ライフサイエンスコーパス: temporal change

1 tudies with hazard ratios in our analyses of temporal changes.

2 Emerging short-chain PFASs showed no temporal changes.

3 wn recently to identify their equilibrium or temporal changes.

4 and less time-consuming means of monitoring temporal changes.

5 that determine foraging niches and possible temporal changes.

6 rength, likely contributed to these observed temporal changes.

7 We presently investigated the temporal changes (1982-2010) in MeO-PBDPB concentrations

8 ncidence of POMI demonstrated no substantial temporal change (2.7% in 2009 to 3.1% in 2014; P = .64 f

9 presence of flow and, second, to measure its temporal change after swim bouts to deduce flow directio

10 e results provide a baseline for determining temporal change and investigations of processes structur

11 nhanced with overlaid time curves to display temporal changes, and novel individual glyphs of state i

12 e in Italy, to identify ketamine spatial and temporal changes, and to confirm the low use of mephedro

13 Temporal changes are difficult to assess in Australia an

14 tions for diverticulitis were calculated and temporal changes assessed.

15 essary phenotypic plasticity for adapting to temporal changes at multiple time scales (seconds-to-min

16 ental property of seismogenic zones, and its temporal changes can increase or decrease the likelihood

17 gel properties was demonstrated to introduce temporal changes, creation of arbitrarily shaped feature

18 thyroid carcinoma in zebrafish that reveals temporal changes due to BRAF(V600E).

19 Temporal changes fit a model incorporating likely select

20 aded live cells demonstrate both spatial and temporal changes for cytoskeletal populations within the

21 Regarding potential temporal changes, from 1960 to 2005 the estimated elasti

22 The direction of temporal change in climatic parameters and in the timing

23 Endpoints included temporal change in FEV1, severity of ACR, and survival.

24 e associations between both baseline GGT and temporal change in GGT, as well as cardiovascular events

25 However, data linking long-term temporal change in hs-cTnT to outcomes are limited, part

26 We analysed extensive data on temporal change in laying date and clutch size of birds

27 However, temporal change in morphological diversity has usually b

28 onstant environment to arbitrary patterns of temporal change in selection coefficients.

29 e climatically sensitive and experience high temporal change in species composition.

30 al-scale vegetation plots, we show that mean temporal change in species diversity over periods of 5-2

31 We evaluate statistical metrics for temporal change in the frequency of individual SNPs, ass

32 re no study has examined if there has been a temporal change in the frequency of inducible myocardial

33 brane lipid composition wherein a spatial or temporal change in the latter can result in a post-assem

34 network, pre-steady-state measurement of the temporal change in the Shh morphogen is a plausible mech

35 ity counterparts, and (iii) characterize the temporal change in the species' functional trait assembl

36 We have determined the temporal changes in (2)H labeling of body water and amin

37 Temporal changes in -volume characteristics provide nove

38 eighborhood foreclosures was associated with temporal changes in 3 objectively measured cardiometabol

39 The temporal changes in [(18)F]FDG uptake and corresponding

40 In this study, we estimate temporal changes in abundance from North American Breedi

41 We compared temporal changes in activation biomarkers of coagulation

42 Temporal changes in AET receipt (estimating the annual p

43 Temporal changes in antibiotic consumption are reflected

44 st-PCI bleeding over time was largely due to temporal changes in antithrombotic strategies.

45 Secondary outcomes included temporal changes in asthma medication prescriptions, the

46 thout moving and, thus, without experiencing temporal changes in attractant concentration.

47 st make continuous adjustment to account for temporal changes in azimuth caused by Earth's rotation.

48 process and provide unique insights into the temporal changes in bacterial populations throughout les

49 The primary study examined both temporal changes in baseline metal concentrations (19 me

50 xcised tissues using gamma spectroscopy, and temporal changes in biodistribution were assessed using

51 he capacity of statistical models to predict temporal changes in bird populations over a 32-year peri

52 We aimed to determine whether temporal changes in birth weight have occurred amongst 2

53 provide tools to investigate the spatial and temporal changes in blood flow within organs of mice at

54 roposed TGSCCA method is able to capture the temporal changes in brain from longitudinal phenotypes b

55 We also find that temporal changes in brain size are not associated with a

56 r defibrillation was performed and evaluated temporal changes in bystander interventions and outcomes

57 The effect of temporal changes in cancer therapy on health status amon

58 Background: The effect of temporal changes in cancer therapy on health status amon

59 senchymal stromal cells in osteogenesis, and temporal changes in cellular composition.

60 Ischemia induces extensive temporal changes in cerebral transcriptome that influenc

61 Identification of temporal changes in chemical structures of process urani

62 n mean annual temperature could help explain temporal changes in CO2 flux.

