyl diphosphate (LPP), and trace quantities of maconelliyl diphosphate (M

65 iphosphate (GPP) and lavandulyl diphosphate (LPP), respectively.

66 nzymes forming labda-13-en-8-ol diphosphate (LPP, TcCPS2) and (+)-copalyl diphosphate (CPP, TcCPS4),

67 t difference in peak bladder pressure during LPP testing whether measured with a transurethral or sup

68 here is no detectable upregulation of either LPP or TRIP6 expression in tissues derived from zyxin-nu

69 tudies showed that CAFs regulate endothelial LPP via a calcium-dependent signaling pathway involving

70 findings suggest that targeting endothelial LPP enhances the efficacy of chemotherapy in ovarian can

71 nt and unpleasant pictures elicited enhanced LPP, as well as heightened BOLD activity in both visual

72 )CRTH2(+) basophils were decreased following LPP treatment at V6 (10 ng/mL, P < .0001) and V8 (10 ng/

73 VPP, 6.1 mg L(-1) for IPP, 0.8 mg L(-1) for LPP and 3.2 mg L(-1) for FP were determined.

74 erminal endocannabinoid signaling needed for LPP-LTP induction and was offset by an agent that enhanc

75 her catheterization method could be used for LPP and/or EUS EMG testing in rats.

76 We previously identified a target gene, LPP/miR-28 (LIM domain containing preferred translocatio

77 ntaining IL2 and IL21, and at 3q28 harboring LPP.

78 o produce molecular constituents, the hybrid LPPs dissolve to produce NPs, with the drug release and

79 These hybrid LPPs exhibit much better flow and aerosolization propert

80 observed with CFHR1, CADM2, LOC730109/IL12A, LPP, LOC63920, SLU7, ADAMTSL1, C10orf64, OR8D4, FAM19A2,

81 C11orf30, STAT6, SLC25A46, HLA-DQB1, IL1RL1, LPP, MYC, IL2 and HLA-B.

82 Mutations that impaired LPP localization to adhesions (mLIM1) or impeded interac

83 tic and cell biological evidence implicating LPPs as negative regulators of lysophospholipid signalin

84 at V6 (all P < .05) and V8 (all P < .05) in LPP-treated group.

85 TS1; 3q28 (rs6444305, p = 1.10 x 10(-10)) in LPP; 18q21.33 (rs17749561, p = 8.28 x 10(-10)) near BCL2

86 n PLCL1 (rs10497813, P=6.1x10(-10)), 3q28 in LPP (rs9860547, P=1.2x10(-9)); 20q13.2 in NFATC2 (rs6021

87 Acute PNT caused a significant decrease in LPP and EMG amplitude and firing rate compared to other

88 ese processes, is significantly decreased in LPP.

89 t of A404 cells induced a strong increase in LPP, as well as SM alpha-actin, SM myosin heavy chain, a

90 ke Experiences group had larger increases in LPP amplitudes as the motivational salience of pleasant

91 of grass pollen-specific IgE was observed in LPP-treated but not placebo-treated group.

92 PNC resulted in a significant reduction in LPP and EMG firing rate 4 days, 3 weeks, and 6 weeks lat

93 potentiation (LTP) had a higher threshold in LPP field potential studies but not in voltage clamped n

94 aluative congruence (N170) and incongruence (LPP) between context and Face_2.

95 Results showed increased LPP amplitudes, increased hemodynamic responses in the c

96 cardin in A404 cells significantly increased LPP mRNA expression.

97 action between SHCA and LPP, TGFbeta-induced LPP localization to cellular adhesions depended on SHCA.

98 al) endocannabinoid messenger that initiates LPP-LTP.

99 SU1 modifies the activity of L. x intermedia LPP synthase (LiLPPS), thus accounting for the relativel

100 In this study we investigated LPP action in rabbit primary intervertebral disc cells c

101 inhibitory peptides, IPP (0.42-0.49 mg/kg), LPP (0.30-0.33 mg/kg), and VPP (0.32-0.35 mg/kg) were fo

102 positive feedback generally induced a larger LPP.

