ライフサイエンスコーパス: second phase

1 gdom (UK) and The Netherlands were analyzed (second phase).

2 ht at home (n = 97 in first phase; n = 17 in second phase).

3 ly has high fatigue resistance but without a second phase.

4 t are large compared with the spacing of the second phase.

5 ranscriptional phase and increase during the second phase.

6 potential to contribute significantly to the second phase.

7 and then exhibited a distinct flat or slower second phase.

8 st phase and 65 patients in 3 centers in the second phase.

9 ceased on the cocaine-paired side during the second phase.

10 e to 96%, 94%, and 83%, respectively, in the second phase.

11 uitment to the enhancer is important for the second phase.

12 hase, and a slow and sustained (24-72 hours) second phase.

13 statistically significant differences in the second phase.

14 demonstrate the role of myosin efflux in the second phase.

15 pe via a DNA end) were not influenced by the second phase.

16 : 23-58) was followed by a slower or plateau second phase.

17 integrity in two phases and apoptosis in the second phase.

18 in two phases, and apoptosis occurred in the second phase.

19 ng materials, whereas the sulfides contained second phases.

20 hrough embedding endotaxially nanostructured second phases.

21 In the second phase, 149 patients underwent education/follow-up

22 In the second phase (20-45 min), p300 is recruited to ERalpha b

23 Initial results from the second phase 3 trial (intravenous to oral therapy design

24 ents were evaluated in 7 centers, and in the second phase 40 patients were evaluated in 2 centers.

25 After the second phase, 54% (95% CI 35-72) tolerated 1400 mg chall

26 In the second phase, 59 scientists, 21 patients, and 31 stakeho

27 In the second phase, 79 slides from patients with BE (23 sample

28 The second phase addresses identification of the aTIS codon

29 During the second phase, after completion of the initial behavioral

30 In the second phase, all stool samples were tested by GDH and X

31 nt, the more homogeneous distribution of the second phase along the boundaries, and the more uniform

32 The second phase also is associated with a spatial transitio

33 a-TNFR1 feedforward signaling, promoting the second phase and driving RIP1 phosphorylation.

34 ed minimum internal electronic short-circuit second phase and external electronic short-circuit decor

35 erved in BiFeO3 based thin films, iron oxide second phases are often detected.

36 h is most effective when spacing between the second phase assumes the critical crack length of the me

37 ic fields (60T) by increasing the density of second phase BaZrO3 nanoparticles.

38 In the second phase, bedside clinicians were additionally assis

39 A second phase begins around week 2.5 to 3, in which relat

40 In the second phase, beta-sheet forms in the polyQ.

41 In the second phase, between days 6 and 13, magnetic resonance

42 fficacy criteria for further analysis in the second phase by reducing renal endpoints 15 to 27% compa

43 In the second phase, Cdk5 activates c-Jun via ROS-mediated acti

44 In the second phase, chains are elongated in a multidirectional

45 f bone marrow-derived macrophages preceded a second phase, characterized by accelerated progression o

46 The second phase, characterized by stable DC-T cell contacts

47 In the second phase content analysis of 33 audio-recorded prima

48 methods to successfully engineer porosities, second phase, crystallography shear-planes and oxygen va

49 In the second phase, de novo synthesis generates ceramide that

50 We show that the rate of second phase decay is determined by the death rate of in

51 First- and second-phase decay rates of plasma HIV-1 were compared i

52 a: -0.29; liver, -0.009; P < 0.001), whereas second-phase decline (posttreatment days 4-15) did not d

53 ath/loss of productively infected cells, the second-phase decline in viral RNA with a dose of 250 U/m

54 o modeling prediction that the more profound second-phase decline observed in IFN-alpha-treated patie

55 model, the C/C genotype predicted a steeper second-phase decline when adjusted for race (P = .01).

56 ents who received ribavirin had a more rapid second-phase decrease, compared with patients who did no

57 The second phase demonstrates how real measurements could be

58 the volume fraction, morphology, and size of second-phase dendrites to confine any initial deformatio

59 damage in causing cell death, whereas in the second phase, depletion of MDMX inhibited cell death.

