ライフサイエンスコーパス: proposed model

1 ividual elementary rate constants within the proposed model.

2 ographic and mutagenesis data supporting the proposed model.

3 values, supporting the predictability of the proposed model.

4 ve control - can further refine the authors' proposed model.

5 ein occupancy profiles, hence supporting our proposed model.

6 may help in operationalizing and testing the proposed model.

7 ed to illustrate the basic principles of the proposed model.

8 lation which is consistent with a previously proposed model.

9 data were found to be in accordance with the proposed model.

10 f IL-7R signaling, in contrast to a recently proposed model.

11 and Arg_Ala) provide strong support for our proposed model.

12 There are two unique aspects to this proposed model.

13 ing empirical support for key aspects of the proposed model.

14 ments further corroborate the utility of the proposed model.

15 fects and make predictions that can test the proposed model.

16 literature, can be well explained using the proposed model.

17 Other types of DNA are also shown to fit the proposed model.

18 plexes to provide additional support for the proposed model.

19 e B3LYP-D3/6-311 G (d,p) levels based on the proposed model.

20 ion is different from that of all previously proposed models.

21 structure did not improve the quality of the proposed models.

22 were less satisfactory in prediction in the proposed models.

23 nsistent with our model than with previously proposed models.

24 , in direct conflict with some (but not all) proposed models.

25 al criteria demonstrated the validity of the proposed models.

26 of the-art techniques, we have revisited the proposed models.

27 compounds using the parametric values of the proposed models.

28 The proposed model accounts for differences in how place and

29 Conclusion The proposed model accurately predicts high- and low-risk RS

30 For the kinetic resolution, the proposed model accurately predicts the faster reacting e

31 k in Saccharomyces cerevisiae has tested the proposed model against real data.

32 es used in other fragment-based methods, the proposed modeling algorithm, SmotifTF, can employ an exh

33 Our findings demonstrate how the proposed model allows delaying the epidemic outbreak and

34 The proposed model allows exploration, visualization and pat

35 The proposed model allows risk stratification of HT candidat

36 When a QTL shows Mendelian effect, the proposed model also outperforms traditional Mendelian mo

37 A comparison between the proposed model and experimental data, of both frequency

38 results provide an experimental test of the proposed model and have identified regions of the N-term

39 vivo HCII-dependent process may utilize the proposed model and suggests a potential for oversulfated

40 he CH1(1) peptide is determined based on the proposed model and temperature-dependent kinetic measure

41 tudies demonstrated the effectiveness of the proposed model and the improvement of the statistical po

42 By simulation studies, we show that the proposed models and tests are very robust in terms of ac

43 isting data on this gradient fit the various proposed models and what aspects of gradient formation t

44 The proposed model approach allowed taking the best advantag

45 The proposed modeling approach may be of use to elucidate th

46 To illustrate the proposed modeling approach we focus on the reductive deh

47 The efficiency and predictive ability of the proposed model are confirmed by comparing the results of

48 use none of the molecules in this previously proposed model are known mediators of intracellular sign

49 The benefits of the proposed model are twofold: not only can the model diffe

50 The proposed models are based on readily available real-time

51 Previously proposed models are based on the volume fraction of the

52 on stereochemistry is also provided, and the proposed models are compared with related systems in the

53 rap resampling (n = 1000) indicates that the proposed models are robust to minor perturbations in inp

54 The proposed models are robust to parameter perturbations an

55 strand ends (DSEs) during TLD, as previously proposed; models are suggested.

56 ical research needed to test and explore the proposed model, are also briefly discussed.