103 nction of context, eliciting somewhat larger LPPs when presented in blocks, and prompting smaller slo

104 Importantly, later (LPP), but not early (EPN), waveforms predicted actual ge

105 Excitatory afferents from lateral (LPP) and medial (MPP) perforant pathways of the EC conne

106 fects of citrus pectins obtained from lemon (LPP), orange (OPP), and bigarade (BPP) peels, at concent

107 Like LPP, palladin, is highly expressed in differentiated smo

108 acterized by the OUD+ group exhibiting lower LPP responses during Regulate compared to View trials re

109 and cigarette-related images prompted lower LPPs than high arousing emotional images in both groups.

110 3C/C2CD4A, FAF1, PTPRD, AP3S2, KCNK16, MAEA, LPP, WFS1, and TMPRSS6 loci.

111 y different and divergent from the mammalian LPPs.

112 Mechanistically, LPP increased focal adhesion and stress fiber formation

113 siRNA-mediated LPP silencing in ovarian tumor-bearing mice improved pac

114 -LTD require different group I mGluR, mGluR5 LPP-GC synapses and mGluR1 MPP-GC synapses.

115 Three-week immunotherapy with 170 mug LPP reduced CPT reactivity significantly and increased p

116 bo or cumulative doses of 70, 170 or 370 mug LPP.

117 ues obtained from modeling the SC's multiple LPP layers are -7.6 and -6.6 cm/s, and that from experim

118 (EPN) and later cognitively controlled (N2, LPP) patterns of neural response while viewing character

119 th autoimmune traits including rs715199 near LPP and rs10858023 near AP4B1.

120 Of note, LPP-based personalized cancer vaccine was administered i

121 counting for the relatively low abundance of LPP-derived irregular monoterpenes in this plant.

122 In neither experiment were there effects of LPP.

123 al adhesion kinase upregulated expression of LPP(2) and now show upregulation of palladin, and paired

124 Both forms of LPP frequency filtering are influenced by presynaptic, a

125 the treatment analysis were the frequency of LPP treatments within 1 year of diagnosis, and the numbe

126 erall, the data suggest that the function of LPP and palladin is context dependent, that they play a

127 stically bound to chromatin for induction of LPP/miR-28 transcription.

128 , the decrease in lymphatic flow and loss of LPP during PLN collapse are consistent with decreased dr

129 monstrate that the immunologic mechanisms of LPP immunotherapy are underscored by immune modulation i

130 ght to investigate immunologic mechanisms of LPP immunotherapy in a subset of patients who participat

131 ntribute to the generation and modulation of LPP are not well understood.

132 AECs expressed LPP1-3, and overexpression of LPP-1 enhanced the hydrolysis of exogenous [(3)H]S1P to

133 s function that triggers the pathogenesis of LPP.

134 pocampal slices during different patterns of LPP stimulation.

135 The palladin interacting region of LPP was mapped to the first and second LIM domains.

136 Down-regulation of LPP-1 by siRNA decreased intracellular S1P production fr

137 oth muscle cells.(1) Using the C-terminus of LPP as bait in a yeast two hybrid system, palladin, an a

138 This shows the ability of LPPs to accurately preserve a sample's genome informatio

139 s only modestly effective as an inhibitor of LPPs, is a potent inhibitor of SPP1; the activity was pa

140 d this was blocked by XY-14, an inhibitor of LPPs.

141 e 1 receptor, which mediates 2-AG effects on LPP-LTP, were similarly unaffected.

142 One LPP was sufficient to capture sequences from <100-500 bp

143 Similar to other LPPs, SPP1 activity was also independent of any cation r

144 lization potential of large porous particle (LPP) systems by spray drying solutions of polymeric and

145 also includes the lipoma preferred partner (LPP) and thyroid receptor-interacting protein 6 (TRIP6).

146 Fs upregulated the lipoma-preferred partner (LPP) gene in microvascular endothelial cells (MECs) and

147 Lipoma preferred partner (LPP) has been identified as a protein highly expressed i

148 Lipoma preferred partner (LPP) is a proline rich LIM domain family protein highly

149 protein (SHCA) and lipoma-preferred partner (LPP) mediate transforming growth factor beta (TGFbeta)-i

150 tein 6 (TRIP6) and lipoma-preferred partner (LPP), but not to zyxin itself.

151 in, zyxin, and the lipoma preferred partner (LPP).