60 In the second phase, different participants were sequentially a

61 itial phase at a constant rate followed by a second phase during which the constriction rate decrease

62 vels decreased approximately 15%, and in the second phase ending at T(release), remaining CaDPA was r

63 shes the molecular circuitry that during the second phase ensures a compatible interaction with the p

64 In the second phase, ERK1/2 is activated by tPA independently o

65 ocytosis was reduced to basal (P < 0.05) and second-phase exocytosis abolished (P < 0.05) by syn1a kn

66 creased, accompanied with the formation of a second phase, FeNi3, which is softer with a lower work f

67 la enterica serotype Typhimurium but lacking second-phase flagellar antigens, has increased considera

68 s to PI3K or Akt attenuated Formalin-induced second-phase flinching behavior, as well as carrageenan-

69 In the second phase, fMRI of response inhibition showed the exp

70 mechanical coupling in solution, providing a second phase for their study and demonstrating the feasi

71 -1A-betaKO islets showed impaired first- and second-phase glucose-stimulated insulin secretion (GSIS)

72 te an essential positive role for Munc18c in second-phase GSIS and suggest novel roles for Munc18c in

73 of Syt-7 in human islets reduced first- and second-phase GSIS attributed to the reduction of exocyto

74 dock) newcomer SGs accounted for the reduced second-phase GSIS.

75 ment of releasable pools required to sustain second-phase GSIS.

76 n, increased islet Ca2+ influx, and enhanced second-phase GSIS.

77 ximately 60% less insulin selectively during second-phase GSIS; RNAi-mediated Munc18c depletion funct

78 In a slow second phase, GtfB recognizes residues that are already

79 rimary afferent sensory neurons, whereas the second phase has been proposed to reflect the combined e

80 ively HCV-infected cells, estimated from the second phase HCV RNA decline slope, is very variable and

81 ndent and swelling intensity correlates with second phase impedance decrease implicating a causative

82 None of the patients with flat second phase in HDV achieved CVR.

83 The observation that a flat second phase in HDV and HBsAg kinetics was associated wi

84 Effectiveness of a second phase in metallic glass heterostructures to impro

85 rms approximately 900-fold less rapidly as a second phase in the reaction under turnover conditions a

86 ase of endosperm proliferation followed by a second phase in which the embryo grows at the expense of

87 m to form a large seed cavity, followed by a second phase in which the embryo grows to replace the en

88 into the band alignment between PbS and the second phases in these materials.

89 This is a pre-requisite for the second phase, in which the Par complex localises to the

90 etection, localization and quantification of second phase inclusions in thin Aurivillius type films.

91 The second phase incorporated findings from phase 1 to devel

92 tolerance test results in improved first and second phase insulin release in response to intravenous

93 ated islets results in the selective loss of second phase insulin release.

94 ads to striking increases in both first- and second-phase insulin release, greatly improved glucose t

95 hesion plaques, multimolecular platforms for second-phase insulin release.

96 oxidation (indirect calorimetry), first- and second-phase insulin secretion (2-h hyperglycemic clamp)

97 quantify the role of incretins in first- and second-phase insulin secretion (ISR) in type 2 diabetes

98 f improvements in indexes of both first- and second-phase insulin secretion (P < 0.02), but with no c

99 First- and second-phase insulin secretion and C-peptide were lower

100 l TALK-1 channels as important modulators of second-phase insulin secretion and suggest a clinically

101 incubation with glucose and the reduction in second-phase insulin secretion induced by blocking R-typ

102 The model indicates that increased second-phase insulin secretion induced by the amplifying

103 Glucose sensitivity of first- and second-phase insulin secretion showed a significant cond

104 Second-phase insulin secretion sustains insulin release

105 kedly decreased in both IFG and IGT, whereas second-phase insulin secretion was decreased only in IGT

106 rglycemic clamp (+125 mg/dL), and first- and second-phase insulin secretion were quantitated.

107 se islets revealed a significant increase in second-phase insulin secretion with a trend toward incre

108 proximal glucose-specific trigger to elicit second-phase insulin secretion, signals downstream to ac

109 n secretion (FPIR), insulin sensitivity, and second-phase insulin secretion.

110 The second phase involved the development of a Markov model

111 2+) from endoplasmic reticulum stores, and a second phase involving STIM 1 (stromal interaction molec

112 on the outcome of any defense response, the second phase is a period of syncytium maintenance (susce

113 reduced by up to approximately 29% when the second phase is added.

114 lds in a biphasic process, in which only the second phase is affected by the known mutations.

115 The second phase is dedicated to the assembly of [4Fe-4S] pr

116 The second phase is defined by A20, whose inducible expressi

117 The second phase is dependent on the activation of the chlor

118 A second phase is exponential, seen in early-onset cancers

119 o a prehairpin intermediate (PHI), while the second phase is marked by transition from the PHI to the

120 Strengthening by precipitation of second phase is the guiding principle for the developmen

121 The second phase is the loss of CR and reduction to the dife

122 utrition perfusion augmented both first- and second-phase ISR but first-phase ISR more in T2DM subjec

123 endin(9-39) significantly reduced first- and second-phase ISR in both HS and T2DM subjects.