63 nt strategies for different bird cohorts and temporal changes in connectivity driven by the invasion

64 Dynamic temporal changes in contact structure and ranging behavi

65 ups if they exceeded 10% of all children and temporal changes in coverage of +/-10% with greater than

66 s and Khyber Pakhtunkhwa regions, as well as temporal changes in coverage.

67 ne use and in-depth studies of, for example, temporal changes in crystallographic grain structure non

68 static cancer undergoing systemic treatment, temporal changes in CTC numbers correlated reasonably we

69 Using quantitative proteomics we monitored temporal changes in diGly site abundance in response to

70 Hence, temporal changes in disparity dynamics are likely constr

71 gradients of species composition also drive temporal changes in diversity--rarely is tested.

72 identified through quantitative analysis of temporal changes in Dorsal target gene expression from o

73 etabololipidomics of murine lungs identified temporal changes in endogenous maresin 1 (MaR1) during s

74 Temporal changes in ex-vivo channel activity and subunit

75 te MNs in an SHH-independent manner and that temporal changes in exposure to patterning factors such

76 hological events in the CNS, we investigated temporal changes in expression levels of ion channels in

77 A portion of the temporal changes in f H is evidenced by a respiratory in

78 Temporal changes in fatty acid levels and misclassificat

79 organismal energy homeostasis in response to temporal changes in feeding and activity or external cha

80 We observed distinct spatial and temporal changes in fluorescence within single cells, re

81 e country- or region-specific information on temporal changes in forest carbon (C) pools to develop a

82 pability of the OPM system to measure spatio-temporal changes in FRET ratio in 3-D in multicellular s

83 s by model fitting of jasplakinolide-induced temporal changes in G-actin concentration.

84 ing the Drosophila wing, we demonstrate that temporal changes in gene expression are accompanied by g

85 We define temporal changes in gene expression from disease onset i

86 IGF-I caused temporal changes in gene expression that were strongly a

87 ironment necessitate and instigate rapid and temporal changes in gene expression within the cells (os

88 e expression, we profiled the sequential and temporal changes in genome-wide expression that accompan

89 Temporal changes in glial fibrillary acidic protein (GFA

90 ing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusi

91 The temporal changes in goethite morphology could not be com

92 Warming temperatures cause temporal changes in growing seasons and prey abundance t

93 tory species, such as salmon, where distinct temporal changes in growth and physiology during develop

94 ur, was used to simulate Pan-European spatio-temporal changes in H. contortus infection pressure unde

95 A systematic quantitative analysis of temporal changes in host and viral proteins throughout t

96 , the two viruses demonstrated very distinct temporal changes in host response genes, although both R

97 he probability of occurrence, extent of, and temporal changes in hybridization increased at sites in

98 nsverse aortic constriction (TAC), including temporal changes in hypertrophy, collagen deposition, ca

99 Striking spatial and temporal changes in immunoexpression of matrix metallopr

100 Temporal changes in imprinting were observed for KCNQ1 a

101 Temporal changes in infection load were species and life

102 nding of the molecular mechanisms underlying temporal changes in intestinal activity might allow us t

103 lga Chlamydomonas reinhardtii and identified temporal changes in intracellular Pb speciation under co

104 However, because temporal changes in intracellular protein abundances can

105 Temporal changes in intratumoral TCR repertoire revealed

106 We propose that temporal changes in islet autoimmunity seroconversion in

107 of detectable cTn to HF outcomes, as well as temporal changes in its magnitude, and its relationship

108 These results demonstrate that temporal changes in lake characteristics due to increase

109 lative impacts of DNA sequence variation and temporal changes in lifestyle and habitat on the human e

110 le among-site variation, partly explained by temporal changes in light availability (a local driver)

111 es were used to characterize the spatial and temporal changes in lipid composition in lung tissue.

112 Moderate calorie restriction causes temporal changes in liver and skeletal muscle metabolism

113 thms and neural circuits that process spatio-temporal changes in luminance to extract visual motion c

114 In this study, we combined temporal changes in LV structure (volume) with alteratio

115 Temporal changes in macaque antibody responses were anal

116 y to show that quartz can resolve late-stage temporal changes in magmatic delta(18)O values.