152 gion, which we term the lateral place patch (LPP), contained a large concentration of scene-selective

153 of LTP expressed by lateral perforant path (LPP) input to the dentate gyrus (DG) was severely impair

154 ollowing capacity by lateral perforant path (LPP) projections from lateral EC to dentate gyrus were u

155 s (DG) branch of the lateral perforant path (LPP) reduces paired-pulse facilitation, is blocked by an

156 manner in which the lateral perforant path (LPP) transforms signals from entorhinal cortex to hippoc

157 jections than in the lateral perforant path (LPP), an effect associated with distinctions in transmit

158 The lateral perforant path (LPP)-dentate gyrus (DG) synapse operates as a low-pass f

159 he structure via the lateral perforant path (LPP).

160 free hydrolysates of Lolium perenne peptide (LPP) immunotherapy for rhinoconjunctivitis with or witho

161 Link protein N-terminal peptide (LPP) is a proteolytic fragment of link protein, an impor

162 gpASIT+) containing Lolium perenne peptides (LPP) and having a short up-dosing phase has been develop

163 lamellar phases: the long periodicity phase (LPP) and the short periodicity phase (SPP).

164 l-atom models of the long periodicity phase (LPP) in the stratum corneum (SC) are studied using bilay

165 ned the role of lipid phosphate phosphatase (LPP)-1 and sphingosine kinase1 (SphK1) in converting exo

166 trolled by two lipid phosphate phosphatases (LPP), wunen (wun) and wunen-2 (wun2).

167 gulated by the lipid phosphate phosphatases (LPPs).

168 wn type 2 lipid phosphate phosphohydrolases (LPPs), but similar to the yeast orthologs, mammalian SPP

169 Lichen planopilaris (LPP) is a form of scarring alopecia associated with prog

170 of the lymphocytic CA, Lichen planopilaris (LPP), compared to normal scalp biopsies identified decre

171 t frequent form of PCA, lichen planopilaris (LPP).

172 han solid targets for laser produced plasma (LPP) for extreme ultraviolet (EUV) and X-ray radiation s

173 ng a highly brilliant laser produced plasma (LPP) source with a scanning-free GEXRF setup, providing

174 lds (v(flow)) inside laser-produced plasmas (LPPs) have rarely been measured, owing to their small si

175 Here, we report Landau-phonon polaritons (LPPs) in magnetized charge-neutral graphene encapsulated

176 ported, and a linear Ppa-conjugated polymer (LPP) is reported as a control.

177 re we report that Lewis pair polymerization (LPP) capable of thermodynamically and kinetically compou

178 echanism by which Lewis pair polymerization (LPP) operates on polar vinyl monomers that allows the co

179 l the nature of a Lewis pair polymerization (LPP) system that has demonstrated itself to be an except

180 control (CSC) by Lewis pair polymerization (LPP) utilizes synergistically both thermodynamic (K(eq))

181 nd vesicle recycling may underlie the potent LPP-DG frequency filtering.

182 - the N170 and the Late Positive Potential (LPP) - in response to faces as putative mechanisms of PA

183 utcome was parietal late positive potential (LPP) and P300 amplitude during positive ER.

184 58) at baseline and late positive potential (LPP) data from 99 children (44 assigned to PCIT-ED vs. 5

185 58) at baseline and late positive potential (LPP) data from 99 children (44 PCIT-ED treatment vs. 55

186 The late positive potential (LPP) is a commonly used event-related potential (ERP) in

187 The late positive potential (LPP) is a reliable electrophysiological index of emotion

188 The late positive potential (LPP) is an event-related potential that is enhanced when

189 lowers), and higher Late Positive Potential (LPP) responses for emotional stimuli.

190 nd a high amplitude Late Positive Potential (LPP) when preceded by emotional contexts, thus showing s

191 tials (ERPs) in the late-positive potential (LPP) window have been observed.

192 nt images while the late positive potential (LPP), an event-related potential component that reflects

193 an emotion-related Late Positive Potential (LPP), both showing distinct latencies and amplitudes bet

194 attention, and the Late Positive Potential (LPP), reflecting sustained attention.

195 as measured by the late positive potential (LPP).

196 (EPN), P3, and the late positive potential (LPP).

197 s prompted a larger late positive potential (LPP, 400-700 ms) and a larger positive slow wave (1-6 s)

198 e same stimuli (the late positive potential [LPP], an event-related potential) in predicting increase

199 back-P3: FB-P3, and Late-Positive Potential: LPP).

200 avatars increased Late Positive Potentials (LPP), in line with previous evidence.