124 sulted in a significantly greater first- and second-phase ISR in HS compared with T2DM subjects.

125 In the second phase, it combines these small seeds to build lar

126 IP10-induction correlated with first- and second-phase kinetics and with ribavirin serum concentra

127 The second phase leads to p27(kip1) down-regulation independ

128 loss of trimeric structure occurring in the second phase, leaving the flexible extracellular loops a

129 which can easily be confounded by unobserved second phase magnetic inclusions.

130 els recovered to baseline, was followed by a second phase marked by an opposing down-regulation of en

131 equatorial ring formation), but also for the second phase (migration towards the animal pole).

132 econd phase's size, and beyond, the specific second phase morphology of the heterostructure is crucia

133 bands between the host PbS and the embedded second phases, MS (M = Cd, Zn, Ca, and Sr).

134 In the second phase, nine articles were excluded from the analy

135 In a second phase, no differentiation occurs while extensive

136 The second phase occurred once the membrane area from preexi

137 with RNA stem loop 3 occurred within 4 ms, a second phase occurred with a time constant of approximat

138 At large positive pressure, a second phase of 2D monolayer ice, i.e. the puckered squa

139 This is the second phase of a 10-year follow-up study of a cohort of

140 This paper reports the findings of the second phase of a study; the first has been reported els

141 learance phase, and then the mice received a second phase of Ag and tocopherol treatments.

142 n and lung lavage fluid were reversible in a second phase of Ag challenge without tocopherols.

143 After this second phase of aggregation, conversion into a fibrillar

144 Cyr61 siRNA inhibited a second phase of Akt phosphorylation measured 12 hours af

145 During the second phase of autophagy, the size of autophagosomes an

146 of the regulatory mechanism controlling the second phase of biphasic WNT activity essential for embr

147 e Hh-dependent module is not limited to this second phase of bone growth: during later larval develop

148 role in open state maintenance and reveals a second phase of CAD/STIM1 binding after channel opening.

149 In contrast, a second phase of calcium influx occurring minutes before

150 quenching of dAP fluorescence followed by a second phase of dAP quenching, which has nearly the same

151 Disruption of the second phase of Delta expression specifically abolishes

152 activated by Delta signaling even during the second phase of delta expression, when this gene is tran

153 of A13 development but are required for the second phase of development and for maintenance of this

154 This second phase of development is dependent on NF-kappaB si

155 econstructions, we further characterized the second phase of development of the A13 nucleus in the mo

156 In the second phase of dissemination, the nonmotile spirochetes

157 ymph gland, the tissue that orchestrates the second phase of Drosophila hematopoiesis.

158 The second phase of ductal growth and branching is driven by

159 esponse to EGFR activation, which leads to a second phase of EGFR-P and subsequent exaggerated mucin

160 t affect the first phase but ameliorated the second phase of endothelial barrier disruption and apopt

161 In the second phase of expression quantitative trait loci analy

162 ncrease in the rate constant of the critical second phase of folding.

163 tment with l-THP significantly inhibited the second phase of formalin-induced pain behavior.

164 rathecal injection and completely blocks the second phase of formalin-induced spontaneous nocifensive

165 Given that Syntaxin 4 functions in the second phase of glucose-stimulated insulin secretion (GS

166 intolerance and substantial reduction of the second phase of glucose-stimulated insulin secretion (GS

167 lta-deficient islets revealed an accelerated second phase of glucose-stimulated insulin secretion.

168 r CD8(+) T cell expansion and the associated second phase of GVHD.

169 and a premature entry into anagen during the second phase of hair cycling without a detectable change

170 HBsAg kinetics of decline paralleled the second phase of HDV decline consistent with HBsAg-produc

171 parasitemia and severe anemia, followed by a second phase of hyperparasitemia, more profound anemia,

172 these data indicate that IRF8 magnifies the second phase of IFN transcription in DCs by prolonging b

173 Subsequently, a second phase of IFN-dependent antiviral gene expression

174 omponent lipoteichoic acid (LTA) governs the second phase of immune responses when high concentration

175 n-12-dependent, Interferon-gamma-independent second phase of inducing the transcription factor T-bet.

176 In 2005 imatinib was added to the second phase of induction (N = 89, early imatinib).

177 The second phase of inflammation could be avoided by using G

178 om isolated islets selectively amplified the second phase of insulin release, consistent with the rol

179 elicit strong host responses, followed by a second phase of intense gene expression.