57 existence and uniqueness of solutions to the proposed model as well as a computationally efficient st

58 nt with experimental results, validating the proposed models as reliable representations of novel glc

59 e) exhibits progressive hearing loss that we proposed models aspects of A1555G-related pathology in h

60 At the ontogenetic level, the proposed model assumes age-dependent interactions betwee

61 Mutant analyses supported this proposed model at a significant proportion of the tested

62 The proposed model based on the atomic force microanalysis s

63 AUC was 0.818 (95% CI: 0.734, 0.902) for the proposed model based on the observations used to create

64 Several theorists have recently proposed model-based reinforcement learning as a candida

65 We also show the validity of the proposed model by investigating the activity of two prot

66 so develop an efficient algorithm to fit the proposed models by incorporating Expectation-Maximizatio

67 The proposed models C and D outperform the current clinical

68 The proposed model can advance our interpretive framework fo

69 The proposed model can also be used to simulate gating prope

70 The study demonstrates that the proposed model can be advantageously used for interrogat

71 The proposed model can be applied to any degradation pathway

72 s problem, namely under which conditions the proposed model can be applied without trip data for cali

73 We show that the proposed model can be further exploited to extract kinet

74 The experimental results have shown that the proposed model can be used for identification of TF-rela

75 The proposed model can be used for optimizing the dialysis r

76 The proposed model can be used to determine appropriate sign

77 The proposed model can be used to study biomolecular dynamic

78 experiments are used to demonstrate how the proposed model can explain a sensorimotor system's abili

79 The proposed model can open a new field in the application o

80 or ovarian cancer patients, showing that the proposed model can potentially uncover key drivers relat

81 The proposed models can fit a large number of effects, inclu

82 Our proposed models can predict two kinds of missing functio

83 The proposed model captures our experimental observations an

84 Numerical simulation results show that the proposed model captures the phenomena occurring in SPME,

85 The proposed model claims effortless monolingual processing.

86 opment in host skin further substantiate the proposed model, consolidating a new concept in parasite

87 er models based on redundancy reduction, the proposed model conveys more information about the origin

88 We envisage that the proposed model could be very useful in physical and engi

89 The proposed model could fit the variance/covariance structu

90 Importantly, the proposed model demonstrates how these elementary percept

91 The proposed model depends upon nonproductive interactions b

92 explicitly rendered unimportant, leaving the proposed model deprived of behavioral feedstock and prox

93 diffraction data and agrees with an earlier proposed model derived by complementary means.

94 provides confirmation of the veracity of the proposed model describing the interactions of copper and

95 Our proposed model divides the region of interest into pixel

96 The proposed model effectively captures population dynamics

97 In the proposed model, egress rates from bone marrow (BM) were

98 Thus, data analysis using the proposed model enables measurement of nanoscale membrane

99 The range of shear rates covered by the proposed model encompass venous and arterial thrombosis,

100 he Fermi level using the redox couple, and a proposed model encompassing these effects are presented.

101 The proposed model explains a wide range of phenomena report

102 Hence, the proposed model explains the dynamics forming the plasmon

103 The proposed model facilitates simulations that span large l

104 We solve the proposed model, finding trade-off conditions on the life

105 This proposed model for aerosol-water distribution underestim

106 In a proposed model for AMPAR assembly, the amino-terminal do

107 A previously proposed model for binding of polyarginine and protamine

108 4 A) with Glu-226, confirming our previously proposed model for cADPR catalysis.

109 nt currents are analyzed in light of a newly proposed model for charge-trapping dynamics that renders

110 The proposed model for ClyA represents a non-classical pathw

111 btained results it can be concluded that the proposed model for converting EC50 into TEAC values and

112 was applied to four data sets, and the best proposed model for each data set was determined by using

113 carrier emission demonstrates that the newly proposed model for ESI is consistent with previously rep

114 The results support a proposed model for high-affinity binding of AdA to Ins(1

115 firm biochemical evidence in support of the proposed model for hydrolysis chemistry.

116 A previously proposed model for ICP8 binding single-stranded DNA (ssD

117 The proposed model for Msp is consistent with the enzymatic

118 The proposed model for prediction of the stability of a dupl

119 Thus our result validates the proposed model for promoter escape and also suggests tha

120 However, the proposed model for speech evolution inadequately integra

121 The proposed model for stereochemical induction is shown to

122 excellent substrate for CPO in accord with a proposed model for the active site of this enzyme.