117 How spatial and temporal changes in major histocompatibility complex/pep

118 Whether temporal changes in maternal weight affect these risks i

119 Temporal changes in MATS coverage underscore the need fo

120 Our aims were to study the temporal changes in MBF in response to EC transplantatio

121 The intricate cross-talk provided by temporal changes in mediators, hormones, metabolites, ne

122 ed plasma mass spectrometry, to characterize temporal changes in mercury exposure and uptake in wild

123 eabird colonies in the Pacific basin exhibit temporal changes in methylmercury levels consistent with

124 Temporal changes in microRNA profile occur at early stag

125 study demonstrates the relationship between temporal changes in microvascular macromolecular flux an

126 y be very useful to reveal important spatial-temporal changes in mitochondrial superoxide production

127 Spatial and temporal changes in molecular expression are essential t

128 ivariable Poisson model was used to evaluate temporal changes in mortality rates.

129 d Cox proportional hazards models to examine temporal changes in mortality, readmission, and hospital

130 We did not find evidence of temporal changes in most aspects of palliative care, fam

131 Temporal changes in MR severity and LV end-systolic volu

132 H3K4me3 marks was found to closely match the temporal changes in mRNA abundance; 22% of genes that in

133 erpinning disease or morphogenesis to spatio-temporal changes in nanoscale mechanical properties such

134 es of transcription factors that coordinates temporal changes in neuronal/glial identity with transit

135 ta gene from a poised structure, we measured temporal changes in NF-kappaB and IFN regulatory factor

136 To investigate the temporal changes in NG2 cell fate, we generated NG2creER

137 The spatial and temporal changes in NK and NKT cells in lethally infecte

138 We also demonstrate, by monitoring temporal changes in Orm phosphorylation and sphingoid ba

139 or patients with advanced heart failure, but temporal changes in outcomes and associations between fa

140 In the paraventricular nucleus, although temporal changes in oxytocin mRNA expression were simila

141 Conclusions and Relevance: Analyses of temporal changes in PAH care reveal a significant decrea

142 A priori knowledge of spatial and temporal changes in partial pressure of oxygen (oxygenat

143 We documented temporal changes in partner availability and used a mixe

144 ion, and Doppler shifts were calculated from temporal changes in phase.

145 actions have been well characterized, spatio-temporal changes in phosphosite availability in response

146 Temporal changes in phytoplankton biomass are governed b

147 c arrest and meiotic resumption, thus spatio-temporal changes in PKA localisation during development

148 Temporal changes in placental function are synchronized

149 datasets are urgently needed to characterize temporal changes in population behaviors, contact networ

150 composition and population differentiation, temporal changes in population were not explained by cor

151 ms may stem from failure to consider dynamic temporal changes in predation risk.

152 A better understanding of the temporal changes in PSMA expression is needed to leverag

153 hat the overall positive correlation between temporal changes in r and r is driven by relatively infr

154 dology for tracking and diagnosing causes of temporal changes in regional-scale aerosol populations i

155 sil and extant mammalian species to test for temporal changes in relative brain size over time.

156 ependence for 4 of 7 antibiotics; background temporal changes in resistance did not explain the tempo

157 124 is important in regulating the intrinsic temporal changes in RGC growth cone sensitivity and sugg

158 reases and these analyses do not account for temporal changes in risk factors.

159 ed cumulative incidence functions to compare temporal changes in risk from predators.

160 ranscription rates determine the majority of temporal changes in RNA levels, but that changes in degr

161 st week after injury and correlated with the temporal changes in S1 extracellular glutamate levels an

162 Temporal changes in SAMS scores were associated with cha

163 s non-nested pattern is a combined effect of temporal changes in selection pressure and partial recog

164 Temporal changes in serotype distributions are well docu

165 Stability and temporal changes in size distributions have been observe

166 the robustness of assortative mating against temporal changes in social conditions.

167 ability among individuals and were robust to temporal changes in social conditions.

168 we characterize the response of H. pylori to temporal changes in sodium chloride concentration and sh

169 cm depth from 1955 to 2016, we evaluated the temporal changes in soil C-N-P stoichiometry across subt

170 ghly weathered Ultisols, and more pronounced temporal changes in soil C:N, N:P, and C:P ratios at low

171 potential confounding effects of spatial and temporal changes in soil microbial communities is unknow

172 Our sensitivity analysis suggests that the temporal changes in soil stoichiometry resulted from ele

173 Temporal changes in solute concentration are sensed by t

174 We tested for temporal changes in standardized incidence rates (SIRs)

175 in28a, let-7, IMP1, and HMGA2 thus regulates temporal changes in stem cell properties.

176 pt their sensitivity depending on localized, temporal changes in stimulation levels.

177 We examined temporal changes in structural and acoustic parameters i

178 nicity versus spontaneous resolution exhibit temporal changes in T(reg) cell function.