180 The second phase of JNK phosphorylation was dependent on aut

181 The second phase of JNK phosphorylation-Bcl-2 phosphorylatio

182 Lack of PXR inhibited the second phase of liver growth, leading to 17% less liver

183 c, but also begins exactly at the onset of a second phase of morphogenesis, when the early bone begin

184 ic neuroblasts (NBs) in Drosophila undergo a second phase of neurogenesis to generate adult-specific

185 Data from the second phase of OHTS also were examined, and control eye

186 s found for eyes that began treatment in the second phase of OHTS, but no significant change in MD or

187 on revealed poor mice exposure; therefore, a second phase of optimization was required.

188 Depletion of betaPix blocks the second phase of p66Shc and FOXO3a phosphorylation and pr

189 A second phase of persistent MT growth requires the cytoso

190 lasia, which developed postnatally, when the second phase of pituitary expansion occurs.

191 The second phase of PKD activation was followed by prolonged

192 The role of Mer kinase in regulating the second phase of platelet activation generates an opportu

193 cal spreading depression wave, we observed a second phase of prolonged, negative direct current shift

194 ring the first 6 to 7 minutes, followed by a second phase of response decay or of no further incremen

195 A second phase of ROS generation that followed after a del

196 consistent with its selective effect on the second phase of secretion.

197 activation of SMADs, TGF-beta also induces a second phase of STAT phosphorylation that requires SMADs

198 The second phase of study was a method development to realiz

199 maturation throughout childhood, a critical second phase of synaptic overproduction and elimination

200 tion rate becomes indistinguishable from the second phase of the bell-shaped curve that was obtained

201 The second phase of the biphasic force decay upon release of

202 In particular, in the second phase of the catalytic cycle, which involves thre

203 During the second phase of the disease, after the onset of neurolog

204 od or cerebrospinal fluid that appear in the second phase of the disease.

205 morph line) served as a reference when, in a second phase of the experiment, either prototype was bri

206 S inhibitor NOArg lowered both the first and second phase of the formalin response.

207 g attenuation of paw licking behavior in the second phase of the formalin test in animals with ACC le

208 e attenuated paw licking behavior during the second phase of the formalin tests as compared to sham l

209 Participants in the second phase of the Marine Resiliency Study (MRS-II) inc

210 As part of the second phase of the North American Prodrome Longitudinal

211 596 clinical high-risk participants from the second phase of the North American Prodrome Longitudinal

212 ected from January 2009 to April 2013 in the second phase of the North American Prodrome Longitudinal

213 Hence, during this second phase of the pandemic, extensive viral migration

214 in a genome-wide association study from the second phase of the Psychiatric Genomics Consortium, and

215 137 publications were scrutinized during the second phase of the review.

216 /polysulfurated forms of SufE accounts for a second phase of the slow catalytic turnover rate.

217 In the second phase of the study, the frequency of these abnorm

218 In a second phase of the study, we use one family-based data

219 improvement in interrater reliability in the second phase of the study.

220 tion and process-focused outcomes during the second phase of the study.

221 s required for recovery of IIS activity in a second phase of the systemic response to DNA damage.

222 dent roles in promoting the progression of a second phase of the viral lytic cycle and that these rol

223 erlies shifted northward, producing a warmer second phase of the YDS in Europe.

224 In a second phase of their migration, the surviving AMG stere

225 r option on POG 9407 after completion of the second phase of therapy.

226 gnificantly later in development, during the second phase of turtle trunk neural crest emigration.

227 While the extremely slow or flat second phase of viral RNA inhibition observed in vitro,

228 ifferent mechanisms underlying the first and second phases of neurovascular dysfunction.

229 gated in detail the effect of CdS and ZnS as second phases on the thermoelectric properties of p-type

230 Furthermore, formalin-induced second-phase pain was suppressed by spinal injection of

231 soriented grains, and the suppression of big second phase particles in this 3.2 mum thick REBa2Cu3Ox

232 In the second phase, phylogenetic footprinting is used to ident

233 In the second phase, predominantly lambda-chain-positive B cell

234 The second phase promotes prolonged, higher level MCP-1 secr

235 slets enhances the first-phase elevation and second-phase pulses of insulin.

236 imed, release-ready granule pools, while the second phase relies on granule mobilization from the res

237 + influx through AMPA receptors, whereas the second phase required release of Ca2+ from internal stor

238 curs in response to StxB1 subunit, while the second phase requires StxA1 subunit activity.