123 and experimentally validated the previously proposed model for the interaction of langerin extracell

124 esults are discussed within the context of a proposed model for the mechanistic coupling of the effic

125 These results are discussed within a proposed model for the role of yeast TFIIF in modulating

126 The proposed model for the sizes of detectable metastases pr

127 suggests that through the application of the proposed model for tumor-microenvironment interactions,

128 scuss these roles in the context of recently proposed models for germline potency and epigenetic inhe

129 This review describes previously proposed models for passive and active Ca(2+) transport,

130 Our experiments differentiate among several proposed models for rhythm generation in the vertebrates

131 These data constrain proposed models for taste transduction and suggest a lin

132 In contrast to proposed models for the homologous ERAP1, no specific re

133 Proposed models for these deletions implicated processin

134 In the proposed model, formic acid is first physisorbed on bism

135 The proposed model framework enables interpretation and desc

136 idea in a mechanical tissue simulation, the proposed model gives rise to efficient spreading and can

137 We show that our proposed model has an anomalous slow diffusion character

138 The proposed model has been shown as a promising mathematica

139 The proposed model has the potential to offer a more complet

140 The proposed model have been applied to a lung cancer datase

141 In the experiments, we show that the proposed models help improve the classification accuraci

142 In this proposed model, high baseline pulvinar activity in depre

143 The proposed model impacts the field by deemphasizing the ro

144 knife test that the accuracy achieved by the proposed model in identifying the m(6)A site was 78.15%.

145 use simulations to show the advantage of our proposed model in terms of variable selection accuracy o

146 interest to evaluate the performance of the proposed model in that situation which is the current fo

147 ntal data demonstrated the usefulness of the proposed model in understanding the general mechanism of

148 This result corroborates the recently proposed model in which "semireverse" electron transfer

149 observations are consistent with a recently proposed model in which drug reacts noncovalently with b

150 ys a role in invasion, but refute a recently proposed model in which parasite replication within the

151 erent points in the growth phase support our proposed model in which quorum sensing downregulates mot

152 This supports the proposed model in which the MLL complex orchestrates bot

153 ing loop within the DBD, consistent with the proposed model in which the transient opening of this re

154 In this study we describe how our recently proposed model, in which oscillator coupling drives the

155 excludes the possibility of other previously proposed models, including the highly oxidized structure

156 Experimental results and the proposed model indicate that band edge alignment can be

157 e RAG complex has not been defined, although proposed models invoke ATM and RAG2's C terminus in main

158 The proposed model involves two DNA damage response proteins

159 This comparison suggests the proposed model is a good approximation but could be impr

160 A key feature of the proposed model is a specific relationship between how od

161 Since the proposed model is capable of incorporating base-specific

162 The proposed model is compared with several other models, by

163 The proposed model is computationally efficient and uses onl

164 The performance of the proposed model is evaluated favorably in simulated, as w

165 The proposed model is expected to be instrumental in underst

166 The proposed model is expressed in the following steps: (1)

167 Besides, the proposed model is flexible and offers an appropriate tre

168 An R program that implements the proposed model is freely available.

169 thetic and real-world networks show that the proposed model is robust against insufficient data and h

170 The proposed model is suited to fit experimental data and to

171 The proposed model is tested by molecular dynamics simulatio

172 The proposed model is that the many TE insertions created ma

173 The proposed model is the simplest solution consistent with

174 The proposed model is used to examine the renaturation of DN

175 The proposed model is validated by its application for the e

176 The proposed model lends itself well to prospective studies

177 onsive patients, and a discussion of how the proposed model might explain individual differences in v

178 The proposed model might facilitate the quantitative evaluat

179 Proposed models mostly focus on the different styles of

180 A newly proposed model named "Escape from Adaptive Conflict" (EA

181 The proposed model naturally incorporates the spatial depend

182 ed volume to evaluate the performance of the proposed model needed in discerning the role of LAD hete

183 Thus, the proposed model not only achieves successful feedforward

184 The proposed model not only provides predictions of active a

185 provides experimental support to the theory-proposed model of active sites in Ni(1-x)Fe(x)OOH.