201 Late positive potentials (LPPs) for 'to-be-remembered' (TBR) relative to 'to-be-fo

202 es prompted larger Late Positive Potentials (LPPs, a robust measure of motivational relevance) than n

203 HCA clustering at the cell membrane preceded LPP recruitment.

204 ference test and the Lateral Paw Preference (LPP) test.

205 In an acute study, leak point pressure (LPP) and external urethral sphincter electromyography (E

206 on methods and order on leak point pressure (LPP) testing.

207 Lymphatic pumping pressure (LPP), measured indirectly by slowly releasing a pressuri

208 o-Pro (VPP), Ile-Pro-Pro (IPP), Leu-Pro-Pro (LPP) and Phe-Pro (FP) were separated on a C18-column cou

209 We used long padlock probes (LPPs) >300 bases in length for the assay, and the increa

210 present the utility of long padlock probes (LPPs) for targeted exon capture followed by array-based

211 oducts, such as lipid peroxidation products (LPP).

212 sequently, a Locality Preserving Projection (LPP) module constructs a shared latent space to achieve

213 om Atp7b(-/-) and Atp7b(+/-) (control) rats (LPP) and mice; some mice were given 5 daily injections o

214 Participants were randomized to receive LPP (n = 21) or placebo (n = 11) for 3 weeks over 4 visi

215 g), and 38.6% (70 mug) of patients receiving LPP vs 25.6% of patients receiving placebo (modified per

216 n, high comorbid participants showed reduced LPPs to negative pictures compared with low comorbid par

217 dy was to determine mechanisms that regulate LPP expression in an in vitro model of SM cell (SMC) dif

218 xamine how domains in zyxin and its relative LPP contribute to cell-cell junction assembly.

219 of invadopodia, a process that also required LPP.

220 um generates a skin pathology that resembles LPP, and that LPP patients show gene expression changes

221 PINB6, P=1.97 x 10(-8)) and 3q28 (rs9815073, LPP, P=3.62 x 10(-8)), as well as a new independent SNP

222 whereas for unpleasant pictures significant LPP-BOLD correlation was observed in ventrolateral prefr

223 t the control audio, corresponded to smaller LPPs to negative images.

224 -dimensional (2D) v(flow) measurements of Sn-LPPs ("double-pulse" scheme with a CO(2) laser) for extr

225 many trials are necessary to obtain a stable LPP?

226 re (mLPP) testing and electrical stimulation LPP (eLPP) testing in female rats to quantify the contri

227 Particularly, victims exhibited stronger LPP modulation and delayed mid-to-late components, sugge

228 In a chronic study, LPP and EMG were tested in 67 rats 4 days, 3 weeks, or 6

229 rovascular endothelial cells (MECs) and that LPP expression levels in intratumoral MECs correlated wi

230 skin pathology that resembles LPP, and that LPP patients show gene expression changes that indicate

231 further demonstrate by microstimulation that LPP is connected with extrastriate visual areas V4V and

232 Our data reveal that LPP promotes disc matrix production, which was evidenced

233 These results suggest that LPP is generated and modulated by an extensive brain net

234 ng cascade initiated by LPP and suggest that LPP may be a useful therapeutic substitute for direct BM

235 The LPP activity was mainly underpinned by brain regions inv

236 The LPP has also been evaluated as a neural marker of affect

237 The LPP predicted both internalizing and externalizing sympt

238 The LPP treatment analysis included all patients with LPP di

239 The LPP-based nanoscopy also tells apart two fundamental man

240 The LPP-formulated mRNA vaccines elicited robust neoantigen-

241 The LPP-LTP defect occurred in conjunction with a pronounced

242 Moreover, interactions between the LPP and stress continued to predict externalizing sympto

243 t episodic encoding is dependent on both the LPP and the endocannabinoid receptor CB1, and is strikin

244 form of synaptic plasticity expressed by the LPP (lppLTP) was profoundly impaired in Fmr1-KOs relativ

245 ong-term potentiation (LTP) expressed by the LPP was profoundly impaired by 8 months in rats and mice

246 d unpleasant information, as measured by the LPP, predispose children to psychiatric symptoms when ex

247 activity were substantially reversed by the LPP-resistant LPA analogue, O-methylphosphothionate.

248 e of SAAs was 32.4 [22.9-49.3] mg/kg for the LPP and 29.6 [18.1-44.3] mg/kg for the HPP (P < 0.05).