179 induced in the vena cava of BALB/C mice, and temporal changes in T1 relaxation time correlated with t

180 ting newt heart, we show dynamic spatial and temporal changes in tenascin-C, hyaluronic acid, and fib

181 cts of the carbon cycle can be assessed from temporal changes in the (13)C/(12)C ratio of oceanic bic

182 igand transport equations, we calculated the temporal changes in the 3-D ligand concentration field.

183 ensity were all responsible for the observed temporal changes in the abundance of two dominant phytop

184 In this study, we quantified and compared temporal changes in the abundance, taxonomic diversity,

185 In this study, temporal changes in the airway microbiome before, at the

186 Previous studies investigated the temporal changes in the association over a few discrete

187 health disparities when bias can arise from temporal changes in the bivariate distribution of educat

188 a strong association of SFTS incidence with temporal changes in the climate within the clusters.

189 of cardiovascular diseases, we investigated temporal changes in the composition of atherosclerotic p

190 The objective was to investigate temporal changes in the concentrations of fecal microbio

191 linear regression (ridge regression), using temporal changes in the distributions of gene expression

192 ythms may have evolved to anticipate regular temporal changes in the environment.

193 mutant mice at 5 and 10 weeks of age exhibit temporal changes in the expression of specific Mullerian

194 Temporal changes in the extent of phosphorylation in res

195 Here, we examined temporal changes in the fine-scale population structure

196 scattering measurements were used to follow temporal changes in the fractal dimension of aggregating

197 We report temporal changes in the genetic composition of the HBV p

198 evel, little attention has been given to the temporal changes in the geographic patterns of heart dis

199 e that individual delta(34)S records reflect temporal changes in the global sulfur cycle; this assump

200 Overall, these data suggest temporal changes in the glycosylation of buttermilk prot

201 In this study, we examined temporal changes in the incidence of primary biliary cir

202 struation would recapitulate the spatial and temporal changes in the inflammatory microenvironment of

203 n, turns are triggered by the integration of temporal changes in the intensity of the stimulus.

204 Temporal changes in the malaria test positivity rate (TP

205 ntary exchange with the oceanic crust, or by temporal changes in the marine inventory for elements th

206 Temporal changes in the median date of salmon migration

207 thogens in ticks may be dependent in part on temporal changes in the microbial community of the tick

208 Our results show temporal changes in the miRNA expression during B-cell d

209 tatistical analysis, has been used to unveil temporal changes in the myelin structure of dissected ne

210 By assessing temporal changes in the occurrence of these states, we d

211 In contrast, temporal changes in the oceanic carbon sink remain poorl

212 t probability of new mutations assuming that temporal changes in the offspring distribution are small

213 To evaluate for temporal changes in the outcomes of warfarin treatment,

214 Temporal changes in the population distribution of age,

215 Temporal changes in the proportion of CPMs among women w

216 In this study, temporal changes in the redox properties of three 0.5 g/

217 Here we explore the implications of temporal changes in the riverine chemical weathering flu

218 bedload and derived suspended load indicates temporal changes in the sediment flux ratio, which imply

219 The current study addresses temporal changes in the serum lipidome from 4 h to 28 d

220 Overall, the data provide a reference of temporal changes in the serum proteome in healthy childr

221 Temporal changes in the site-wide maximum concentrations

222 ed computational modeling to investigate the temporal changes in the spatial distributions of the key

223 virus Y, and describes, at high resolution, temporal changes in the structure of viral populations w

224 otide composition, even if we allow for slow temporal changes in the substitution matrix.

225 is tool should help epidemiologists quantify temporal changes in the transmission intensity of future

226 Additionally, the impact of temporal changes in the use and restriction of phthalate

227 ur results reveal 63 miRNAs with significant temporal changes in their expression during normal PCD.

228 It is unknown whether temporal changes in therapy are associated with changes

229 The temporal changes in these marks suggest distinct functio

230 opic expression of XCdc6 leads to apoptosis; temporal changes in this protein are critical for proper

231 P < 0.001), whereas WT mice did not show any temporal changes in tracer uptake during the interval of

232 These data indicate that dynamic spatial and temporal changes in traction force and local strain may

233 METHODS AND We profiled the temporal changes in transcriptome and chromatin accessib

234 To quantify the association between temporal changes in treatment dosing and subsequent neop

235 Temporal changes in treatment exposures were not associa

236 15)N) and carbon (delta(13)C) to control for temporal changes in trophic structure and diet.

237 Temporal changes in virus prevalence occur, and season m

238 ing tissue to near-infrared (NIR) light, the temporal changes in vitreous concentrations of a biomole

239 d consider the flux of (129)I in response to temporal changes in wetland hydrologic and chemical cond

240 t(1/2) = 20.4 min) as (11)CO(2), we captured temporal changes in whole-plant carbon movement and part

241 of phytoplankton in the lake underwent major temporal changes, in correlation with known climatic eve

242 changes (northward species range shifts) and temporal changes (increases in the total abundances of w

243 isotope compositions may reflect spatial or temporal changes influenced by photochemical processes.