186 Previous experimental work has led to a proposed model of adsorption that involves an unusual cl

187 This would be consistent with a recently proposed model of an autoinhibited form of the plant ACA

188 A proposed model of axon degeneration is that nerve insult

189 y ectopic synapsis in NAHR together with our proposed model of chromosomal compression/extension/loop

190 otype, which is consistent with a previously proposed model of cooperation between EZH2 WT and Y641N

191 These findings support a proposed model of DOHH-eIF5A binding in which the amino

192 In contrast to the previously proposed model of eggshell patterning, we show that the

193 While this finding supports a proposed model of G stimulation, we also find from addit

194 A current proposed model of GRK1 activation involves the binding o

195 y human HAT-B, in further agreement with the proposed model of H4 tail binding.

196 ypothetical stalk-intermediate, supports the proposed model of how the surfactant proteins promote ad

197 near-physiological conditions, confirming a proposed model of hyaluronan structural organization.

198 Our results support a previously proposed model of hypertrophy in which hypertrophy can p

199 Using a recently proposed model of locomotor wave propagation, we show th

200 Findings are consistent with the proposed model of mental and physical health disparities

201 ht, a feature not captured in any previously proposed model of path integration.

202 ssed samples, which is in agreement with the proposed model of protein interaction at the air-liquid

203 ns and tests two assumptions that underlie a proposed model of receptor dynamics.

204 s in NS5B are structurally consistent with a proposed model of regulation of RNA binding by cyclophil

205 By fitting the parameters of the proposed model of reversible MB interactions to the expe

206 n of sGC are discussed in the context of the proposed model of sGC/NO interactions and dynamic transf

207 are most readily explained using a recently proposed model of substituent effects in the benzene san

208 Further, this study supports a proposed model of synergistic interaction between AMPK a

209 proof-of-concept implementation is fit by a proposed model of the CEP process.

210 This proposed model of the electron-transfer complex between

211 so compare features of old and more recently proposed models of eyespot development and propose a sch

212 However, the recently proposed models of filamentous actin (F-actin) did not e

213 Our results are inconsistent with recently proposed models of Gaussian disorder in the energy lands

214 , we discuss J chain in light of the various proposed models of its expression and regulation, with a

215 Thus, proposed models of neural crest evolution postulate vert

216 PhoB family of RRs in contrast to previously proposed models of OmpR activation.

217 ls, has been a long-appreciated obstacle for proposed models of prebiotic organophosphate formation.

218 Among the many proposed models of the cohesin complex, the 'core' cohes

219 tide 1a are fundamentally different than the proposed models of the fibrils formed by alpha-synuclein

220 The proposed model offers direct interfaces to material indu

221 e way for future clinical application of the proposed model on individual patients, including estimat

222 The proposed model outlines a quality control program that a

223 The proposed model overlooks the contribution of a relationa

224 However, this widely proposed model overlooks the fact, established 100 years

225 The proposed model possesses the key feature of combing the

226 The proposed model predicts that such signal amplification s

227 The proposed modeling process will apply as long as the basi

228 The proposed model provides a basis for computational simula

229 The proposed model provides a basis for understanding the me

230 The proposed model provides a framework to optimize treatmen

231 The proposed model provides a mechanical explanation for sev

232 The proposed model provides a statistical tool to correct or

233 In this setting, our proposed model provides higher sensitivity than existing

234 structure and computational innovations, the proposed model provides testable hypotheses of the physi

235 at the time evolution of the dynamics in the proposed model qualitatively agrees with the real-world

236 there is little consensus for the LCA, with proposed models ranging from African ape to orangutan or