239 The second phase requires the activity of a pool of myosin t

240 The second phase, responsible for leukocyte exit from the gl

241 orylation and activation of Src, whereas the second phase resulted from the sequestration of activate

242 en removal rate continued to decrease in the second phase, resulting in an overall removal rate of 80

243 In the first and second phases, rising metabolite levels and increased po

244 This spacing should coincide with the second phase's size, and beyond, the specific second pha

245 During the second phase (sampled at E38-E45), the loosely banded S-

246 Second-phase secretion was similar across all NGT and IG

247 as proximal and Rac1 as distal regulators of second-phase secretion.

248 In the second phase, SHB1 enhances embryo cell proliferation an

249 However, the second phase slope of viral decline was improved with SA

250 sing a biphasic model to describe first- and second-phase slopes of viral decay during therapy.

251 In the second phase specific T cells invade the infected organ,

252 In the second phase, Src family kinases phosphorylate tyrosyl r

253 tants had a shorter first phase and a longer second phase than the wild-type protein, one mutant had

254 synthesis-independent manner, followed by a second phase that is more delayed and dependent on prote

255 rst phases and a 3.5-millisecond rectilinear second phase that was half the voltage of the first phas

256 In the second phase (the oxidase phase), oxidation of alkenes a

257 In the second phase, the CD8+ population emigrates to the tissu

258 In the second phase, the critically short telomeres lead to gen

259 In the second phase, the NC domain binds RNA, and the bound for

260 During the second phase, the WAVE (WASP-family verprolin homologous

261 In the second phase, these effector cells seek out and eliminat

262 In the second phase, they answered with respect to two predefin

263 In the second phase, they were divided into four treatment grou

264 sic waveform had a 60% first-phase and a 50% second-phase tilt.

265 microstructures can arrest shear bands at a second phase to prevent cracks from exceeding critical s

266 ng the microstructural length scales (of the second phase) to mechanical crack-length scales.

267 ric light (n = 243 in first phase; n = 25 in second phase) to those with electric light at home (n =

268 Induction of second phase transcription required IRF8.

269 Sofosbuvir + ribavirin are cost-effective as second-phase treatments following peginterferon + ribavi

270 In the second phase, type II genes (hCGbeta1 and -2) were forme

271 amellar scaffolds are often infiltrated by a second phase, typically a soft polymer matrix, a hard ce

272 The second-phase viral decay rate was also faster in the 3-d

273 ared empirical Bayes estimates of first- and second-phase viral decay rates between treatment arms an

274 a favorable genotype had greater first- and second-phase viral kinetics (P = 0.004 and P = 0.036, re

275 tained virological response as the first- or second-phase viral kinetics responses.

276 First- and second-phase viral kinetics were evaluated.

277 gamma-producing NK cells was greater in fast second-phase virological responders than in slow respond

278 in vitro stimulation by IFN-alpha during the second-phase virological response.

279 In the second phase, viruses with linked MDR mutations rapidly

280 This second phase was actively regulated by potently suppress

281 The slowly upward shift in the second phase was consistent with the slowly increasing t

282 first was mainly ozone controlled, while the second phase was more related to HO(*) reactions.

283 hanism for the Rac2-led PLD2 inhibition (the second phase), we used leukocytes from wild-type (WT) an

284 In a second phase, we applied an unbiased machine learning pr

285 For the second phase, we assessed the effect on mortality in tri

286 In the second phase, we carry out the alignment in the compress

287 lthough much remains to be learned about the second phase, we feel that an understanding of the first

288 In the second phase, we genotyped 343 SNPs from 123 regions mos

289 In the second phase, we included all 218 subjects with mild cog

290 In the second phase, we prospectively implemented the algorithm

291 In this second phase, we release a new server-side specification

292 o increased synaptic strength, we identify a second phase where this potentiation is profoundly reduc

293 Linoleic acid in pastures was highest in the second phase which coincided with mid-lactation days (p<

294 healthcare centers Lagos State, Nigeria and second phase which consists of definitive clinical evalu

295 The second phase, which followed the most energetic explosio

296 complex, NFATc1.STAT-3, to its promoter, the second phase, which is more robust, depends on NFATc1-me

297 Critical design aspect is a soft second phase, which is most effective when spacing betwe

298 tantly, the transition from the first to the second phase, which is the main determinant of the final

299 ex enhances the activity associated with the second phase, while modestly inhibiting the activity ass

300 ontrol participants underwent OIT during the second phase, with subsequent DBPCFC.