244 nd comparison between plot-scale treatments, temporal change is a significant influence.

245 After Kelch13-C580Y, the strongest temporal change is seen at a SNP in phosphatidylinositol

246 e from a number of Earth systems that abrupt temporal changes known as regime shifts are important, t

247 y of acute kidney injury is gleaned from the temporal change markers of renal injury (urine neutrophi

248 tion, with different causative organisms and temporal changes, might influence this heterogeneity.

249 variable degrees of parietal with or without temporal changes; no case had strikingly focal or asymme

250 technique is powerful in detecting possible temporal change of medium.

251 tance speckle and tested the hypothesis that temporal change of RNFL speckle reveals axonal dynamic a

252 results obtained in this study suggest that temporal change of RNFL speckle reveals structural chang

253 fit to the time course was used to evaluate temporal change of speckle pattern.

254 To relate temporal change of speckle to axonal activity, in vitro

255 teins provided new insights into the diverse temporal changes of biological cascades associated with

256 we were for the first time able to trace the temporal changes of cell death during the combination tr

257 individuals exhibited significant (P < 0.05) temporal changes of core clock (PER1, PER2, PER3, CRY2,

258 geneity within the viral populations and the temporal changes of drug-resistant viruses found in this

259 isions regarding cancer therapy are based on temporal changes of EF.

260 rs, and assigns cluster memberships based on temporal changes of gene expressions.

261 Temporal changes of H3K4me2, unmethylated CpG, and H2A.Z

262 s significantly associated with the relative temporal changes of hs-cTnT (p < 0.01, corrected for mul

263 The diverse spectra and temporal changes of HSV drug resistance were determined

264 high-throughput screening system to monitor temporal changes of IP(3) is essential for screening of

265 tation of ligands on Janus particles and the temporal changes of membrane dynamics revealed in this w

266 Here we studied temporal changes of microbial communities in Tengchong h

267 genomic sequences based on the similarity of temporal changes of multiple epigenomic marks during a c

268 SL-MRI allows quantification of temporal changes of regional MBF in response to EC treat

269 teractions, inferring causality and modeling temporal changes of regulation behaviors.

270 paired samples were available, and assessed temporal changes of routinely available biomarkers, outc

271 this diet shift partially accounted for the temporal changes of summation operatorMeO-PBDPB levels i

272 Here we report temporal changes of surface wave velocity over a large a

273 ng AD progression, little is known about the temporal changes of tau accumulation in this region.

274 phores that allow simultaneous monitoring of temporal changes of the content and membrane.

275 The analysis reveals temporal changes of the effective reproductive number th

276 remains unclear what can be learned from the temporal changes of the epigenome.

277 The temporal changes of the images enable studies of the vis

278 Detecting temporal changes of the medium associated with major ear

279 these methods yield correct inferences about temporal change only under limited conditions.

280 i were identified that showed no significant temporal change or association with leukocyte population

281 This research examined continuous temporal changes (potentially nonlinear) in mortality re

282 Source stability (or easy predictable temporal changes, similar to those observed in the case

283 he results provide an expression analysis of temporal changes that occur in LVN neurons in nonregener

284 Similarly, temporal changes to actin-sequestering proteins beta-thy

285 In particular, we studied the temporal changes to chromatin during UV light exposure,

286 However, our knowledge about the temporal changes to the epigenome during fetal brain dev

287 Here we compare the temporal changes to the intact rhizosphere pore structur

288 t mechanisms of protein-protein interaction; temporal changes under nonequilibrium conditions; locali

289 e Energy Transfer (SM-FRET) assay to monitor temporal changes upon binding of NS5B to surface immobil

290 s in key signaling pathways therefore confer temporal changes upon stem cell self-renewal and tumor s

291 This temporal change was statistically significant but not st

292 The differences and temporal changes we found in causes of blindness and MSV

293 Individual growth models of temporal change were estimated.

294 However, these temporal changes were attributable to the increasing com

295 xes to the sediment and the magnitude of the temporal changes were generally much lower in Lake Annec

296 These temporal changes were necessary and sufficient to mainta

297 However, temporal changes were striking.

298 Temporal changes were tested in centers that participate

299 lation (>/=14ng/l) as well as their relative temporal changes were used as continuous variables of in

300 ic inactivity, are particularly sensitive to temporal change, whereas the sustained components of bro