237 This proposed model reconciles previous contradictory evidenc

238 The proposed model reduces the loss of (99)Mo by decay and a

239 The proposed model reliably learns the error distribution by

240 Most of the proposed models rely on reaction-diffusion equations, bu

241 The proposed model represents a useful tool to analyze strat

242 Our proposed model represents an advance in the ability of s

243 We show that the proposed model represents RBC membrane with the appropri

244 The proposed model reproduces the regime in which spontaneou

245 The processing in the proposed model requires little computational resources a

246 cal trip data is available, we show that the proposed model's estimation accuracy is as good as other

247 We show that the proposed model satisfies several cognitive face effects

248 The proposed model serves as a useful tool for predicting th

249 The proposed model sheds light on the evolution of cooperati

250 The proposed models show that carrying capacities of T cell

251 sible catalyst conformations, culminating in proposed models showing possible interactions of farneso

252 According to the proposed model, spectrin's quaternary structure and mech

253 The proposed modeling strategy can help to explore certain f

254 ng its progression rate; the dynamics of the proposed model suggest that by increasing the host immun

255 Recently proposed models suggest that long-range force transmissi

256 The proposed model suggests a general mechanism for the form

257 The proposed model suggests an involvement of the Ca(2+)-dep

258 One proposed model suggests that synaptic activity leads to

259 Moreover, the structure combined with the proposed model suggests that the shift from the 'open-ri

260 These results lead to a proposed model that centrioles may duplicate via a templ

261 These observations support a previously proposed model that invokes net membrane deposition at t

262 ciated sterility, consistent with previously proposed models that nuclear genomes can regulate the ph

263 Within the proposed model, the impact of coupling factor of network

264 Following the proposed model, the joined dynamics of the protein parti

265 In the proposed model, the NTT does not clash with either mRNA

266 In the proposed model, the strongly reducing surface site is as

267 significant differences among the previously proposed models, they all agree with our experimental fi

268 currently used phylodynamic methods with our proposed model through clinically-relevant, seasonal hum

269 We compare the performance of our proposed model to existing analysis methods for bead arr

270 The proposed model took into account the interaction effect

271 The proposed model treats each time series as a random field

272 iation to distinguish it from the previously proposed models (type-N) where galectin-3 molecules bind

273 The proposed models use prior distributions for the genetic

274 The proposed model uses background stratification to provide

275 The proposed model uses dimensionality reduction for preproc

276 The proposed model uses Equalization-Cancellation (EC) proce

277 The proposed model uses the approximation of an effective sp

278 The proposed model uses the Finite Element (FE) method to di

279 We evaluated the performance of the proposed model using simulation studies and subsequently

280 We compare the four proposed models using two criteria: the approximate Baye

281 The proposed model was applied to three case studies concern

282 The success of the proposed model was evaluated by comparing a drug and its

283 The proposed model was fitted to two data sets from wheat an

284 Satisfactory performance of the proposed model was found for both simulated datasets and

285 The proposed model was therefore able to explain that freque

286 The proposed model was used to systematically examine area-l

287 In contrast to previously proposed models, we find that Nmu does not promote arous

288 iological and statistical assumptions in the proposed models, we were able to identify the assumption

289 The experimental results and proposed model were corroborated by ab initio Car-Parrin

290 The rates of correct classifications for the proposed models were higher than 90% and their performan

291 Current and proposed models were tested for survival prognostication

292 lusivity analysis in support of a previously proposed model where APOBEC activity is the underlying p

293 We synthesize several recent findings into a proposed model where the transcription of lncRNAs can se

294 r its accumulation, consistent with recently proposed models where the semiquinone is destabilized to

295 Moreover, the expression in the proposed model, which has clear physical meanings in all

296 with behavioral outputs, we test whether the proposed model, which is designed to account for neural

297 The RSM showed a good fit to the proposed model with R(2)>0.83, 0.79 and 0.69 for viscosi

298 Comparing results of the proposed model with those in literature, it is clear tha

299 The proposed model, with the allocation of deMELD, has the p

300 Analysis of the proposed model yields a quantitative description as foll