249 lit-half reliabilities were computed for the LPP and for difference waves revealing emotion effects (

250 iriform cortex were similar to those for the LPP, whereas adenosine modulation again correlated with

251 from the lavandulyl carbocation to form the LPP product.

252 Furthermore, the LPP varies little after 8 trials are added to the averag

253 However, the LPP component associated with the cognitive evaluation o

254 Prior work has implicated the LPP in episodic memory.

255 l of 170 children from 141 households in the LPP and 169 children from 138 households in the HPP comp

256 onse to erotica and smaller increases in the LPP as the motivational salience of pleasant images incr

257 osite pattern of results was obtained in the LPP branch that innervates the distal dendrites of CA3:

258 ed with MORE showed greater increases in the LPP during Regulate compared with View trials than patie

259 ograde trophic signaling-were reduced in the LPP terminal field.

260 elease probability, were much greater in the LPP than in CA3-CA1 connections.

261 t-risk groups showed larger increases in the LPP to threatening images but smaller increases to mutil

262 This arrangement of lipids in the LPP unit cell corresponds with the location of their lip

263 t the pollen season (-53.7%, P = .03) in the LPP-treated group compared with those in the placebo-tre

264 ut potent type of frequency filtering in the LPP.

265 questions: how internally consistent is the LPP, and how many trials are necessary to obtain a stabl

266 (performing mathematics) would modulate the LPP while participants viewed emotionally arousing stimu

267 The affective modulation of the LPP is believed to reflect the increased attention to, a

268 We used the mean amplitude of the LPP to assess the affective significance that participan

269 esults are further discussed in terms of the LPP's role in motivated attention and implications for r

270 ikingly, 250 ms before the occurrence of the LPP, P200 amplitude increased due to the experience of l

271 ly verified atomistic sandwich models of the LPP, will aid in the design and optimization of transder

272 ormation on the molecular arrangement of the LPP.

273 ly moderated the effect of meditation on the LPP, such that less sleepiness during meditation, but no

274 For pleasant pictures, the LPP amplitude was coupled with BOLD in occipitotemporal

275 Second, the LPP amplitude across three picture categories was signif

276 ndings of the current study suggest that the LPP demonstrates good internal consistency and can be ad

277 This suggests that the LPP may not be ideally suited to discriminate neurophysi

278 Results indicated that the LPP was larger following pleasant and unpleasant stimuli

279 In conclusion, we demonstrated that the LPP-based mRNA vaccine can elicit strong antitumor immun

280 tribution by each of these structures to the LPP modulation is valence specific.

281 ls nine diffraction orders attributed to the LPP with a repeating unit of 129.4 +/- 0.5 A.

282 To further validate the LPP model, umbrella sampling was used to calculate ethan

283 and rest was positively correlated with the LPP even after controlling for sleepiness.

284 To engineer the LPPs, we developed a method that generates ssDNA molecul

285 different enzymological properties than the LPPs: the aliphatic cation propanolol, which is an effec

286 ion properties than the NPs; yet, unlike the LPPs, which dissolve in physiological conditions to prod

287 tween male and female smokers with regard to LPP responses to cigarette-related images.

288 on of two dimethylallyl diphosphate units to LPP in vitro with apparent Km and kcat values of 208 +/-

289 the problem by correlating the single-trial LPP amplitude evoked by affective pictures with the bloo

290 Differences in the two LPP termination sites were also noted for frequency faci

291 d demonstrate the improved efficacy of using LPP-targeting siRNA in combination with cytotoxic drugs.

292 In stented pig coronary vessels, LPP was expressed in the neointima of cells lacking smoo

293 dized prevalence estimates of US adults with LPP across age, sex, and racial groups.

294 random sample and identified US adults with LPP diagnoses between 2017 and 2019.

295 ce and treatment patterns for US adults with LPP in a representative sample.

296 The N-terminus of palladin interacted with LPP both in vitro and in vivo, but not solely through it

297 reatment analysis included all patients with LPP diagnoses between 2016 and 2020 and a dermatologist

298 Most patients with LPP received treatment, and many received multiple treat

299 age-related increase in synaptophysin within LPP terminals, an effect suggestive of incipient patholo

300 Dominant-negative zyxin/LPP mutants reduce the rate of adhesion, lower VASP leve